Method and apparatus for neuroenhancement to facilitate learning and performance

Information

  • Patent Grant
  • 11717686
  • Patent Number
    11,717,686
  • Date Filed
    Tuesday, December 4, 2018
    5 years ago
  • Date Issued
    Tuesday, August 8, 2023
    9 months ago
Abstract
A method of facilitating a skill learning process or improving performance of a task, comprising: determining a brainwave pattern reflecting neuronal activity of a skilled subject while engaged in a respective skill or task; processing the determined brainwave pattern with at least one automated processor; and subjecting a subject training in the respective skill or task to brain entrainment by a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed temporal pattern extracted from brainwaves reflecting neuronal activity of the skilled subject.
Description
FIELD OF THE INVENTION

The present invention generally relates to the field of neuroenhancement and more specifically to systems and methods for determining brain activity patterns corresponding to tasks, and inducing brain activity patterns of the desired type in a subject through, inter alia, brain entrainment.


BACKGROUND OF THE INVENTION

Each reference and document cited herein is expressly incorporated herein by reference in its entirety, for all purposes.


Time in a Biological Matter


Almost everything in biology is subject to change over time. These changes occur on many different time scales, which vary greatly. For example, there are evolutionary changes that affect entire populations over time rather than a single organism. Evolutionary changes are often slower than a human time scale that spans many years (usually a human lifetime). Faster variations of the timing and duration of biological activity in living organisms occur, for example, in many essential biological processes in everyday life: in humans and animals, these variations occur, for example, in eating, sleeping, mating, hibernating, migration, cellular regeneration, etc. Other fast changes may include the transmission of a neural signal, for example, through a synapse such as the calyx of held, a particularly large synapse in the auditory central nervous system of mammals that can reach transmission frequencies of up to 50 Hz. With recruitment modulation, the effective frequencies can be higher. A single nerve impulse can reach a speed as high as one hundred meters (0.06 mile) per second (Kraus, David. Concepts in Modern Biology. New York: Globe Book Company, 1969:170.). Myelination of axons can increase the speed of transmission by segmenting the membrane depolarization process.


Many of these changes over time are repetitive or rhythmic and are described as some frequency or oscillation. The field of chronobiology, for example, examines such periodic (cyclic) phenomena in living organisms and their adaptation, for example, to solar and lunar-related rhythms [DeCoursey, et al. (2003).] These cycles are also known as biological rhythms. The related terms chronomics and chronome have been used in some cases to describe either the molecular mechanisms involved in chronobiological phenomena or the more quantitative aspects of chronobiology, particularly where comparison of cycles between organisms is required. Chronobiological studies include, but are not limited to, comparative anatomy, physiology, genetics, molecular biology and behavior of organisms within biological rhythms mechanics [DeCoursey et al. (2003).]. Other aspects include epigenetics, development, reproduction, ecology, and evolution.


The most important rhythms in chronobiology are the circadian rhythms, roughly 24-hour cycles shown by physiological processes in all these organisms. It is regulated by circadian clocks. The circadian rhythms can be further broken down into routine cycles during the 24-hour day [Nelson R J. 2005. An Introduction to Behavioral Endocrinology. Sinauer Associates, Inc.: Massachusetts. Pg. 587.] All animals can be classified according to their activity cycles: Diurnal, which describes organisms active during daytime; Nocturnal, which describes organisms active in the night; and Crepuscular, which describes animals primarily active during the dawn and dusk hours (ex: white-tailed deer, some bats).


While circadian rhythms are defined as regulated by endogenous processes, other biological cycles may be regulated by exogenous signals. In some cases, multi-trophic systems may exhibit rhythms driven by the circadian clock of one of the members (which may also be influenced or reset by external factors).


Many other important cycles are also studied, including: Infradian rhythms, which are cycles longer than a day. Examples include circannual or annual cycles that govern migration or reproduction cycles in many plants and animals, or the human menstrual cycle; Ultradian rhythms, which are cycles shorter than 24 hours, such as the 90-minute REM cycle, the 4-hour nasal cycle, or the 3-hour cycle of growth hormone production; Tidal rhythms, commonly observed in marine life, which follow the roughly 12.4-hour transition from high to low tide and back; Lunar rhythms, which follow the lunar month (29.5 days). They are relevant, for example, to marine life, as the level of the tides is modulated across the lunar cycle; and Gene oscillations—some genes are expressed more during certain hours of the day than during other hours.


Within each cycle, the time period during which the process is more active is called the acrophase, see Refinetti, Roberto (2006). Circadian Physiology. CRC Press/Taylor & Francis Group. ISBN 0-8493-2233-2. When the process is less active, the cycle is in its bathyphase, or trough phase. The particular moment of highest activity is the peak or maximum; the lowest point is the nadir. How high (or low) the process gets is measured by the amplitude.


The Sleep Cycle and the Ultradian Rhythms


The normal cycle of sleep and wakefulness implies that, at specific times, various neural systems are being activated while others are being turned off. A key to the neurobiology of sleep is therefore to understand the various stages of sleep. In 1953, Nathaniel Kleitman and Eugene Aserinksy showed, using electroencephalographic (EEG) recordings from normal human subjects, that sleep comprises different stages that occur in a characteristic sequence.


Humans descend into sleep in stages that succeed each other over the first hour or so after retiring. These characteristic stages are defined primarily by electroencephalographic criteria. Initially, during “drowsiness,” the frequency spectrum of the electroencephalogram (EEG) is shifted toward lower values, and the amplitude of the cortical waves slightly increases. This drowsy period, called stage I sleep, eventually gives way to light or stage II sleep, which is characterized by a further decrease in the frequency of the EEG waves and an increase in their amplitude, together with intermittent high-frequency spike clusters called sleep spindles. Sleep spindles are periodic bursts of activity at about 10-12 Hz that generally last 1 or 2 seconds and arise as a result of interactions between thalamic and cortical neurons. In stage III sleep, which represents moderate to deep sleep, the number of spindles decreases, whereas the amplitude of low-frequency waves increases still more. In the deepest level of sleep, stage IV sleep, the predominant EEG activity consists of low-frequency (1-4 Hz), high-amplitude fluctuations called delta waves, the characteristic slow waves for which this phase of sleep is named. The entire sequence from drowsiness to deep stage IV sleep usually takes about an hour.


These four sleep stages are called non-rapid eye movement (non-REM) sleep, and its most prominent feature is the slow-wave (stage IV) sleep. It is most difficult to awaken people from slow-wave sleep; hence it is considered to be the deepest stage of sleep. Following a period of slow-wave sleep, however, EEG recordings show that the stages of sleep reverse to reach a quite different state called rapid eye movement, or REM, sleep. In REM sleep, the EEG recordings are remarkably similar to that of the awake state. This mode is bizarre: a dreamer's brain becomes highly active while the body's muscles are paralyzed, and breathing and heart rate become erratic. After about 10 minutes in REM sleep, the brain typically cycles back through the non-REM sleep stages. Slow-wave sleep usually occurs again in the second period of this continual cycling, but not during the rest of the night. On average, four additional periods of REM sleep occur, each having longer than the preceding cycle durations.


In summary, the typical 8 hours of sleep experienced each night actually comprise several cycles that alternate between non-REM and REM sleep, the brain being quite active during much of this supposedly dormant, restful time. For reasons that are not clear, the amount of REM sleep each day decreases from about 8 hours at birth to 2 hours at 20 years, to only about 45 minutes at 70 years of age.


Falling Asleep


When falling asleep, a series of highly orchestrated events puts the brain to sleep in the above-mentioned stages. Technically sleep starts in the brain areas that produce slow-wave sleep (SWS). It has been shown that two groups of cells—the ventrolateral preoptic nucleus in the hypothalamus and the parafacial zone in the brain stem—are involved in prompting SWS. When these cells are activated, it triggers a loss of consciousness. After SWS, REM sleep begins. The purpose of REM sleep remains a biological mystery, despite our growing understanding of its biochemistry and neurobiology. It has been shown that a small group of cells in the brain stem, called the subcoeruleus nucleus, control REM sleep. When these cells become injured or diseased, people do not experience the muscle paralysis associated with REM sleep, which can lead to REM sleep behavior disorder—a serious condition in which the afflicted violently act out their dreams.


Neural Correlates


A neural correlate of a brain state is an electro-neuro-biological state or the state assumed by some biophysical subsystem of the brain, whose presence necessarily and regularly correlates with such specific states. All properties credited to the mind, including consciousness, emotion, and desires are thought to have direct neural correlates.


Mental State


A mental state is a state of mind that a subject is in. Some mental states are pure and unambiguous, while humans are capable of complex states that are a combination of mental representations, which may have in their pure state contradictory characteristics. There are several paradigmatic states of mind that a subject has: love, hate, pleasure, fear, and pain. Mental states can also include a waking state, a sleeping state, a flow (or being in the “zone”), and a mood (a mental state). A mental state is a hypothetical state that corresponds to thinking and feeling, and consists of a conglomeration of mental representations. A mental state is related to an emotion, though it can also relate to cognitive processes. Because the mental state itself is complex and potentially possess inconsistent attributes, clear interpretation of mental state through external analysis (other than self-reporting) is difficult or impossible. However, some studies report that certain attributes of mental state or thought processes may, in fact, be determined through passive monitoring, such as EEG, or fMRI with some degree of statistical reliability. In most studies, the characterization of mental state was an endpoint, and the raw signals, after statistical classification or semantic labeling, are superseded. The remaining signal energy treated as noise. Current technology does not permit a precise abstract encoding or characterization of the full range of mental states based on neural correlates of mental state.


Brain


The brain is a key part of the central nervous system, enclosed in the skull. In humans, and mammals more generally, the brain controls both autonomic processes, as well as cognitive processes. The brain (and to a lesser extent, the spinal cord) controls all volitional functions of the body and interprets information from the outside world. Intelligence, memory, emotions, speech, thoughts, movements and creativity are controlled by the brain. The central nervous system also controls autonomic functions and many homeostatic and reflex actions, such as breathing, heart rate, etc. The human brain consists of the cerebrum, cerebellum, and brainstem. The brainstem includes the midbrain, the pons, and the medulla oblongata. Sometimes the diencephalon, the caudal part of the forebrain, is included.


The brain is composed of neurons, neuroglia (a.k.a., glia), and other cell types in connected networks that integrate sensory inputs, control movements, facilitate learning and memory, activate and express emotions, and control all other behavioral and cognitive functions. Neurons communicate primarily through electrochemical pulses that transmit signals between connected cells within and between brain areas. Thus, the desire to noninvasively capture and replicate neural activity associated with cognitive states has been a subject of interest to behavioral and cognitive neuroscientists.


Technological advances now allow for non-invasive recording of large quantities of information from the brain at multiple spatial and temporal scales. Examples include electroencephalogram (“EEG”) data using multi-channel electrode arrays placed on the scalp or inside the brain, magnetoencephalography (“MEG”), magnetic resonance imaging (“MRI”), functional data using functional magnetic resonance imaging (“fMRI”), positron emission tomography (“PET”), near-infrared spectroscopy (“NIRS”), single-photon emission computed tomography (“SPECT”), and others.


Noninvasive neuromodulation technologies have also been developed that can modulate the pattern of neural activity, and thereby cause altered behavior, cognitive states, perception, and motor output. Integration of noninvasive measurement and neuromodulation techniques for identifying and transplanting brain states from neural activity would be very valuable for clinical therapies, such as brain stimulation and related technologies often attempting to treat disorders of cognition.


The brainstem provides the main motor and sensory innervation to the face and neck via the cranial nerves. Of the twelve pairs of cranial nerves, ten pairs come from the brainstem. This is an extremely important part of the brain, as the nerve connections of the motor and sensory systems from the main part of the brain to the rest of the body pass through the brainstem. This includes the corticospinal tract (motor), the posterior column-medial lemniscus pathway (fine touch, vibration sensation, and proprioception), and the spinothalamic tract (pain, temperature, itch, and crude touch). The brainstem also plays an important role in the regulation of cardiac and respiratory function. It also regulates the central nervous system and is pivotal in maintaining consciousness and regulating the sleep cycle. The brainstem has many basic functions including controlling heart rate, breathing, sleeping, and eating.


The function of the skull is to protect delicate brain tissue from injury. The skull consists of eight fused bones: the frontal, two parietal, two temporal, sphenoid, occipital and ethmoid. The face is formed by 14 paired bones including the maxilla, zygoma, nasal, palatine, lacrimal, inferior nasal conchae, mandible, and vomer. The bony skull is separated from the brain by the dura, a membranous organ, which in turn contains cerebrospinal fluid. The cortical surface of the brain typically is not subject to localized pressure from the skull. The skull, therefore, imposes a barrier to electrical access to the brain functions, and in a healthy human, breaching the dura to access the brain is highly disfavored. The result is that electrical readings of brain activity are filtered by the dura, the cerebrospinal fluid, the skull, the scalp, skin appendages (e.g., hair), resulting in a loss of potential spatial resolution and amplitude of signals emanating from the brain. While magnetic fields resulting from brain electrical activity are accessible, the spatial resolution using feasible sensors is also limited.


The cerebrum is the largest part of the brain and is composed of right and left hemispheres. It performs higher functions, such as interpreting inputs from the senses, as well as speech, reasoning, emotions, learning, and fine control of movement. The surface of the cerebrum has a folded appearance called the cortex. The human cortex contains about 70% of the nerve cells (neurons) and gives an appearance of gray color (grey matter). Beneath the cortex are long connecting fibers between neurons, called axons, which make up the white matter.


The cerebellum is located behind the cerebrum and brainstem. It coordinates muscle movements, helps to maintain balance and posture. The cerebellum may also be involved in some cognitive functions such as attention and language, as well as in regulating fear and pleasure responses. There is considerable evidence that the cerebellum plays an essential role in some types of motor learning. The tasks where the cerebellum most clearly comes into play are those in which it is necessary to make fine adjustments to the way an action is performed. There is a dispute about whether learning takes place within the cerebellum itself, or whether it merely serves to provide signals that promote learning in other brain structures. Cerebellum also plays an important role in sleep and long-term memory formation.


The brain communicates with the body through the spinal cord and twelve pairs of cranial nerves. Ten of the twelve pairs of cranial nerves that control hearing, eye movement, facial sensations, taste, swallowing and movement of the face, neck, shoulder and tongue muscles originate in the brainstem. The cranial nerves for smell and vision originate in the cerebrum.


The right and left hemispheres of the brain are joined by a structure consisting of fibers called the corpus callosum. Each hemisphere controls the opposite side of the body. The right eye sends visual signals to the left hemisphere and vice versa. However, the right ear sends signals to the right hemisphere, and the left ear sends signals to the left hemisphere. Not all functions of the hemispheres are shared. For example, speech is processed exclusively in the left hemisphere.


The cerebral hemispheres have distinct structures, which divide the brain into lobes. Each hemisphere has four lobes: frontal, temporal, parietal, and occipital. There are very complex relationships between the lobes of the brain and between the right and left hemispheres:


Frontal lobes control judgment, planning, problem-solving, behavior, emotions, personality, speech, self-awareness, concentration, intelligence, body movements.


Temporal lobes control understanding of language, memory, organization, and hearing.


Parietal lobes control the interpretation of language; input from vision, hearing, sensory, and motor; temperature, pain, tactile signals, memory, spatial and visual perception.


Occipital lobes interpret visual input (movement, light, color).


A neuron is a fundamental unit of the nervous system, which comprises the autonomic nervous system and the central nervous system.


Brain structures and particular areas within brain structures include but are not limited to Hindbrain structures (e.g., Myelencephalon structures (e.g., Medulla oblongata, Medullary pyramids, Olivary body, Inferior olivary nucleus, Respiratory center, Cuneate nucleus, Gracile nucleus, Intercalated nucleus, Medullary cranial nerve nuclei, Inferior salivatory nucleus, Nucleus ambiguous, Dorsal nucleus of vagus nerve, Hypoglossal nucleus, Solitary nucleus, etc.), Metencephalon structures (e.g., Pons, Pontine cranial nerve nuclei, chief or pontine nucleus of the trigeminal nerve sensory nucleus (V), Motor nucleus for the trigeminal nerve (V), Abducens nucleus (VI), Facial nerve nucleus (VII), vestibulocochlear nuclei (vestibular nuclei and cochlear nuclei) (VIII), Superior salivatory nucleus, Pontine tegmentum, Respiratory centers, Pneumotaxic center, Apneustic center, Pontine micturition center (Barrington's nucleus), Locus coeruleus, Pedunculopontine nucleus, Laterodorsal tegmental nucleus, Tegmental pontine reticular nucleus, Superior olivary complex, Paramedian pontine reticular formation, Cerebellar peduncles, Superior cerebellar peduncle, Middle cerebellar peduncle, Inferior cerebellar peduncle, Fourth ventricle, Cerebellum, Cerebellar vermis, Cerebellar hemispheres, Anterior lobe, Posterior lobe, Flocculonodular lobe, Cerebellar nuclei, Fastigial nucleus, Interposed nucleus, Globose nucleus, Emboliform nucleus, Dentate nucleus, etc.)), Midbrain structures (e.g., Tectum, Corpora quadrigemina, inferior colliculi, superior colliculi, Pretectum, Tegmentum, Periaqueductal gray, Parabrachial area, Medial parabrachial nucleus, Lateral parabrachial nucleus, Subparabrachial nucleus (Kolliker-Fuse nucleus), Rostral interstitial nucleus of medial longitudinal fasciculus, Midbrain reticular formation, Dorsal raphe nucleus, Red nucleus, Ventral tegmental area, Substantia nigra, Pars compacta, Pars reticulata, Interpeduncular nucleus, Cerebral peduncle, Cms cerebri, Mesencephalic cranial nerve nuclei, Oculomotor nucleus (III), Trochlear nucleus (IV), Mesencephalic duct (cerebral aqueduct, aqueduct of Sylvius), etc.), Forebrain structures (e.g., Diencephalon, Epithalamus structures (e.g., Pineal body, Habenular nuclei, Stria medullares, Taenia thalami, etc.) Third ventricle, Thalamus structures (e.g., Anterior nuclear group, Anteroventral nucleus (aka ventral anterior nucleus), Anterodorsal nucleus, Anteromedial nucleus, Medial nuclear group, Medial dorsal nucleus, Midline nuclear group, Paratenial nucleus, Reuniens nucleus, Rhomboidal nucleus, Intralaminar nuclear group, Centromedial nucleus, Parafascicular nucleus, Paracentral nucleus, Central lateral nucleus, Central medial nucleus, Lateral nuclear group, Lateral dorsal nucleus, Lateral posterior nucleus, Pulvinar, Ventral nuclear group, Ventral anterior nucleus, Ventral lateral nucleus, Ventral posterior nucleus, Ventral posterior lateral nucleus, Ventral posterior medial nucleus, Metathalamus, Medial geniculate body, Lateral geniculate body, Thalamic reticular nucleus, etc.), Hypothalamus structures (e.g., Anterior, Medial area, Parts of preoptic area, Medial preoptic nucleus, Suprachiasmatic nucleus, Paraventricular nucleus, Supraoptic nucleus (mainly), Anterior hypothalamic nucleus, Lateral area, Parts of preoptic area, Lateral preoptic nucleus, Anterior part of Lateral nucleus, Part of supraoptic nucleus, Other nuclei of preoptic area, median preoptic nucleus, periventricular preoptic nucleus, Tuberal, Medial area, Dorsomedial hypothalamic nucleus, Ventromedial nucleus, Arcuate nucleus, Lateral area, Tuberal part of Lateral nucleus, Lateral tuberal nuclei, Posterior, Medial area, Mammillary nuclei (part of mammillary bodies), Posterior nucleus, Lateral area, Posterior part of Lateral nucleus, Optic chiasm, Subfomical organ, Periventricular nucleus, Pituitary stalk, Tuber cinereum, Tuberal nucleus, Tuberomammillary nucleus, Tuberal region, Mammillary bodies, Mammillary nucleus, etc.), Subthalamus structures (e.g., Thalamic nucleus, Zona incerta, etc.), Pituitary gland structures (e.g., neurohypophysis, Pars intermedia (Intermediate Lobe), adenohypophysis, etc.), Telencephalon structures, white matter structures (e.g., Corona radiata, Internal capsule, External capsule, Extreme capsule, Arcuate fasciculus, Uncinate fasciculus, Perforant Path, etc.), Subcortical structures (e.g., Hippocampus (Medial Temporal Lobe), Dentate gyrus, Comu ammonis (CA fields), Comu ammonis area 1, Comu ammonis area 2, Comu ammonis area 3, Comu ammonis area 4, Amygdala (limbic system) (limbic lobe), Central nucleus (autonomic nervous system), Medial nucleus (accessory olfactory system), Cortical and basomedial nuclei (main olfactory system), Lateral[disambiguation needed] and basolateral nuclei (frontotemporal cortical system), Claustrum, Basal ganglia, Striatum, Dorsal striatum (aka neostriatum), Putamen, Caudate nucleus, Ventral striatum, Nucleus accumbens, Olfactory tubercle, Globus pallidus (forms nucleus lentiformis with putamen), Subthalamic nucleus, Basal forebrain, Anterior perforated substance, Substantia innominata, Nucleus basalis, Diagonal band of Broca, Medial septal nuclei, etc.), Rhinencephalon structures (e.g., Olfactory bulb, Piriform cortex, Anterior olfactory nucleus, Olfactory tract, Anterior commissure, Uncus, etc.), Cerebral cortex structures (e.g., Frontal lobe, Cortex, Primary motor cortex (Precentral gyrus, M1), Supplementary motor cortex, Premotor cortex, Prefrontal cortex, Gyri, Superior frontal gyrus, Middle frontal gyrus, Inferior frontal gyrus, Brodmann areas: 4, 6, 8, 9, 10, 11, 12, 24, 25, 32, 33, 44, 45, 46, 47, Parietal lobe, Cortex, Primary somatosensory cortex (51), Secondary somatosensory cortex (52), Posterior parietal cortex, Gyri, Postcentral gyrus (Primary somesthetic area), Other, Precuneus, Brodmann areas 1, 2, 3 (Primary somesthetic area); 5, 7, 23, 26, 29, 31, 39, 40, Occipital lobe, Cortex, Primary visual cortex (V1), V2, V3, V4, V5/MT, Gyri, Lateral occipital gyrus, Cuneus, Brodmann areas 17 (V1, primary visual cortex); 18, 19, Temporal lobe, Cortex, Primary auditory cortex (A1), secondary auditory cortex (A2), Inferior temporal cortex, Posterior inferior temporal cortex, Superior temporal gyrus, Middle temporal gyrus, Inferior temporal gyrus, Entorhinal Cortex, Perirhinal Cortex, Parahippocampal gyrus, Fusiform gyrus, Brodmann areas: 9, 20, 21, 22, 27, 34, 35, 36, 37, 38, 41, 42, Medial superior temporal area (MST), Insular cortex, Cingulate cortex, Anterior cingulate, Posterior cingulate, Retrosplenial cortex, Indusium griseum, Subgenual area 25, Brodmann areas 23, 24; 26, 29, 30 (retrosplenial areas); 31, 32, etc.)).


Neurons


Neurons are electrically excitable cells that receive, process, and transmit information, and based on that information sends a signal to other neurons, muscles, or glands through electrical and chemical signals. These signals between neurons occur via specialized connections called synapses. Neurons can connect to each other to form neural networks. The basic purpose of a neuron is to receive incoming information and, based upon that information send a signal to other neurons, muscles, or glands. Neurons are designed to rapidly send signals across physiologically long distances. They do this using electrical signals called nerve impulses or action potentials. When a nerve impulse reaches the end of a neuron, it triggers the release of a chemical, or neurotransmitter. The neurotransmitter travels rapidly across the short gap between cells (the synapse) and acts to signal the adjacent cell. See www.biologyreference.com/Mo-Nu/Neuron.html#ixzz5AVxCuM5a.


Neurons can receive thousands of inputs from other neurons through synapses. Synaptic integration is a mechanism whereby neurons integrate these inputs before the generation of a nerve impulse, or action potential. The ability of synaptic inputs to effect neuronal output is determined by a number of factors: Size, shape and relative timing of electrical potentials generated by synaptic inputs; the geometric structure of the target neuron; the physical location of synaptic inputs within that structure; and the expression of voltage-gated channels in different regions of the neuronal membrane.


Neurons within a neural network receive information from, and send information to, many other cells, at specialized junctions called synapses. Synaptic integration is the computational process by which an individual neuron processes its synaptic inputs and converts them into an output signal. Synaptic potentials occur when neurotransmitter binds to and opens ligand-operated channels in the dendritic membrane, allowing ions to move into or out of the cell according to their electrochemical gradient. Synaptic potentials can be either excitatory or inhibitory depending on the direction and charge of ion movement. Action potentials occur if the summed synaptic inputs to a neuron reach a threshold level of depolarisation and trigger regenerative opening of voltage-gated ion channels. Synaptic potentials are often brief and of small amplitude, therefore summation of inputs in time (temporal summation) or from multiple synaptic inputs (spatial summation) is usually required to reach action potential firing threshold.


There are two types of synapses: electrical synapses and chemical synapses. Electrical synapses are a direct electrical coupling between two cells mediated by gap junctions, which are pores constructed of connexin proteins—essentially result in the passing of a gradient potential (may be depolarizing or hyperpolarizing) between two cells. Electrical synapses are very rapid (no synaptic delay). It is a passive process where signal can degrade with distance and may not produce a large enough depolarization to initiate an action potential in the postsynaptic cell. Electrical synapses are bidirectional, i.e., postsynaptic cell can actually send messages to the “presynaptic cell.


Chemical synapses are a coupling between two cells through neuro-transmitters, ligand or voltage gated channels, receptors. They are influenced by the concentration and types of ions on either side of the membrane. Among the neurotransmitters, Glutamate, sodium, potassium, and cadium are positively charged. GABA and chloride are negatively charged. Neurotransmitter junctions provide an opportunity for pharmacological intervention, and many different drugs, including illicit drugs, act at synapses.


An excitatory postsynaptic potential (EPSP) is a postsynaptic potential that makes the postsynaptic neuron more likely to fire an action potential. An electrical charge (hyperpolarization) in the membrane of a postsynaptic neuron is caused by the binding of an inhibitory neurotransmitter from a presynaptic cell to a postsynaptic receptor. It makes it more difficult for a postsynaptic neuron to generate an action potential. An electrical change (depolarization) in the membrane of a postsynaptic neuron caused by the binding of an excitatory neurotransmitter from a presynaptic cell to a postsynaptic receptor. It makes it more likely for a postsynaptic neuron to generate an action potential. In a neuronal synapse that uses glutamate as receptor, for example, receptors open ion channels that are non-selectively permeable to cations. When these glutamate receptors are activated, both Na+ and K+ flow across the postsynaptic membrane. The reversal potential (Erev) for the post—synaptic current is approximately 0 mV. The resting potential of neurons is approximately −60 mV. The resulting EPSP will depolarize the post synaptic membrane potential, bringing it toward 0 mV.


An inhibitory postsynaptic potential (IPSP) is a kind of synaptic potential that makes a postsynaptic neuron less likely to generate an action potential. An example of inhibitory post synaptic s action is a neuronal synapse that uses y-Aminobutyric acid (GABA) as its transmitter. At such synapses, the GABA receptors typically open channels that are selectively permeable to Cl—. When these channels open, negatively charged chloride ions can flow across the membrane. The postsynaptic neuron has a resting potential of −60 mV and an action potential threshold of −40 mV. Transmitter release at this synapse will inhibit the postsynaptic cell. Since ECl is more negative than the action potential threshold, e.g., −70 mV, it reduces the probability that the postsynaptic cell will fire an action potential.


Some types of neurotransmitters, such as glutamate, consistently result in EPSPs. Others, such as GABA, consistently result in IPSPs. The action potential lasts about one millisecond (1 msec). In contrast, the EPSPs and IPSPs can last as long as 5 to 10 msec. This allows the effect of one postsynaptic potential to build upon the next and so on.


Membrane leakage, and to a lesser extent, potentials per se, can be influenced by external electrical and magnetic fields. These fields may be generated focally, such as through implanted electrodes, or less specifically, such as through transcranial stimulation. Transcranial stimulation may be subthreshold or superthreshold. In the former case, the external stimulation acts to modulate resting membrane potential, making nerves more or less excitable. Such stimulation may be direct current or alternating current. In the latter case, this will tend to synchronize neuron depolarization with the signals. Superthreshold stimulation can be painful (at least because the stimulus directly excites pain neurons) and must be pulsed. Since this has correspondence to electroconvulsive therapy, superthresold transcranial stimulation is sparingly used.


A number of neurotransmitters are known, as are pharmaceutical interventions and therapies that influence these compounds. Typically, the major neurotransmitters are small monoamine molecules, such as dopamine, epinephrine, norepinephrine, serotonin, GABA, histamine, etc., as well as acetylcholine. In addition, neurotransmitters also include amino acids, gas molecules such as nitric oxide, carbon monoxide, carbon dioxide, and hydrogen sulfide, as well as peptides. The presence, metabolism, and modulation of these molecules may influence learning and memory. Supply of neurotransmitter precursors, control of oxidative and mental stress conditions, and other influences on learning and memory-related brain chemistry, may be employed to facilitate memory, learning, and learning adaption transfer.


The neuropeptides, as well as their respective receptors, are widely distributed throughout the mammalian central nervous system. During learning and memory processes, besides structural synaptic remodeling, changes are observed at molecular and metabolic levels with the alterations in neurotransmitter and neuropeptide synthesis and release. While there is a consensus that brain cholinergic neurotransmission plays a critical role in the processes related to learning and memory, it is also well known that these functions are influenced by a tremendous number of neuropeptides and non-peptide molecules. Arginine vasopressin (AVP), oxytocin, angiotensin II, insulin, growth factors, serotonin (5-HT), melanin-concentrating hormone, histamine, bombesin and gastrin-releasing peptide (GRP), glucagon-like peptide-1 (GLP-1), cholecystokinin (CCK), dopamine, corticotropin-releasing factor (CRF) have modulatory effects on learning and memory. Among these peptides, CCK, 5-HT, and CRF play strategic roles in the modulation of memory processes under stressful conditions. CRF is accepted as the main neuropeptide involved in both physical and emotional stress, with a protective role during stress, possibly through the activation of the hypothalamo-pituitary (HPA) axis. The peptide CCK has been proposed to facilitate memory processing, and CCK-like immunoreactivity in the hypothalamus was observed upon stress exposure, suggesting that CCK may participate in the central control of stress response and stress-induced memory dysfunction. On the other hand, 5-HT appears to play a role in behaviors that involve a high cognitive demand and stress exposure activates serotonergic systems in a variety of brain regions. See:

  • Mehmetali Guilpmar, Berrak C Ye{hacek over (g)}en, “The Physiology of Learning and Memory: Role of Peptides and Stress”, Current Protein and Peptide Science, 2004 (5)
  • www.researchgate.net/publication/8147320_The_Physiology_of_Learning_and_Memory_Role_of_Peptides_and_Stress.Deep brain stimulation is described in NIH Research Matters, “A noninvasive deep brain stimulation technique”, (2017),
  • Brainworks, “QEEG Brain Mapping”.
  • Carmnnon, A., Mor, J., & Goldberg, J. (1976). Evoked cerebral responses to noxious thermal stimuli in humans. Experimental Brain Research, 25(1), 103-107.


Mental State


A number of studies report that certain attributes of mental state or thought processes may in fact be determined through passive monitoring, such as EEG, with some degree of statistical reliability. In most studies, the characterization of mental state was an endpoint, and the raw signals, after statistically classification or semantic labelling, are superseded and the remaining signal energy treated as noise.


Neural Correlates


A neural correlate of a mental state is an electro-neuro-biological state or the state assumed by some biophysical subsystem of the brain, whose presence necessarily and regularly correlates with such specific mental state. All properties credited to the en.wikipedia.org/wiki/Mind, including consciousness, emotion, and desires are thought to have direct neural correlates. For our purposes, neural correlates of a mental state can be defined as the minimal set of neuronal oscillations that correspond to the given mental state. Neuroscientists use empirical approaches to discover neural correlates of subjective mental states.


Brainwaves


At the root of all our thoughts, emotions and behaviors is the communication between neurons within our brains, a rhythmic or repetitive neural activity in the central nervous system. The oscillation can be produced by a single neuron or by synchronized electrical pulses from ensembles of neurons communicating with each other. The interaction between neurons can give rise to oscillations at a different frequency than the firing frequency of individual neurons. The synchronized activity of large numbers of neurons produces macroscopic oscillations, which can be observed in an electroencephalogram. They are divided into bandwidths to describe their purported functions or functional relationships. Oscillatory activity in the brain is widely observed at different levels of organization and is thought to play a key role in processing neural information. Numerous experimental studies support a functional role of neural oscillations. A unified interpretation, however, is still not determined. Neural oscillations and synchronization have been linked to many cognitive functions such as information transfer, perception, motor control and memory. Electroencephalographic (EEG) signals are relatively easy and safe to acquire, have a long history of analysis, and can have high dimensionality, e.g., up to 128 or 256 separate recording electrodes. While the information represented in each electrode is not independent of the others, and the noise in the signals high, there is much information available through such signals that has not been fully characterized to date.


Brain waves have been widely studied in neural activity generated by large groups of neurons, mostly by EEG. In general, EEG signals reveal oscillatory activity (groups of neurons periodically firing in synchrony), in specific frequency bands: alpha (7.5-125 Hz) that can be detected from the occipital lobe during relaxed wakefulness and which increases when the eyes are closed; delta (1-4 Hz), theta (4-8 Hz), beta (13-30 Hz), low gamma (30-70 Hz), and high gamma (70-150 Hz) frequency bands, where faster rhythms such as gamma activity have been linked to cognitive processing. Higher frequencies imply multiple groups of neurons firing in coordination, either in parallel or in series, or both, since individual neurons do not fire at rates of 100 Hz. Neural oscillations of specific characteristics have been linked to cognitive states, such as awareness and consciousness and different sleep stages.


Nyquist Theorem states that the highest frequency that can be accurately represented is one-half of the sampling rate. Practically, the sampling rate should be ten times higher than the highest frequency of the signal. (See, www.slideshare.net/ertvk/eeg-examples). While EEG signals are largely band limited, the superimposed noise may not be. Further, the EEG signals themselves represent components from a large number of neurons, which fire independently. Therefore, large bandwidth signal acquisition may have utility.


It is a useful analogy to think of brainwaves as musical notes. Like in symphony, the higher and lower frequencies link and cohere with each other through harmonics, especially when one considers that neurons may be coordinated not only based on transitions, but also on phase delay. Oscillatory activity is observed throughout the central nervous system at all levels of organization. The dominant neuro oscillation frequency is associated with a respective mental state.


The functions of brain waves are wide-ranging and vary for different types of oscillatory activity. Neural oscillations also play an important role in many neurological disorders.


In standard EEG recording practice, 19 recording electrodes are placed uniformly on the scalp (the International 10-20 System). In addition, one or two reference electrodes (often placed on earlobes) and a ground electrode (often placed on the nose to provide amplifiers with reference voltages) are required. However, additional electrodes may add minimal useful information unless supplemented by computer algorithms to reduce raw EEG data to a manageable form. When large numbers of electrodes are employed, the potential at each location may be measured with respect to the average of all potentials (the common average reference), which often provides a good estimate of potential at infinity. The common average reference is not appropriate when electrode coverage is sparse (perhaps less than 64 electrodes). See, Paul L. Nunez and Ramesh Srinivasan (2007) Electroencephalogram. Scholarpedia, 2(2):1348, scholarpedia.org/article/Electroencephalogram. Dipole localization algorithms may be useful to determine spatial emission patterns in EEG.


Scalp potential may be expressed as a volume integral of dipole moment per unit volume over the entire brain provided is defined generally rather than in columnar terms. For the important case of dominant cortical sources, scalp potential may be approximated by the following integral over the cortical volume If the volume element is defined in terms of cortical columns, the volume integral may be reduced to an integral over the folded cortical surface. The time-dependence of scalp potential is the weighted sum of all dipole time variations in the brain, although deep dipole volumes typically make negligible contributions. The vector Green's function contains all geometric and conductive information about the head volume conductor and weights the integral accordingly. Thus, each scalar component of the Green's function is essentially an inverse electrical distance between each source component and scalp location. For the idealized case of sources in an infinite medium of constant conductivity, the electrical distance equals the geometric distance. The Green's function accounts for the tissue's finite spatial extent and its inhomogeneity and anisotropy. The forward problem in EEG consists of choosing a head model to provide and carrying out the integral for some assumed source distribution. The inverse problem consists of using the recorded scalp potential distribution plus some constraints (usual assumptions) on to find the best fit source distribution Since the inverse problem has no unique solution, any inverse solution depends critically on the chosen constraints, for example, only one or two isolated sources, distributed sources confined to the cortex, or spatial and temporal smoothness criteria. High-resolution EEG uses the experimental scalp potential to predict the potential on the dura surface (the unfolded membrane surrounding the cerebral cortex) This may be accomplished using a head model Green's function or by estimating the surface Laplacian with either spherical or 3D splines. These two approaches typically provide very similar dura potentials VD(r,t); the estimates of dura potential distribution are unique subject to head model, electrode density, and noise issues.


In an EEG recording system, each electrode is connected to one input of a differential amplifier (one amplifier per pair of electrodes); a common system reference electrode (or synthesized reference) is connected to the other input of each differential amplifier. These amplifiers amplify the voltage between the active electrode and the reference (typically 1,000-100,000 times, or 60-100 dB of voltage gain). The amplified signal is digitized via an analog-to-digital converter, after being passed through an anti-aliasing filter. Analog-to-digital sampling typically occurs at 256-512 Hz in clinical scalp EEG; sampling rates of up to 20 kHz are used in some research applications. The EEG signals can be captured with open source hardware such as OpenBCI, and the signal can be processed by freely available EEG software such as EEGLAB or the Neurophysiological Biomarker Toolbox. A typical adult human EEG signal is about 10 μV to 100 μV in amplitude when measured from the scalp and is about 10-20 mV when measured from subdural electrodes.


Delta wave (en.wikipedia.org/wiki/Delta_wave) is the frequency range up to 4 Hz. It tends to be the highest in amplitude and the slowest waves. It is normally seen in adults in NREM (en.wikipedia.org/wiki/NREM). It is also seen normally in babies. It may occur focally with subcortical lesions and in general distribution with diffuse lesions, metabolic encephalopathy hydrocephalus or deep midline lesions. It is usually most prominent frontally in adults (e.g., FIRDA—frontal intermittent rhythmic delta) and posteriorly in children (e.g., OIRDA—occipital intermittent rhythmic delta).


Theta is the frequency range from 4 Hz to 7 Hz. Theta is normally seen in young children. It may be seen in drowsiness or arousal in older children and adults; it can also be seen in meditation. Excess theta for age represents abnormal activity. It can be seen as a focal disturbance in focal subcortical lesions; it can be seen in generalized distribution in diffuse disorder or metabolic encephalopathy or deep midline disorders or some instances of hydrocephalus. On the contrary, this range has been associated with reports of relaxed, meditative, and creative states.


Alpha is the frequency range from 7 Hz to 14 Hz. This was the “posterior basic rhythm” (also called the “posterior dominant rhythm” or the “posterior alpha rhythm”), seen in the posterior regions of the head on both sides, higher in amplitude on the dominant side. It emerges with the closing of the eyes and with relaxation and attenuates with eye opening or mental exertion. The posterior basic rhythm is actually slower than 8 Hz in young children (therefore technically in the theta range). In addition to the posterior basic rhythm, there are other normal alpha rhythms such as the sensorimotor, or mu rhythm (alpha activity in the contralateral sensory and motor cortical areas) that emerges when the hands and arms are idle; and the “third rhythm” (alpha activity in the temporal or frontal lobes). Alpha can be abnormal; for example, an EEG that has diffuse alpha occurring in coma and is not responsive to external stimuli is referred to as “alpha coma.”


Beta is the frequency range from 15 Hz to about 30 Hz. It is usually seen on both sides in symmetrical distribution and is most evident frontally. Beta activity is closely linked to motor behavior and is generally attenuated during active movements. Low-amplitude beta with multiple and varying frequencies is often associated with active, busy or anxious thinking and active concentration. Rhythmic beta with a dominant set of frequencies is associated with various pathologies, such as Dup15q syndrome, and drug effects, especially benzodiazepines. It may be absent or reduced in areas of cortical damage. It is the dominant rhythm in patients who are alert or anxious or who have their eyes open.


Gamma is the frequency range approximately 30-100 Hz. Gamma rhythms are thought to represent binding of different populations of neurons together into a network to carry out a certain cognitive or motor function.


Mu range is 8-13 Hz and partly overlaps with other frequencies. It reflects the synchronous firing of motor neurons in a rest state. Mu suppression is thought to reflect motor mirror neuron systems, because when an action is observed, the pattern extinguishes, possibly because of the normal neuronal system and the mirror neuron system “go out of sync” and interfere with each other. (en.wikipedia.org/wiki/Electroencephalography).


See: Abeles M, Local Cortical Circuits (1982) New York: Springer-Verlag.

  • Braitenberg V and Schuz A (1991) Anatomy of the Cortex. Statistics and Geometry. New York: Springer-Verlag.
  • Ebersole J S (1997) Defining epileptogenic foci: past, present, future. J. Clin. Neurophysiology 14: 470-483.
  • Edelman G M and Tononi G (2000) A Universe of Consciousness, New York: Basic Books.
  • Freeman W J (1975) Mass Action in the Nervous System, New York: Academic Press.
  • Gevins A S and Cutillo B A (1995) Neuroelectric measures of mind. In: P L Nunez (Au), Neocortical Dynamics and Human EEG Rhythms. NY: Oxford U. Press, pp. 304-338.
  • Gevins A S, Le J, Martin N, Brickett P, Desmond J, and Reutter B (1994) High resolution EEG: 124-channel recording, spatial enhancement, and MRI integration methods. Electroencephalography and Clin. Neurophysiology 90: 337-358.
  • Gevins A S, Smith M E, McEvoy L and Yu D (1997) High-resolution mapping of cortical activation related to working memory: effects of task difficulty, type of processing, and practice. Cerebral Cortex 7: 374-385.
  • Haken H (1983) Synergetics: An Introduction, 3rd Edition, Springer-Verlag.
  • Haken H (1999) What can synergetics contribute to the understanding of brain functioning? In: Analysis of Neurophysiological Brain Functioning, C Uhl (Ed), Berlin: Springer-Verlag, pp 7-40.
  • Ingber L (1995) Statistical mechanics of multiple scales of neocortical interactions. In: P L Nunez (Au), Neocortical Dynamics and Human EEG Rhythms. NY: Oxford U. Press, 628-681.
  • Izhikevich E M (1999) Weakly connected quasi-periodic oscillators, FM interactions, and multiplexing in the brain, SIAM J. Applied Mathematics 59: 2193-2223.
  • Jirsa V K and Haken H (1997) A derivation of a macroscopic field theory of the brain from the quasi-microscopic neural dynamics. Physica D 99: 503-526.
  • Jirsa V K and Kelso J A S (2000) Spatiotemporal pattern formation in continuous systems with heterogeneous connection topologies. Physical Review E 62: 8462-8465.
  • Katznelson R D (1981) Normal modes of the brain: Neuroanatomical basis and a physiological theoretical model. In PL Nunez (Au), Electric Fields of the Brain: The Neurophysics of EEG, 1st Edition, NY: Oxford U. Press, pp 401-442.
  • Klimesch W (1996) Memory processes, brain oscillations and EEG synchronization. International J. Psychophysiology 24: 61-100.
  • Law S K, Nunez P L and Wijesinghe R S (1993) High resolution EEG using spline generated surface Laplacians on spherical and ellipsoidal surfaces. IEEE Transactions on Biomedical Engineering 40:145-153.
  • Liley D T J, Cadusch P J and Dafilis M P (2002) A spatially continuous mean field theory of electrocortical activity network. Computation in Neural Systems 13:67-113.
  • Malmuvino J and Plonsey R (1995) Bioelectromagetism. NY: Oxford U. Press.
  • Niedermeyer E and Lopes da Silva F H (Eds) (2005) Electroencephalography. Basic Principals, Clin. Applications, and Related Fields. Fifth Edition. London: Williams and Wilkins.
  • Nunez P L (1989) Generation of human EEG by a combination of long and short range neocortical interactions. Brain Topography 1:199-215.
  • Nunez P L (1995) Neocortical Dynamics and Human EEG Rhythms. NY: Oxford U. Press.
  • Nunez P L (2000) Toward a large-scale quantitative description of neocortical dynamic function and EEG (Target article), Behavioral and Brain Sciences 23: 371-398.
  • Nunez P L (2000) Neocortical dynamic theory should be as simple as possible, but not simpler (Response to 18 commentaries on target article), Behavioral and Brain Sciences 23: 415-437.
  • Nunez P L (2002) EEG. In V S Ramachandran (Ed) Encyclopedia of the Human Brain, La Jolla: Academic Press, 169-179.
  • Nunez P L and Silberstein R B (2001) On the relationship of synaptic activity to macroscopic measurements: Does co-registration of EEG with fMRI make sense? Brain Topog. 13:79-96.
  • Nunez P L and Srinivasan R (2006) Electric Fields of the Brain: The Neurophysics of EEG, 2nd Edition, NY: Oxford U. Press.
  • Nunez P L and Srinivasan R (2006) A theoretical basis for standing and traveling brain waves measured with human EEG with implications for an integrated consciousness. Clin. Neurophysiology 117: 2424-2435.
  • Nunez P L, Srinivasan R, Westdorp A F, Wijesinghe R S, Tucker D M, Silberstein R B, and Cadusch P J (1997) EEG coherency I: Statistics, reference electrode, volume conduction, Laplacians, cortical imaging, and interpretation at multiple scales. Electroencephalography and Clin. Neurophysiology 103: 516-527.
  • Nunez P L. Wingeier B M and Silberstein R B (2001) Spatial-temporal structures of human alpha rhythms: theory, micro-current sources, multiscale measurements, and global binding of local networks, Human Brain Mapping 13:125-164.
  • Nuwer M (1997) Assessment of digital EEG, quantitative EEG, and EEG brain mapping: report of the American Academy of Neurology and the American Clin. Neurophysiology Society. Neurology 49: 277-292.
  • Penfield W and Jasper H D (1954) Epilepsy and the Functional Anatomy of the Human Brain. London: Little, Brown and Co.
  • Robinson P A, Rennie U, Rowe D L and O'Conner S C (2004) Estimation of multiscale neurophysiologic parameters by electroencephalographic means. Human Brain Mapping 23: 53-72.
  • Scott A C (1995) Stairway to the Mind. New York: Springer-Verlag.
  • Silberstein R B, Danieli F and Nunez P L (2003) Fronto-parietal evoked potential synchronization is increased during mental rotation, NeuroReport 14: 67-71.
  • Silberstein R B, Song J, Nunez P L and Park W (2004) Dynamic sculpting of brain functional connectivity is correlated with performance, Brain Topography 16: 240-254.
  • Srinivasan R and Petrovic 5 (2006) MEG phase follows conscious perception during binocular rivalry induced by visual stream segregation. Cerebral Cortex, 16: 597-608.
  • Srinivasan R, Nunez P L and Silberstein R B (1998) Spatial filtering and neocortical dynamics: estimates of EEG coherence. IEEE Trans. on Biomedical Engineering, 45: 814-825.
  • Srinivasan R, Russell D P, Edelman G M, and Tononi G (1999) Frequency tagging competing stimuli in binocular rivalry reveals increased synchronization of neuromagnetic responses during conscious perception. J. Neuroscience 19: 5435-5448.
  • Uhl C (Ed) (1999) Analysis of Neurophysiological Brain Functioning. Berlin: Springer-Verlag,
  • Wingeier B M, Nunez P L and Silberstein R B (2001) Spherical harmonic decomposition applied to spatial-temporal analysis of human high-density electroencephalogram. Physical Review E 64: 051916-1 to 9.
  • en.wikipedia.org/wiki/Electroencephalography









TABLE 1







Comparison of EEG bands












Freq.





Band
(Hz)
Location
Normally
Pathologically





Delta
<4
frontally in adults,
adult slow-wave sleep
subcortical lesions




posteriorly in
in babies
diffuse lesions




children; high-
Has been found during some
metabolic encephalopathy hydrocephalus




amplitude waves
continuous-attention tasks
deep midline lesions


Theta
4-7
Found in locations
higher in young children
focal subcortical lesions




not related to task at
drowsiness in adults and teens
metabolic encephalopathy




hand
idling
deep midline disorders





Associated with inhibition of elicited
some instances of hydrocephalus





responses (has been found to spike in






situations where a person is actively






trying to repress a response or action).



Alpha
8-15
posterior regions of
relaxed/reflecting
Coma




head, both sides,
closing the eyes





higher in amplitude
Also associated with inhibition control,





on dominant side.
seemingly with the purpose of timing





Central sites (c3-c4)
inhibitory activity in different locations





at rest
across the brain.



Beta
16-
both sides,
range span: active calm → intense →
Benzodiazepines (en.wikipedia.org/wiki/



31
symmetrical
stressed → mild obsessive
Benzodiazepines)




distribution, most
active thinking, focus, high alert,
Dup15g syndrome




evident frontally;
anxious





low-amplitude waves




Gamma
>32
Somatosensory
Displays during cross-modal sensory





cortex
processing (perception that combines
A decrease in gamma-band activity may





two different senses, such as sound and
be associated with cognitive decline,





sight)
especially when related to the theta band;





Also is shown during short-term
however, this has not been proven for use





memory matching of recognized objects,
as a clinical diagnostic measurement





sounds, or tactile sensations



Mu
8-12
Sensorimotor cortex
Shows rest-state motor neurons.
Mu suppression could indicate that motor






mirror neurons are working. Deficits in Mu






suppression, and thus in mirror neurons,






might play a role in autism.









EEG AND qEEG


An EEG electrode will mainly detect the neuronal activity in the brain region just beneath it. However, the electrodes receive the activity from thousands of neurons. One square millimeter of cortex surface, for example, has more than 100,000 neurons. It is only when the input to a region is synchronized with electrical activity occurring at the same time that simple periodic waveforms in the EEG become distinguishable. The temporal pattern associated with specific brainwaves can be digitized and encoded a non-transient memory, and embodied in or referenced by, computer software.


EEG (electroencephalography) and MEG (magnetoencephalography) are available technologies to monitor brain electrical activity. Each generally has sufficient temporal resolution to follow dynamic changes in brain electrical activity. Electroencephalography (EEG) and quantitative electroencephalography (qEEG) are electrophysiological monitoring methods that analyze the electrical activity of the brain to measure and display patterns that correspond to cognitive states and/or diagnostic information. It is typically noninvasive, with the electrodes placed on the scalp, although invasive electrodes are also used in some cases. EEG signals may be captured and analyzed by a mobile device, often referred as “brain wearables”. There are a variety of “brain wearables” readily available on the market today. EEGs can be obtained with a non-invasive method where the aggregate oscillations of brain electric potentials are recorded with numerous electrodes attached to the scalp of a person. Most EEG signals originate in the brain's outer layer (the cerebral cortex), believed largely responsible for our thoughts, emotions, and behavior. Cortical synaptic action generates electrical signals that change in the 10 to 100-millisecond range. Transcutaneous EEG signals are limited by the relatively insulating nature of the skull surrounding the brain, the conductivity of the cerebrospinal fluid and brain tissue, relatively low amplitude of individual cellular electrical activity, and distances between the cellular current flows and the electrodes. EEG is characterized by: (1) Voltage; (2) Frequency; (3) Spatial location; (4) Inter-hemispheric symmetries; (5) Reactivity (reaction to state change); (6) Character of waveform occurrence (random, serial, continuous); and (7) Morphology of transient events. EEGs can be separated into two main categories. Spontaneous EEG which occur in the absence of specific sensory stimuli and evoked potentials (EPs) which are associated with sensory stimuli like repeated light flashes, auditory tones, finger pressure or mild electric shocks. The latter is recorded for example by time averaging to remove effects of spontaneous EEG. Non-sensory triggered potentials are also known. EP's typically are time synchronized with the trigger, and thus have an organization principle. Event-related potentials (ERPs) provide evidence of a direct link between cognitive events and brain electrical activity in a wide range of cognitive paradigms. It has generally been held that an ERP is the result of a set of discrete stimulus-evoked brain events. Event-related potentials (ERPs) are recorded in the same way as EPs, but occur at longer latencies from the stimuli and are more associated with an endogenous brain state.


Typically, a magnetic sensor with sufficient sensitivity to individual cell depolarization or small groups is a superconducting quantum interference device (SQIUD), which requires cryogenic temperature operation, either at liquid nitrogen temperatures (high temperature superconductors, HTS) or at liquid helium temperatures (low temperature superconductors, LTS). However, current research shows possible feasibility of room temperature superconductors (20C). Magnetic sensing has an advantage, due to the dipole nature of sources, of having better potential volumetric localization; however, due to this added information, complexity of signal analysis is increased.


In general, the electromagnetic signals detected represent action potentials, an automatic response of a nerve cell to depolarization beyond a threshold, which briefly opens conduction channels. The cells have ion pumps which seek to maintain a depolarized state. Once triggered, the action potential propagates along the membrane in two-dimensions, causing a brief high level of depolarizing ion flow. There is a quiescent period after depolarization that generally prevents oscillation within a single cell. Since the exon extends from the body of the neuron, the action potential will typically proceed along the length of the axon, which terminates in a synapse with another cell. While direct electrical connections between cells occur, often the axon releases a neurotransmitter compound into the synapse, which causes a depolarization or hyperpolarization of the target cell. Indeed, the result may also be release of a hormone or peptide, which may have a local or more distant effect.


The electrical fields detectable externally tend to not include signals which low frequency signals, such as static levels of polarization, or cumulative depolarizating or hyperpolarizing effects between action potentials. In myelinated tracts, the current flows at the segments tend to be small, and therefore the signals from individual cells are small. Therefore, the largest signal components are from the synapses and cell bodies. In the cerebrum and cerebellum, these structures are mainly in the cortex, which is largely near the skull, making electroencephalography useful, since it provides spatial discrimination based on electrode location. However, deep signals are attenuated, and poorly localized. Magnetoencephalography detects dipoles, which derive from current flow, rather than voltage changes. In the case of a radially or spherically symmetric current flow within a short distance, the dipoles will tend to cancel, while net current flows long axons will reinforce. Therefore, an electroencephalogram reads a different signal than a magnetoencephalogram.


EEG-based studies of emotional specificity at the single-electrode level demonstrated that asymmetric activity at the frontal site, especially in the alpha (8-12 Hz) band, is associated with emotion. Voluntary facial expressions of smiles of enjoyment produce higher left frontal activation. Decreased left frontal activity is observed during the voluntary facial expressions of fear. In addition to alpha band activity, theta band power at the frontal midline (Fm) has also been found to relate to emotional states. Pleasant (as opposed to unpleasant) emotions are associated with an increase in frontal midline theta power. Many studies have sought to utilize pattern classification, such as neural networks, statistical classifiers, clustering algorithms, etc., to differentiate between various emotional states reflected in EEG.


EEG-based studies of emotional specificity at the single-electrode level demonstrated that asymmetric activity at the frontal site, especially in the alpha (8-12 Hz) band, is associated with emotion. Ekman and Davidson found that voluntary facial expressions of smiles of enjoyment produced higher left frontal activation (Ekman P, Davidson R J (1993) Voluntary Smiling Changes Regional Brain Activity. Psychol Sci 4: 342-345). Another study by Coan et al. found decreased left frontal activity during the voluntary facial expressions of fear (Coan J A, Allen J J, Harmon-Jones E (2001) Voluntary facial expression and hemispheric asymmetry over the frontal cortex. Psychophysiology 38: 912-925). In addition to alpha band activity, theta band power at the frontal midline (Fm) has also been found to relate to emotional states. Sammler and colleagues, for example, showed that pleasant (as opposed to unpleasant) emotion is associated with an increase in frontal midline theta power (Sammler D, Grigutsch M, Fritz T, Koelsch 5 (2007) Music and emotion: Electrophysiological correlates of the processing of pleasant and unpleasant music. Psychophysiology 44: 293-304). To further demonstrate whether these emotion-specific EEG characteristics are strong enough to differentiate between various emotional states, some studies have utilized a pattern classification analysis approach. See, for example:

  • Dan N, Xiao-Wei W, Li-Chen 5, Bao-Liang L. EEG-based emotion recognition during watching movies; 2011 Apr. 27, 2011-May 1.2011: 667-670;
  • Lin Y P, Wang C H, Jung T P, Wu T L, Jeng S K, et al. (2010) EEG-Based Emotion Recognition in Music Listening. Ieee T Bio Med Eng 57:1798-1806;
  • Murugappan M, Nagarajan R, Yaacob S (2010) Classification of human emotion from EEG using discrete wavelet transform. J Biomed Sci Eng 3: 390-396;
  • Murugappan M, Nagarajan R, Yaacob S (2011) Combining Spatial Filtering and Wavelet Transform for Classifying Human Emotions Using EEG Signals. J Med. Bio. Eng. 31:45-51.


Detecting different emotional states by EEG may be more appropriate using EEG-based functional connectivity. There are various ways to estimate EEG-based functional brain connectivity: correlation, coherence and phase synchronization indices between each pair of EEG electrodes had been used. The assumption is that a higher correlation map indicates a stronger relationship between two signals. (Brazier M A, Casby J U (1952) Cross-correlation and autocorrelation studies of electroencephalographic potentials. Electroen clin neuro 4: 201-211). Coherence gives information similar to correlation, but also includes the covariation between two signals as a function of frequency. (Cantero J L, Atienza M, Salas R M, Gomez C M (1999) Alpha EEG coherence in different brain states: an electrophysiological index of the arousal level in human subjects. Neurosci lett 271:167-70.) The assumption is that higher correlation indicates a stronger relationship between two signals. (Guevara M A, Corsi-Cabrera M (1996) EEG coherence or EEG correlation? Int J Psychophysiology 23: 145-153; Cantero J L, Atienza M, Salas R M, Gomez C M (1999) Alpha EEG coherence in different brain states: an electrophysiological index of the arousal level in human subjects. Neurosci lett 271: 167-70; Adler G, Brassen 5, Jajcevic A (2003) EEG coherence in Alzheimer's dementia. J Neural Transm 110: 1051-1058; Deeny S P, Hillman C H, Janelle C M, Hatfield B D (2003) Cortico-cortical communication and superior performance in skilled marksmen: An EEG coherence analysis. J Sport Exercise Psy 25:188-204.) Phase synchronization among the neuronal groups estimated based on the phase difference between two signals is another way to estimate the EEG-based functional connectivity among brain areas. It is. (Franaszczuk P, Bergey G K (1999) An autoregressive method for the measurement of synchronization of interictal and ictal EEG signals. Biol Cybern 81: 3-9.)


A number of groups have examined emotional specificity using EEG-based functional brain connectivity. For example, Shin and Park showed that, when emotional states become more negative at high room temperatures, correlation coefficients between the channels in temporal and occipital sites increase (Shin J-H, Park D-H. (2011) Analysis for Characteristics of Electroencephalogram (EEG) and Influence of Environmental Factors According to Emotional Changes. In Lee G, Howard D, Ślçzak D, editors. Convergence and Hybrid Information Technology. Springer Berlin Heidelberg, 488-500.) Hinrichs and Machleidt demonstrated that coherence decreases in the alpha band during sadness, compared to happiness (Hinrichs H, Machleidt W (1992) Basic emotions reflected in EEG-coherences. Int J Psychophysiol 13: 225-232). Miskovic and Schmidt found that EEG coherence between the prefrontal cortex and the posterior cortex increased while viewing highly emotionally arousing (i.e., threatening) images, compared to viewing neutral images (Miskovic V, Schmidt L A (2010) Cross-regional cortical synchronization during affective image viewing. Brain Res 1362:102-111). Costa and colleagues applied the synchronization index to detect interaction in different brain sites under different emotional states (Costa T, Rognoni E, Galati D (2006) EEG phase synchronization during emotional response to positive and negative film stimuli. Neurosci Lett 406:159-164). Costa's results showed an overall increase in the synchronization index among frontal channels during emotional stimulation, particularly during negative emotion (i.e., sadness). Furthermore, phase synchronization patterns were found to differ between positive and negative emotions. Costa also found that sadness was more synchronized than happiness at each frequency band and was associated with a wider synchronization both between the right and left frontal sites and within the left hemisphere. In contrast, happiness was associated with a wider synchronization between the frontal and occipital sites.


Different connectivity indices are sensitive to different characteristics of EEG signals. Correlation is sensitive to phase and polarity, but is independent of amplitudes. Changes in both amplitude and phase lead to a change in coherence (Guevara M A, Corsi-Cabrera M (1996) EEG coherence or EEG correlation? Int J Psychophysiol 23:145-153). The phase synchronization index is only sensitive to a change in phase (Lachaux J P, Rodriguez E, Martinerie J, Varela F J (1999) Measuring phase synchrony in brain signals. Hum Brain Mapp 8:194-208).


A number of studies have tried to classify emotional states by means of recording and statistically analyzing EEG signals from the central nervous systems. See for example:

  • Lin Y P, Wang C H, Jung T P, Wu T L, Jeng S K, et al. (2010) EEG-Based Emotion Recognition in Music Listening. IEEE T Bio Med Eng 57:1798-1806
  • Murugappan M, Nagarajan R, Yaacob S (2010) Classification of human emotion from EEG using discrete wavelet transform. J Biomed Sci Eng 3: 390-396.
  • Murugappan M, Nagarajan R, Yaacob S (2011) Combining Spatial Filtering and Wavelet Transform for Classifying Human Emotions Using EEG Signals. J Med. Bio. Eng. 31:45-51.
  • Berkman E, Wong D K, Guimaraes M P, Uy E T, Gross J J, et al. (2004) Brain wave recognition of emotions in EEG. Psychophysiology 41: 571-571.
  • Chanel G, Kronegg J, Grandjean D, Pun T (2006) Emotion assessment: Arousal evaluation using EEG's and peripheral physiological signals. Multimedia Content Representation, Classification and Security 4105: 530-537.
  • Hagiwara KlaM (2003) A Feeling Estimation System Using a Simple Electroencephalograph. IEEE International Conference on Systems, Man and Cybemetics. 4204-4209.
  • You-Yun Lee and Shulan Hsieh studied different emotional states by means of EEG-based functional connectivity patterns. They used emotional film clips to elicit three different emotional states.


The dimensional theory of emotion, which asserts that there are neutral, positive, and negative emotional states, may be used to classify emotional states, because numerous studies have suggested that the responses of the central nervous system correlate with emotional valence and arousal. (See for example, Davidson R J (1993) Cerebral Asymmetry and Emotion—Conceptual and Methodological Conundrums. Cognition Emotion 7:115-138; Jones N A, Fox N A (1992) Electroencephalogram asymmetry during emotionally evocative films and its relation to positive and negative affectivity. Brain Cogn 20: 280-299; Schmidt L A, Trainor U (2001) Frontal brain electrical activity (EEG) distinguishes valence and intensity of musical emotions. Cognition Emotion 15: 487-500; Tomarken A J, Davidson R J, Henriques J B (1990) Resting frontal brain asymmetry predicts affective responses to films. J Pers Soc Psychol 59: 791-801.) As suggested by Mauss and Robins (2009), “measures of emotional responding appear to be structured along dimensions (e.g., valence, arousal) rather than discrete emotional states (e.g., sadness, fear, anger)”.


EEG-based functional connectivity change was found to be significantly different among emotional states of neutral, positive, or negative. Lee Y-Y, Hsieh 5 (2014) Classifying Different Emotional States by Means of EEG-Based Functional Connectivity Patterns. PLoS ONE 9(4): e95415. doi.org/10.1371/journal.pone.0095415. A connectivity pattern may be detected by pattern classification analysis using Quadratic Discriminant Analysis. The results indicated that the classification rate was better than chance. They concluded that estimating EEG-based functional connectivity provides a useful tool for studying the relationship between brain activity and emotional states.


Emotions affects learning. Intelligent Tutoring Systems (ITS) learner model initially composed of a cognitive module was extended to include a psychological module and an emotional module. Alicia Heraz et al. introduced an emomental agent. It interacts with an ITS to communicate the emotional state of the learner based upon his mental state. The mental state was obtained from the learner's brainwaves. The agent learns to predict the learner's emotions by using machine learning techniques. (Alicia Heraz, Ryad Razaki; Claude Frasson, “Using machine learning to predict learner emotional state from brainwaves” Advanced Learning Technologies, 2007. ICALT 2007. Seventh IEEE International Conference on Advanced Learning Technologies (ICALT 2007)) See also:

  • Ella T. Mampusti, Jose S. Ng, Jarren James I. Quinto, Grizelda L. Teng, Merlin Teodosia C. Suarez, Rhia S. Trogo, “Measuring Academic Affective States of Students via Brainwave Signals”, Knowledge and Systems Engineering (KSE) 2011 Third International Conference on, pp. 226-231, 2011
  • Judith J. Azcarraga, John Francis Ibanez Jr., Ianne Robert Lim, Nestor Lumanas Jr., “Use of Personality Profile in Predicting Academic Emotion Based on Brainwaves Signals and Mouse Behavior”, Knowledge and Systems Engineering (KSE) 2011 Third International Conference on, pp. 239-244, 2011.
  • Yi-Hung Liu, Chien-Te Wu, Yung-Hwa Kao, Ya-Ting Chen, “Single-trial EEG-based emotion recognition using kernel Eigen-emotion pattern and adaptive support vector machine”, Engineering in Medicine and Biology Society (EMBC) 2013 35th Annual International Conference of the IEEE, pp. 4306-4309, 2013, ISSN 1557-170X.
  • Thong Tri Vo, Nam Phuong Nguyen, Toi Vo Van, IFMBE Proceedings, vol. 63, pp. 621, 2018, ISSN 1680-0737, ISBN 978-981-10-4360-4.
  • Adrian Rodriguez Aguiñaga, Miguel Angel Lopez Ramirez, Lecture Notes in Computer Science, vol. 9456, pp. 177, 2015, ISSN 0302-9743, ISBN 978-3-319-26507-0.
  • Judith Azcarraga, Merlin Teodosia Suarez, “Recognizing Student Emotions using Brainwaves and Mouse Behavior Data”, International Journal of Distance Education Technologies, vol. 11, pp. 1, 2013, ISSN 1539-3100.
  • Tri Thong Vo, Phuong Nam Nguyen, Van Toi Vo, IFMBE Proceedings, vol. 61, pp. 67, 2017, ISSN 1680-0737, ISBN 978-981-10-4219-5.
  • Alicia Heraz, Claude Frasson, Lecture Notes in Computer Science, vol. 5535, pp. 367, 2009, ISSN 0302-9743, ISBN 978-3-642-02246-3.
  • Hamwira Yaacob, Wahab Abdul, Norhaslinda Kamaruddin, “Classification of EEG signals using MLP based on categorical and dimensional perceptions of emotions”, Information and Communication Technology for the Muslim World (ICT4M) 2013 5th International Conference on, pp. 1-6, 2013.
  • Yuan-Pin Lin, Chi-Hong Wang, Tzyy-Ping Jung, Tien-Lin Wu, Shyh-Kang Jeng, Jeng-Ren Duann, Jyh-Horng Chen, “EEG-Based Emotion Recognition in Music Listening”, Biomedical Engineering IEEE Transactions on, vol. 57, pp. 1798-1806, 2010, ISSN 0018-9294.
  • Yi-Hung Liu, Wei-Teng Cheng, Yu-Tsung Hsiao, Chien-Te Wu, Mu-Der Jeng, “EEG-based emotion recognition based on kernel Fisher's discriminant analysis and spectral powers”, Systems Man and Cybernetics (SMC) 2014 IEEE International Conference on, pp. 2221-2225, 2014.


Using EEG to assess the emotional state has numerous practical applications. One of the first such applications was the development of a travel guide based on emotions by measuring brainwaves by the Singapore tourism group. “By studying the brainwaves of a family on vacation, the researchers drew up the Singapore Emotion Travel Guide, which advises future visitors of the emotions they can expect to experience at different attractions.” (www.lonelyplanet.com/news/2017/04/12/singapore-emotion-travel-guide) Joel Pearson at University of New South Wales and his group developed the protocol of measuring brainwaves of travelers using EEG and decoding specific emotional states.


Another recently released application pertains to virtual reality (VR) technology. On Sep. 18, 2017 Looxid Labs launched a technology that harnesses EEG from a subject waring a VR headset. Looxid Labs intention is to factor in brain waves into VR applications in order to accurately infer emotions. Other products such as MindMaze and even Samsung have tried creating similar applications through facial muscles recognition. (scottamyx.com/2017/10/13/looxid-labs-vr-brain-waves-human-emotions/). According to its website (looxidlabs.com/device-2/), the Looxid Labs Development Kit provides a VR headset embedded with miniaturized eye and brain sensors. It uses 6 EEG channels: Fp1, Fp2, AF7, AF8, AF3, AF4 in international 10-20 system.


To assess a user's state of mind, a computer may be used to analyze the EEG signals produced by the brain of the user. However, the emotional states of a brain are complex, and the brain waves associated with specific emotions seem to change over time. Wei-Long Zheng at Shanghai Jiao Tong University used machine learning to identify the emotional brain states and to repeat it reliably. The machine learning algorithm found a set of patterns that clearly distinguished positive, negative, and neutral emotions that worked for different subjects and for the same subjects over time with an accuracy of about 80 percent. (See Wei-Long Zheng, Jia-Yi Zhu, Bao-Liang Lu, Identifying Stable Patterns over Time for Emotion Recognition from EEG, arxiv.org/abs/1601.02197; see also How One Intelligent Machine Learned to Recognize Human Emotions, MIT Technology Review, Jan. 23, 2016.)


MEG


Magnetoencephalography (MEG) is a functional neuroimaging technique for mapping brain activity by recording magnetic fields produced by electrical currents occurring naturally in the brain, using very sensitive magnetometers. Arrays of SQUIDs (superconducting quantum interference devices) are currently the most common magnetometer, while the SERF (spin exchange relaxation-free) magnetometer is being investigated (Hämäläinen, Matti; Hari, Riitta; Ilmoniemi, Risto J.; Knuutila, Jukka; Lounasmaa, Olli V. (1993). “Magnetoencephalography-theory, instrumentation, and applications to noninvasive studies of the working human brain”. Reviews of Modern Physics. 65 (2): 413-497. ISSN 0034-6861. doi:10.1103/RevModPhys.65.413.) It is known that “neuronal activity causes local changes in cerebral blood flow, blood volume, and blood oxygenation” (Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. K. K. Kwong, J. W. Belliveau, D. A. Chesler, I. E. Goldberg, R. M. Weisskoff, B. P. Poncelet, D. N. Kennedy, B. E. Hoppel, M. S. Cohen, and R. Turner). Using “a 122-channel D.C. SQUID magnetometer with a helmet-shaped detector array covering the subject's head” it has been shown that the “system allows simultaneous recording of magnetic activity all over the head.” (122-channel squid instrument for investigating the magnetic signals from the human brain.) A. I. Ahonen, M. S. Hämäläinen, M. J. Kajola, J. E. T. Knuutila, P. P. Laine, O. V. Lounasmaa, L. T. Parkkonen, J. T. Simola, and C. D. Tesche Physica Scripta, Volume 1993, T49A).


In some cases, magnetic fields cancel, and thus the detectable electrical activity may fundamentally differ from the detectable electrical activity obtained via EEG. However, the main types of brain rhythms are detectable by both methods.


See: U.S. Pub. App. Nos. and U.S. Pat. Nos. 5,059,814; 5,118,606; 5,136,687; 5,224,203; 5,303,705; 5,325,862; 5,461,699; 5,522,863; 5,640,493; 5,715,821; 5,719,561; 5,722,418; 5,730,146; 5,736,543; 5,737,485; 5,747,492; 5,791,342; 5,816,247; 6,497,658; 6,510,340; 6,654,729; 6,893,407; 6,950,697; 8,135,957; 8,620,206; 8,644,754; 9,118,775; 9,179,875; 9,642,552; 20030018278; 20030171689; 20060293578; 20070156457; 20070259323; 20080015458; 20080154148; 20080229408; 20100010365; 20100076334; 20100090835; 20120046531; 20120052905; 20130041281; 20150081299; 20150262016. See EP1304073A2; EP1304073A3; WO2000025668A1; and WO2001087153A1.


MEGs seek to detect the magnetic dipole emission from an electrical discharge in cells, e.g., neural action potentials. Typical sensors for MEGs are superconducting quantum interference devices (SQUIDs). These currently require cooling to liquid nitrogen or liquid helium temperatures. However, the development of room temperature, or near room temperature superconductors, and miniature cryocoolers, may permit field deployments and portable or mobile detectors. Because MEGs are less influenced by medium conductivity and dielectric properties, and because they inherently detect the magnetic field vector, MEG technology permits volumetric mapping of brain activity and distinction of complementary activity that might suppress detectable EEG signals. MEG technology also supports vector mapping of fields, since magnetic emitters are inherently dipoles, and therefore a larger amount of information is inherently available.


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 4,862,359; 5,027,817; 5,198,977; 5,230,346; 5,269,315; 5,309,923; 5,325,862; 5,331,970; 5,546,943; 5,568,816; 5,662,109; 5,724,987; 5,797,853; 5,840,040; 5,845,639; 6,042,548; 6,080,164; 6,088,611; 6,097,980; 6,144,872; 6,161,031; 6,171,239; 6,240,308; 6,241,686; 6,280,393; 6,309,361; 6,319,205; 6,322,515; 6,356,781; 6,370,414; 6,377,833; 6,385,479; 6,390,979; 6,402,689; 6,419,629; 6,466,816; 6,490,472; 6,526,297; 6,527,715; 6,530,884; 6,547,746; 6,551,243; 6,553,252; 6,622,036; 6,644,976; 6,648,880; 6,663,571; 6,684,098; 6,697,660; 6,728,564; 6,740,032; 6,743,167; 6,773,400; 6,907,280; 6,947,790; 6,950,698; 6,963,770; 6,963,771; 6,996,261; 7,010,340; 7,011,814; 7,022,083; 7,092,748; 7,104,947; 7,105,824; 7,120,486; 7,130,673; 7,171,252; 7,177,675; 7,231,245; 7,254,500; 7,283,861; 7,286,871; 7,338,455; 7,346,395; 7,378,056; 7,461,045; 7,489,964; 7,490,085; 7,499,745; 7,510,699; 7,539,528; 7,547,284; 7,565,193; 7,567,693; 7,577,472; 7,613,502; 7,627,370; 7,647,098; 7,653,433; 7,697,979; 7,729,755; 7,754,190; 7,756,568; 7,766,827; 7,769,431; 7,778,692; 7,787,937; 7,787,946; 7,794,403; 7,831,305; 7,840,250; 7,856,264; 7,860,552; 7,899,524; 7,904,139; 7,904,144; 7,933,645; 7,962,204; 7,983,740; 7,986,991; 8,000,773; 8,000,793; 8,002,553; 8,014,847; 8,036,434; 8,065,360; 8,069,125; 8,086,296; 8,121,694; 8,190,248; 8,190,264; 8,197,437; 8,224,433; 8,233,682; 8,233,965; 8,236,038; 8,262,714; 8,280,514; 8,295,914; 8,306,607; 8,306,610; 8,313,441; 8,326,433; 8,337,404; 8,346,331; 8,346,342; 8,356,004; 8,358,818; 8,364,271; 8,380,289; 8,380,290; 8,380,314; 8,391,942; 8,391,956; 8,423,125; 8,425,583; 8,429,225; 8,445,851; 8,457,746; 8,467,878; 8,473,024; 8,498,708; 8,509,879; 8,527,035; 8,532,756; 8,538,513; 8,543,189; 8,554,325; 8,562,951; 8,571,629; 8,586,932; 8,591,419; 8,606,349; 8,606,356; 8,615,479; 8,626,264; 8,626,301; 8,632,750; 8,644,910; 8,655,817; 8,657,756; 8,666,478; 8,679,009; 8,684,926; 8,690,748; 8,696,722; 8,706,205; 8,706,241; 8,706,518; 8,712,512; 8,717,430; 8,725,669; 8,738,395; 8,761,869; 8,761,889; 8,768,022; 8,805,516; 8,814,923; 8,831,731; 8,834,546; 8,838,227; 8,849,392; 8,849,632; 8,852,103; 8,855,773; 8,858,440; 8,868,174; 8,888,702; 8,915,741; 8,918,162; 8,938,289; 8,938,290; 8,951,189; 8,951,192; 8,956,277; 8,965,513; 8,977,362; 8,989,836; 8,998,828; 9,005,126; 9,020,576; 9,022,936; 9,026,217; 9,026,218; 9,028,412; 9,033,884; 9,037,224; 9,042,201; 9,050,470; 9,067,052; 9,072,905; 9,084,896; 9,089,400; 9,089,683; 9,092,556; 9,095,266; 9,101,276; 9,107,595; 9,116,835; 9,133,024; 9,144,392; 9,149,255; 9,155,521; 9,167,970; 9,167,976; 9,167,977; 9,167,978; 9,171,366; 9,173,609; 9,179,850; 9,179,854; 9,179,858; 9,179,875; 9,192,300; 9,198,637; 9,198,707; 9,204,835; 9,211,077; 9,211,212; 9,213,074; 9,242,067; 9,247,890; 9,247,924; 9,248,288; 9,254,097; 9,254,383; 9,268,014; 9,268,015; 9,271,651; 9,271,674; 9,282,930; 9,289,143; 9,302,110; 9,308,372; 9,320,449; 9,322,895; 9,326,742; 9,332,939; 9,336,611; 9,339,227; 9,357,941; 9,367,131; 9,370,309; 9,375,145; 9,375,564; 9,387,320; 9,395,425; 9,402,558; 9,403,038; 9,414,029; 9,436,989; 9,440,064; 9,463,327; 9,470,728; 9,471,978; 9,474,852; 9,486,632; 9,492,313; 9,560,967; 9,579,048; 9,592,409; 9,597,493; 9,597,494; 9,615,789; 9,616,166; 9,655,573; 9,655,669; 9,662,049; 9,662,492; 9,669,185; 9,675,292; 9,682,232; 9,687,187; 9,707,396; 9,713,433; 9,713,444; 20010020127; 20010021800; 20010051774; 20020005784; 20020016552; 20020017994; 20020042563; 20020058867; 20020099273; 20020099295; 20020103428; 20020103429; 20020128638; 20030001098; 20030009096; 20030013981; 20030032870; 20030040660; 20030068605; 20030074032; 20030093004; 20030093005; 20030120140; 20030128801; 20030135128; 20030153818; 20030163027; 20030163028; 20030181821; 20030187359; 20030204135; 20030225335; 20030236458; 20040030585; 20040059241; 20040072133; 20040077960; 20040092809; 20040096395; 20040097802; 20040116798; 20040122787; 20040122790; 20040144925; 20040204656; 20050004489; 20050007091; 20050027284; 20050033122; 20050033154; 20050033379; 20050079474; 20050079636; 20050106713; 20050107654; 20050119547; 20050131311; 20050136002; 20050159670; 20050159671; 20050182456; 20050192514; 20050222639; 20050283053; 20060004422; 20060015034; 20060018525; 20060036152; 20060036153; 20060051814; 20060052706; 20060058683; 20060074290; 20060074298; 20060078183; 20060084858; 20060100526; 20060111644; 20060116556; 20060122481; 20060129324; 20060173510; 20060189866; 20060241373; 20060241382; 20070005115; 20070007454; 20070008172; 20070015985; 20070032737; 20070055145; 20070100251; 20070138886; 20070179534; 20070184507; 20070191704; 20070191727; 20070203401; 20070239059; 20070250138; 20070255135; 20070293760; 20070299370; 20080001600; 20080021332; 20080021340; 20080033297; 20080039698; 20080039737; 20080042067; 20080058664; 20080091118; 20080097197; 20080123927; 20080125669; 20080128626; 20080154126; 20080167571; 20080221441; 20080230702; 20080230705; 20080249430; 20080255949; 20080275340; 20080306365; 20080311549; 20090012387; 20090018407; 20090018431; 20090018462; 20090024050; 20090048507; 20090054788; 20090054800; 20090054958; 20090062676; 20090078875; 20090082829; 20090099627; 20090112117; 20090112273; 20090112277; 20090112278; 20090112279; 20090112280; 20090118622; 20090131995; 20090137923; 20090156907; 20090156955; 20090157323; 20090157481; 20090157482; 20090157625; 20090157662; 20090157751; 20090157813; 20090163777; 20090164131; 20090164132; 20090171164; 20090172540; 20090177050; 20090179642; 20090191131; 20090209845; 20090216091; 20090220429; 20090221928; 20090221930; 20090246138; 20090264785; 20090267758; 20090270694; 20090287271; 20090287272; 20090287273; 20090287274; 20090287467; 20090292180; 20090292713; 20090292724; 20090299169; 20090304582; 20090306531; 20090306534; 20090318773; 20090318794; 20100021378; 20100030073; 20100036233; 20100036453; 20100041962; 20100042011; 20100049276; 20100069739; 20100069777; 20100076274; 20100082506; 20100087719; 20100094154; 20100094155; 20100099975; 20100106043; 20100113959; 20100114193; 20100114237; 20100130869; 20100143256; 20100163027; 20100163028; 20100163035; 20100168525; 20100168529; 20100168602; 20100189318; 20100191095; 20100191124; 20100204748; 20100248275; 20100249573; 20100261993; 20100298735; 20100324441; 20110004115; 20110004412; 20110009777; 20110015515; 20110015539; 20110028859; 20110034821; 20110046491; 20110054345; 20110054562; 20110077503; 20110092800; 20110092882; 20110112394; 20110112426; 20110119212; 20110125048; 20110125238; 20110129129; 20110144521; 20110160543; 20110160607; 20110160608; 20110161011; 20110178359; 20110178441; 20110178442; 20110207988; 20110208094; 20110213200; 20110218405; 20110230738; 20110257517; 20110263962; 20110263968; 20110270074; 20110270914; 20110275927; 20110295143; 20110295166; 20110301448; 20110306845; 20110306846; 20110307029; 20110313268; 20110313487; 20120004561; 20120021394; 20120022343; 20120022884; 20120035765; 20120046531; 20120046971; 20120053449; 20120053483; 20120078327; 20120083700; 20120108998; 20120130228; 20120130229; 20120149042; 20120150545; 20120163689; 20120165899; 20120165904; 20120197163; 20120215114; 20120219507; 20120226091; 20120226185; 20120232327; 20120232433; 20120245493; 20120253219; 20120253434; 20120265267; 20120271148; 20120271151; 20120271376; 20120283502; 20120283604; 20120296241; 20120296253; 20120296569; 20120302867; 20120310107; 20120310298; 20120316793; 20130012804; 20130063434; 20130066350; 20130066391; 20130066394; 20130072780; 20130079621; 20130085678; 20130096441; 20130096454; 20130102897; 20130109996; 20130110616; 20130116561; 20130131755; 20130138177; 20130172716; 20130178693; 20130184728; 20130188854; 20130204085; 20130211238; 20130226261; 20130231580; 20130238063; 20130245422; 20130245424; 20130245486; 20130261506; 20130274586; 20130281879; 20130281890; 20130289386; 20130304153; 20140000630; 20140005518; 20140031703; 20140057232; 20140058241; 20140058292; 20140066763; 20140081115; 20140088377; 20140094719; 20140094720; 20140111335; 20140114207; 20140119621; 20140128763; 20140135642; 20140148657; 20140151563; 20140155952; 20140163328; 20140163368; 20140163409; 20140171749; 20140171757; 20140171819; 20140180088; 20140180092; 20140180093; 20140180094; 20140180095; 20140180096; 20140180097; 20140180099; 20140180100; 20140180112; 20140180113; 20140180176; 20140180177; 20140193336; 20140194726; 20140200414; 20140211593; 20140228649; 20140228702; 20140243614; 20140243652; 20140243714; 20140249360; 20140249445; 20140257073; 20140270438; 20140275807; 20140275851; 20140275891; 20140276013; 20140276014; 20140276187; 20140276702; 20140279746; 20140296646; 20140296655; 20140303425; 20140303486; 20140316248; 20140323849; 20140330268; 20140330394; 20140335489; 20140336489; 20140340084; 20140343397; 20140357962; 20140364721; 20140371573; 20140378830; 20140378941; 20150011866; 20150011877; 20150018665; 20150018905; 20150024356; 20150025408; 20150025422; 20150025610; 20150029087; 20150033245; 20150033258; 20150033259; 20150033262; 20150033266; 20150035959; 20150038812; 20150038822; 20150038869; 20150039066; 20150073237; 20150080753; 20150088120; 20150119658; 20150119689; 20150119698; 20150140528; 20150141529; 20150141773; 20150150473; 20150151142; 20150157266; 20150165239; 20150174418; 20150182417; 20150196800; 20150201879; 20150208994; 20150219732; 20150223721; 20150227702; 20150230744; 20150246238; 20150247921; 20150257700; 20150290420; 20150297106; 20150297893; 20150305799; 20150305800; 20150305801; 20150306340; 20150313540; 20150317796; 20150320591; 20150327813; 20150335281; 20150335294; 20150339363; 20150343242; 20150359431; 20150360039; 20160001065; 20160001096; 20160001098; 20160008620; 20160008632; 20160015289; 20160022165; 20160022167; 20160022168; 20160022206; 20160027342; 20160029946; 20160029965; 20160038049; 20160038559; 20160048659; 20160051161; 20160051162; 20160058354; 20160058392; 20160066828; 20160066838; 20160081613; 20160100769; 20160120480; 20160128864; 20160143541; 20160143574; 20160151018; 20160151628; 20160157828; 20160158553; 20160166219; 20160184599; 20160196393; 20160199241; 20160203597; 20160206380; 20160206871; 20160206877; 20160213276; 20160235324; 20160235980; 20160235983; 20160239966; 20160239968; 20160245670; 20160245766; 20160270723; 20160278687; 20160287118; 20160287436; 20160296746; 20160302720; 20160303397; 20160303402; 20160320210; 20160339243; 20160341684; 20160361534; 20160366462; 20160371721; 20170021161; 20170027539; 20170032098; 20170039706; 20170042474; 20170043167; 20170065349; 20170079538; 20170080320; 20170085855; 20170086729; 20170086763; 20170087367; 20170091418; 20170112403; 20170112427; 20170112446; 20170112577; 20170147578; 20170151435; 20170160360; 20170164861; 20170164862; 20170164893; 20170164894; 20170172527; 20170173262; 20170185714; 20170188862; 20170188866; 20170188868; 20170188869; 20170188932; 20170189691; 20170196501; and 20170202633.

  • Allen, Philip B., et al. High-temperature superconductivity. Springer Science & Business Media, 2012;
  • Fausti, Daniele, et al. “Light-induced superconductivity in a stripe-ordered cuprate.” Science 331.6014 (2011): 189-191;
  • Inoue, Mitsuteru, et al. “Investigating the use of magnonic crystals as extremely sensitive magnetic field sensors at room temperature.” Applied Physics Letters 98.13 (2011): 132511;
  • Kaiser, Stefan, et al. “Optically induced coherent transport far above Tc in underdoped YBa2 Cu306+δ.” Physical Review B 89.18 (2014): 184516;
  • Malik, M. A., and B. A. Malik. “High Temperature Superconductivity: Materials, Mechanism and Applications.” Bulgarian J. Physics 41.4 (2014).
  • Mankowsky, Roman, et al. “Nonlinear lattice dynamics as a basis for enhanced superconductivity in YBa2Cu306. 5.” arXiv preprint arXiv:1405.2266 (2014);
  • Mcfetridge, Grant. “Room temperature superconductor.” U.S. Pub. App. No. 20020006875.
  • Mitrano, Matteo, et al. “Possible light-induced superconductivity in K3C60 at high temperature.” Nature 530.7591 (2016): 461-464;
  • Mourachkine, Andrei. Room-temperature superconductivity. Cambridge Int Science Publishing, 2004;
  • Narlikar, Anant V., ed. High Temperature Superconductivity 2. Springer Science & Business Media, 2013;
  • Pickett, Warren E. “Design for a room-temperature superconductor.” J. superconductivity and novel magnetism 193 (2006): 291-297;
  • Sleight, Arthur W. “Room temperature superconductors.” Accounts of chemical research 28.3 (1995): 103-108.
  • Hämäläinen, Matti; Hari, Riitta; Ilmoniemi, Risto J.; Knuutila, Jukka; Lounasmaa, Olli V. (1993). “Magnetoencephalography-theory, instrumentation, and applications to noninvasive studies of the working human brain”. Reviews of Modern Physics. 65 (2): 413-497. ISSN 0034-6861. doi:10.1103/RevModPhys.65.413.


EEGs and MEGs can monitor the state of consciousness. For example, states of deep sleep are associated with slower EEG oscillations of larger amplitude. Various signal analysis methods allow for robust identifications of distinct sleep stages, depth of anesthesia, epileptic seizures and connections to detailed cognitive events.


Positron Emission Tomography (PET) Scan


A PET scan is an imaging test that helps reveal how tissues and organs are functioning (Bailey, D. L; D. W. Townsend; P. E. Valk; M. N. Maisey (2005). Positron Emission Tomography: Basic Sciences. Secaucus, N.J.: Springer-Verlag. ISBN 1-85233-798-2.). A PET scan uses a radioactive drug (positron-emitting tracer) to show this activity. It uses this radiation to produce 3-D, images colored for the different activity of the brain. See, e.g.:

  • Jarden, Jens O., Vijay Dhawan, Alexander Poltorak, Jerome B. Posner, and David A. Rottenberg. “Positron emission tomographic measurement of blood-to-brain and blood-to-tumor transport of 82Rb: The effect of dexamethasone and whole-brain radiation therapy.” Annals of neurology 18, no. 6 (1985): 636-646.
  • Dhawan, V. I. J. A. Y., A. Poltorak, J. R. Moeller, J. O. Jarden, S. C. Strother, H. Thaler, and D. A. Rottenberg. “Positron emission tomographic measurement of blood-to-brain and blood-to-tumour transport of 82Rb. I: Error analysis and computer simulations.” Physics in medicine and biology 34, no.12 (1989): 1773.


U.S. Pub. App. Nos. and U.S. Pat. Nos. 4,977,505; 5,331,970; 5,568,816; 5,724,987; 5,825,830; 5,840,040; 5,845,639; 6,053,739; 6,132,724; 6,161,031; 6,226,418; 6,240,308; 6,266,453; 6,364,845; 6,408,107; 6,490,472; 6,547,746; 6,615,158; 6,633,686; 6,644,976; 6,728,424; 6,775,405; 6,885,886; 6,947,790; 6,996,549; 7,117,026; 7,127,100; 7,150,717; 7,254,500; 7,309,315; 7,355,597; 7,367,807; 7,383,237; 7,483,747; 7,583,857; 7,627,370; 7,647,098; 7,678,047; 7,738,683; 7,778,490; 7,787,946; 7,876,938; 7,884,101; 7,890,155; 7,901,211; 7,904,144; 7,961,922; 7,983,762; 7,986,991; 8,002,553; 8,069,125; 8,090,164; 8,099,299; 8,121,361; 8,126,228; 8,126,243; 8,148,417; 8,148,418; 8,150,796; 8,160,317; 8,167,826; 8,170,315; 8,170,347; 8,175,359; 8,175,360; 8,175,686; 8,180,125; 8,180,148; 8,185,186; 8,195,593; 8,199,982; 8,199,985; 8,233,689; 8,233,965; 8,249,815; 8,303,636; 8,306,610; 8,311,747; 8,311,748; 8,311,750; 8,315,812; 8,315,813; 8,315,814; 8,321,150; 8,356,004; 8,358,818; 8,374,411; 8,379,947; 8,386,188; 8,388,529; 8,423,118; 8,430,816; 8,463,006; 8,473,024; 8,496,594; 8,520,974; 8,523,779; 8,538,108; 8,571,293; 8,574,279; 8,577,103; 8,588,486; 8,588,552; 8,594,950; 8,606,356; 8,606,361; 8,606,530; 8,606,592; 8,615,479; 8,630,812; 8,634,616; 8,657,756; 8,664,258; 8,675,936; 8,675,983; 8,680,119; 8,690,748; 8,706,518; 8,724,871; 8,725,669; 8,734,356; 8,734,357; 8,738,395; 8,754,238; 8,768,022; 8,768,431; 8,785,441; 8,787,637; 8,795,175; 8,812,245; 8,812,246; 8,838,201; 8,838,227; 8,861,819; 8,868,174; 8,871,797; 8,913,810; 8,915,741; 8,918,162; 8,934,685; 8,938,102; 8,980,891; 8,989,836; 9,025,845; 9,034,911; 9,037,224; 9,042,201; 9,053,534; 9,064,036; 9,076,212; 9,078,564; 9,081,882; 9,082,169; 9,087,147; 9,095,266; 9,138,175; 9,144,392; 9,149,197; 9,152,757; 9,167,974; 9,171,353; 9,171,366; 9,177,379; 9,177,416; 9,179,854; 9,186,510; 9,198,612; 9,198,624; 9,204,835; 9,208,430; 9,208,557; 9,211,077; 9,221,755; 9,226,672; 9,235,679; 9,256,982; 9,268,902; 9,271,657; 9,273,035; 9,275,451; 9,282,930; 9,292,858; 9,295,838; 9,305,376; 9,311,335; 9,320,449; 9,328,107; 9,339,200; 9,339,227; 9,367,131; 9,370,309; 9,390,233; 9,396,533; 9,401,021; 9,402,558; 9,412,076; 9,418,368; 9,434,692; 9,436,989; 9,449,147; 9,451,303; 9,471,978; 9,472,000; 9,483,613; 9,495,684; 9,556,149; 9,558,558; 9,560,967; 9,563,950; 9,567,327; 9,582,152; 9,585,723; 9,600,138; 9,600,778; 9,604,056; 9,607,377; 9,613,186; 9,652,71; 9,662,083; 9,697,330; 9,706,925; 9,717,461; 9,729,252; 9,732,039; 9,734,589; 9,734,601; 9,734,632; 9,740,710; 9,740,946; 9,741,114; 9,743,835; RE45336; RE45337; 20020032375; 20020183607; 20030013981; 20030028348; 20030031357; 20030032870; 20030068605; 20030128801; 20030233039; 20030233250; 20030234781; 20040049124; 20040072133; 20040116798; 20040151368; 20040184024; 20050007091; 20050065412; 20050080124; 20050096311; 20050118286; 20050144042; 20050215889; 20050244045; 20060015153; 20060074290; 20060084858; 20060129324; 20060188134; 20070019846; 20070032737; 20070036402; 20070072857; 20070078134; 20070081712; 20070100251; 20070127793; 20070280508; 20080021340; 20080069446; 20080123927; 20080167571; 20080219917; 20080221441; 20080241804; 20080247618; 20080249430; 20080279436; 20080281238; 20080286453; 20080287774; 20080287821; 20080298653; 20080298659; 20080310697; 20080317317; 20090018407; 20090024050; 20090036781; 20090048507; 20090054800; 20090074279; 20090099783; 20090143654; 20090148019; 20090156907; 20090156955; 20090157323; 20090157481; 20090157482; 20090157625; 20090157660; 20090157751; 20090157813; 20090163777; 20090164131; 20090164132; 20090164302; 20090164401; 20090164403; 20090164458; 20090164503; 20090164549; 20090171164; 20090172540; 20090221904; 20090246138; 20090264785; 20090267758; 20090270694; 20090271011; 20090271120; 20090271122; 20090271347; 20090290772; 20090292180; 20090292478; 20090292551; 20090299435; 20090312595; 20090312668; 20090316968; 20090316969; 20090318773; 20100004762; 20100010316; 20100010363; 20100014730; 20100014732; 20100015583; 20100017001; 20100022820; 20100030089; 20100036233; 20100041958; 20100041962; 20100041964; 20100042011; 20100042578; 20100063368; 20100069724; 20100069777; 20100076249; 20100080432; 20100081860; 20100081861; 20100094155; 20100100036; 20100125561; 20100130811; 20100130878; 20100135556; 20100142774; 20100163027; 20100163028; 20100163035; 20100168525; 20100168529; 20100168602; 20100172567; 20100179415; 20100189318; 20100191124; 20100219820; 20100241449; 20100249573; 20100260402; 20100268057; 20100268108; 20100274577; 20100274578; 20100280332; 20100293002; 20100305962; 20100305963; 20100312579; 20100322488; 20100322497; 20110028825; 20110035231; 20110038850; 20110046451; 20110077503; 20110125048; 20110152729; 20110160543; 20110229005; 20110230755; 20110263962; 20110293193; 20120035765; 20120041318; 20120041319; 20120041320; 20120041321; 20120041322; 20120041323; 20120041324; 20120041498; 20120041735; 20120041739; 20120053919; 20120053921; 20120059246; 20120070044; 20120080305; 20120128683; 20120150516; 20120207362; 20120226185; 20120263393; 20120283502; 20120288143; 20120302867; 20120316793; 20120321152; 20120321160; 20120323108; 20130018596; 20130028496; 20130054214; 20130058548; 20130063434; 20130064438; 20130066618; 20130085678; 20130102877; 20130102907; 20130116540; 20130144192; 20130151163; 20130188830; 20130197401; 20130211728; 20130226464; 20130231580; 20130237541; 20130243287; 20130245422; 20130274586; 20130318546; 20140003696; 20140005518; 20140018649; 20140029830; 20140058189; 20140063054; 20140063055; 20140067740; 20140081115; 20140107935; 20140119621; 20140133720; 20140133722; 20140148693; 20140155770; 20140163627; 20140171757; 20140194726; 20140207432; 20140211593; 20140222113; 20140222406; 20140226888; 20140236492; 20140243663; 20140247970; 20140249791; 20140249792; 20140257073; 20140270438; 20140343397; 20140348412; 20140350380; 20140355859; 20140371573; 20150010223; 20150012466; 20150019241; 20150029087; 20150033245; 20150033258; 20150033259; 20150033262; 20150033266; 20150073141; 20150073722; 20150080753; 20150088015; 20150088478; 20150150530; 20150150753; 20150157266; 20150161326; 20150161348; 20150174418; 20150196800; 20150199121; 20150201849; 20150216762; 20150227793; 20150257700; 20150272448; 20150287223; 20150294445; 20150297106; 20150306340; 20150317796; 20150324545; 20150327813; 20150332015; 20150335303; 20150339459; 20150343242; 20150363941; 20150379230; 20160004396; 20160004821; 20160004957; 20160007945; 20160019693; 20160027178; 20160027342; 20160035093; 20160038049; 20160038770; 20160048965; 20160067496; 20160070436; 20160073991; 20160082319; 20160110517; 20160110866; 20160110867; 20160113528; 20160113726; 20160117815; 20160117816; 20160117819; 20160128661; 20160133015; 20160140313; 20160140707; 20160151018; 20160155005; 20160166205; 20160180055; 20160203597; 20160213947; 20160217586; 20160217595; 20160232667; 20160235324; 20160239966; 20160239968; 20160246939; 20160263380; 20160284082; 20160296287; 20160300352; 20160302720; 20160364859; 20160364860; 20160364861; 20160366462; 20160367209; 20160371455; 20160374990; 20170024886; 20170027539; 20170032524; 20170032527; 20170032544; 20170039706; 20170053092; 20170061589; 20170076452; 20170085855; 20170091418; 20170112577; 20170128032; 20170147578; 20170148213; 20170168566; 20170178340; 20170193161; 20170198349; 20170202621; 20170213339; 20170216595; 20170221206; and 20170231560.


fMRI


Functional magnetic resonance imaging or functional MRI (fMRI) is a functional neuroimaging procedure using MRI technology that measures brain activity by detecting changes associated with blood flow (“Magnetic Resonance, a critical peer-reviewed introduction; functional MRI”. European Magnetic Resonance Forum. Retrieved 17 Nov. 2014; Huettel, Song & McCarthy (2009)).


Yukiyasu Kamitani et al., Neuron (DOI:10.1016/j.neuron.2008.11.004) used an image of brain activity taken in a functional MRI scanner to recreate a black-and-white image from scratch. See also ‘Mind-reading’ software could record your dreams” By Celeste Biever. New Scientist, 12 Dec. 2008. (www.newscientist.com/article/dn16267-mind-reading-software-could-record-your-dreams/)


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 6,622,036; 7,120,486; 7,177,675; 7,209,788; 7,489,964; 7,697,979; 7,754,190; 7,856,264; 7,873,411; 7,962,204; 8,060,181; 8,224,433; 8,315,962; 8,320,649; 8,326,433; 8,356,004; 8,380,314; 8,386,312; 8,392,253; 8,532,756; 8,562,951; 8,626,264; 8,632,750; 8,655,817; 8,679,009; 8,684,742; 8,684,926; 8,698,639; 8,706,241; 8,725,669; 8,831,731; 8,849,632; 8,855,773; 8,868,174; 8,915,871; 8,918,162; 8,939,903; 8,951,189; 8,951,192; 9,026,217; 9,037,224; 9,042,201; 9,050,470; 9,072,905; 9,084,896; 9,095,266; 9,101,276; 9,101,279; 9,135,221; 9,161,715; 9,192,300; 9,230,065; 9,248,286; 9,248,288; 9,265,458; 9,265,974; 9,292,471; 9,296,382; 9,302,110; 9,308,372; 9,345,412; 9,367,131; 9,420,970; 9,440,646; 9,451,899; 9,454,646; 9,463,327; 9,468,541; 9,474,481; 9,475,502; 9,489,854; 9,505,402; 9,538,948; 9,579,247; 9,579,457; 9,615,746; 9,693,724; 9,693,734; 9,694,155; 9,713,433; 9,713,444; 20030093129; 20030135128; 20040059241; 20050131311; 20050240253; 20060015034; 20060074822; 20060129324; 20060161218; 20060167564; 20060189899; 20060241718; 20070179534; 20070244387; 20080009772; 20080091118; 20080125669; 20080228239; 20090006001; 20090009284; 20090030930; 20090062676; 20090062679; 20090082829; 20090132275; 20090137923; 20090157662; 20090164132; 20090209845; 20090216091; 20090220429; 20090270754; 20090287271; 20090287272; 20090287273; 20090287467; 20090290767; 20090292713; 20090297000; 20090312808; 20090312817; 20090312998; 20090318773; 20090326604; 20090327068; 20100036233; 20100049276; 20100076274; 20100094154; 20100143256; 20100145215; 20100191124; 20100298735; 20110004412; 20110028827; 20110034821; 20110092882; 20110106750; 20110119212; 20110256520; 20110306845; 20110306846; 20110313268; 20110313487; 20120035428; 20120035765; 20120052469; 20120060851; 20120083668; 20120108909; 20120165696; 20120203725; 20120212353; 20120226185; 20120253219; 20120265267; 20120271376; 20120296569; 20130031038; 20130063550; 20130080127; 20130085678; 20130130799; 20130131755; 20130158883; 20130185145; 20130218053; 20130226261; 20130226408; 20130245886; 20130253363; 20130338803; 20140058528; 20140114889; 20140135642; 20140142654; 20140154650; 20140163328; 20140163409; 20140171757; 20140200414; 20140200432; 20140211593; 20140214335; 20140243652; 20140276549; 20140279746; 20140309881; 20140315169; 20140347265; 20140371984; 20150024356; 20150029087; 20150033245; 20150033258; 20150033259; 20150033262; 20150033266; 20150038812; 20150080753; 20150094962; 20150112899; 20150119658; 20150164431; 20150174362; 20150174418; 20150196800; 20150227702; 20150248470; 20150257700; 20150290453; 20150290454; 20150297893; 20150305685; 20150324692; 20150327813; 20150339363; 20150343242; 20150351655; 20150359431; 20150360039; 20150366482; 20160015307; 20160027342; 20160031479; 20160038049; 20160048659; 20160051161; 20160051162; 20160055304; 20160107653; 20160120437; 20160144175; 20160152233; 20160158553; 20160206380; 20160213276; 20160262680; 20160263318; 20160302711; 20160306942; 20160324457; 20160357256; 20160366462; 20170027812; 20170031440; 20170032098; 20170042474; 20170043160; 20170043167; 20170061034; 20170065349; 20170085547; 20170086727; 20170087302; 20170091418; 20170113046; 20170188876; 20170196501; 20170202476; 20170202518; and 20170206913.


Functional Near Infrared Spectroscopy (fNIRS)


fNIR is a non-invasive imaging method involving the quantification of chromophore concentration resolved from the measurement of near infrared (NIR) light attenuation or temporal or phasic changes. NIR spectrum light takes advantage of the optical window in which skin, tissue, and bone are mostly transparent to NIR light in the spectrum of 700-900 nm, while hemoglobin (Hb) and deoxygenated-hemoglobin (deoxy-Hb) are stronger absorbers of light. Differences in the absorption spectra of deoxy-Hb and oxy-Hb allow the measurement of relative changes in hemoglobin concentration through the use of light attenuation at multiple wavelengths. Two or more wavelengths are selected, with one wavelength above and one below the isosbestic point of 810 nm at which deoxy-Hb and oxy-Hb have identical absorption coefficients. Using the modified Beer-Lambert law (mBLL), relative concentration can be calculated as a function of total photon path length. Typically, the light emitter and detector are placed ipsilaterally on the subject's skull so recorded measurements are due to back-scattered (reflected) light following elliptical pathways. The use of fNIR as a functional imaging method relies on the principle of neuro-vascular coupling also known as the haemodynamic response or blood-oxygen-level dependent (BOLD) response. This principle also forms the core of fMRI techniques. Through neuro-vascular coupling, neuronal activity is linked to related changes in localized cerebral blood flow. fNIR and fMRI are sensitive to similar physiologic changes and are often comparative methods. Studies relating fMRI and fNIR show highly correlated results in cognitive tasks. fNIR has several advantages in cost and portability over fMRI, but cannot be used to measure cortical activity more than 4 cm deep due to limitations in light emitter power and has more limited spatial resolution. fNIR includes the use of diffuse optical tomography (DOT/NIRDOT) for functional purposes. Multiplexing fNIRS channels can allow 2D topographic functional maps of brain activity (e.g. with Hitachi ETG-4000 or Artinis Oxymon) while using multiple emitter spacings may be used to build 3D tomographic maps.


Beste Yuksel and Robert Jacob, Brain Automated Chorales (BACh), ACM CHI 2016, DOI: 10.1145/2858036.2858388, provides a system that helps beginners learn to play Bach chorales on piano by measuring how hard their brains are working. This is accomplished by estimating the brain's workload using functional Near-Infrared Spectroscopy (fNIRS), a technique that measures oxygen levels in the brain—in this case in the prefrontal cortex. A brain that's working hard pulls in more oxygen. Sensors strapped to the player's forehead talk to a computer, which delivers the new music, one line at a time. See also “Mind-reading tech helps beginners quickly learn to play Bach.” By Anna Nowogrodzki, New Scientist, 9 Feb. 2016 available online at www.newscientist.com/article/2076899-mind-reading-tech-helps-beginners-quickly-learn-to-play-bach/.


LORETA


Low-resolution brain electromagnetic tomography often referred as LORETA is a functional imaging technology usually using a linearly constrained minimum variance vector beamformer in the time-frequency domain as described in Gross et al., ““Dynamic imaging of coherent sources: Studying neural interactions in the human brain””, PNAS 98, 694-699, 2001. It allows to the image (mostly 3D) evoked and induced oscillatory activity in a variable time-frequency range, where time is taken relative to a triggered event. There are three categories of imaging related to the technique used for LORETA. See, wiki.besa.deindex.ph p?title=Source_Analysis_3D_Imaging#Multiple_Source_Beamformer_0.28MSBF.29. The Multiple Source Beamformer (MSBF) is a tool for imaging brain activity. It is applied in the time-frequency domain and based on single-trial data. Therefore, it can image not only evoked, but also induced activity, which is not visible in time-domain averages of the data. Dynamic Imaging of Coherent Sources (DICS) can find coherence between any two pairs of voxels in the brain or between an external source and brain voxels. DICS requires time-frequency-transformed data and can find coherence for evoked and induced activity. The following imaging methods provides an image of brain activity based on a distributed multiple source model: CLARA is an iterative application of LORETA images, focusing the obtained 3D image in each iteration step. LAURA uses a spatial weighting function that has the form of a local autoregressive function. LORETA has the 3D Laplacian operator implemented as spatial weighting prior. sLORETA is an unweighted minimum norm that is standardized by the resolution matrix. swLORETA is equivalent to sLORETA, except for an additional depth weighting. SSLOFO is an iterative application of standardized minimum norm images with consecutive shrinkage of the source space. A User-defined volume image allows experimenting with the different imaging techniques. It is possible to specify user-defined parameters for the family of distributed source images to create a new imaging technique. If no individual MRI is available, the minimum norm image is displayed on a standard brain surface and computed for standard source locations. If available, an individual brain surface is used to construct the distributed source model and to image the brain activity. Unlike classical LORETA, cortical LORETA is not computed in a 3D volume, but on the cortical surface. Unlike classical CLARA, cortical CLARA is not computed in a 3D volume, but on the cortical surface. The Multiple Source Probe Scan (MSPS) is a tool for the validation of a discrete multiple source model. The Source Sensitivity image displays the sensitivity of a selected source in the current discrete source model and is, therefore, data independent.


See U.S. Pat. Appl. Nos. and U.S. Pat. Nos. 4,562,540; 4,594,662; 5,650,726; 5,859,533; 6,026,173; 6,182,013; 6,294,917; 6,332,087; 6,393,363; 6,534,986; 6,703,838; 6,791,331; 6,856,830; 6,863,127; 7,030,617; 7,092,748; 7,119,553; 7,170,294; 7,239,731; 7,276,916; 7,286,871; 7,295,019; 7,353,065; 7,363,164; 7,454,243; 7,499,894; 7,648,498; 7,804,441; 7,809,434; 7,841,986; 7,852,087; 7,937,222; 8,000,795; 8,046,076; 8,131,526; 8,174,430; 8,188,749; 8,244,341; 8,263,574; 8,332,191; 8,346,365; 8,362,780; 8,456,166; 8,538,700; 8,565,883; 8,593,154; 8,600,513; 8,706,205; 8,711,655; 8,731,987; 8,756,017; 8,761,438; 8,812,237; 8,829,908; 8,958,882; 9,008,970; 9,035,657; 9,069,097; 9,072,449; 9,091,785; 9,092,895; 9,121,964; 9,133,709; 9,165,472; 9,179,854; 9,320,451; 9,367,738; 9,414,749; 9,414,763; 9,414,764; 9,442,088; 9,468,541; 9,513,398; 9,545,225; 9,557,439; 9,562,988; 9,568,635; 9,651,706; 9,675,254; 9,675,255; 9,675,292; 9,713,433; 9,715,032; 20020000808; 20020017905; 20030018277; 20030093004; 20040097802; 20040116798; 20040131998; 20040140811; 20040145370; 20050156602; 20060058856; 20060069059; 20060136135; 20060149160; 20060152227; 20060170424; 20060176062; 20060184058; 20060206108; 20070060974; 20070159185; 20070191727; 20080033513; 20080097235; 20080125830; 20080125831; 20080183072; 20080242976; 20080255816; 20080281667; 20090039889; 20090054801; 20090082688; 20090099783; 20090216146; 20090261832; 20090306534; 20090312663; 20100010366; 20100030097; 20100042011; 20100056276; 20100092934; 20100132448; 20100134113; 20100168053; 20100198519; 20100231221; 20100238763; 20110004115; 20110050232; 20110160607; 20110308789; 20120010493; 20120011927; 20120016430; 20120083690; 20120130641; 20120150257; 20120162002; 20120215448; 20120245474; 20120268272; 20120269385; 20120296569; 20130091941; 20130096408; 20130141103; 20130231709; 20130289385; 20130303934; 20140015852; 20140025133; 20140058528; 20140066739; 20140107519; 20140128763; 20140155740; 20140161352; 20140163328; 20140163893; 20140228702; 20140243714; 20140275944; 20140276012; 20140323899; 20150051663; 20150112409; 20150119689; 20150137817; 20150145519; 20150157235; 20150167459; 20150177413; 20150248615; 20150257648; 20150257649; 20150301218; 20150342472; 20160002523; 20160038049; 20160040514; 20160051161; 20160051162; 20160091448; 20160102500; 20160120436; 20160136427; 20160187524; 20160213276; 20160220821; 20160223703; 20160235983; 20160245952; 20160256109; 20160259085; 20160262623; 20160298449; 20160334534; 20160345856; 20160356911; 20160367812; 20170001016; 20170067323; 20170138132; and 20170151436.


Neurofeedback


Neurofeedback (NFB), also called neurotherapy or neurobiofeedback, is a type of biofeedback that uses real-time displays of brain activity-most commonly electroencephalography (EEG), to teach self-regulation of brain function. Typically, sensors are placed on the scalp to measure activity, with measurements displayed using video displays or sound. The feedback may be in various other forms as well. Typically, the feedback is sought to be presented through primary sensory inputs, but this is not a limitation on the technique.


The applications of neurofeedback to enhance performance extend to the arts in fields such as music, dance, and acting. A study with conservatoire musicians found that alpha-theta training benefitted the three music domains of musicality, communication, and technique. Historically, alpha-theta training, a form of neurofeedback, was created to assist creativity by inducing hypnagogia, a “borderline waking state associated with creative insights”, through facilitation of neural connectivity. Alpha-theta training has also been shown to improve novice singing in children. Alpha-theta neurofeedback, in conjunction with heart rate variability training, a form of biofeedback, has also produced benefits in dance by enhancing performance in competitive ballroom dancing and increasing cognitive creativity in contemporary dancers. Additionally, neurofeedback has also been shown to instill a superior flow state in actors, possibly due to greater immersion while performing.


Several studies of brain wave activity in experts while performing a task related to their respective area of expertise revealed certain characteristic telltale signs of so-called “flow” associated with top-flight performance. Mihaly Csikszentmihalyi (University of Chicago) found that the most skilled chess players showed less EEG activity in the prefrontal cortex, which is typically associated with higher cognitive processes such as working memory and verbalization, during a game.


Chris Berka et al., Advanced Brain Monitoring, Carlsbad, Calif., The International J. Sport and Society, vol 1, p 87, looked at the brain waves of Olympic archers and professional golfers. A few seconds before the archers fired off an arrow or the golfers hit the ball, the team spotted a small increase in alpha band patterns. This may correspond to the contingent negative variation observed in evoked potential studies, and the Bereitschaftspotential or BP (from German, “readiness potential”), also called the pre-motor potential or readiness potential (RP), a measure of activity in the motor cortex and supplementary motor area of the brain leading up to voluntary muscle movement. Berka also trained novice marksmen using neurofeedback. Each person was hooked up to electrodes that tease out and display specific brain waves, along with a monitor that measured their heartbeat. By controlling their breathing and learning to deliberately manipulate the waveforms on the screen in front of them, the novices managed to produce the alpha waves characteristic of the flow state. This, in turn, helped them improve their accuracy at hitting the targets.


Low Energy Neurofeedback System (LENS)


The LENS, or Low Energy Neurofeedback System, uses a very low power electromagnetic field, to carry feedback to the person receiving it. The feedback travels down the same wires carrying the brain waves to the amplifier and computer. Although the feedback signal is weak, it produces a measurable change in the brainwaves without conscious effort from the individual receiving the feedback. The system is software controlled, to receive input from EEG electrodes, to control the stimulation. Through the scalp. Neurofeedback uses a feedback frequency that is different from, but correlates with, the dominant brainwave frequency. When exposed to this feedback frequency, the EEG amplitude distribution changes in power. Most of the time the brain waves reduce in power; but at times they also increase in power. In either case the result is a changed brainwave state, and much greater ability for the brain to regulate itself.


Content-Based Brainwave Analysis


Memories are not unique. Janice Chen, Nature Neuroscience, DOI: 10.1038/nn.4450, showed that when people describe the episode from Sherlock Holmes drama, their brain activity patterns were almost exactly the same as each other's, for each scene. Moreover, there's also evidence that, when a person tells someone else about it, they implant that same activity into their brain as well. Moreover, research in which people who have not seen a movie listen to someone else's description of it, Chen et al. have found that the listener's brain activity looks much like that of the person who has seen it. See also “Our brains record and remember things in exactly the same way” by Andy Coghlan, New Scientist, Dec. 5, 2016 (www.newscientist.com/artie/2115093-our-brains-record-and-remember-things-in-exactly-the-same-way/)


Brian Pasley, Frontiers in Neuroengineering, doi.org/whb, developed a technique for reading thoughts. The team hypothesized that hearing speech and thinking to oneself might spark some of the same neural signatures in the brain. They supposed that an algorithm trained to identify speech heard out loud might also be able to identify words that are thought. In the experiment, the decoder trained on speech was able to reconstruct which words several of the volunteers were thinking, using neural activity alone. See also “Hearing our inner voice” by Helen Thomson. New Scientist, Oct. 29, 2014 (www.newscientist.com/article/mg22429934-000-brain-decoder-can-eavesdrop-on-your-inner-voice/)


Jack Gallant et al. were able to detect which of a set of images someone was looking at from a brain scan, using software that compared the subject's brain activity while looking at an image with that captured while they were looking at “training” photographs. The program then picked the most likely match from a set of previously unseen pictures.


Ann Graybiel and Mark Howe used electrodes to analyze brainwaves in the ventromedial striatum of rats while they were taught to navigate a maze. As rats were learning the task, their brain activity showed bursts of fast gamma waves. Once the rats mastered the task, their brainwaves slowed to almost a quarter of their initial frequency, becoming beta waves. Graybiel's team posited that this transition reflects when learning becomes a habit.


Bernard Balleine, Proceedings of the National Academy of Sciences, DOI: 10.1073/pnas.1113158108. See also “Habits form when brainwaves slow down” by Wendy Zukerman. New Scientist, Sep. 26, 2011 (www.newscientist.com/article/dn20964-habits-form-when-brainwaves-slow-down/) posits that the slower brainwaves may be the brain weeding out excess activity to refine behavior. He suggests it might be possible to boost the rate at which they learn a skill by enhancing such beta-wave activity.


U.S. Pat. No. 9,763,592 provides a system for instructing a user behavior change comprising: collecting and analyzing bioelectrical signal datasets; and providing a behavior change suggestion based upon the analysis. A stimulus may be provided to prompt an action by the user, which may be visual, auditory, or haptic. See also U.S. Pat. Nos. 9,622,660, 20170041699; 20130317384; 20130317382; 20130314243; 20070173733; and 20070066914.


The chess game is a good example of a cognitive task which needs a lot of training and experience. A number of EEG studies have been done on chess players. Pawel Stepien, Wlodzimierz Klonowski and Nikolay Suvorov, Nonlinear analysis of EEG in chess players, EPJ Nonlinear Biomedical Physics 20153:1, showed better applicability of Higuchi Fractal Dimension method for analysis of EEG signals related to chess tasks than that of Sliding Window Empirical Mode Decomposition. The paper shows that the EEG signal during the game is more complex, non-linear, and non-stationary even when there are no significant differences between the game and relaxed state in the contribution of different EEG bands to total power of the signal. There is the need of gathering more data from more chess experts and of comparing them with data from novice chess players. See also Junior, L. R. S., Cesar, F. H. G., Rocha, F. T., and Thomaz, C. E. EEG and Eye Movement Maps of Chess Players. Proceedings of the Sixth International Conference on Pattern Recognition Applications and Methods. (ICPRAM 2017) pp. 343-441. (fei.edu.br/˜cet/icpram17_LaercioJunior.pdf).


Estimating EEG-based functional connectivity provides a useful tool for studying the relationship between brain activity and emotional states. See You-Yun Lee, Shulan Hsieh. Classifying Different Emotional States by Means of EEG-Based Functional Connectivity Patterns. Apr. 17, 2014, (doi.org/10.1371/journal.pone.0095415), which aimed to classify different emotional states by means of EEG-based functional connectivity patterns, and showed that the EEG-based functional connectivity change was significantly different among emotional states. Furthermore, the connectivity pattern was detected by pattern classification analysis using Quadratic Discriminant Analysis. The results indicated that the classification rate was better than chance. Estimating EEG-based functional connectivity provides a useful tool for studying the relationship between brain activity and emotional states.


Neuromodulation/Neuroenhancement


Neuromodulation is the alteration of nerve activity through targeted delivery of a stimulus, such as electrical stimulation or chemical agents, to specific neurological sites in the body. It is carried out to normalize—or modulate—nervous tissue function. Neuromodulation is an evolving therapy that can involve a range of electromagnetic stimuli such as a magnetic field (TMS, rTMS), an electric current (TES, e.g., tDCS, HD-tDCS, tACS, electrosleep), or a drug instilled directly in the subdural space (intrathecal drug delivery). Emerging applications involve targeted introduction of genes or gene regulators and light (optogenetics). The most clinical experience has been with electrical stimulation. Neuromodulation, whether electrical or magnetic, employs the body's natural biological response by stimulating nerve cell activity that can influence populations of nerves by releasing transmitters, such as dopamine, or other chemical messengers such as the peptide Substance P, that can modulate the excitability and firing patterns of neural circuits. There may also be more direct electrophysiological effects on neural membranes. According to some applications, the end effect is a “normalization” of a neural network function from its perturbed state. Presumed mechanisms of action for neurostimulation include depolarizing blockade, stochastic normalization of neural firing, axonal blockade, reduction of neural firing keratosis, and suppression of neural network oscillations. Although the exact mechanisms of neurostimulation are not known, the empirical effectiveness has led to considerable application clinically.


Neuroenhancement refers to the targeted enhancement and extension of cognitive and affective abilities based on an understanding of their underlying neurobiology in healthy persons who do not have any mental illness. As such, it can be thought of as an umbrella term that encompasses pharmacological and non-pharmacological methods of improving cognitive, affective, and motor functionality, as well as the overarching ethico-legal discourse that accompanies these aims. Critically, for any agent to qualify as a neuroenhancer, it must reliably engender substantial cognitive, affective, or motor benefits beyond normal functioning in healthy individuals (or in select groups of individuals having pathology), whilst causing few side effects: at most at the level of commonly used comparable legal substances or activities, such as caffeine, alcohol, and sleep-deprivation. Pharmacological neuroenhancement agents include the well-validated nootropics, such as racetam, vinpocetine, and phosphatidylserine, as well as other drugs used for treating patients suffering from neurological disorders. Non-pharmacological measures include non-invasive brain stimulation, which has been employed to improve various cognitive and affective functions, and brain-machine interfaces, which hold much potential to extend the repertoire of motor and cognitive actions available to humans.


Brain Stimulation


Non-invasive brain stimulation (NIBS) bypasses the correlative approaches of other imaging techniques, making it possible to establish a causal relationship between cognitive processes and the functioning of specific brain areas. NIBS can provide information about where a particular process occurs. NIBS offers the opportunity to study brain mechanisms beyond process localization, providing information about when activity in a given brain region is involved in a cognitive process, and even how it is involved. When using NIBS to explore cognitive processes, it is important to understand not only how NIBS functions but also the functioning of the neural structures themselves. Non-invasive brain stimulation (NIBS) methods, which include transcranial magnetic stimulation (TMS) and transcranial electric stimulation (TES), are used in cognitive neuroscience to induce transient changes in brain activity and thereby alter the behavior of the subject.


The application of NIBS aims at establishing the role of a given cortical area in an ongoing specific motor, perceptual or cognitive process. Physically, NIBS techniques affect neuronal states through different mechanisms. In TMS, a solenoid (coil) is used to deliver a strong and transient magnetic field, or “pulse,” to induce a transitory electric current at the cortical surface beneath the coil. The pulse causes the rapid and above-threshold depolarization of cell membranes affected by the current, followed by the transynaptic depolarization or hyperpolarization of interconnected neurons. Therefore, strong TMS can induce a current that elicits action potentials in neurons, while weak (subthreshold) can modify susceptibility of cells to depolarization. A complex set of coils can deliver a complex 3D excitation field. By contrast, in TES techniques, the stimulation involves the application of weak electrical currents directly to the scalp through a pair of electrodes. As a result, TES induces a subthreshold polarization of cortical neurons that is too weak to generate an action potential. (Superthreshold tES corresponds to electroconvulsive therapy, which is a currently disfavored, but apparently effective treatment for depression). However, by changing the intrinsic neuronal excitability, TES can induce changes in the resting membrane potential and the postsynaptic activity of cortical neurons. This, in turn, can alter the spontaneous firing rate of neurons and modulate their response to afferent signals, leading to changes in synaptic efficacy. The typical application of NIBS involves different types of protocols: TMS can be delivered as a single pulse (spTMS) at a precise time, as pairs of pulses separated by a variable interval, or as a series of stimuli in conventional or patterned protocols of repetitive TMS (rTMS). In TES, different protocols are established by the electrical current used and by its polarity, which can be direct (anodal or cathodal transcranial direct current stimulation: tDCS), alternating at a fix frequency (transcranial alternating current stimulation: tACS), oscillating transcranial direct current stimulation (osc-tDCS), high-definition transcranial direct current stimulation (HD-tDCS), or at random frequencies (transcranial random noise stimulation: tRNS).


In general, the final effects of NIBS on the central nervous system depend on a lengthy list of parameters (e.g., frequency, temporal characteristics, intensity, geometric configuration of the coil/electrode, current direction), when it is delivered before (off-line) or during (on-line) the task as part of the experimental procedure. In addition, these factors interact with several variables related to the anatomy (e.g., properties of the brain tissue and its location), as well as physiological (e.g., gender and age) and cognitive states of the stimulated area/subject. The entrainment hypothesis, suggests the possibility of inducing a particular oscillation frequency in the brain using an external oscillatory force (e.g., rTMS, but also tACS). The physiological basis of oscillatory cortical activity lies in the timing of the interacting neurons; when groups of neurons synchronize their firing activities, brain rhythms emerge, network oscillations are generated, and the basis for interactions between brain areas may develop. Because of the variety of experimental protocols for brain stimulation, limits on descriptions of the actual protocols employed, and limited controls, consistency of reported studies is lacking, and extrapolability is limited. Thus, while there is some consensus in various aspects of the effects of extra cranial brain stimulation, the results achieved have a degree of uncertainty dependent on details of implementation. On the other hand, within a specific experimental protocol, it is possible to obtain statistically significant and repeatable results. This implies that feedback control might be effective to control implementation of the stimulation for a given purpose; however, prior studies that employ feedback control are lacking.


Changes in the neuronal threshold result from changes in membrane permeability (Liebetanz et al., 2002), which influence the response of the task-related network. The same mechanism of action may be responsible for both TES methods and TMS, i.e., the induction of noise in the system. However, the neural activity induced by TES will be highly influenced by the state of the system because it is a neuromodulatory method (Paulus, 2011), and its effect will depend on the activity of the stimulated area. Therefore, the final result will depend strongly on the task characteristics, the system state and the way in which TES will interact with such a state.


In TMS, the magnetic pulse causes a rapid increase in current flow, which can in some cases cause and above-threshold depolarization of cell membranes affected by the current, triggering an action potential, and leading to the trans-synaptic depolarization or hyperpolarization of connected cortical neurons, depending on their natural response to the firing of the stimulated neuron(s). Therefore, TMS activates a neural population that, depending on several factors, can be congruent (facilitate) or incongruent (inhibit) with task execution. TES induces a polarization of cortical neurons at a subthreshold level that is too weak to evoke an action potential. However, by inducing a polarity shift in the intrinsic neuronal excitability, TES can alter the spontaneous firing rate of neurons and modulate the response to afferent signals. In this sense, TES-induced effects are even more bound to the state of the stimulated area that is determined by the conditions. In short, NIBS leads to a stimulation-induced modulation of the state that can be substantially defined as noise induction. Induced noise will not be just random activity, but will depend on the interaction of many parameters, from the characteristics of the stimulation to the state.


The noise induced by NIBS will be influenced by the state of the neural population of the stimulated area. Although the types and number of neurons “triggered” by NIBS are theoretically random, the induced change in neuronal activity is likely to be correlated with ongoing activity, yet even if we are referring to a non-deterministic process, the noise introduced will not be a totally random element. Because it will be partially determined by the experimental variables, the level of noise that will be introduced by the stimulation and by the context can be estimated, as well as the interaction between the two levels of noise (stimulation and context). Known transcranial stimulation does not permit stimulation with a focused and highly targeted signal to a clearly defined area of the brain to establish a unique brain-behavior relationship; therefore, the known introduced stimulus activity in the brain stimulation is ‘noise.’


Cosmetic neuroscience has emerged as a new field of research. Roy Hamilton, Samuel Messing, and Anjan Chatterjee, “Rethinking the thinking cap—Ethics of neural enhancement using noninvasive brain stimulation.” Neurology, Jan. 11, 2011, vol. 76 no. 2187-193. (www.neurology.org/content/76/2/187.) discuss the use noninvasive brain stimulation techniques such as transcranial magnetic stimulation and transcranial direct current stimulation to enhance neurologic function: cognitive skills, mood, and social cognition.


Electrical brain stimulation (EBS), or focal brain stimulation (FBS), is a form of clinical neurobiology electrotherapy used to stimulate a neuron or neural network in the brain through the direct or indirect excitation of cell membranes using an electric current. See, en.wikipedia.org/wiki/Electrical_brain_stimulation; U.S. Pub. App. Nos. and U.S. Pat. Nos. 7,753,836; 7,94673; 8,545,378; 9,345,901; 9,610,456; 9,694,178; 20140330337; 20150112403; and 20150119689.


Motor skills can be affected by CNS stimulation.


See, U.S. Pat. Nos. 5,343,871; 5,742,748; 6,057,846; 6,390,979; 6,644,976; 6,656,137; 7,063,535; 7,558,622; 7,618,381; 7,733,224; 7,829,562; 7,863,272; 8,016,597; 8,065,240; 8,069,125; 8,108,036; 8,126,542; 8,150,796; 8,195,593; 8,356,004; 8,449,471; 8,461,988; 8,525,673; 8,525,687; 8,531,291; 8,591,419; 8,606,592; 8,615,479; 8,680,991; 8,682,449; 8,706,518; 8,747,336; 8,750,971; 8,764,651; 8,784,109; 8,858,440; 8,862,236; 8,938,289; 8,962,042; 9,005,649; 9,064,036; 9,107,586; 9,125,788; 9,138,579; 9,149,599; 9,173,582; 9,204,796; 9,211,077; 9,265,458; 9,351,640; 9,358,361; 9,380,976; 9,403,038; 9,418,368; 9,468,541; 9,495,684; 9,545,515; 9,549,691; 9,560,967; 9,577,992; 9,590,986; 20030068605; 20040072133; 20050020483; 20050032827; 20050059689; 20050153268; 20060014753; 20060052386; 20060106326; 20060191543; 20060229164; 20070031798; 20070138886; 20070276270; 20080001735; 20080004904; 20080243005; 20080287821; 20080294019; 20090005654; 20090018407; 20090024050; 20090118593; 20090119154; 20090132275; 20090156907; 20090156955; 20090157323; 20090157481; 20090157482; 20090157625; 20090157660; 20090157751; 20090157813; 20090163777; 20090164131; 20090164132; 20090164302; 20090164401; 20090164403; 20090164458; 20090164503; 20090164549; 20090171164; 20090172540; 20090221928; 20090267758; 20090271011; 20090271120; 20090271347; 20090312595; 20090312668; 20090318773; 20090318779; 20090319002; 20100004762; 20100015583; 20100017001; 20100022820; 20100041958; 20100042578; 20100063368; 20100069724; 20100076249; 20100081860; 20100081861; 20100100036; 20100125561; 20100130811; 20100145219; 20100163027; 20100163035; 20100168525; 20100168602; 20100280332; 20110015209; 20110015469; 20110082154; 20110105859; 20110115624; 20110152284; 20110178441; 20110181422; 20110288119; 20120092156; 20120092157; 20120130300; 20120143104; 20120164613; 20120177716; 20120316793; 20120330109; 20130009783; 20130018592; 20130034837; 20130053656; 20130054215; 20130085678; 20130121984; 20130132029; 20130137717; 20130144537; 20130184728; 20130184997; 20130211291; 20130231574; 20130281890; 20130289385; 20130330428; 20140039571; 20140058528; 20140077946; 20140094720; 20140104059; 20140148479; 20140155430; 20140163425; 20140207224; 20140235965; 20140249429; 20150025410; 20150025422; 20150068069; 20150071907; 20150141773; 20150208982; 20150265583; 20150290419; 20150294067; 20150294085; 20150294086; 20150359467; 20150379878; 20160001096; 20160007904; 20160007915; 20160030749; 20160030750; 20160067492; 20160074657; 20160120437; 20160140834; 20160198968; 20160206671; 20160220821; 20160303402; 20160351069; 20160360965; 20170046971; 20170065638; 20170080320; 20170084187; 20170086672; 20170112947; 20170127727; 20170131293; 20170143966; 20170151436; 20170157343; and 20170193831.

  • See: Abraham, W. C., 2008. Metaplasticity: tuning synapses and networks for plasticity. Nature Reviews Neuroscience 9, 387.
  • Abrahamyan, A., Clifford, C. W., Arabzadeh, E., Harris, J. A., 2011. Improving visual sensitivity with subthreshold transcranial magnetic stimulation. J. Neuroscience 31, 3290-3294.
  • Adrian, E. D., 1928. The Basis of Sensation. W. W. Norton, New York.
  • Amassian, V. E., Cracco, R. Q., Maccabee, P. J., Cracco, J. B., Rudell, A., Eberle, L., 1989. Suppression of visual perception by magnetic coil stimulation of human occipital cortex. Electroencephalography and Clin. Neurophysiology 74, 458-462.
  • Amassian, V. E., Eberle, L., Maccabee, P. J., Cracco, R. Q., 1992. Modelling magnetic coil excitation of human cerebral cortex with a peripheral nerve immersed in a brain-shaped volume conductor the significance of fiber bending in excitation. Electroencephalography and Clin. Neurophysiology 85, 291-301.
  • Antal, A., Boros, K., Poreisz, C., Chaieb, L., Terney, D., Paulus, W., 2008. Comparatively weak after-effects of transcranial alternating current stimulation (tACS) on cortical excitability in humans. Brain Stimulation 1, 97-105.
  • Antal, A., Nitsche, M. A., Kruse, W., Kincses, T. Z., Hoffmann, K. P., Paulus, W., 2004. Direct current stimulation over V5 enhances visuomotor coordination by improving motion perception in humans. J. Cognitive Neuroscience 16, 521-527.
  • Ashbridge, E., Walsh, V., Cowey, A., 1997. Temporal aspects of visual search studied by transcranial magnetic stimulation. Neuropsychologia 35, 1121-1131.
  • Barker, A. T., Freeston, I. L., Jalinous, R., Jarratt, J. A., 1987. Magnetic stimulation of the human brain and peripheral nervous system: an introduction and the results of an initial clinical evaluation. Neurosurgery 20, 100-109.
  • Barker, A. T., Jalinous, R., Freeston, I. L., 1985. Non-invasive magnetic stimulation of human motor cortex. Lancet 1, 1106-1107.
  • Bi, G., Poo, M., 2001. Synaptic modification by correlated activity: Hebb's postulate revisited. Annual Review of Neuroscience 24, 139-166.
  • Bialek, W., Rieke, F., 1992. Reliability and information transmission in spiking neurons. Trends in Neurosciences 15, 428-434.
  • Bienenstock, E. L., Cooper, L. N., Munro, P. W., 1982. Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex. J. Neuroscience 2, 32-48.
  • Bindman, L. J., Lippold, O. C., Milne, A. R., 1979. Prolonged changes in excitability of pyramidal tract neurones in the cat: a post-synaptic mechanism. J. Physiology 286, 457-477.
  • Bindman, L. J., Lippold, O. C., Redfeam, J. W., 1962. Long-lasting changes in the level of the electrical activity of the cerebral cortex produced by polarizing currents. Nature 196, 584-585.
  • Bindman, L. J., Lippold, O. C., Redfeam, J. W., 1964. The action of brief polarizing currents on the cerebral cortex of the rat (1) during current flow and (2) in the production of long-lasting after-effects. J. Physiology 172, 369-382.
  • Brignani, D., Ruzzoli, M., Mauri, P., Miniussi, C., 2013. Is transcranial alternating current stimulation effective in modulating brain oscillations? PLoS ONE 8, e56589. Buzsaki, G., 2006. Rhythms of the Brain. Oxford University Press, Oxford.
  • Canolty, R. T., Knight, R. T., 2010. The functional role of cross-frequency coupling. Trends in Cognitive Sciences 14, 506-515.
  • Carandini, M., Ferster, D., 1997. A tonic hyperpolarization underlying contrast adaptation in cat visual cortex. Science 276, 949-952.
  • Cattaneo, L., Sandrini, M., Schwarzbach, J., 2010. State-dependent TMS reveals a hierarchical representation of observed acts in the temporal, parietal, and premotor cortices. Cerebral Cortex 20, 2252-2258.
  • Cattaneo, Z., Rota, F., Vecchi, T., Silvanto, J., 2008. Using state-dependency of trans-cranial magnetic stimulation (TMS) to investigate letter selectivity in the left posterior parietal cortex: a comparison of TMS-priming and TMS-adaptation paradigms. Eur. J. Neuroscience 28, 1924-1929.
  • Chambers, C. D., Payne, J. M., Stokes, M. G., Mattingley, J. B., 2004. Fast and slow parietal pathways mediate spatial attention. Nature Neuroscience 7, 217-218.
  • Corthout, E., Uttl, B., Walsh, V., Hallett, M., Cowey, A., 1999. Timing of activity in early visual cortex as revealed by transcranial magnetic stimulation. Neuroreport 10, 2631-2634.
  • Creutzfeldt, O. D., Fromm, G. H., Kapp, H., 1962. Influence of transcortical d-c currents on cortical neuronal activity. Experimental Neurology 5, 436-452.
  • Deans, J. K., Powell, A. D., Jefferys, J. G., 2007. Sensitivity of coherent oscillations in rat hippocampus to A C electric fields. J. Physiology 583, 555-565.
  • Dockery, C. A., Hueckel-Weng, R., Birbaumer, N., Plewnia, C., 2009. Enhancement of planning ability by transcranial direct current stimulation. J. Neuroscience 29, 7271-7277.
  • Ermentrout, G. B., Galan, R. F., Urban, N. N., 2008. Reliability, synchrony and noise. Trends in Neurosciences 31, 428-434.
  • Epstein, C. M., Rothwell, J. C., 2003. Therapeutic uses of rTMS. Cambridge University Press, Cambridge, pp. 246-263.
  • Faisal, A. A., Selen, L. P., Wolpert, D. M., 2008. Noise in the nervous system. Nature Reviews Neuroscience 9, 292-303.
  • Ferbert, A., Caramia, D., Priori, A., Bertolasi, L., Rothwell, J. C., 1992. Cortical projection to erector spinae muscles in man as assessed by focal transcranial magnetic stimulation. Electroencephalography and Clin. Neurophysiology 85, 382-387.
  • Fertonani, A., Pirulli, C., Miniussi, C., 2011. Random noise stimulation improves neuroplasticity in perceptual learning. J. Neuroscience 31, 15416-15423. Feurra, M., Galli, G., Rossi, 5., 2012. Transcranial alternating current stimulation affects decision making. Frontiers in Systems Neuroscience 6, 39.
  • Guyonneau, R., Vanrullen, R., Thorpe, S. J., 2004. Temporal codes and sparse representations: a key to understanding rapid processing in the visual system. J. Physiology, Paris 98, 487-497.
  • Hallett, M., 2000. Transcranial magnetic stimulation and the human brain. Nature 406, 147-150.
  • Harris, I. M., Miniussi, C., 2003. Parietal lobe contribution to mental rotation demonstrated with rTMS. J. Cognitive Neuroscience 15, 315-323.
  • Harris, J. A., Clifford, C. W., Miniussi, C., 2008. The functional effect of transcranial magnetic stimulation: signal suppression or neural noise generation. J. Cognitive Neuroscience 20, 734-740.
  • Hebb, D. O., 1949. The Organization of Behavior; A Neuropsychological Theory. Wiley, New York.
  • Hutcheon, B., Yarom, Y., 2000. Resonance, oscillation and the intrinsic frequency preferences of neurons. Trends in Neurosciences 23, 216-222.
  • Jacobson, L., Koslowsky, M., Lavidor, M., 2011. tDCS polarity effects in motor and cognitive domains: a meta-analytical review. Experimental Brain Research 216, 1-10.
  • Joundi, R. A., Jenkinson, N., Brittain, J. S., Aziz, T. Z., Brown, P., 2012. Driving oscillatory activity in the human cortex enhances motor performance. Current Biology 22, 403-407.
  • Kahn, I., Pascual-Leone, A., Theoret, H., Fregni, F., Clark, D., Wagner, A. D., 2005. Transient disruption of ventrolateral prefrontal cortex during verbal encoding affects subsequent memory performance. J. Neurophysiology 94, 688-698.
  • Kanai, R., Chaieb, L., Antal, A., Walsh, V., Paulus, W., 2008. Frequency-dependent electrical stimulation of the visual cortex. Current Biology 18, 1839-1843.
  • Kitajo, K., Doesburg, S. M., Yamanaka, K., Nozaki, D., Ward, L. M., Yamamoto, Y., 2007. Noise-induced large-scale phase synchronization of human-brain activity associated with behavioral stochastic resonance. EPL—Europhysics Letters, 80.
  • Kitajo, K., Nozaki, D., Ward, L. M., Yamamoto, Y., 2003. Behavioral stochastic resonance within the human brain. Physical Review Letters 90, 218103.
  • Landi, D., Rossini, P. M., 2010. Cerebral restorative plasticity from normal aging to brain diseases: a never-ending story. Restorative Neurology and Neuroscience 28, 349-366.
  • Lang, N., Rothkegel, H., Reiber, H., Hasan, A., Sueske, E., Tergau, F., Ehrenreich, H., Wuttke, W., Paulus, W., 2011. Circadian modulation of GABA-mediated cortical inhibition. Cerebral Cortex 21, 2299-2306.
  • Laycock, R., Crewther, D. P., Fitzgerald, P. B., Crewther, S. G., 2007. Evidence for fast signals and later processing in human V1/V2 and V5/MT+. A TMS study of motion perception. J. Neurophysiology 98, 1253-1262.
  • Liebetanz, D., Nitsche, M. A., Tergau, F., Paulus, W., 2002. Pharmacological approach to the mechanisms of transcranial D C-stimulation-induced after-effects of human motor cortex excitability. Brain 125, 2238-2247.
  • Longtin, A., 1997. Autonomous stochastic resonance in bursting neurons. Physical Review E 55, 868-876.
  • Manenti, R., Cappa, S. F., Rossini, P. M., Miniussi, C., 2008. The role of the prefrontal cortex in sentence comprehension: an rTMS study. Cortex 44, 337-344.
  • Marzi, C. A., Miniussi, C., Maravita, A., Bertolasi, L., Zanette, G., Rothwell, J. C., Sanes, J. N., 1998. Transcranial magnetic stimulation selectively impairs interhemispheric transfer of visuo-motor information in humans. Experimental Brain Research 118, 435-438.
  • Masquelier, T., Thorpe, S. J., 2007. Unsupervised learning of visual features through spike timing dependent plasticity. PLOS Computational Biology 3, e31.
  • Miniussi, C., Brignani, D., Pellicciari, M. C., 2012a. Combining transcranial electrical stimulation with electroencephalography: a multimodal approach. Clin. EEG and Neuroscience 43, 184-191.
  • Miniussi, C., Paulus, W., Rossini, P. M., 2012b. Transcranial Brain Stimulation. CRC Press, Boca Raton, Fla.
  • Miniussi, C., Ruzzoli, M., Walsh, V., 2010. The mechanism of transcranial magnetic stimulation in cognition. Cortex 46, 128-130.
  • Moliadze, V., Zhao, Y., Eysel, U., Funke, K., 2003. Effect of transcranial magnetic stimulation on single-unit activity in the cat primary visual cortex. J. Physiology 553, 665-679.
  • Moss, F., Ward, L. M., Sannita, W. G., 2004. Stochastic resonance and sensory information processing: a tutorial and review of application. Clin. Neurophysiology 115, 267-281.
  • Mottaghy, F. M., Gangitano, M., Krause, B J., Pascual-Leone, A., 2003. Chronometry of parietal and prefrontal activations in verbal working memory revealed by transcranial magnetic stimulation. Neuroimage 18, 565-575.
  • Nachmias, J., Sansbury, R. V., 1974. Grating contrast: discrimination may be better than detection. Vision Research 14, 1039-1042.
  • Nitsche, M. A., Cohen, L. G., Wassermann, E. M., Priori, A., Lang, N., Antal, A., Paulus, W., Hummel, F., Boggio, P. S., Fregni, F., Pascual-Leone, A., 2008. Transcranial direct current stimulation: state of the art 2008. Brain Stimulation 1, 206-223.
  • Nitsche, M. A., Liebetanz, D., Lang, N., Antal, A., Tergau, F., Paulus, W., 2003a. Safety criteria for transcranial direct current stimulation (tDCS) in humans. Clin. Neurophysiology 114, 2220-2222, author reply 2222-2223.
  • Nitsche, M. A., Niehaus, L., Hoffmann, K. T., Hengst, S., Liebetanz, D., Paulus, W., Meyer, B. U., 2004. MRI study of human brain exposed to weak direct current stimulation of the frontal cortex. Clin. Neurophysiology 115, 2419-2423.
  • Nitsche, M. A., Nitsche, M. S., Klein, C. C., Tergau, F., Rothwell, J. C., Paulus, W., 2003b. Level of action of cathodal D C polarisation induced inhibition of the human motor cortex. Clin. Neurophysiology 114, 600-604.
  • Nitsche, M. A., Paulus, W., 2000. Excitability changes induced in the human motor cortex by weak transcranial direct current stimulation. J. Physiology 527 (Pt 3), 633-639.
  • Nitsche, M. A., Paulus, W., 2011. Transcranial direct current stimulation—update 2011. Restorative Neurology and Neuroscience 29, 463-492.


Nitsche, M. A., Seeber, A., Frommann, K., Klein, C. C., Rochford, C., Nitsche, M. S., Fricke, K., Liebetanz, D., Lang, N., Antal, A., Paulus, W., Tergau, F., 2005. Modulating parameters of excitability during and after transcranial direct current stimulation of the human motor cortex. J. Physiology 568, 291-303.

  • Pascual-Leone, A., Walsh, V., Rothwell, J., 2000. Transcranial magnetic stimulation in cognitive neuroscience-virtual lesion, chronometry, and functional connectivity. Current Opinion in Neurobiology 10, 232-237.
  • Pasley, B. N., Allen, E A., Freeman, R. D., 2009. State-dependent variability of neuronal responses to transcranial magnetic stimulation of the visual cortex. Neuron 62, 291-303.
  • Paulus, W., 2011. Transcranial electrical stimulation (tES-tDCS; tRNS, tACS) methods. Neuropsychological Rehabilitation 21, 602-617.
  • Plewnia, C., Rilk, A. J., Soekadar, S. R., Arfeller, C., Huber, H S., Sauseng, P., Hummel, F., Geroff, C., 2008. Enhancement of long-range EEG coherence by synchronous bifocal transcranial magnetic stimulation. European J. Neuroscience 27, 1577-1583.
  • Pogosyan, A., Gaynor, L. D., Eusebio, A., Brown, P., 2009. Boosting cortical activity at Beta-band frequencies slows movement in humans. Current Biology 19, 1637-1641.
  • Priori, A., Berardelli, A., Rona, S., Accornero, N., Manfredi, M., 1998. Polarization of the human motor cortex through the scalp. Neuroreport 9, 2257-2260.
  • Radman, T., Datta, A., Peterchev, A. V., 2007. In vitro modulation of endogenous rhythms by A C electric fields: syncing with clinical brain stimulation. J. Physiology 584, 369-370.
  • Rahnev, D. A., Maniscalco, B., Luber, B., Lau, H., Lisanby, S. H., 2012. Direct injection of noise to the visual cortex decreases accuracy but increases decision confidence. J. Neurophysiology 107, 1556-1563.
  • Reato, D., Rahman, A., Bikson, M., Parra, L. C., 2010. Low-intensity electrical stimulation affects network dynamics by modulating population rate and spike timing. J. Neuroscience 30, 15067-15079.
  • Ridding, M. C., Ziemann, U., 2010. Determinants of the induction of cortical plasticity by non-invasive brain stimulation in healthy subjects. J. Physiology 588, 2291-2304.
  • Rosanova, M., Casali, A., Bellina, V., Resta, F., Mariotti, M., Massimini, M., 2009. Natural frequencies of human corticothalamic circuits. J. Neuroscience 29, 7679-7685.
  • Rossi, S., Hallett, M., Rossini, P. M., Pascual-Leone, A., Safety of TMS Consensus Group, 2009. Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research. Clin. Neurophysiology 120, 2008-2039.
  • Roth, B. J., 1994. Mechanisms for electrical stimulation of excitable tissue. Critical Reviews in Biomedical Engineering 22, 253-305.
  • Rothwell, J. C., Day, B. L., Thompson, P. D., Dick, J. P., Marsden, C. D., 1987. Some experiences of techniques for stimulation of the human cerebral motor cortex through the scalp. Neurosurgery 20, 156-163.
  • Ruohonen, J., 2003. Background physics for magnetic stimulation. Supplements to Clin. Neurophysiology 56, 3-12.
  • Ruzzoli, M., Abrahamyan, A., Clifford, C. W., Marzi, C. A., Miniussi, C., Harris, J. A., 2011. The effect of TMS on visual motion sensitivity: an increase in neural noise or a decrease in signal strength. J. Neurophysiology 106, 138-143.
  • Ruzzoli, M., Marzi, C. A., Miniussi, C., 2010. The neural mechanisms of the effects of transcranial magnetic stimulation on perception. J. Neurophysiology 103, 2982-2989.
  • Sack, A. T., Linden, D. E., 2003. Combining transcranial magnetic stimulation and functional imaging in cognitive brain research: possibilities and limitations. Brain Research: Brain Research Reviews 43, 41-56.
  • Sandrini, M., Umilta, C., Rusconi, E., 2011. The use of transcranial magnetic stimulation in cognitive neuroscience: a new synthesis of methodological issues. Neuroscience and Biobehavioral Reviews 35, 516-536.
  • Schutter, D. J., Hortensius, R., 2010. Retinal origin of phosphenes to transcranial alternating current stimulation. Clin. Neurophysiology 121, 1080-1084.
  • Schwarzkopf, D. S., Silvanto, J., Rees, G., 2011. Stochastic resonance effects reveal the neural mechanisms of transcranial magnetic stimulation. J. Neuro-science 31, 3143-3147.
  • Schwiedrzik, C. M., 2009. Retina or visual cortex? The site of phosphene induction by transcranial alternating current stimulation. Frontiers in Integrative Neuro-science 3, 6.
  • Sclar, G., Lennie, P., DePriest, D. D., 1989. Contrast adaptation in striate cortex of macaque. Vision Research 29, 747-755.
  • Seyal, M., Masuoka, L. K., Browne, J. K., 1992. Suppression of cutaneous perception by magnetic pulse stimulation of the human brain. Electroencephalography and Clin. Neurophysiology 85, 397-401.
  • Siebner, H. R., Lang, N., Rizzo, V., Nitsche, M. A., Paulus, W., Lemon, R. N., Rothwell, J. C., 2004. Preconditioning of low-frequency repetitive transcranial magnetic stimulation with transcranial direct current stimulation: evidence for homeostatic plasticity in the human motor cortex. The J. Neuroscience 24, 3379-3385.
  • Silvanto, J., Muggleton, N., Walsh, V., 2008. State-dependency in brain stimulation studies of perception and cognition. Trends in Cognitive Sciences 12, 447-454.
  • Silvanto, J., Muggleton, N. G., Cowey, A., Walsh, V., 2007. Neural adaptation reveals state-dependent effects of transcranial magnetic stimulation. Eur. J. Neuroscience 25, 1874-1881.
  • Solomon, J. A., 2009. The history of dipper functions. Attention, Perception, and Psychophysics 71, 435-443.
  • Stein, R. B., Gossen, E. R., Jones, K. E., 2005. Neuronal variability: noise or part of the signal? Nature Reviews Neuroscience 6, 389-397.
  • Terney, D., Chaieb, L., Moliadze, V., Antal, A., Paulus, W., 2008. Increasing human brain excitability by transcranial high-frequency random noise stimulation. J. Neuroscience 28, 14147-14155.
  • Thut, G., Miniussi, C., 2009. New insights into rhythmic brain activity from TMS-EEG studies. Trends in Cognitive Sciences 13, 182-189.
  • Thut, G., Miniussi, C., Gross, J., 2012. The functional importance of rhythmic activity in the brain. Current Biology 22, R658-R663.
  • Thut, G., Schyns, P. G., Gross, J., 2011a. Entrainment of perceptually relevant brain oscillations by non-invasive rhythmic stimulation of the human brain. Front. Psychology 2,170.
  • Thut, G., Veniero, D., Romei, V., Miniussi, C., Schyns, P., Gross, J., 2011b. Rhythmic TMS causes local entrainment of natural oscillatory signatures. Current Biology 21, 1176-1185.
  • Vallar, G., Bolognini, N., 2011. Behavioural facilitation following brain stimula-tion: implications for neurorehabilitation. Neuropsychological Rehabilitation 21, 618-649.
  • Varela, F., Lachaux, J. P., Rodriguez, E., Martinerie, J., 2001. The brainweb: phase synchronization and large-scale integration. Nature Reviews Neuroscience 2, 229-239.
  • Veniero, D., Brignani, D., Thut, G., Miniussi, C., 2011. Alpha-generation as basic response-signature to transcranial magnetic stimulation (TMS) targeting the human resting motor cortex: a TMS/EEG co-registration study. Psychophysiology 48, 1381-1389.
  • Walsh, V., Cowey, A., 2000. Transcranial magnetic stimulation and cognitive neuroscience. Nature Reviews Neuroscience 1, 73-79.
  • Walsh, V., Ellison, A., Battelli, L., Cowey, A., 1998. Task-specific impairments and enhancements induced by magnetic stimulation of human visual area V5. Proceedings: Biological Sciences 265, 537-543.
  • Walsh, V., Pascual-Leone, A., 2003. Transcranial Magnetic Stimulation: A Neurochronometrics of Mind. MIT Press, Cambridge, Mass.
  • Walsh, V., Rushworth, M., 1999. A primer of magnetic stimulation as a tool for neuropsychology. Neuropsychologia 37, 125-135.
  • Ward, L M., Doesburg, S. M., Kitajo, K., MacLean, S. E., Roggeveen, A. B., 2006. Neural synchrony in stochastic resonance, attention, and consciousness. Canadian J. Experimental Psychology 60, 319-326.
  • Wassermann, E. M., Epstein, C., Ziemann, U., Walsh, V., Paus, T., Lisanby, 5., 2008.
  • Handbook of Transcranial Stimulation. Oxford University Press, Oxford, U K.
  • Waterston, M. L, Pack, C. C., 2010. Improved discrimination of visual stimuli following repetitive transcranial magnetic stimulation. PLoS ONE 5, e10354.
  • Wu, S., Amari, S., Nakahara, H., 2002. Population coding and decoding in a neural field: a computational study. Neural Computation 14, 999-1026.
  • Zaehle, T., Rach, S., Herrmann, C. S., 2010. Transcranial alternating current stimulation enhances individual alpha activity in human EEG. PLoS ONE 5, e13766.


Transcranial Electrical Stimulation (tES)


tES (tDCS, tACS, and tRNS) is a set of noninvasive method of cortical stimulation, using weak direct currents to polarize target brain regions. The most used and best-known method is tDCS, as all considerations for the use of tDCS have been extended to the other tES methods. The hypotheses concerning the application of tDCS in cognition are very similar to those of TMS, with the exception that tOCS was never considered a virtual lesion method. tDCS can increase or decrease cortical excitability in the stimulated brain regions and facilitate or inhibit behavior accordingly. tES does not induce action potentials but instead modulates the neuronal response threshold so that it can be defined as subthreshold stimulation.


Michael A. Nitsche, and Armin Kibele. “Noninvasive brain stimulation and neural entrainment enhance athletic performance—a review.” J. Cognitive Enhancement 1.1 (2017): 73-79, discusses that non-invasive brain stimulation (NIBS) bypasses the correlative approaches of other imaging techniques, making it possible to establish a causal relationship between cognitive processes and the functioning of specific brain areas. NIBS can provide information about where a particular process occurs. NIBS offers the opportunity to study brain mechanisms beyond process localization, providing information about when activity in a given brain region is involved in a cognitive process, and even how it is involved. When using NIBS to explore cognitive processes, it is important to understand not only how NIBS functions but also the functioning of the neural structures themselves. Non-invasive brain stimulation (NIBS) methods, which include transcranial magnetic stimulation (TMS) and transcranial electric stimulation (tES), are used in cognitive neuroscience to induce transient changes in brain activity and thereby alter the behavior of the subject. The application of NIBS aims at establishing the role of a given cortical area in an ongoing specific motor, perceptual or cognitive process (Hallett, 2000; Walsh and Cowey, 2000). Physically, NIBS techniques affect neuronal states through different mechanisms. In TMS, a solenoid (coil) is used to deliver a strong and transient magnetic field, or “pulse,” to induce a transitory electric current at the cortical surface beneath the coil. (US 2004078056) The pulse causes the rapid and above-threshold depolarization of cell membranes affected by the current (Barker et al., 1985, 1987), followed by the transynaptic depolarization or hyperpolarization of interconnected neurons. Therefore, TMS induces a current that elicits action potentials in neurons. A complex set of coils can deliver a complex 3D excitation field. By contrast, in tES techniques, the stimulation involves the application of weak electrical currents directly to the scalp through a pair of electrodes (Nitsche and Paulus, 2000; Priori et al., 1998). As a result, tES induces a subthreshold polarization of cortical neurons that is too weak to generate an action potential. However, by changing the intrinsic neuronal excitability, tES can induce changes in the resting membrane potential and the postsynaptic activity of cortical neurons. This, in turn, can alter the spontaneous firing rate of neurons and modulate their response to afferent signals (Bindman et al., 1962, 1964, 1979; Creutzfeldt et al., 1962), leading to changes in synaptic efficacy. The typical application of NIBS involves different types of protocols: TMS can be delivered as a single pulse (spTMS) at a precise time, as pairs of pulses separated by a variable interval, or as a series of stimuli in conventional or patterned protocols of repetitive TMS (rTMS) (for a complete classification see Rossi et al., 2009). In tES, different protocols are established by the electrical current used and by its polarity, which can be direct (anodal or cathodal transcranial direct current stimulation: tDCS), high-definition transcranial direct current stimulation (HD-tDCS), oscillating transcranial direct current stimulation (osc-tDCS), alternating at a fix frequency (transcranial alternating current stimulation: tACS) or at random frequencies (transcranial random noise stimulation: tRNS) (Nitsche et al., 2008; Paulus, 2011). In general, the final effects of NIBS on the central nervous system depend on a lengthy list of parameters (e.g., frequency, temporal characteristics, intensity, geometric configuration of the coil/electrode, current direction), when it is delivered before (off-line) or during (on-line) the task as part of the experimental procedure (e.g., Jacobson et al., 2011; Nitsche and Paulus, 2011; Sandrini et al., 2011). In addition, these factors interact with several variables related to the anatomy (e.g., properties of the brain tissue and its location, Radman et al., 2007), as well as physiological (e.g., gender and age, Landi and Rossini, 2010; Lang et al., 2011; Ridding and Ziemann, 2010) and cognitive (e.g., Miniussi et al., 2010; Silvanto et al., 2008; Walsh et al., 1998) states of the stimulated area/subject.


Transcranial Direct Current Stimulation (tDCS)


Cranial electrotherapy stimulation (CES) is a form of non-invasive brain stimulation that applies a small, pulsed electric current across a person's head to treat a variety of conditions such as anxiety, depression and insomnia. See, en.wikipedia.org/wiki/Cranial_electrotherapy_stimulation. Transcranial direct current stimulation (tDCS) is a form of neurostimulation that uses constant, low current delivered to the brain area of interest via electrodes on the scalp. It was originally developed to help patients with brain injuries or psychiatric conditions like major depressive disorder. tDCS appears to have some potential for treating depression. See, en.wikipedia.org/wiki/Transcranial_direct-current_stimulation.


tDCS is being studied for acceleration of learning. The mild electrical shock (usually, a 2-milliamp current) is used to depolarize the neuronal membranes, making the cells more excitable and responsive to inputs. Weisend, Experimental Brain Research, vol 213, p 9 (DARPA) showed that tDCS accelerates the formation of new neural pathways during the time that someone practices a skill. tDCS appears to bring about the flow state. The movements of the subjects become more automatic; they report calm, focused concentration, and their performance improves immediately. (See Adee, Sally, “Zap your brain into the zone: Fast track to pure focus”, New Scientist, No. 2850, Feb. 1, 2012, www.newscientist.com/article/mg21328501-600-zap-your-brain-into-the-zone-fast-track-to-pure-focus/).


U.S. Pub. App. Nos. and U.S. Pat. Nos. 7,856,264; 8,706,241; 8,725,669; 9,037,224; 9,042,201; 9,095,266; 9,248,286; 9,349,178; 9,629,568; 9,693,725; 9,713,433; 20040195512; 20070179534; 20110092882; 20110311021; 20120165696; 20140142654; 20140200432; 20140211593; 20140316243; 20140347265; 20150099946; 20150174418; 20150257700; 20150327813; 20150343242; 20150351655; 20160000354; 20160038049; 20160113569; 20160144175; 20160148371; 20160148372; 20160180042; 20160213276; 20160228702; and 20160235323.


Reinhart, Robert M G. “Disruption and rescue of interareal theta phase coupling and adaptive behavior.” Proceedings of the National Academy of Sciences (2017): provide evidence for a causal relation between interareal theta phase synchronization in frontal cortex and multiple components of adaptive human behavior. Reinhart's results support the idea that the precise timing of rhythmic population activity spatially distributed in frontal cortex conveys information to direct behavior. Given prior work showing that phase synchronization can change spike time-dependent plasticity, together with Reihart's findings showing stimulation effects on neural activity and behavior can outlast a 20-min period of electrical stimulation, it is reasonable to suppose that the externally modulated interareal coupling changed behavior by causing neuroplastic modifications in functional connectivity. Reinhart suggests that we may be able to noninvasively intervene in the temporal coupling of distant rhythmic activity in the human brain to optimize (or impede) the postsynaptic effect of spikes from one area on the other, improving (or impairing) the cross-area communication necessary for cognitive action control and learning. Moreover, these neuroplastic alterations in functional connectivity were induced with a 0° phase, suggesting that inducing synchronization does not require a meticulous accounting of the communication delay between regions such as MFC and IPFC to effectively modify behavior and learning. This conforms to work showing that despite long axonal conduction delays between distant brain areas, theta phase synchronizations at 0° phase lag can occur between these regions and underlie meaningful functions of cognition and action. It is also possible that a third subcortical or posterior region with a nonzero time lag interacted with these two frontal areas to drive changes in goal-directed behavior.

  • Alexander W H & Brown J W (2011) Medial prefrontal cortex as an action-outcome predictor. Nature Neuroscience 14(10):1338-1344.
  • Alexander W H & Brown J W (2015) Hierarchical error representation: A computational model of anterior cingulate and dorsolateral prefrontal cortex. Neural Computation 27:2354-2410.
  • Anguera J A, et al. (2013) Video game training enhances cognitive control in older adults. Nature 501:97-101.
  • Aron A R, Fletcher P C, Bullmore E T, Sahakian B J, Robbins T W (2003) Stop-signal inhibition disrupted by damage to right inferior frontal gyrus in humans. Nat Neurosci 6:115-116.
  • Au J, et al. (2015) Improving fluid intelligence with training on working memory: a meta-analysis. Psychonomic Bulletin & Review 22:366-377.
  • Bellman R, Kalaba R (1959) A mathematical theory of adaptive control processes. Proc Natl Acad Sci USA 45:1288-1290.
  • Bibbig A, Traub R D, Whittington M A (2002) Long-range synchronization of gamma and beta oscillations and the plasticity of excitatory and inhibitory synapses: A network model. J Neurophysiol 88:1634-1654.
  • Botvinick M M (2012) Hierarchical reinforcement learning and decision making. Current Opinion in Neurobiology 22(6):956-962.
  • Botvinick M M, Braver T S, Barch D M, Carter C S, & Cohen J D (2001) Conflict monitoring and cognitive control. Psychological Review 108(3):624-652.
  • Bryck R L & Fisher P A (2012) Training the brain: practical applications of neural plasticity from the intersection of cognitive neuroscience, developmental psychology, and prevention science. American Psychologist 67:87-100.
  • Cavanagh J F, Cohen M X, & Allen J J (2009) Prelude to and resolution of an error EEG phase synchrony reveals cognitive control dynamics during action monitoring. Journal of Neuroscience 29(1):98-105.
  • Cavanagh J F, Frank M J (2014) Frontal theta as a mechanism for cognitive control. Trends Cogn Sci 18:414-421.
  • Christie G J, Tata M S (2009) Right frontal cortex generates reward-related theta-band oscillatory activity. Neuroimage 48:415-422.
  • Cohen M X, Wilmes K, Vijver Iv (2011) Cortical electrophysiological network dynamics of feedback learning. Trends Cogn Sci 15558-566.
  • Corbett A, et al. (2015) The effect of an online cognitive training package in healthy older adults: An online randomized controlled trial. J Am Med Dir Assoc 16:990-997.
  • Dale A M & Sereno M I (1993) Improved localization of cortical activity by combining EEG and MEG with MRI cortical surface reconstruction: A linear approach. Journal of Cognitive Neuroscience 5:162-176.
  • Dalley J W, Robbins T W (2017) Fractionating impulsivity: Neuropsychiatric implications. Nat Rev Neurosci 18:158-171.
  • Delorme A & Makeig S (2004) EEGLAB: An open source toolbox for analysis of singel-trial EEG dynamics including independent component analysis. Journal of Neuroscience Methods 134(1).9-21.
  • Diamond A & Lee K (2011) Interventions and programs demonstrated to aid executive function development in children 4-12 years of age. Science 333:959964.
  • Engel A K, Fries P, Singer W (2001) Dynamic predictions: Oscillations and synchrony in top-down processing. Nat Rev Neurosci 2:704-716.
  • Fairclough S H & Houston K (2004) A metabolic measure of mental effort. Biological Psychology 66:177-190.
  • Fell J, Axmacher N (2011) The role of phase synchronization in memory processes. Nat Rev Neurosci 12:105-118.
  • Fitzgerald K D, et al. (2005) Error-related hyperactivity of the anterior cingulate cortex in obsessive-compulsive disorder. Biol Psychiatry 57:287-294.
  • Foti D, Weinberg A, Dien J, Hajcak G (2011) Event-related potential activity in the basal ganglia differentiates rewards from nonrewards: Temporospatial principal components analysis and source localization of the feedback negativity. Hum Brain Mapp 32:2207-2216.
  • Fuchs M, Drenckhahn R, Wischmann H A, & Wagner M (1998) An improved boundary element method for realistic volume-conductor modeling. IEEE Trans Biomed Eng 45(8):980-997.
  • Gailliot M T & Baumeister R F (2007) The physiology of willpower: linking blood glucose to self-control. Personality and Social Psychology Review 11(4)303-327.
  • Gandiga P, Hummel F, & Cohen L (2006) Transcranial D C stimulation (tDCS): A tool for double-blind sham-controlled clinical studies in brain stimulation. Clinical Neurophysiology 117(4):845-850.
  • Gregoriou G G, Gotts S J, Zhou H, Desimone R (2009) High-frequency, long-range coupling between prefrontal and visual cortex during attention. Science 324:1207-1210.
  • Hillman C H, Erickson K I, & Kramer A F (2008) Be smart, exercise your heart: exercise effects on brain and cognition. Nature Reviews Neuroscience 9(1)5865.
  • Holroyd C B & Yeung N (2012) Motivation of extended behaviors by anterior cingulate cortex. Trends in Cognitive Sciences 16:122-128.
  • Inzlicht M, Schmeichel B J, & Macrae C N (2014) Why self-control seems (but may not be) limited. Trends in Cognitive Sciences 18(3):127-133.
  • Jennings J R & Wood C C (1976) The e-adjustment procedure for repeated measures analyses of variance. Psychophysiology 13:277-278.
  • Kanai R, Chaieb L, Antal A, Walsh V, & Paulus W (2008) Frequency-dependent electrical stimulation of the visual cortex. Current Biology 18(23):1839-1843.
  • Kayser J & Tenke C E (2006) Principal components analysis of Laplacian waveforms as a generic method for identifying estimates: II. Adequacy of low density estimates. Clinical Neurophysiology 117.369-380.
  • Kramer A F & Erickson K I (2007) Capitalizing on cortical plasticity: influence of physical activity on cognition and brain function. Trends in Cognitive Sciences 11:342-348.
  • Kurland J, Baldwin K, Tauer C (2010) Treatment-induced neuroplasticity following intensive naming therapy in a case of chronic wernicke's aphasia. Aphasiology 24:737-751.
  • Lachaux J P, Rodriguez E, Martinerie J, & Varela F J (1999) Measuring phase synchrony in brain signals. Human Brain Mapping 8:194-208.
  • Lennie P (2003) The cost of cortical computation. Current Biology 13:493-497.
  • Luft C D B, Nolte G, & Bhattacharya J (2013) High-learners present larger midfrontal theta power and connectivity in response to incorrect performance feedback. Journal of Neuroscience 33(5):2029-2038.
  • Luft C D B, Nolte G, Bhattacharya J (2013) High-learners present larger mid-frontal theta power and connectivity in response to incorrect performance feedback. J Neurosci 33:2029-2038.
  • Marco-Pallares J, et al. (2008) Human oscillatory activity associated to reward processing in a gambling task. Neuropsychologia 46:241-248.
  • Marcora S M, Staiano W, & Manning V (2009) Mental fatigue impairs physical performance in humans. Journal of Applied Physiology 106:857-864.
  • Miltner W H R, Braun C H, & Coles M G H (1997) Event-related brain potentials following incorrect feedback in a time-estimation task: evidence for a “generic” neural system for error detection. Journal of Cognitive Neuroscience 9.788-798.
  • Noury N, Hipp J F, Siegel M (2016) Physiological processes non-linearly affect electrophysiological recordings during transcranial electric stimulation. Neuroimage 140: 99-109.
  • Oostenveld R, Fries P, Maris E, & Schoffelen J M (2011) FieldTrip: Open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data. Computational Intelligence and Neuroscience 2011:1-9.
  • Owen A M, et al. (2010) Putting brain training to the test. Nature 465:775-778.
  • Pascual-Marqui R D (2002) Standardized low-resolution brain electromagnetic tomography (sLORETA): technical details. Methods & Findings in Experimental & Clinical Pharmacology 24:5-12.
  • Paulus W (2010) On the difficulties of separating retinal from cortical origins of phosphenes when using transcranial alternating current stimulation (tACS). Clinical Neurophysiology 121:987-991.
  • Poreisz C, Boros K, Antal A, & Paulus W (2007) Safety aspects of transcranial direct current stimulation concerning healthy subjects and patients. Brain Research Bulletin 72(4-6):208-214.
  • Raichle M E & Mintun M A (2006) Brain work and brain imaging. Annual Review of Neuroscience 29.449-476.
  • Reinhart R M G & Woodman G F (2014) Causal control of medial-frontal cortex governs electrophysiological and behavioral indices of performance monitoring and learning. Journal of Neuroscience 34(12):4214-4227.
  • Reinhart R M G & Woodman G F (2015) Enhancing long-term memory with stimulation tunes visual attention in one trial. Proceedings of the National Academy of Sciences of the USA 112(2):625-630.
  • Reinhart R M G, Cosman J D, Fukuda K, & Woodman G F (2017) Using transcranial direct-current stimulation (tDCS) to understand cognitive processing. Attention, Perception & Psychophysics 79(1)3-23.
  • Reinhart R M G, Woodman G F (2014) Oscillatory coupling reveals the dynamic reorganization of large-scale neural networks as cognitive demands change. J Cogn Neurosci 26:175-188.
  • Reinhart R M G, Xiao W, McClenahan L, & Woodman G F (2016) Electrical stimulation of visual cortex can immediately improve spatial vision. Current Biology 25(14):1867-1872.
  • Reinhart R M G, Zhu J, Park 5S, & Woodman G F (2015) Medial-frontal stimulation enhances learning in schizophrenia by restoring prediction-error signaling. Journal of Neuroscience 35(35):12232-12240.
  • Reinhart R M G, Zhu J, Park 5S, & Woodman G F (2015) Synchronizing theta oscillations with direct-current stimulation strengthens adaptive control in the human brain. Proceedings of the National Academy of Sciences of the USA 112(30).9448-9453.
  • Ridderinkhof K R, Ullsperger M, Crone E A, & Nieuwenhuis 5 (2004) The role of the medial frontal cortex in cognitive control. Science 306:443-447.
  • Salinas E, Sejnowski T J (2001) Correlated neuronal activity and the flow of neural information. Nat Rev Neurosci 2539-550.
  • Schnitzler A, Gross J (2005) Normal and pathological oscillatory communication in the brain. Nat Rev Neurosci 6:285-296.
  • Schutter D J & Hortensius R (2010) Retinal origin of phosphenes to transcranial alternating current stimulation. Clinical Neurophysiology 121(7):1080-1084.
  • Shallice T, Gazzaniga M S (2004) The fractionation of supervisory control. The Cognitive Neuroscience (MIT Press, Cambridge, Mass.), pp 943-956.
  • Shenhav A, Botvinick M M, & Cohen J D (2013) The expected value of control: An integrative theory of anterior cingulate cortex function. Neuron 79:217-240.
  • Shenhav A, Cohen J D, & Botvinick M M (2016) Dorsal anterior cingulate cortex and the value of control. Nature Neuroscience 19:1286-1291.
  • Siegel M, Donner T H, Engel A K (2012) Spectral fingerprints of large-scale neuronal interactions. Nat Rev Neurosci 13:121-134.
  • Srinivasan R, Winter W R, Ding J, & Nunez P L (2007) EEG and MEG coherence: measures of functional connectivity at distinct spatial scales of neocortical dynamics. Journal of Neuroscience Methods 166(1):41-52.
  • Tang Y, et al. (2010) Short term mental training induces white-matter changes in the anterior cingulate. Proceedings of the National Academy of Sciences 107:16649-16652.
  • Tang Y Y, et al. (2009) Central and autonomic nervous system interaction is altered by short term meditation. Proceedings of the National Academy of Sciences 106:8865-8870.
  • Thrane G, Friborg O, Anke A, Indredavik B (2014) A meta-analysis of constraint-induced movement therapy after stroke. J Rehabil Med 46:833-842.
  • Uhlhaas P, Singer W (2006) Neural synchrony in brain disorders: Relevance for cognitive dysfunctions and pathophysiology. Neuron 52:155-168.
  • Uhlhaas P, Singer W (2010) Abnormal neural oscillations and synchrony in schizophrenia. Nat Rev Neurosci 11:100-113.
  • van de Vijver I, Ridderinkhof K R, & Cohen M X (2011) Frontal oscillatory dynamics predict feedback learning and action adjustment. Journal of Cognitive Neuroscience 23:4106-4121.
  • van Driel J, Ridderinkhof K R, & Cohen M X (2012) Not all errors are alike: Theta and alpha EEG dynamics relate to differences in error-processing dynamics. Journal of Neuroscience 32(47):16795-16806.
  • van Meel C S, Heslenfeld D J, Oosterlaan J, Sergeant J A (2007) Adaptive control deficits in attention-deficit/hyperactivity disorder (ADHD): The role of error processing. Psychiatry Res 151:211-220.
  • Varela F, Lachaux J P, Rodriguez E, Martinerie J (2001) The brainweb: Phase synchronization and large-scale integration. Nat Rev Neurosci 2:229-239.
  • Velligan D I, Ritch J L, Sui D, DiCocco M, Huntzinger C D (2002) Frontal systems behavior scale in schizophrenia: Relationships with psychiatric symptomatology, cognition and adaptive function. Psychiatry Res 113:227-236.
  • Vicente R, Gollo L L, Mirasso C R, Fischer I, Pipa G (2008) Dynamical relaying can yield zero time lag neuronal synchrony despite long conduction delays. Proc Natl Acad Sci USA 105:17157-17162.
  • Wagner M, Fuchs M, & Kastner J (2007) SWARM: sLORETA-weighted accurate minimum norm inverse solutions. International Congress Series 1300:185-188.
  • Wang X J (2010) Neurophysiological and computational principles of cortical rhythms in cognition. Physiol Rev 90.1195-1268.
  • Wolpert D M, Diedrichsen J, & Flanagan J R (2011) Principles of sensorimotor learning. Nature Reviews Neuroscience 12:739-751.
  • Xue S, Tang Y Y, Tang R, & Posner M I (2014) Short-term meditation induces changes in brain resting EEG theta networks. Brain & Cognition 87:1-6
  • Zatorre R J, Fields R D, & Johansen-Berg H (2012) Plasticity in gray and white: neuroimaging changes in brain structure during learning. Nature Neuroscience 15(4)528-536. See, Daniel Stevenson. “Intro to Transcranial Direct Current Stimulation (tDCS)” (Mar. 26, 2017) (www.slideshare.net/DanieStevenson27/intro-to-transcranial-direct-curent-stimulation-tdcs).


High-Definition-tDCS


High-Definition transcranial Direct Current Stimulation (HD-tDCS) was invented at The City University of New York with the introduction of the 4×1 HD-tDCS montage. The 4×1 HD-tDCS montage allows precise targeting of cortical structures. The region of current flow is circumscribed by the area of the 4× ring, such that decreasing ring radius increases focality. 4×1 HD-tDCS allows for unifocal stimulation, meaning the polarity of the center 1× electrode will determine the direction of neuromodulation under the ring. This is in contrast to conventional tDCS where the need for one anode and one cathode always produces bidirectional modulation (even when an extra-cephalic electrode is used). 4×1 HD-tDCS thus provides the ability not only to select a cortical brain region to target, but to modulate the excitability of that brain region with a designed polarity without having to consider return counter-electrode flow.


Transcranial Alternative Current Stimulation (tACS)


Transcranial alternating current stimulation (tACS) is a noninvasive means by which alternating electrical current applied through the skin and skull entrains in a frequency-specific fashion the neural oscillations of the underlying brain. See, en.wikipedia.org/wiki/Transcranial_alternating_current_stimulation.


U.S. Pub. App. No. 20170197081 discloses transdermal electrical stimulation of nerves to modify or induce a cognitive state using transdermal electrical stimulation (TES).


Transcranial alternating current stimulation (tACS) is a noninvasive means by which alternating electrical current applied through the skin and skull entrains in a frequency-specific fashion the neural oscillations of the underlying brain. See, en.wikipedia.org/wiki/Transcranial_alternating_current_stimulation; U.S. Pub. App. Nos. and U.S. Pat. Nos. 6,804,558; 7,149,773; 7,181,505; 7,278,966; 9,042,201; 9,629,568; 9,713,433; 20010051787; 20020013613; 20020052539; 20020082665; 20050171410; 20140211593; 20140316243; 20150174418; 20150343242; 20160000354; 20160038049; 20160106513; 20160213276; 20160228702; 20160232330; 20160235323; and 20170113056.


Transcranial Random Noise Stimulation (tRNS)


Transcranial random noise stimulation (tRNS) is a non-invasive brain stimulation technique and a form of transcranial electrical stimulation (tES). See, en.wikipedia.org/wiki/Transcranial_random_noise_stimulation; U.S. Pub. App. Nos. and U.S. Pat. Nos. 9,198,733; 9,713,433; 20140316243; 20160038049; and 20160213276.


The stimulus may comprise transcranial pulsed current stimulation (tPCS). See:

  • Shapour Jaberzadeh, Andisheh Bastani, Maryam Zoghi, “Anodal transcranial pulsed current stimulation: A novel technique to enhance corticospinal excitability,” Clin. Neurophysiology, Volume 125, Issue 2, February 2014, Pages 344-351, doi.org/10.1016/j.clin ph.2013.08.025;
  • earthpulse.net/tpcs-transcranial-pulsed-current-stimulation/; help.foc.us/article/16-tpcs-transcranial-pulsed-current-stimulation.


Transcranial Magnetic Stimulation


Transcranial magnetic stimulation (TMS) is a method in which a changing magnetic field is used to cause electric current to flow in a small region of the brain via electromagnetic induction. During a TMS procedure, a magnetic field generator, or “coil”, is placed near the head of the person receiving the treatment. The coil is connected to a pulse generator, or stimulator, that delivers a changing electric current to the coil. TMS is used diagnostically to measure the connection between the central nervous system and skeletal muscle to evaluate damage in a wide variety of disease states, including stroke, multiple sclerosis, amyotrophic lateral sclerosis, movement disorders, and motor neuron diseases. Evidence is available suggesting that TMS is useful in treating neuropathic pain, major depressive disorder, and other conditions.


See, en.wikipedia.org/wiki/Transcranial_magnetic_stimulation,


See U.S. Pub. App. Nos. and U.S. Pat. Nos. 4,296,756; 4,367,527; 5,069,218; 5,088,497; 5,359,363; 5,384,588; 5,459,536; 5,711,305; 5,877,801; 5,891,131; 5,954,662; 5,971,923; 6,188,924; 6,259,399; 6,487,441; 6,603,502; 7,714,936; 7,844,324; 7,856,264; 8,221,330; 8,655,817; 8,706,241; 8,725,669; 8,914,115; 9,037,224; 9,042,201; 9,095,266; 9,149,195; 9,248,286; 9,265,458; 9,414,776; 9,445,713; 9,713,433; 20020097332; 20040088732; 20070179534; 20070249949; 20080194981; 20090006001; 20110004412; 20110007129; 20110087127; 20110092882; 20110119212; 20110137371; 20120165696; 20120296569; 20130339043; 20140142654; 20140163328; 20140200432; 20140211593; 20140257047; 20140279746; 20140316243; 20140350369; 20150065803; 20150099946; 20150148617; 20150174418; 20150257700; 20150327813; 20150343242; 20150351655; 20160038049; 20160140306; 20160144175; 20160213276; 20160235323; 20160284082; 20160306942; 20160317077; 20170084175; and 20170113056.


PEMF


Pulsed electromagnetic field (PEMF) when applied to the brain is referred to as Transcranial magnetic stimulation, and has been FDA approved since 2008 for use in people who failed to respond to antidepressants. Weak magnetic stimulation of the brain is often called transcranial pulsed electromagnetic field (tPEMF) therapy. See, en.wikipedia.org/wiki/Pulsed_electromagnetk_field_therapy,


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 7,280,861; 8,343,027; 8,415,123; 8,430,805; 8,435,166; 8,571,642; 8,657,732; 8,775,340; 8,961,385; 8,968,172; 9,002,477; 9,005,102; 9,278,231; 9,320,913; 9,339,641; 9,387,338; 9,415,233; 9,427,598; 9,433,797; 9,440,089; 9,610,459; 9,630,004; 9,656,096; 20030181791; 20060129022; 20100057655; 20100197993; 20120101544; 20120116149; 20120143285; 20120253101; 20130013339; 20140213843; 20140213844; 20140221726; 20140228620; 20140303425; 20160235983; 20170087367; and 20170165496.


Deep Brain Stimulation (DBS)


Deep brain stimulation (DBS) is a neurosurgical procedure involving the implantation of a medical device called a neurostimulator (sometimes referred to as a ‘brain pacemaker’), which sends electrical impulses, through implanted electrodes, to specific targets in the brain (brain nuclei) for the treatment of movement and neuropsychiatric disorders. See, en.wikipedia.org/wiki/Deep-brain_stimulation;


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 6,539,263; 6,671,555; 6,959,215; 6,990,377; 7,006,872; 7,010,351; 7,024,247; 7,079,977; 7,146,211; 7,146,217; 7,149,572; 7,174,206; 7,184,837; 7,209,787; 7,221,981; 7,231,254; 7,236,830; 7,236,831; 7,239,926; 7,242,983; 7,242,984; 7,252,090; 7,257,439; 7,267,644; 7,277,758; 7,280,867; 7,282,030; 7,299,096; 7,302,298; 7,305,268; 7,313,442; 7,321,837; 7,324,851; 7,346,382; 7,353,064; 7,403,820; 7,437,196; 7,463,927; 7,483,747; 7,499,752; 7,565,199; 7,565,200; 7,577,481; 7,582,062; 7,594,889; 7,603,174; 7,606,405; 7,610,096; 7,617,002; 7,620,456; 7,623,928; 7,624,293; 7,629,889; 7,670,838; 7,672,730; 7,676,263; 7,680,526; 7,680,540; 7,684,866; 7,684,867; 7,715,919; 7,725,192; 7,729,773; 7,742,820; 7,747,325; 7,747,326; 7,756,584; 7,769,464; 7,775,993; 7,822,481; 7,831,305; 7,853,322; 7,853,323; 7,853,329; 7,856,264; 7,860,548; 7,894,903; 7,899,545; 7,904,134; 7,908,009; 7,917,206; 7,917,225; 7,930,035; 7,933,646; 7,945,330; 7,957,797; 7,957,809; 7,976,465; 7,983,762; 7,991,477; 8,000,794; 8,000,795; 8,005,534; 8,027,730; 8,031,076; 8,032,229; 8,050,768; 8,055,348; 8,065,012; 8,073,546; 8,082,033; 8,092,549; 8,121,694; 8,126,567; 8,126,568; 8,135,472; 8,145,295; 8,150,523; 8,150,524; 8,160,680; 8,180,436; 8,180,601; 8,187,181; 8,195,298; 8,195,300; 8,200,340; 8,223,023; 8,229,559; 8,233,990; 8,239,029; 8,244,347; 8,249,718; 8,262,714; 8,280,517; 8,290,596; 8,295,934; 8,295,935; 8301,257; 8,303,636; 8,308,661; 8,315,703; 8,315,710; 8,326,420; 8,326,433; 8,332,038; 8,332,041; 8,346,365; 8,364,271; 8,364,272; 8,374,703; 8,379,952; 8,380,314; 8,388,555; 8,396,565; 8,398,692; 8,401,666; 8,412,335; 8,433,414; 8,437,861; 8,447,392; 8,447,411; 8,456,309; 8,463,374; 8,463,387; 8,467,877; 8,475,506; 8,504,150; 8,506,469; 8,512,219; 8,515,549; 8,515,550; 8,538,536; 8,538,543; 8,543,214; 8,554,325; 8,565,883; 8,565,886; 8,574,279; 8,579,786; 8,579,834; 8,583,238; 8,583,252; 8,588,899; 8,588,929; 8,588,933; 8,589,316; 8,594,798; 8,603,790; 8,606,360; 8,606,361; 8,644,945; 8,649,845; 8,655,817; 8,660,642; 8,675,945; 8,676,324; 8,676,330; 8,684,921; 8,690,748; 8,694,087; 8,694,092; 8,696,722; 8,700,174; 8,706,237; 8,706,241; 8,708,934; 8,716,447; 8,718,777; 8,725,243; 8,725,669; 8,729,040; 8,731,656; 8,734,498; 8,738,136; 8,738,140; 8,751,008; 8,751,011; 8,755,901; 8,758,274; 8,761,889; 8,762,065; 8,768,718; 8,774,923; 8,781,597; 8,788,033; 8,788,044; 8,788,055; 8,792,972; 8,792,991; 8,805,518; 8,815,582; 8,821,559; 8,825,166; 8,831,731; 8,834,392; 8,834,546; 8,843,201; 8,843,210; 8,849,407; 8,849,632; 8,855,773; 8,855,775; 8,868,172; 8,868,173; 8,868,201; 8,886,302; 8,892,207; 8,900,284; 8,903,486; 8,903,494; 8,906,360; 8,909,345; 8,910,638; 8,914,115; 8,914,119; 8,918,176; 8,918,178; 8,918,183; 8,926,959; 8,929,991; 8,932,562; 8,934,979; 8,936,629; 8,938,290; 8,942,817; 8,945,006; 8,951,203; 8,956,363; 8,958,870; 8,962,589; 8,965,513; 8,965,514; 8,974,365; 8,977,362; 8,983,155; 8,983,620; 8,983,628; 8,983,629; 8,989,871; 9,008,780; 9,011,329; 9,014,823; 9,020,598; 9,020,612; 9,020,789; 9,022,930; 9,026,217; 9,037,224; 9,037,254; 9,037,256; 9,042,201; 9,042,988; 9,043,001; 9,044,188; 9,050,470; 9,050,471; 9,061,153; 9,063,643; 9,072,832; 9,072,870; 9,072,905; 9,079,039; 9,079,940; 9,081,488; 9,084,885; 9,084,896; 9,084,900; 9,089,713; 9,095,266; 9,101,690; 9,101,759; 9,101,766; 9,113,801; 9,126,050; 9,135,400; 9,149,210; 9,167,976; 9,167,977; 9,167,978; 9,173,609; 9,174,055; 9,175,095; 9,179,850; 9,179,875; 9,186,510; 9,187,745; 9,198,563; 9,204,838; 9,211,411; 9,211,417; 9,215,298; 9,220,917; 9,227,056; 9,233,245; 9,233,246; 9,235,685; 9,238,142; 9,238,150; 9,248,280; 9,248,286; 9,248,288; 9,248,296; 9,249,200; 9,249,234; 9,254,383; 9,254,387; 9,259,591; 9,271,674; 9,272,091; 9,272,139; 9,272,153; 9,278,159; 9,284,353; 9,289,143; 9,289,595; 9,289,603; 9,289,609; 9,295,838; 9,302,103; 9,302,110; 9,302,114; 9,302,116; 9,308,372; 9,308,392; 9,309,296; 9,310,985; 9,314,190; 9,320,900; 9,320,914; 9,327,070; 9,333,350; 9,340,589; 9,348,974; 9,352,156; 9,357,949; 9,358,381; 9,358,398; 9,359,449; 9,360,472; 9,364,665; 9,364,679; 9,365,628; 9,375,564; 9,375,571; 9,375,573; 9,381,346; 9,387,320; 9,393,406; 9,393,418; 9,394,347; 9,399,134; 9,399,144; 9,403,001; 9,403,010; 9,408,530; 9,411,935; 9,414,776; 9,415,219; 9,415,222; 9,421,258; 9,421,373; 9,421,379; 9,427,581; 9,427,585; 9,439,150; 9,440,063; 9,440,064; 9,440,070; 9,440,084; 9,452,287; 9,453,215; 9,458,208; 9,463,327; 9,474,903; 9,480,841; 9,480,845; 9,486,632; 9,498,628; 9,501,829; 9,505,17; 9,517,020; 9,522,278; 9,522,288; 9,526,902; 9,526,913; 9,526,914; 9,533,148; 9,533,150; 9,538,951; 9,545,510; 9,561,380; 9,566,426; 9,579,247; 9,586,053; 9,592,004; 9,592,387; 9,592,389; 9,597,493; 9,597,494; 9,597,501; 9,597,504; 9,604,056; 9,604,067; 9,604,073; 9,613,184; 9,615,789; 9,622,675; 9,622,700; 9,623,240; 9,623,241; 9,629,548; 9,630,011; 9,636,185; 9,642,552; 9,643,015; 9,643,017; 9,643,019; 9,649,439; 9,649,494; 9,649,501; 9,656,069; 9,656,078; 9,662,502; 9,697,336; 9,706,957; 9,713,433; 9,717,920; 9,724,517; 9,729,252; 20020087201; 20020091419; 20020188330; 20030088274; 20030097159; 20030097161; 20030125786; 20030130706; 20030181955; 20040133118; 20040133119; 20040133120; 20040133248; 20040133390; 20040138516; 20040138517; 20040138518; 20040138536; 20040138580; 20040138581; 20040138647; 20040138711; 20040152958; 20040158119; 20040158298; 20050021105; 20050060001; 20050060007; 20050060008; 20050060009; 20050060010; 20050065427; 20050124848; 20050154425; 20050154426; 20050182389; 20050209512; 20050222522; 20050240253; 20050267011; 20060004422; 20060015153; 20060064138; 20060069415; 20060100671; 20060106274; 20060106430; 20060149337; 20060155348; 20060155495; 20060161218; 20060161384; 20060167370; 20060195155; 20060200206; 20060212090; 20060217781; 20060224421; 20060239482; 20060241718; 20070000372; 20070014454; 20070025608; 20070027486; 20070027498; 20070027499; 20070027500; 20070027501; 20070032834; 20070043401; 20070060974; 20070066915; 20070100278; 20070100389; 20070100392; 20070100398; 20070118197; 20070129769; 20070129774; 20070142874; 20070150026; 20070150029; 20070179534; 20070179558; 20070225774; 20070250119; 20070276441; 20080009772; 20080015459; 20080033503; 20080033508; 20080045775; 20080046012; 20080046035; 20080058773; 20080064934; 20080071150; 20080071326; 20080097553; 20080103547; 20080103548; 20080109050; 20080125829; 20080154331; 20080154332; 20080157980; 20080161700; 20080161879; 20080161880; 20080161881; 20080162182; 20080183097; 20080208285; 20080215112; 20080228239; 20080269812; 20080269843; 20080275526; 20080281381; 20080288018; 20090018462; 20090076567; 20090082829; 20090093862; 20090099627; 20090105785; 20090112273; 20090112277; 20090112278; 20090112279; 20090112280; 20090118786; 20090118787; 20090163982; 20090192556; 20090210018; 20090216288; 20090234419; 20090264789; 20090264954; 20090264955; 20090264956; 20090264957; 20090264958; 20090264967; 20090281594; 20090287035; 20090287271; 20090287272; 20090287273; 20090287274; 20090287467; 20090299126; 20090299435; 20090306491; 20090306741; 20090312808; 20090312817; 20090319000; 20090319001; 20090326604; 20100004500; 20100010383; 20100010388; 20100010391; 20100010392; 20100010571; 20100010572; 20100010573; 20100010574; 20100010575; 20100010576; 20100010577; 20100010578; 20100010579; 20100010580; 20100010584; 20100010585; 20100010587; 20100010588; 20100010589; 20100010590; 20100016783; 20100045467; 20100049276; 20100057159; 20100057160; 20100070001; 20100076525; 20100114237; 20100114272; 20100121415; 20100131030; 20100145427; 20100191305; 20100198090; 20100222845; 20100241020; 20100256592; 20100274106; 20100274141; 20100274147; 20100274305; 20100280334; 20100280335; 20100280500; 20100280571; 20100280574; 20100280579; 20100292602; 20110004270; 20110009928; 20110021970; 20110022981; 20110028798; 20110028799; 20110034812; 20110040356; 20110040546; 20110040547; 20110082522; 20110092882; 20110093033; 20110106206; 20110112590; 20110119212; 20110137371; 20110137381; 20110160796; 20110172554; 20110172562; 20110172564; 20110172567; 20110172738; 20110172743; 20110172927; 20110184487; 20110191275; 20110208012; 20110208264; 20110213222; 20110230701; 20110238130; 20110238136; 20110245734; 20110257501; 20110270348; 20110275927; 20110276107; 20110307030; 20110307079; 20110313268; 20110313487; 20110319726; 20110319975; 20120016430; 20120016432; 20120016435; 20120022340; 20120022611; 20120041498; 20120046531; 20120046715; 20120053508; 20120089205; 20120108998; 20120109020; 20120116244; 20120116475; 20120157963; 20120165696; 20120165898; 20120179071; 20120179228; 20120184801; 20120185020; 20120195860; 20120197322; 20120209346; 20120253421; 20120253429; 20120253442; 20120265267; 20120271148; 20120271183; 20120271189; 20120271374; 20120271375; 20120271376; 20120271380; 20120277833; 20120289869; 20120290058; 20120302912; 20120303087; 20120310050; 20120316630; 20130018435; 20130066392; 20130066394; 20130066395; 20130073022; 20130090706; 20130102919; 20130104066; 20130116578; 20130116748; 20130123568; 20130123684; 20130131746; 20130131753; 20130131755; 20130138176; 20130138177; 20130144353; 20130150921; 20130178913; 20130184781; 20130184792; 20130197401; 20130211183; 20130218232; 20130218819; 20130226261; 20130231709; 20130231716; 20130231721; 20130238049; 20130238050; 20130245466; 20130245486; 20130245711; 20130245712; 20130281758; 20130281811; 20130282075; 20130289385; 20130310909; 20130317474; 20130317568; 20130317580; 20130338526; 20130338738; 20140005743; 20140005744; 20140025133; 20140039577; 20140058289; 20140066796; 20140074060; 20140074179; 20140074180; 20140081071; 20140081347; 20140107397; 20140107398; 20140107728; 20140122379; 20140135642; 20140135886; 20140142654; 20140142669; 20140148872; 20140163627; 20140180194; 20140180358; 20140194720; 20140194726; 20140211593; 20140213842; 20140222113; 20140237073; 20140243613; 20140243926; 20140243934; 20140249396; 20140249445; 20140257047; 20140257437; 20140257438; 20140276185; 20140277282; 20140277286; 20140279746; 20140296646; 20140309614; 20140323924; 20140323946; 20140324118; 20140324138; 20140330334; 20140330335; 20140330345; 20140350634; 20140350636; 20140358024; 20140358199; 20140364721; 20140371515; 20150005680; 20150012057; 20150018699; 20150025408; 20150025421; 20150025610; 20150032178; 20150038822; 20150039066; 20150065831; 20150073505; 20150088224; 20150088228; 20150119689; 20150119898; 20150134031; 20150142082; 20150174406; 20150174418; 20150190636; 20150190637; 20150196246; 20150202447; 20150223721; 20150231395; 20150231397; 20150238693; 20150238765; 20150245781; 20150251016; 20150254413; 20150257700; 20150265207; 20150265830; 20150265836; 20150273211; 20150273223; 20150283379; 20150290453; 20150290454; 20150297893; 20150306391; 20150321000; 20150327813; 20150343215; 20150343242; 20150352363; 20150360026; 20150360039; 20150366482; 20150374983; 20160001065; 20160001096; 20160001098; 20160008600; 20160008632; 20160016014; 20160030666; 20160030749; 20160030750; 20160038049; 20160044841; 20160058359; 20160066789; 20160067494; 20160067496; 20160067526; 20160074661; 20160095546; 20160096025; 20160106997; 20160120437; 20160121114; 20160121116; 20160136429; 20160136430; 20160136443; 20160144175; 20160144186; 20160147964; 20160151628; 20160158553; 20160184596; 20160199662; 20160206380; 20160213276; 20160213314; 20160220821; 20160220850; 20160228204; 20160228640; 20160228702; 20160228705; 20160235323; 20160249846; 20160250473; 20160256690; 20160256691; 20160256693; 20160263380; 20160263393; 20160278870; 20160279410; 20160279417; 20160287436; 20160287869; 20160287889; 20160296746; 20160303322; 20160317077; 20160317824; 20160325111; 20160331970; 20160339243; 20160342762; 20160346542; 20160361540; 20160367808; 20160375259; 20170007820; 20170007828; 20170014625; 20170014630; 20170021161; 20170036024; 20170042474; 20170042713; 20170043167; 20170043178; 20170050046; 20170056642; 20170056663; 20170065349; 20170079573; 20170080234; 20170095670; 20170095676; 20170100591; 20170106193; 20170113046; 20170120043; 20170120052; 20170120054; 20170136238; 20170143966; 20170151433; 20170151435; 20170151436; 20170156622; 20170157410; 20170164895; 20170165481; 20170173326; 20170182285; 20170185741; 20170189685; 20170189686; 20170189687; 20170189688; 20170189689; 20170189700; 20170197080; 20170197086; 20170216595; 20170224990; 20170239486; and 20170239489.


Transcranial Pulse Ultrasound (TPU)


Transcranial pulsed ultrasound (TPU) uses low intensity, low frequency ultrasound (LILFU) as a method to stimulate the brain. See, en.wikipedia.org/wiki/Transcranial_pulsed_ultrasound;


U.S. Pat. Nos. 8,591,419; 8,858,440; 8,903,494; 8,921,320; 9,002,458; 9,014,811; 9,036,844; 9,042,201; 9,061,133; 9,233,244; 9,333,334; 9,399,126; 9,403,038; 9,440,070; 9,630,029; 9,669,239; 20120259249; 20120283502; 20120289869; 20130079621; 20130144192; 20130184218; 20140058219; 20140211593; 20140228653; 20140249454; 20140316243; 20150080327; 20150133716; 20150343242; 20160143541; 20160176053; and 20160220850.


Sensory Stimulation


Light, sound or electromagnetic fields may be used to remotely convey a temporal pattern of brainwaves. See:


U.S. Pub. App. Nos. and U.S. Pat. Nos. 5,293,187; 5,422,689; 5,447,166; 5,491,492; 5,546,943; 5,622,168; 5,649,061; 5,720,619; 5,740,812; 5,983,129; 6,050,962; 6,092,058; 6,149,586; 6,325,475; 6,377,833; 6,394,963; 6,428,490; 6,482,165; 6,503,085; 6,520,921; 6,522,906; 6,527,730; 6,556,695; 6,565,518; 6,652,458; 6,652,470; 6,701,173; 6,726,624; 6,743,182; 6,746,409; 6,758,813; 6,843,774; 6,896,655; 6,996,261; 7,037,260; 7,070,571; 7,107,090; 7,120,486; 7,212,851; 7,215,994; 7,260,430; 7,269,455; 7,280,870; 7,392,079; 7,407,485; 7,463,142; 7,478,108; 7,488,294; 7,515,054; 7,567,693; 7,647,097; 7,740,592; 7,751,877; 7,831,305; 7,856,264; 7,881,780; 7,970,734; 7,972,278; 7,974,787; 7,991,461; 8,012,107; 8,032,486; 8,033,996; 8,060,194; 8,095,209; 8,209,224; 8,239,030; 8,262,714; 8,320,649; 8,358,818; 8,376,965; 8,380,316; 8,386,312; 8,386,313; 8,392,250; 8,392,253; 8,392,254; 8,392,255; 8,437,844; 8,464,288; 8,475,371; 8,483,816; 8,494,905; 8,517,912; 8,533,042; 8,545,420; 8,560,041; 8,655,428; 8,672,852; 8,682,687; 8,684,742; 8,694,157; 8,706,241; 8,706,518; 8,738,395; 8,753,296; 8,762,202; 8,764,673; 8,768,022; 8,788,030; 8,790,255; 8,790,297; 8,821,376; 8,838,247; 8,864,310; 8,872,640; 8,888,723; 8,915,871; 8,938,289; 8,938,301; 8,942,813; 8,955,010; 8,955,974; 8,958,882; 8,964,298; 8,971,936; 8,989,835; 8,992,230; 8,998,828; 9,004,687; 9,060,671; 9,101,279; 9,135,221; 9,142,145; 9,165,472; 9,173,582; 9,179,855; 9,208,558; 9,215,978; 9,232,984; 9,241,665; 9,242,067; 9,254,099; 9,271,660; 9,275,191; 9,282,927; 9,292,858; 9,292,920; 9,320,450; 9,326,705; 9,330,206; 9,357,941; 9,396,669; 9,398,873; 9,414,780; 9,414,907; 9,424,761; 9,445,739; 9,445,763; 9,451,303; 9,451,899; 9,454,646; 9,462,977; 9,468,541; 9,483,117; 9,492,120; 9,504,420; 9,504,788; 9,526,419; 9,541,383; 9,545,221; 9,545,222; 9,545,225; 9,560,967; 9,560,984; 9,563,740; 9,582,072; 9,596,224; 9,615,746; 9,622,702; 9,622,703; 9,626,756; 9,629,568; 9,642,699; 9,649,030; 9,651,368; 9,655,573; 9,668,694; 9,672,302; 9,672,617; 9,682,232; 9,693,734; 9,694,155; 9,704,205; 9,706,910; 9,710,788; RE44408; RE45766; 20020024450; 20020103428; 20020103429; 20020112732; 20020128540; 20030028081; 20030028121; 20030070685; 20030083596; 20030100844; 20030120172; 20030149351; 20030158496; 20030158497; 20030171658; 20040019257; 20040024287; 20040068172; 20040092809; 20040101146; 20040116784; 20040143170; 20040267152; 20050010091; 20050019734; 20050025704; 20050038354; 20050113713; 20050124851; 20050148828; 20050228785; 20050240253; 20050245796; 20050267343; 20050267344; 20050283053; 20060020184; 20060061544; 20060078183; 20060087746; 20060102171; 20060129277; 20060161218; 20060189866; 20060200013; 20060241718; 20060252978; 20060252979; 20070050715; 20070179534; 20070191704; 20070238934; 20070273611; 20070282228; 20070299371; 20080004550; 20080009772; 20080058668; 20080081963; 20080119763; 20080123927; 20080132383; 20080228239; 20080234113; 20080234601; 20080242521; 20080255949; 20090018419; 20090058660; 20090062698; 20090076406; 20090099474; 20090112523; 20090221928; 20090267758; 20090270687; 20090270688; 20090270692; 20090270693; 20090270694; 20090270786; 20090281400; 20090287108; 20090297000; 20090299169; 20090311655; 20090312808; 20090312817; 20090318794; 20090326604; 20100004977; 20100010289; 20100010366; 20100041949; 20100069739; 20100069780; 20100163027; 20100163028; 20100163035; 20100165593; 20100168525; 20100168529; 20100168602; 20100268055; 20100293115; 20110004412; 20110009777; 20110015515; 20110015539; 20110043759; 20110054272; 20110077548; 20110092882; 20110105859; 20110130643; 20110172500; 20110218456; 20110256520; 20110270074; 20110301488; 20110307079; 20120004579; 20120021394; 20120036004; 20120071771; 20120108909; 20120108995; 20120136274; 20120150545; 20120203130; 20120262558; 20120271377; 20120310106; 20130012804; 20130046715; 20130063434; 20130063550; 20130080127; 20130120246; 20130127980; 20130185144; 20130189663; 20130204085; 20130211238; 20130226464; 20130242262; 20130245424; 20130281759; 20130289360; 20130293844; 20130308099; 20130318546; 20140058528; 20140155714; 20140171757; 20140200432; 20140214335; 20140221866; 20140243608; 20140243614; 20140243652; 20140276130; 20140276944; 20140288614; 20140296750; 20140300532; 20140303508; 20140304773; 20140313303; 20140315169; 20140316191; 20140316192; 20140316235; 20140316248; 20140323899; 20140335489; 20140343408; 20140347491; 20140350353; 20140350431; 20140364721; 20140378810; 20150002815; 20150003698; 20150003699; 20150005640; 20150005644; 20150006186; 20150012111; 20150038869; 20150045606; 20150051663; 20150099946; 20150112409; 20150120007; 20150124220; 20150126845; 20150126873; 20150133812; 20150141773; 20150145676; 20150154889; 20150174362; 20150196800; 20150213191; 20150223731; 20150234477; 20150235088; 20150235370; 20150235441; 20150235447; 20150241705; 20150241959; 20150242575; 20150242943; 20150243100; 20150243105; 20150243106; 20150247723; 20150247975; 20150247976; 20150248169; 20150248170; 20150248787; 20150248788; 20150248789; 20150248791; 20150248792; 20150248793; 20150290453; 20150290454; 20150305685; 20150306340; 20150309563; 20150313496; 20150313539; 20150324692; 20150325151; 20150335288; 20150339363; 20150351690; 20150366497; 20150366504; 20150366656; 20150366659; 20150369864; 20150370320; 20160000354; 20160004298; 20160005320; 20160007915; 20160008620; 20160012749; 20160015289; 20160022167; 20160022206; 20160029946; 20160029965; 20160038069; 20160051187; 20160051793; 20160066838; 20160073886; 20160077547; 20160078780; 20160106950; 20160112684; 20160120436; 20160143582; 20160166219; 20160167672; 20160176053; 20160180054; 20160198950; 20160199577; 20160202755; 20160216760; 20160220439; 20160228640; 20160232625; 20160232811; 20160235323; 20160239084; 20160248994; 20160249826; 20160256108; 20160267809; 20160270656; 20160287157; 20160302711; 20160306942; 20160313798; 20160317060; 20160317383; 20160324478; 20160324580; 20160334866; 20160338644; 20160338825; 20160339300; 20160345901; 20160357256; 20160360970; 20160363483; 20170000324; 20170000325; 20170000326; 20170000329; 20170000330; 20170000331; 20170000332; 20170000333; 20170000334; 20170000335; 20170000337; 20170000340; 20170000341; 20170000342; 20170000343; 20170000345; 20170000454; 20170000683; 20170001032; 20170006931; 20170007111; 20170007115; 20170007116; 20170007122; 20170007123; 20170007165; 20170007182; 20170007450; 20170007799; 20170007843; 20170010469; 20170010470; 20170017083; 20170020447; 20170020454; 20170020627; 20170027467; 20170027651; 20170027812; 20170031440; 20170032098; 20170035344; 20170043160; 20170055900; 20170060298; 20170061034; 20170071523; 20170071537; 20170071546; 20170071551; 20170080320; 20170086729; 20170095157; 20170099479; 20170100540; 20170103440; 20170112427; 20170112671; 20170113046; 20170113056; 20170119994; 20170135597; 20170135633; 20170136264; 20170136265; 20170143249; 20170143442; 20170148340; 20170156662; 20170162072; 20170164876; 20170164878; 20170168568; 20170173262; 20170173326; 20170177023; 20170188947; 20170202633; 20170209043; 20170209094; and 20170209737.


Light Stimulation


The functional relevance of brain oscillations in the alpha frequency range (8-13 Hz) has been repeatedly investigated through the use of rhythmic visual stimulation. There are two hypotheses on the origin of steady-state visual evoked potential (SSVEP) measured in EEG during rhythmic stimulation: entrainment of brain oscillations and superposition of event-related responses (ERPs). The entrainment but not the superposition hypothesis justifies rhythmic visual stimulation as a means to manipulate brain oscillations, because superposition assumes a linear summation of single responses, independent from ongoing brain oscillations. Participants stimulated with rhythmic flickering light of different frequencies and intensities, and entrainment was measured by comparing the phase coupling of brain oscillations stimulated by rhythmic visual flicker with the oscillations induced by arrhythmic jittered stimulation, varying the time, stimulation frequency, and intensity conditions. Phase coupling was found to be more pronounced with increasing stimulation intensity as well as at stimulation frequencies closer to each participant's intrinsic frequency. Even in a single sequence of an SSVEP, non-linear features (intermittency of phase locking) was found that contradict the linear summation of single responses, as assumed by the superposition hypothesis. Thus, evidence suggests that visual rhythmic stimulation entrains brain oscillations, validating the approach of rhythmic stimulation as a manipulation of brain oscillations. See, Notbohm A, Kurths J, Herrmann C S, Modification of Brain Oscillations via Rhythmic Light Stimulation Provides Evidence for Entrainment but Not for Superposition of Event-Related Responses, Front Hum Neurosci. 2016 Feb. 3; 10:10. doi: 10.3389/fnhum.2016.00010. eCollection 2016.


It is also known that periodic visual stimulation can trigger epileptic seizures.


Cochlear Implant


A cochlear implant is a surgically implanted electronic device that provides a sense of sound to a person who is profoundly deaf or severely hard of hearing in both ears. See, en.wikipedia.org/wiki/Cochlear_implant;


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 5,999,856; 6,354,299; 6,427,086; 6,430,443; 6,665,562; 6,873,872; 7,359,837; 7,440,806; 7,493,171; 7,610,083; 7,610,100; 7,702,387; 7,747,318; 7,765,088; 7,853,321; 7,890,176; 7,917,199; 7,920,916; 7,957,806; 8,014,870; 8,024,029; 8,065,017; 8,108,033; 8,108,042; 8,140,152; 8,165,687; 8,175,700; 8,195,295; 8,209,018; 8,224,431; 8,315,704; 8,332,024; 8,401,654; 8,433,410; 8,478,417; 8,515,541; 8,538,543; 8,560,041; 8,565,864; 8,574,164; 8,577,464; 8,577,465; 8,577,466; 8,577,467; 8,577,468; 8,577,472; 8,577,478; 8,588,941; 8,594,800; 8,644,946; 8,644,957; 8,652,187; 8,676,325; 8,696,724; 8,700,183; 8,718,776; 8,768,446; 8,768,477; 8,788,057; 8,798,728; 8,798,773; 8,812,126; 8,864,806; 8,868,189; 8,929,999; 8,968,376; 8,989,868; 8,996,120; 9,002,471; 9,044,612; 9,061,132; 9,061,151; 9,095,713; 9,135,400; 9,186,503; 9,235,685; 9,242,067; 9,248,290; 9,248,291; 9,259,177; 9,302,093; 9,314,613; 9,327,069; 9,352,145; 9,352,152; 9,358,392; 9,358,393; 9,403,009; 9,409,013; 9,415,215; 9,415,216; 9,421,372; 9,432,777; 9,501,829; 9,526,902; 9,533,144; 9,545,510; 9,550,064; 9,561,380; 9,578,425; 9,592,389; 9,604,067; 9,616,227; 9,643,017; 9,649,493; 9,674,621; 9,682,232; 9,743,197; 9,744,358; 20010014818; 20010029391; 20020099412; 20030114886; 20040073273; 20050149157; 20050182389; 20050182450; 20050182467; 20050182468; 20050182469; 20050187600; 20050192647; 20050209664; 20050209665; 20050209666; 20050228451; 20050240229; 20060064140; 20060094970; 20060094971; 20060094972; 20060095091; 20060095092; 20060161217; 20060173259; 20060178709; 20060195039; 20060206165; 20060235484; 20060235489; 20060247728; 20060282123; 20060287691; 20070038264; 20070049988; 20070156180; 20070198063; 20070213785; 20070244407; 20070255155; 20070255531; 20080049376; 20080140149; 20080161886; 20080208280; 20080235469; 20080249589; 20090163980; 20090163981; 20090243756; 20090259277; 20090270944; 20090280153; 20100030287; 20100100164; 20100198282; 20100217341; 20100231327; 20100241195; 20100268055; 20100268288; 20100318160; 20110004283; 20110060382; 20110166471; 20110295344; 20110295345; 20110295346; 20110295347; 20120035698; 20120116179; 20120116741; 20120150255; 20120245655; 20120262250; 20120265270; 20130165996; 20130197944; 20130235550; 20140032512; 20140098981; 20140200623; 20140249608; 20140275847; 20140330357; 20140350634; 20150018699; 20150045607; 20150051668; 20150065831; 20150066124; 20150080674; 20150328455; 20150374986; 20150374987; 20160067485; 20160243362; 20160261962; 20170056655; 20170087354; 20170087355; 20170087356; 20170113046; 20170117866; 20170135633; and 20170182312.


Vagus Nerve Stimulation


Vagus nerve stimulation (VNS) is a medical treatment that involves delivering electrical impulses to the vagus nerve. It is used as an adjunctive treatment for certain types of intractable epilepsy and treatment-resistant depression. See, en.wikipedia.org/wiki/Vagus_nerve_stimulation;


See, U.S. Pub. Pat. Nos. and U.S. Pat. Nos. 5,215,086; 5,231,988; 5,299,569; 5,335,657; 5,571,150; 5,928,272; 5,995,868; 6,104,956; 6,167,311; 6,205,359; 6,208,902; 6,248,126; 6,269,270; 6,339,725; 6,341,236; 6,356,788; 6,366,814; 6,418,344; 6,497,699; 6,549,804; 6,556,868; 6,560,486; 6,587,727; 6,591,137; 6,597,954; 6,609,030; 6,622,047; 6,665,562; 6,671,556; 6,684,105; 6,708,064; 6,735,475; 6,782,292; 6,788,975; 6,873,872; 6,879,859; 6,882,881; 6,920,357; 6,961,618; 7,003,352; 7,151,961; 7,155,279; 7,167,751; 7,177,678; 7,203,548; 7,209,787; 7,228,167; 7,231,254; 7,242,984; 7,277,758; 7,292,890; 7,313,442; 7,324,851; 7,346,395; 7,366,571; 7,386,347; 7,389,144; 7,403,820; 7,418,290; 7,422,555; 7,444,184; 7,454,245; 7,457,665; 7,463,927; 7,486,986; 7,493,172; 7,499,752; 7,561,918; 7,620,455; 7,623,927; 7,623,928; 7,630,757; 7,634,317; 7,643,881; 7,653,433; 7,657,316; 7,676,263; 7,680,526; 7,684,858; 7,706,871; 7,711,432; 7,734,355; 7,736,382; 7,747,325; 7,747,326; 7,769,461; 7,783,362; 7,801,601; 7,805,203; 7,840,280; 7,848,803; 7,853,321; 7,853,329; 7,860,548; 7,860,570; 7,865,244; 7,869,867; 7,869,884; 7,869,885; 7,890,185; 7,894,903; 7,899,539; 7,904,134; 7,904,151; 7,904,175; 7,908,008; 7,920,915; 7,925,353; 7,945,316; 7,957,796; 7,962,214; 7,962,219; 7,962,220; 7,974,688; 7,974,693; 7,974,697; 7,974,701; 7,996,079; 8,000,788; 8,027,730; 8,036,745; 8,041,418; 8,041,419; 8,046,076; 8,064,994; 8,068,911; 8,097,926; 8,108,038; 8,112,148; 8,112,153; 8,116,883; 8,150,508; 8,150,524; 8,160,696; 8,172,759; 8,180,601; 8,190,251; 8,190,264; 8,204,603; 8,209,009; 8,209,019; 8,214,035; 8,219,188; 8,224,444; 8,224,451; 8,229,559; 8,239,028; 8,260,426; 8,280,505; 8,306,627; 8,315,703; 8,315,704; 8,326,418; 8,337,404; 8,340,771; 8,346,354; 8,352,031; 8,374,696; 8,374,701; 8,379,952; 8,382,667; 8,401,634; 8,412,334; 8,412,338; 8,417,344; 8,423,155; 8,428,726; 8,452,387; 8,454,555; 8,457,747; 8,467,878; 8,478,428; 8,485,979; 8,489,185; 8,498,699; 8,515,538; 8,536,667; 8,538,523; 8,538,543; 8,548,583; 8,548,594; 8,548,604; 8,560,073; 8,562,536; 8,562,660; 8,565,867; 8,571,643; 8,571,653; 8,588,933; 8,591,419; 8,600,521; 8,603,790; 8,606,360; 8,615,309; 8,630,705; 8,634,922; 8,641,646; 8,644,954; 8,649,871; 8,652,187; 8,660,666; 8,666,501; 8,676,324; 8,676,330; 8,684,921; 8,694,118; 8,700,163; 8,712,547; 8,716,447; 8,718,779; 8,725,243; 8,738,126; 8,744,562; 8,761,868; 8,762,065; 8,768,471; 8,781,597; 8,815,582; 8,827,912; 8,831,732; 8,843,210; 8,849,409; 8,852,100; 8,855,775; 8,858,440; 8,864,806; 8,868,172; 8,868,177; 8,874,205; 8,874,218; 8,874,227; 8,888,702; 8,914,122; 8,918,178; 8,934,967; 8,942,817; 8,945,006; 8,948,855; 8,965,514; 8,968,376; 8,972,004; 8,972,013; 8,983,155; 8,983,628; 8,983,629; 8,985,119; 8,989,863; 8,989,867; 9,014,804; 9,014,823; 9,020,582; 9,020,598; 9,020,789; 9,026,218; 9,031,655; 9,042,201; 9,042,988; 9,043,001; 9,044,188; 9,050,469; 9,056,195; 9,067,054; 9,067,070; 9,079,940; 9,089,707; 9,089,719; 9,095,303; 9,095,314; 9,108,041; 9,113,801; 9,119,533; 9,135,400; 9,138,580; 9,162,051; 9,162,052; 9,174,045; 9,174,066; 9,186,060; 9,186,106; 9,204,838; 9,204,998; 9,220,910; 9,233,246; 9,233,258; 9,235,685; 9,238,150; 9,241,647; 9,242,067; 9,242,092; 9,248,286; 9,249,200; 9,249,234; 9,254,383; 9,259,591; 9,265,660; 9,265,661; 9,265,662; 9,265,663; 9,265,931; 9,265,946; 9,272,145; 9,283,394; 9,284,353; 9,289,599; 9,302,109; 9,309,296; 9,314,633; 9,314,635; 9,320,900; 9,326,720; 9,332,939; 9,333,347; 9,339,654; 9,345,886; 9,358,381; 9,359,449; 9,364,674; 9,365,628; 9,375,571; 9,375,573; 9,381,346; 9,394,347; 9,399,133; 9,399,134; 9,402,994; 9,403,000; 9,403,001; 9,403,038; 9,409,022; 9,409,028; 9,415,219; 9,415,222; 9,427,581; 9,440,063; 9,458,208; 9,468,761; 9,474,852; 9,480,845; 9,492,656; 9,492,678; 9,501,829; 9,504,390; 9,505,817; 9,522,085; 9,522,282; 9,526,902; 9,533,147; 9,533,151; 9,538,951; 9,545,226; 9,545,510; 9,561,380; 9,566,426; 9,579,506; 9,586,047; 9,592,003; 9,592,004; 9,592,409; 9,604,067; 9,604,073; 9,610,442; 9,622,675; 9,623,240; 9,643,017; 9,643,019; 9,656,075; 9,662,069; 9,662,490; 9,675,794; 9,675,809; 9,682,232; 9,682,241; 9,700,256; 9,700,716; 9,700,723; 9,707,390; 9,707,391; 9,717,904; 9,729,252; 9,737,230; 20010003799; 20010029391; 20020013612; 20020072776; 20020072782; 20020099417; 20020099418; 20020151939; 20030023282; 20030045914; 20030083716; 20030114886; 20030181954; 20030195574; 20030236557; 20030236558; 20040015204; 20040015205; 20040073273; 20040138721; 20040153129; 20040172089; 20040172091; 20040172094; 20040193220; 20040243182; 20040260356; 20050027284; 20050033379; 20050043774; 20050049651; 20050137645; 20050149123; 20050149157; 20050154419; 20050154426; 20050165458; 20050182288; 20050182450; 20050182453; 20050182467; 20050182468; 20050182469; 20050187600; 20050192644; 20050192647; 20050197590; 20050197675; 20050197678; 20050209654; 20050209664; 20050209665; 20050209666; 20050216070; 20050216071; 20050251220; 20050267542; 20060009815; 20060047325; 20060052657; 20060064138; 20060064139; 20060064140; 20060079936; 20060111644; 20060129202; 20060142802; 20060155348; 20060167497; 20060173493; 20060173494; 20060173495; 20060195154; 20060206155; 20060212090; 20060212091; 20060217781; 20060224216; 20060259077; 20060282123; 20060293721; 20060293723; 20070005115; 20070021800; 20070043401; 20070060954; 20070060984; 20070066997; 20070067003; 20070067004; 20070093870; 20070100377; 20070100378; 20070100392; 20070112404; 20070150024; 20070150025; 20070162085; 20070173902; 20070198063; 20070213786; 20070233192; 20070233193; 20070255320; 20070255379; 20080021341; 20080027347; 20080027348; 20080027515; 20080033502; 20080039904; 20080065183; 20080077191; 20080086182; 20080091240; 20080125829; 20080140141; 20080147137; 20080154332; 20080161894; 20080167571; 20080183097; 20080269542; 20080269833; 20080269834; 20080269840; 20090018462; 20090036950; 20090054946; 20090088680; 20090093403; 20090118780; 20090163982; 20090171405; 20090187230; 20090234419; 20090276011; 20090276012; 20090280153; 20090326605; 20100003656; 20100004705; 20100004717; 20100057159; 20100063563; 20100106217; 20100114190; 20100114192; 20100114193; 20100125219; 20100125304; 20100145428; 20100191304; 20100198098; 20100198296; 20100204749; 20100268288; 20100274303; 20100274308; 20100292602; 20110009920; 20110021899; 20110028799; 20110029038; 20110029044; 20110034912; 20110054569; 20110077721; 20110092800; 20110098778; 20110105998; 20110125203; 20110130615; 20110137381; 20110152967; 20110152988; 20110160795; 20110166430; 20110166546; 20110172554; 20110172725; 20110172732; 20110172739; 20110178441; 20110178442; 20110190569; 20110201944; 20110213222; 20110224602; 20110224749; 20110230701; 20110230938; 20110257517; 20110264182; 20110270095; 20110270096; 20110270346; 20110270347; 20110276107; 20110276112; 20110282225; 20110295344; 20110295345; 20110295346; 20110295347; 20110301529; 20110307030; 20110311489; 20110319975; 20120016336; 20120016432; 20120029591; 20120029601; 20120046711; 20120059431; 20120078323; 20120083700; 20120083701; 20120101326; 20120116741; 20120158092; 20120179228; 20120184801; 20120185020; 20120191158; 20120203079; 20120209346; 20120226130; 20120232327; 20120265262; 20120303080; 20120310050; 20120316622; 20120330369; 20130006332; 20130018438; 20130018439; 20130018440; 20130019325; 20130046358; 20130066350; 20130066392; 20130066395; 20130072996; 20130089503; 20130090454; 20130096441; 20130131753; 20130165846; 20130178913; 20130184639; 20130184792; 20130204144; 20130225953; 20130225992; 20130231721; 20130238049; 20130238050; 20130238053; 20130244323; 20130245464; 20130245486; 20130245711; 20130245712; 20130253612; 20130261703; 20130274625; 20130281890; 20130289653; 20130289669; 20130296406; 20130296637; 20130304159; 20130309278; 20130310909; 20130317580; 20130338450; 20140039290; 20140039336; 20140039578; 20140046203; 20140046407; 20140052213; 20140056815; 20140058189; 20140058292; 20140074188; 20140081071; 20140081353; 20140094720; 20140100633; 20140107397; 20140107398; 20140113367; 20140128938; 20140135680; 20140135886; 20140142653; 20140142654; 20140142669; 20140155772; 20140155952; 20140163643; 20140213842; 20140213961; 20140214135; 20140235826; 20140236272; 20140243613; 20140243714; 20140257118; 20140257132; 20140257430; 20140257437; 20140257438; 20140275716; 20140276194; 20140277255; 20140277256; 20140288620; 20140303452; 20140324118; 20140330334; 20140330335; 20140330336; 20140336514; 20140336730; 20140343463; 20140357936; 20140358067; 20140358193; 20140378851; 20150005592; 20150005839; 20150012054; 20150018893; 20150025422; 20150032044; 20150032178; 20150051655; 20150051656; 20150051657; 20150051658; 20150051659; 20150057715; 20150072394; 20150073237; 20150073505; 20150119689; 20150119794; 20150119956; 20150142082; 20150148878; 20150157859; 20150165226; 20150174398; 20150174405; 20150174407; 20150182753; 20150182756; 20150190636; 20150190637; 20150196246; 20150202428; 20150208978; 20150216469; 20150231330; 20150238761; 20150265830; 20150265836; 20150283265; 20150297719; 20150297889; 20150306392; 20150343222; 20150352362; 20150360030; 20150366482; 20150374973; 20150374993; 20160001096; 20160008620; 20160012749; 20160030666; 20160045162; 20160045731; 20160051818; 20160058359; 20160074660; 20160081610; 20160114165; 20160121114; 20160121116; 20160135727; 20160136423; 20160144175; 20160151628; 20160158554; 20160175607; 20160199656; 20160199662; 20160206236; 20160222073; 20160232811; 20160243381; 20160249846; 20160250465; 20160263376; 20160279021; 20160279022; 20160279023; 20160279024; 20160279025; 20160279267; 20160279410; 20160279435; 20160287869; 20160287895; 20160303396; 20160303402; 20160310070; 20160331952; 20160331974; 20160331982; 20160339237; 20160339238; 20160339239; 20160339242; 20160346542; 20160361540; 20160361546; 20160367808; 20160375245; 20170007820; 20170027812; 20170043160; 20170056467; 20170056642; 20170066806; 20170079573; 20170080050; 20170087364; 20170095199; 20170095670; 20170113042; 20170113057; 20170120043; 20170120052; 20170143550; 20170143963; 20170143986; 20170150916; 20170150921; 20170151433; 20170157402; 20170164894; 20170189707; 20170198017; and 20170224994.


Brain-To-Brain Interface


A brain-brain interface is a direct communication pathway between the brain of one animal and the brain of another animal. Brain to brain interfaces have been used to help rats collaborate with each other. When a second rat was unable to choose the correct lever, the first rat noticed (not getting a second reward), and produced a round of task-related neuron firing that made the second rat more likely to choose the correct lever. Human studies have also been conducted.


In 2013, researcher from the University of Washington were able to use electrical brain recordings and a form of magnetic stimulation to send a brain signal to a recipient, which caused the recipient to hit the fire button on a computer game. In 2015, researchers linked up multiple brains, of both monkeys and rats, to form an “organic computer.” It is hypothesized that by using brain-to-brain interfaces (BTBIs) a biological computer, or brain-net, could be constructed using animal brains as its computational units. Initial exploratory work demonstrated collaboration between rats in distant cages linked by signals from cortical microelectrode arrays implanted in their brains. The rats were rewarded when actions were performed by the “decoding rat” which conformed to incoming signals and when signals were transmitted by the “encoding rat” which resulted in the desired action. In the initial experiment the rewarded action was pushing a lever in the remote location corresponding to the position of a lever near a lighted LED at the home location. About a month was required for the rats to acclimate themselves to incoming “brainwaves.” When a decoding rat was unable to choose the correct lever, the encoding rat noticed (not getting an expected reward), and produced a round of task-related neuron firing that made the second rat more likely to choose the correct lever.


In another study, electrical brain readings were used to trigger a form of magnetic stimulation, to send a brain signal based on brain activity on a subject to a recipient, which caused the recipient to hit the fire button on a computer game.


Brain-To-Computer Interface


A brain-computer interface (BCI), sometimes called a neural-control interface (NCI), mind-machine interface (MMI), direct neural interface (DNI), or brain-machine interface (BMI), is a direct communication pathway between an enhanced or wired brain and an external device. BCI differs from neuromodulation in that it allows for bidirectional information flow. BCIs are often directed at researching, mapping, assisting, augmenting, or repairing human cognitive or sensory-motor functions.


Synthetic telepathy, also known as techlepathy or psychotronics (geeldon.wordpress.com/2010/09/06/synthetic-telepathy-also-known-as-techlepathy-or-psychotronics/), describes the process of use of brain-computer interfaces by which human thought (as electromagnetic radiation) is intercepted, processed by computer and a return signal generated that is perceptible by the human brain. Dewan, E. M., “Occipital Alpha Rhythm Eye Position and Lens Accommodation.” Nature 214, 975-977 (3 Jun. 1967), demonstrates the mental control of Alpha waves, turning them on and off, to produce Morse code representations of words and phrases by thought alone. U.S. Pat. No. 3,951,134 proposes remotely monitoring and altering brainwaves using radio, and references demodulating the waveform, displaying it to an operator for viewing and passing this to a computer for further analysis. In 1988, Farwell, L. A., & Donchin, E. (1988). Talking off the top of your head: toward a mental prosthesis utilizing event-related brain potentials. Electroencephalography and Clinical Neurophysiology, 70(6), 510-523 describes a method of transmitting linguistic information using the P300 response system, which combines matching observed information to what the subject was thinking of. In this case, being able to select a letter of the alphabet that the subject was thinking of. In theory, any input could be used and a lexicon constructed. U.S. Pat. No. 6,011,991 describes a method of monitoring an individual's brain waves remotely, for the purposes of communication, and outlines a system that monitors an individual's brainwaves via a sensor, then transmits this information, specifically by satellite, to a computer for analysis. This analysis would determine if the individual was attempting to communicate a “word, phrase, or thought corresponding to the matched stored normalized signal.”


Approaches to synthetic telepathy can be categorized into two major groups, passive and active. Like sonar, the receiver can take part or passively listen. Passive reception is the ability to “read” a signal without first broadcasting a signal. This can be roughly equated to tuning into a radio station—the brain generates electromagnetic radiation which can be received at a distance. That distance is determined by the sensitivity of the receiver, the filters used and the bandwidth required. Most universities would have limited budgets, and receivers, such as EEG (and similar devices), would be used. A related military technology is the surveillance system TEMPEST. Robert G. Malech's approach requires a modulated signal to be broadcast at the target. The method uses an active signal, which is interfered with by the brain's modulation. Thus, the return signal can be used to infer the original brainwave.


Computer mediation falls into two basic categories, interpretative and interactive. Interpretative mediation is the passive analysis of signals coming from the human brain. A computer “reads” the signal then compares that signal against a database of signals and their meanings. Using statistical analysis and repetition, false-positives are reduced over time. Interactive mediation can be in a passive-active mode or active-active mode. In this case, passive and active denote the method of reading and writing to the brain and whether or not they make use of a broadcast signal. Interactive mediation can also be performed manually or via artificial intelligence. Manual interactive mediation involves a human operator producing return signals such as speech or images. A.I. mediation leverages the cognitive system of the subject to identify images, pre-speech, objects, sounds and other artifacts, rather than developing A.I. routines to perform such activities. A.I. based systems may incorporate natural language processing interfaces that produce sensations, mental impressions, humor and conversation to provide a mental picture of a computerized personality. Statistical analysis and machine learning techniques, such as neural networks can be used.


ITV News Service, in March 1991, produced a report of ultrasound piggybacked on a commercial radio broadcast (100 Mhz) aimed at entraining the brains of Iraqi troops and creating feelings of despair. U.S. Pat. No. 5,159,703 that refers to a “silent communications system in which nonaural carriers, in the very low or very high audio frequency range or in the adjacent ultrasonic frequency spectrum, are amplitude or frequency modulated with the desired intelligence and propagated acoustically or vibrationally, for inducement into the brain, typically through the use of loudspeakers, earphones or piezoelectric transducers.” See:

  • Dr Nick Begich—Controlling the Human Mind, Earth Pulse Press Anchorage—isbn=1-890693-54-5
    • cbcg.org/gjcs1.htm %7C God's Judgment Cometh Soon
    • cnslab.ss.uci.edu/muri/research.html, #Dewan, #FarwellDonchin, #ImaginedSpeechProduction, #Overview, MURI:


      Synthetic Telepathy
  • daprocess.com/01.welcome.htmlDaProcess of A Federal Investigation
  • deepthought.newsvine.com/_news/2012/01/01/9865851-nsa-disinformation-watch-the-watchers-with-me
  • deepthought.newsvine.com/_news/2012/01/09/10074589-nsa-disinformation-watch-the-watchers-with-me-part-2
  • deepthought.newsvine.com/_news/2012/01/16/10169491-the-nsa-behind-the-curtain
  • genamason.wordpress.com/2009/10/18/more-on-synthetic-telepathy/
  • io9.com/5065304/tips-and-tricks-for-mind-control-from-the-us-military
  • newdawnmagazine.com.au/Artide/Brain_Zapping_Part_One.html
  • pinktentacle.com/2008/12/scientists-extract-images-directly-from-brain/Scientists extract images directly from brain
  • timesofindia.indiatimes.com/HealthScUS_army_developing_synthetic_telepathy/
  • www.bibliotecapleyades.net/ciencia/cienciα_nonlethalweapons02.htm Eleanor White—New Devices That ‘Talk’ To The Human Mind Need Debate, Controls
  • www.cbsnews.com/stories/2008/12/31/60 minutes/main4694713.shtml 60 Minutes: Incredible Research Lets Scientists Get A Glimpse At Your Thoughts
  • www.cbsnews.com/video/watch/?id=5119805n&amptag=related;photovideo 60 Minutes: Video-Mind Reading
  • www.charlesreh n.com/charlesreh n/books/aconversationwithamerica/essays/myessays/The %20NSA.doc
  • www.govtrack.us/congress/billtext.xpd?bill=h107-2977 Space Preservation Act of 2001
  • www.informaworld.com/smpp/content-db=all-content=a785359968 Partial Amnesia for a Narrative Following


Application of Theta Frequency Electromagnetic Fields

  • www.msnbc.msn.com/id/27162401/
  • www.psychology.nottingham.ac.uk/staff/Ipxdts/TMS %20info.html Transcranial Magnetic Stimulation
  • www.ravenl.net/silsoun2.htm Psy-Ops Weaponry Used In The Persian Gulf War
  • www.scribd.com/doc/24531011/Operation-Mind-Control
  • www.scribd.com/doc/6508206/synthetic-telepathy-and-the-early-mind-wars
  • www.slavery.org.uk/Bioeffects_of_Selected_Non-Lethal_Weapons.pdf-Bioeffects of selected non-lethal weapons
  • www.sst.ws/tempstandards.php?pab=1_1 TEMPEST measurement standards
  • www.uwe.ac.uk/hlss/research/cpss/Journal_Psycho-Social_Studies/v2-2/SmithC.shtml Journal of Psycho-Social Studies—Vol 2 (2) 2003—On the Need for New Criteria of Diagnosis of Psychosis in the Light of Mind Invasive Technology by Dr. Carole Smith
  • www.wired.com/dangerroom/2009/05/pentagon-preps-soldier-telepathy-push
  • www.wired.com/wired/archive/7.11/persinger.html This Is Your Brain on God
  • Noah, Shachtman—Pentagon's PCs Bend to Your Brain www.wired.com/dangerroom/2007/03/the_us_military Soldier-Telepathy” Drummond, Katie—Pentagon Preps Soldier Telepathy Push U.S. Pat. No. 3,951,134
  • U.S. Pat. No. 5,159,703 Silent subliminal presentation system
  • U.S. Pat. No. 6,011,991
  • U.S. Pat. No. 6,587,729 Apparatus for audibly communicating speech using the radio frequency hearing effect Wall, Judy, “Military Use of Mind Control Weapons”, NEXUS, 5/06, October-November 1998


It is known to analyze EEG patterns to extract an indication of certain volitional activity (U.S. Pat. No. 6,011,991). This technique describes that an EEG recording can be matched against a stored normalized signal using a computer. This matched signal is then translated into the corresponding reference. The patent application describes a method “a system capable of identifying particular nodes in an individual's brain, the firings of which affect characteristics such as appetite, hunger, thirst, communication skills” and “devices mounted to the person (e.g. underneath the scalp) may be energized in a predetermined manner or sequence to remotely cause particular identified brain node(s) to be fired in order to cause a predetermined feeling or reaction in the individual” without technical description of implementation. This patent also describes, that “brain activity [is monitored] by way of electroencephalograph (EEG) methods, magnetoencephalograph (MEG) methods, and the like. For example, see U.S. Pat. Nos. 5,816,247 and 5,325,862.


See also, U.S. Pub. App. Nos. and U.S. Pat. Nos. 3,951,134; 4,437,064; 4,591,787; 4,613,817; 4,689,559; 4,693,000; 4,700,135; 4,733,180; 4,736,751; 4,749,946; 4,753,246; 4,761,611; 4,771,239; 4,801,882; 4,862,359; 4,913,152; 4,937,525; 4,940,058; 4,947,480; 4,949,725; 4,951,674; 4,974,602; 4,982,157; 4,983,912; 4,996,479; 5,008,622; 5,012,190; 5,020,538; 5,061,680; 5,092,835; 5,095,270; 5,126,315; 5,158,932; 5,159,703; 5,159,928; 5,166,614; 5,187,327; 5,198,977; 5,213,338; 5,241,967; 5,243,281; 5,243,517; 5,263,488; 5,265,611; 5,269,325; 5,282,474; 5,283,523; 5,291,888; 5,303,705; 5,307,807; 5,309,095; 5,311,129; 5,323,777; 5,325,862; 5,326,745; 5,339,811; 5,417,211; 5,418,512; 5,442,289; 5,447,154; 5,458,142; 5,469,057; 5,476,438; 5,496,798; 5,513,649; 5,515,301; 5,552,375; 5,579,241; 5,594,849; 5,600,243; 5,601,081; 5,617,856; 5,626,145; 5,656,937; 5,671,740; 5,682,889; 5,701,909; 5,706,402; 5,706,811; 5,729,046; 5,743,854; 5,743,860; 5,752,514; 5,752,911; 5,755,227; 5,761,332; 5,762,611; 5,767,043; 5,771,261; 5,771,893; 5,771,894; 5,797,853; 5,813,993; 5,815,413; 5,842,986; 5,857,978; 5,885,976; 5,921,245; 5,938,598; 5,938,688; 5,970,499; 6,002,254; 6,011,991; 6,023,161; 6,066,084; 6,069,369; 6,080,164; 6,099,319; 6,144,872; 6,154,026; 6,155,966; 6,167,298; 6,167,311; 6,195,576; 6,230,037; 6,239,145; 6,263,189; 6,290,638; 6,354,087; 6,356,079; 6,370,414; 6,374,131; 6,385,479; 6,418,344; 6,442,948; 6,470,220; 6,488,617; 6,516,246; 6,526,415; 6,529,759; 6,538,436; 6,539,245; 6,539,263; 6,544,170; 6,547,746; 6,557,558; 6,587,729; 6,591,132; 6,609,030; 6,611,698; 6,648,822; 6,658,287; 6,665,552; 6,665,553; 6,665,562; 6,684,098; 6,687,525; 6,695,761; 6,697,660; 6,708,051; 6,708,064; 6,708,184; 6,725,080; 6,735,460; 6,774,929; 6,785,409; 6,795,724; 6,804,661; 6,815,949; 6,853,186; 6,856,830; 6,873,872; 6,876,196; 6,885,192; 6,907,280; 6,926,921; 6,947,790; 6,978,179; 6,980,863; 6,983,184; 6,983,264; 6,996,261; 7,022,083; 7,023,206; 7,024,247; 7,035,686; 7,038,450; 7,039,266; 7,039,547; 7,053,610; 7,062,391; 7,092,748; 7,105,824; 7,116,102; 7,120,486; 7,130,675; 7,145,333; 7,171,339; 7,176,680; 7,177,675; 7,183,381; 7,186,209; 7,187,169; 7,190,826; 7,193,413; 7,196,514; 7,197,352; 7,199,708; 7,209,787; 7,218,104; 7,222,964; 7,224,282; 7,228,178; 7,231,254; 7,242,984; 7,254,500; 7,258,659; 7,269,516; 7,277,758; 7,280,861; 7,286,871; 7,313,442; 7,324,851; 7,334,892; 7,338,171; 7,340,125; 7,340,289; 7,346,395; 7,353,064; 7,353,065; 7,369,896; 7,371,365; 7,376,459; 7,394,246; 7,400,984; 7,403,809; 7,403,820; 7,409,321; 7,418,290; 7,420,033; 7,437,196; 7,440,789; 7,453,263; 7,454,387; 7,457,653; 7,461,045; 7,462,155; 7,463,024; 7,466,132; 7,468,350; 7,482,298; 7,489,964; 7,502,720; 7,539,528; 7,539,543; 7,553,810; 7,565,200; 7,565,809; 7,567,693; 7,570,054; 7,573,264; 7,573,268; 7,580,798; 7,603,174; 7,608,579; 7,613,502; 7,613,519; 7,613,520; 7,620,456; 7,623,927; 7,623,928; 7,625,340; 7,627,370; 7,647,098; 7,649,351; 7,653,433; 7,672,707; 7,676,263; 7,678,767; 7,697,979; 7,706,871; 7,715,894; 7,720,519; 7,729,740; 7,729,773; 7,733,973; 7,734,340; 7,737,687; 7,742,820; 7,746,979; 7,747,325; 7,747,326; 7,747,551; 7,756,564; 7,763,588; 7,769,424; 7,771,341; 7,792,575; 7,800,493; 7,801,591; 7,801,686; 7,831,305; 7,834,627; 7,835,787; 7,840,039; 7,840,248; 7,840,250; 7,853,329; 7,856,264; 7,860,552; 7,873,411; 7,881,760; 7,881,770; 7,882,135; 7,891,814; 7,892,764; 7,894,903; 7,895,033; 7,904,139; 7,904,507; 7,908,009; 7,912,530; 7,917,221; 7,917,225; 7,929,693; 7,930,035; 7,932,225; 7,933,727; 7,937,152; 7,945,304; 7,962,204; 7,974,787; 7,986,991; 7,988,969; 8,000,767; 8,000,794; 8,001,179; 8,005,894; 8,010,178; 8,014,870; 8,027,730; 8,029,553; 8,032,209; 8,036,736; 8,055,591; 8,059,879; 8,065,360; 8,069,125; 8,073,631; 8,082,215; 8,083,786; 8,086,563; 8,116,874; 8,116,877; 8,121,694; 8,121,695; 8,150,523; 8,150,796; 8,155,726; 8,160,273; 8,185,382; 8,190,248; 8,190,264; 8,195,593; 8,209,224; 8,212,556; 8,222,378; 8,224,433; 8,229,540; 8,239,029; 8,244,552; 8,244,553; 8,248,069; 8,249,316; 8,270,814; 8,280,514; 8,285,351; 8,290,596; 8,295,934; 8,301,222; 8,301,257; 8,303,636; 8,304,246; 8,305,078; 8,308,646; 8,315,703; 8,334,690; 8,335,715; 8,335,716; 8,337,404; 8,343,066; 8,346,331; 8,350,804; 8,354,438; 8,356,004; 8,364,271; 8,374,412; 8,374,696; 8,380,314; 8,380,316; 8,380,658; 8,386,312; 8,386,313; 8,388,530; 8,392,250; 8,392,251; 8,392,253; 8,392,254; 8,392,255; 8,396,545; 8,396,546; 8,396,744; 8,401,655; 8,406,838; 8,406,848; 8,412,337; 8,423,144; 8,423,297; 8,429,225; 8,431,537; 8,433,388; 8,433,414; 8,433,418; 8,439,845; 8,444,571; 8,445,021; 8,447,407; 8,456,164; 8,457,730; 8,463,374; 8,463,378; 8,463,386; 8,463,387; 8,464,288; 8,467,878; 8,473,345; 8,483,795; 8,484,081; 8,487,760; 8,492,336; 8,494,610; 8,494,857; 8,494,905; 8,498,697; 8,509,904; 8,519,705; 8,527,029; 8,527,035; 8,529,463; 8,532,756; 8,532,757; 8,533,042; 8,538,513; 8,538,536; 8,543,199; 8,548,786; 8,548,852; 8,553,956; 8,554,325; 8,559,645; 8,562,540; 8,562,548; 8,565,606; 8,568,231; 8,571,629; 8,574,279; 8,586,019; 8,587,304; 8,588,933; 8,591,419; 8,593,141; 8,600,493; 8,600,696; 8,603,790; 8,606,592; 8,612,005; 8,613,695; 8,613,905; 8,614,254; 8,614,873; 8,615,293; 8,615,479; 8,615,664; 8,618,799; 8,626,264; 8,628,328; 8,635,105; 8,648,017; 8,652,189; 8,655,428; 8,655,437; 8,655,817; 8,658,149; 8,660,649; 8,666,099; 8,679,009; 8,682,441; 8,690,748; 8,693,765; 8,700,167; 8,703,114; 8,706,205; 8,706,206; 8,706,241; 8,706,518; 8,712,512; 8,716,447; 8,721,695; 8,725,243; 8,725,668; 8,725,669; 8,725,796; 8,731,650; 8,733,290; 8,738,395; 8,762,065; 8,762,202; 8,768,427; 8,768,447; 8,781,197; 8,781,597; 8,786,624; 8,798,717; 8,814,923; 8,815,582; 8,825,167; 8,838,225; 8,838,247; 8,845,545; 8,849,390; 8,849,392; 8,855,775; 8,858,440; 8,868,173; 8,874,439; 8,888,702; 8,893,120; 8,903,494; 8,907,668; 8,914,119; 8,918,176; 8,922,376; 8,933,696; 8,934,965; 8,938,289; 8,948,849; 8,951,189; 8,951,192; 8,954,293; 8,955,010; 8,961,187; 8,974,365; 8,977,024; 8,977,110; 8,977,362; 8,993,623; 9,002,458; 9,014,811; 9,015,087; 9,020,576; 9,026,194; 9,026,218; 9,026,372; 9,031,658; 9,034,055; 9,034,923; 9,037,224; 9,042,074; 9,042,201; 9,042,988; 9,044,188; 9,053,516; 9,063,183; 9,064,036; 9,069,031; 9,072,482; 9,074,976; 9,079,940; 9,081,890; 9,095,266; 9,095,303; 9,095,618; 9,101,263; 9,101,276; 9,102,717; 9,113,801; 9,113,803; 9,116,201; 9,125,581; 9,125,788; 9,138,156; 9,142,185; 9,155,373; 9,161,715; 9,167,979; 9,173,609; 9,179,854; 9,179,875; 9,183,351; 9,192,300; 9,198,621; 9,198,707; 9,204,835; 9,211,076; 9,211,077; 9,213,074; 9,229,080; 9,230,539; 9,233,244; 9,238,150; 9,241,665; 9,242,067; 9,247,890; 9,247,911; 9,248,003; 9,248,288; 9,249,200; 9,249,234; 9,251,566; 9,254,097; 9,254,383; 9,259,482; 9,259,591; 9,261,573; 9,265,943; 9,265,965; 9,271,679; 9,280,784; 9,283,279; 9,284,353; 9,285,249; 9,289,595; 9,302,069; 9,309,296; 9,320,900; 9,329,758; 9,331,841; 9,332,939; 9,333,334; 9,336,535; 9,336,611; 9,339,227; 9,345,609; 9,351,651; 9,357,240; 9,357,298; 9,357,970; 9,358,393; 9,359,449; 9,364,462; 9,365,628; 9,367,738; 9,368,018; 9,370,309; 9,370,667; 9,375,573; 9,377,348; 9,377,515; 9,381,352; 9,383,208; 9,392,955; 9,394,347; 9,395,425; 9,396,669; 9,401,033; 9,402,558; 9,403,038; 9,405,366; 9,410,885; 9,411,033; 9,412,233; 9,415,222; 9,418,368; 9,421,373; 9,427,474; 9,438,650; 9,440,070; 9,445,730; 9,446,238; 9,448,289; 9,451,734; 9,451,899; 9,458,208; 9,460,400; 9,462,733; 9,463,327; 9,468,541; 9,471,978; 9,474,852; 9,480,845; 9,480,854; 9,483,117; 9,486,381; 9,486,389; 9,486,618; 9,486,632; 9,492,114; 9,495,684; 9,497,017; 9,498,134; 9,498,634; 9,500,722; 9,505,817; 9,517,031; 9,517,222; 9,519,981; 9,521,958; 9,534,044; 9,538,635; 9,539,118; 9,556,487; 9,558,558; 9,560,458; 9,560,967; 9,560,984; 9,560,986; 9,563,950; 9,568,564; 9,572,996; 9,579,035; 9,579,048; 9,582,925; 9,584,928; 9,588,203; 9,588,490; 9,592,384; 9,600,138; 9,604,073; 9,612,295; 9,618,591; 9,622,660; 9,622,675; 9,630,008; 9,642,553; 9,642,554; 9,643,019; 9,646,248; 9,649,501; 9,655,573; 9,659,186; 9,664,856; 9,665,824; 9,665,987; 9,675,292; 9,681,814; 9,682,232; 9,684,051; 9,685,600; 9,687,562; 9,694,178; 9,694,197; 9,713,428; 9,713,433; 9,713,444; 9,713,712; D627476; RE44097; RE46209; 20010009975; 20020103428; 20020103429; 20020158631; 20020173714; 20030004429; 20030013981; 20030018277; 20030081818; 20030093004; 20030097159; 20030105408; 20030158495; 20030199749; 20040019370; 20040034299; 20040092809; 20040127803; 20040186542; 20040193037; 20040210127; 20040210156; 20040263162; 20050015205; 20050033154; 20050043774; 20050059874; 20050216071; 20050256378; 20050283053; 20060074822; 20060078183; 20060100526; 20060135880; 20060225437; 20070005391; 20070036355; 20070038067; 20070043392; 20070049844; 20070083128; 20070100251; 20070165915; 20070167723; 20070191704; 20070197930; 20070239059; 20080001600; 20080021340; 20080091118; 20080167571; 20080249430; 20080304731; 20090018432; 20090082688; 20090099783; 20090149736; 20090179642; 20090216288; 20090299169; 20090312624; 20090318794; 20090319001; 20090319004; 20100010366; 20100030097; 20100049482; 20100056276; 20100069739; 20100092934; 20100094155; 20100113959; 20100131034; 20100174533; 20100197610; 20100219820; 20110015515; 20110015539; 20110046491; 20110082360; 20110110868; 20110150253; 20110182501; 20110217240; 20110218453; 20110270074; 20110301448; 20120021394; 20120143104; 20120150262; 20120191542; 20120232376; 20120249274; 20120253168; 20120271148; 20130012804; 20130013667; 20130066394; 20130072780; 20130096453; 20130150702; 20130165766; 20130211238; 20130245424; 20130251641; 20130255586; 20130304472; 20140005518; 20140058241; 20140062472; 20140077612; 20140101084; 20140121565; 20140135873; 20140142448; 20140155730; 20140159862; 20140206981; 20140243647; 20140243652; 20140245191; 20140249445; 20140249447; 20140271483; 20140275891; 20140276013; 20140276014; 20140276187; 20140276702; 20140277582; 20140279746; 20140296733; 20140297397; 20140300532; 20140303424; 20140303425; 20140303511; 20140316248; 20140323899; 20140328487; 20140330093; 20140330394; 20140330580; 20140335489; 20140336489; 20140336547; 20140343397; 20140343882; 20140348183; 20140350380; 20140354278; 20140357507; 20140357932; 20140357935; 20140358067; 20140364721; 20140370479; 20140371573; 20140371611; 20140378815; 20140378830; 20150005840; 20150005841; 20150008916; 20150011877; 20150017115; 20150018665; 20150018702; 20150018705; 20150018706; 20150019266; 20150025422; 20150025917; 20150026446; 20150030220; 20150033363; 20150044138; 20150065838; 20150065845; 20150069846; 20150072394; 20150073237; 20150073249; 20150080695; 20150080703; 20150080753; 20150080985; 20150088024; 20150088224; 20150091730; 20150091791; 20150096564; 20150099962; 20150105844; 20150112403; 20150119658; 20150119689; 20150119698; 20150119745; 20150123653; 20150133811; 20150133812; 20150133830; 20150140528; 20150141529; 20150141773; 20150148619; 20150150473; 20150150475; 20150151142; 20150154721; 20150154764; 20150157271; 20150161738; 20150174403; 20150174418; 20150178631; 20150178978; 20150182417; 20150186923; 20150192532; 20150196800; 20150201879; 20150202330; 20150206051; 20150206174; 20150212168; 20150213012; 20150213019; 20150213020; 20150215412; 20150216762; 20150219729; 20150219732; 20150220830; 20150223721; 20150226813; 20150227702; 20150230719; 20150230744; 20150231330; 20150231395; 20150231405; 20150238104; 20150248615; 20150253391; 20150257700; 20150264492; 20150272461; 20150272465; 20150283393; 20150289813; 20150289929; 20150293004; 20150294074; 20150297108; 20150297139; 20150297444; 20150297719; 20150304048; 20150305799; 20150305800; 20150305801; 20150306057; 20150306390; 20150309582; 20150313496; 20150313971; 20150315554; 20150317447; 20150320591; 20150324544; 20150324692; 20150327813; 20150328330; 20150335281; 20150335294; 20150335876; 20150335877; 20150343242; 20150359431; 20150360039; 20150366503; 20150370325; 20150374250; 20160000383; 20160005235; 20160008489; 20160008598; 20160008620; 20160008632; 20160012011; 20160012583; 20160015673; 20160019434; 20160019693; 20160022165; 20160022168; 20160022207; 20160022981; 20160023016; 20160029958; 20160029959; 20160029998; 20160030666; 20160030834; 20160038049; 20160038559; 20160038770; 20160048659; 20160048948; 20160048965; 20160051161; 20160051162; 20160055236; 20160058322; 20160063207; 20160063883; 20160066838; 20160070436; 20160073916; 20160073947; 20160081577; 20160081793; 20160082180; 20160082319; 20160084925; 20160086622; 20160095838; 20160097824; 20160100769; 20160103487; 20160103963; 20160109851; 20160113587; 20160116472; 20160116553; 20160120432; 20160120436; 20160120480; 20160121074; 20160128589; 20160128632; 20160129249; 20160131723; 20160135748; 20160139215; 20160140975; 20160143540; 20160143541; 20160148077; 20160148400; 20160151628; 20160157742; 20160157777; 20160157828; 20160158553; 20160162652; 20160164813; 20160166207; 20160166219; 20160168137; 20160170996; 20160170998; 20160171514; 20160174862; 20160174867; 20160175557; 20160175607; 20160184599; 20160198968; 20160203726; 20160204937; 20160205450; 20160206581; 20160206871; 20160206877; 20160210872; 20160213276; 20160219345; 20160220163; 20160220821; 20160222073; 20160223622; 20160223627; 20160224803; 20160235324; 20160238673; 20160239966; 20160239968; 20160240212; 20160240765; 20160242665; 20160242670; 20160250473; 20160256130; 20160257957; 20160262680; 20160275536; 20160278653; 20160278662; 20160278687; 20160278736; 20160279267; 20160287117; 20160287308; 20160287334; 20160287895; 20160299568; 20160300252; 20160300352; 20160302711; 20160302720; 20160303396; 20160303402; 20160306844; 20160313408; 20160313417; 20160313418; 20160321742; 20160324677; 20160324942; 20160334475; 20160338608; 20160339300; 20160346530; 20160357003; 20160360970; 20160361532; 20160361534; 20160371387; 20170000422; 20170014080; 20170020454; 20170021158; 20170021161; 20170027517; 20170032527; 20170039591; 20170039706; 20170041699; 20170042474; 20170042476; 20170042827; 20170043166; 20170043167; 20170045601; 20170052170; 20170053082; 20170053088; 20170053461; 20170053665; 20170056363; 20170056467; 20170056655; 20170065199; 20170065349; 20170065379; 20170065816; 20170066806; 20170079538; 20170079543; 20170080050; 20170080256; 20170085547; 20170085855; 20170086729; 20170087367; 20170091418; 20170095174; 20170100051; 20170105647; 20170107575; 20170108926; 20170119270; 20170119271; 20170120043; 20170131293; 20170133576; 20170133577; 20170135640; 20170140124; 20170143986; 20170146615; 20170146801; 20170147578; 20170148213; 20170148592; 20170150925; 20170151435; 20170151436; 20170154167; 20170156674; 20170165481; 20170168121; 20170168568; 20170172446; 20170173391; 20170178001; 20170178340; 20170180558; 20170181252; 20170182176; 20170188932; 20170189691; 20170190765; 20170196519; 20170197081; 20170198017; 20170199251; 20170202476; 20170202518; 20170206654; 20170209044; 20170209062; 20170209225; 20170209389; and 20170212188.


Brain Entrainment


Brain entrainment, also referred to as brainwave synchronization and neural entrainment, refers to the capacity of the brain to naturally synchronize its brainwave frequencies with the rhythm of periodic external stimuli, most commonly auditory, visual, or tactile. Brainwave entrainment technologies are used to induce various brain states, such as relaxation or sleep, by creating stimuli that occur at regular, periodic intervals to mimic electrical cycles of the brain during the desired states, thereby “training” the brain to consciously alter states. Recurrent acoustic frequencies, flickering lights, or tactile vibrations are the most common examples of stimuli applied to generate different sensory responses. It is hypothesized that listening to these beats of certain frequencies one can induce a desired state of consciousness that corresponds with specific neural activity. Patterns of neural firing, measured in Hz, correspond with alertness states such as focused attention, deep sleep, etc.


Neural oscillations are rhythmic or repetitive electrochemical activity in the brain and central nervous system. Such oscillations can be characterized by their frequency, amplitude and phase. Neural tissue can generate oscillatory activity driven by mechanisms within individual neurons, as well as by interactions between them. They may also adjust frequency to synchronize with the periodic vibration of external acoustic or visual stimuli. The functional role of neural oscillations is still not fully understood; however, they have been shown to correlate with emotional responses, motor control, and a number of cognitive functions including information transfer, perception, and memory. Specifically, neural oscillations, in particular theta activity, are extensively linked to memory function, and coupling between theta and gamma activity is considered to be vital for memory functions, including episodic memory. Electroencephalography (EEG) has been most widely used in the study of neural activity generated by large groups of neurons, known as neural ensembles, including investigations of the changes that occur in electroencephalographic profiles during cycles of sleep and wakefulness. EEG signals change dramatically during sleep and show a transition from faster frequencies to increasingly slower frequencies, indicating a relationship between the frequency of neural oscillations and cognitive states including awareness and consciousness.


The term ‘entrainment’ has been used to describe a shared tendency of many physical and biological systems to synchronize their periodicity and rhythm through interaction. This tendency has been identified as specifically pertinent to the study of sound and music generally, and acoustic rhythms specifically. The most ubiquitous and familiar examples of neuromotor entrainment to acoustic stimuli is observable in spontaneous foot or finger tapping to the rhythmic beat of a song. Exogenous rhythmic entrainment, which occurs outside the body, has been identified and documented for a variety of human activities, which include the way people adjust the rhythm of their speech patterns to those of the subject with whom they communicate, and the rhythmic unison of an audience clapping. Even among groups of strangers, the rate of breathing, locomotive and subtle expressive motor movements, and rhythmic speech patterns have been observed to synchronize and entrain, in response to an auditory stimulus, such as a piece of music with a consistent rhythm. Furthermore, motor synchronization to repetitive tactile stimuli occurs in animals, including cats and monkeys as well as humans, with accompanying shifts in electroencephalogram (EEG) readings. Examples of endogenous entrainment, which occurs within the body, include the synchronizing of human circadian sleep-wake cycles to the 24-hour cycle of light and dark, and the frequency following response of humans to sounds and music.


Brainwaves, or neural oscillations, share the fundamental constituents with acoustic and optical waves, including frequency, amplitude and periodicity. The synchronous electrical activity of cortical neural ensembles can synchronize in response to external acoustic or optical stimuli and also entrain or synchronize their frequency and phase to that of a specific stimulus. Brainwave entrainment is a colloquialism for such ‘neural entrainment’, which is a term used to denote the way in which the aggregate frequency of oscillations produced by the synchronous electrical activity in ensembles of cortical neurons can adjust to synchronize with the periodic vibration of an external stimuli, such as a sustained acoustic frequency perceived as pitch, a regularly repeating pattern of intermittent sounds, perceived as rhythm, or of a regularly rhythmically intermittent flashing light.


Changes in neural oscillations, demonstrable through electroencephalogram (EEG) measurements, are precipitated by listening to music, which can modulate autonomic arousal ergotropically and trophotropically, increasing and decreasing arousal respectively. Musical auditory stimulation has also been demonstrated to improve immune function, facilitate relaxation, improve mood, and contribute to the alleviation of stress.


The Frequency following response (FFR), also referred to as Frequency Following Potential (FFP), is a specific response to hearing sound and music, by which neural oscillations adjust their frequency to match the rhythm of auditory stimuli. The use of sound with intent to influence cortical brainwave frequency is called auditory driving, by which frequency of neural oscillation is ‘driven’ to entrain with that of the rhythm of a sound source.


See, en.wikipedia.org/wiki/Brainwave_entrainment;


U.S. Pub. App. Nos. and U.S. Pat. Nos. 5,070,399; 5,306,228; 5,409,445; 6,656,137; 7,749,155; 7,819,794; 7,988,613; 8,088,057; 8,167,784; 8,213,670; 8,267,851; 8,298,078; 8,517,909; 8,517,912; 8,579,793; 8,579,795; 8,597,171; 8,636,640; 8,638,950; 8,668,496; 8,852,073; 8,932,218; 8,968,176; 9,330,523; 9,357,941; 9,459,597; 9,480,812; 9,563,273; 9,609,453; 9,640,167; 9,707,372; 20050153268; 20050182287; 20060106434; 20060206174; 20060281543; 20070066403; 20080039677; 20080304691; 20100010289; 20100010844; 20100028841; 20100056854; 20100076253; 20100130812; 20100222640; 20100286747; 20100298624; 20110298706; 20110319482; 20120003615; 20120053394; 20120150545; 20130030241; 20130072292; 20130131537; 20130172663; 20130184516; 20130203019; 20130234823; 20130338738; 20140088341; 20140107401; 20140114242; 20140154647; 20140174277; 20140275741; 20140309484; 20140371516; 20150142082; 20150283019; 20150296288; 20150313496; 20150313949; 20160008568; 20160019434; 20160055842; 20160205489; 20160235980; 20160239084; 20160345901; 20170034638; 20170061760; 20170087330; 20170094385; 20170095157; 20170099713; 20170135597; and 20170149945.

  • Carter, J., and H. Russell. “A pilot investigation of auditory and visual entrainment of brain wave activity in learning disabled boys.” Texas Researcher 4.1 (1993): 65-75;
  • Casciaro, Francesco, et al. “Alpha-rhythm stimulation using brain entrainment enhances heart rate variability in subjects with reduced HRV.” World J. Neuroscience 3.04 (2013): 213;
  • Helfrich, Randolph F., et al. “Entrainment of brain oscillations by transcranial alternating current stimulation.” Current Biology 243 (2014): 333-339;
  • Huang, Tina L., and Christine Charyton. “A comprehensive review of the psychological effects of brainwave entrainment.” Alternative therapies in health and medicine 14.5 (2008): 38;
  • Joyce, Michael, and Dave Siever. “Audio-visual entrainment program as a treatment for behavior disorders in a school setting.” J. Neurotherapy 4.2 (2000): 9-25;
  • Keitel, Christian, Cliodhna Quigley, and Philipp Ruhnau. “Stimulus-driven brain oscillations in the alpha range: entrainment of intrinsic rhythms or frequency-following response?” J. Neuroscience 34.31 (2014): 10137-10140;
  • Lakatos, Peter, et al. “Entrainment of neuronal oscillations as a mechanism of attentional selection.” Science 320.5872 (2008): 110-113;
  • Mori, Toshio, and Shoichi Kai. “Noise-induced entrainment and stochastic resonance in human brain waves.” Physical review letters 88.21 (2002): 218101;
  • Padmanabhan, R., A. J. Hildreth, and D. Laws. “A prospective, randomised, controlled study examining binaural beat audio and pre-operative anxiety in patients undergoing general anaesthesia for day case surgery.” Anaesthesia 60.9 (2005): 874-877;
  • Schalles, Matt D., and Jaime A. Pineda. “Musical sequence learning and EEG correlates of audiomotor processing.” Behavioural neurology 2015 (2015). www.hindawi.com/journals/bn/2015/638202/Thaut,
  • Michael H., David A. Peterson, and Gerald C. McIntosh. “Temporal entrainment of cognitive functions.” Annals of the New York Academy of Sciences 1060.1 (2005): 243-254.
  • Thut, Gregor, Philippe G. Schyns, and Joachim Gross. “Entrainment of perceptually relevant brain oscillations by non-invasive rhythmic stimulation of the human brain.” Frontiers in Psychology 2 (2011);
  • Trost, Wiebke, et al. “Getting the beat: entrainment of brain activity by musical rhythm and pleasantness.” NeuroImage 103 (2014): 55-64;
  • Will, Udo, and Eric Berg. “Brain wave synchronization and entrainment to periodic acoustic stimuli.” Neuroscience letters 424.1 (2007): 55-60; and
  • Zhuang, Tianbao, Hong Zhao, and Zheng Tang. “A study of brainwave entrainment based on EEG brain dynamics.” Computer and information science 2.2 (2009): 80.


A baseline correction of event-related time-frequency measure may be made to take pre-event baseline activity into consideration. In general, a baseline period is defined by the average of the values within a time window preceding the time-locking event. There are at least four common methods for baseline correction in time-frequency analysis. The methods include various baseline value normalizations. See,

  • Spencer K M, Nestor P G, Perlmutter R, et al. Neural synchrony indexes disordered perception and cognition in schizophrenia. Proc Natl Acad Sci USA. 2004; 101:17288-17293;
  • Hoogenboom N, Schoffelen J M, Oostenveld R, Parkes L M, Fries P. Localizing human visual gamma-band activity in frequency, time and space. Neuroimage. 2006; 29:764-773;
  • Le Van Quyen M, Foucher J, Lachaux J, et al. Comparison of Hilbert transform and wavelet methods for the analysis of neuronal synchrony. J Neurosci Methods. 2001; 111:83-98, Lachaux J P, Rodriguez E, Martinerie J, Varela F J. Measuring phase synchrony in brain signals. Hum Brain Mapp. 1999; 8:194-208,
  • Rodriguez E, George N, Lachaux J P, Martinerie J, Renault B, Varela F J. Perception's shadow: long-distance synchronization of human brain activity. Nature. 1999; 397:430-433.,
  • Canolty R T, Edwards E, Dalal S S, et al. High gamma power is phase-locked to theta oscillations in human neocortex. Science. 2006; 313:1626-1628.


The question of whether different emotional states are associated with specific patterns of physiological response has long being a subject of neuroscience research See, for example:

  • James W (1884.) What is an emotion? Mind 9: 188-205; Lacey J I, Bateman D E, Vanlehn R (1953) Autonomic response specificity; an experimental study. Psychosom Med 15: 8-21;
  • Levenson R W, Heider K, Ekman P, Friesen W V (1992) Emotion and Autonomic Nervous-System Activity in the Minangkabau of West Sumatra. J Pers Soc Psychol 62: 972-988.


Some studies have indicated that the physiological correlates of emotions are likely to be found in the central nervous system (CNS). See, for example:

  • Buck R (1999) The biological affects: A typology. Psychological Review 106: 301-336; Izard C E (2007) Basic Emotions, Natural Kinds, Emotion Schemas, and a New Paradigm. Perspect Psychol Sci 2: 260-280;
  • Panksepp J (2007) Neurologizing the Psychology of Affects How Appraisal-Based Constructivism and Basic Emotion Theory Can Coexist. Perspect Psychol Sci 2: 281-296.


Electroencephalograms (EEG) and functional Magnetic Resonance Imaging, fMRI have been used to study specific brain activity associated with different emotional states. Mauss and Robinson, in their review paper, have indicated that “emotional state is likely to involve circuits rather than any brain region considered in isolation” (Mauss I B, Robinson M D (2009) Measures of emotion: A review. Cogn Emot 23: 209-237.)


The amplitude, latency from the stimulus, and covariance (in the case of multiple electrode sites) of each component can be examined in connection with a cognitive task (ERP) or with no task (EP). Steady-state visually evoked potentials (SSVEPs) use a continuous sinusoidally-modulated flickering light, typically superimposed in front of a TV monitor displaying a cognitive task. The brain response in a narrow frequency band containing the stimulus frequency is measured. Magnitude, phase, and coherence (in the case of multiple electrode sites) may be related to different parts of the cognitive task. Brain entrainment may be detected through EEG or MEG activity.

  • Brain entrainment may be detected through EEG or MEG activity. See:
  • Abeln, Vera, et al. “Brainwave entrainment for better sleep and post-sleep state of young elite soccer players-A pilot study.” European J. Sport science 14.5 (2014): 393-402;
  • Acton, George. “Methods for independent entrainment of visual field zones.” U.S. Pat. No. 9,629,976. 25 Apr. 2017;
  • Albouy, Philippe, et al. “Selective entrainment of theta oscillations in the dorsal stream causally enhances auditory working memory performance.” Neuron 94.1 (2017): 193-206.
  • Amengual, J., et al. “P018 Local entrainment and distribution across cerebral networks of natural oscillations elicited in implanted epilepsy patients by intracranial stimulation: Paving the way to develop causal connectomics of the healthy human brain.” Clin. Neurophysiology 1283 (2017): e18;
  • Argento, Emanuele, et al. “Augmented Cognition via Brainwave Entrainment in Virtual Reality: An Open, Integrated Brain Augmentation in a Neuroscience System Approach.” Augmented Human Research 2.1 (2017): 3;
  • Bello, Nicholas P. “Altering Cognitive and Brain States Through Cortical Entrainment.” (2014); Costa-Faidella, Jordi, Elyse S.
  • Sussman, and Caries Escera. “Selective entrainment of brain oscillations drives auditory perceptual organization.” NeuroImage (2017);
  • Börgers, Christoph. “Entrainment by Excitatory Input Pulses.” An Introduction to Modeling Neuronal Dynamics. Springer International Publishing, 2017.183-192;
  • Calderone, Daniel J., et al. “Entrainment of neural oscillations as a modifiable substrate of attention.” Trends in cognitive sciences 18.6 (2014): 300-309;
  • Casciaro, Francesco, et al. “Alpha-rhythm stimulation using brain entrainment enhances heart rate variability in subjects with reduced HRV.” World J. Neuroscience 3.04 (2013): 213;
  • Chang, Daniel Wonchul. “Method and system for brain entertainment.” U.S. Pat. No. 8,636,640. 28 Jan. 2014;
  • Colzato, Lorenza S., Amengual, Juli L., et al. “Local entrainment of oscillatory activity induced by direct brain stimulation in humans.” Scientific Reports 7 (2017);
  • Conte, Elio, et al. “A Fast Fourier Transform analysis of time series data of heart rate variability during alfa-rhythm stimulation in brain entrainment.” NeuroQuantology 11.3 (2013);
  • Dikker, Suzanne, et al. “Brain-to-brain synchrony tracks real-world dynamic group interactions in the classroom.” Current Biology 27.9 (2017): 1375-1380;
  • Ding, Nai, and Jonathan Z. Simon. “Cortical entrainment to continuous speech: functional roles and interpretations.” Frontiers in human neuroscience 8 (2014);
  • Doherty, Cormac. “A comparison of alpha brainwave entrainment, with and without musical accompaniment.” (2014);
  • Falk, Simone, Cosima Lanzilotti, and Daniele Schön. “Tuning neural phase entrainment to speech.” J. Cognitive Neuroscience (2017);
  • Gao, Junling, et al. “Entrainment of chaotic activities in brain and heart during MBSR mindfulness training.” Neuroscience letters 616 (2016): 218-223;
  • Gooding-Williams, Gerard, Hongfang Wang, and Klaus Kessler. “THETA-Rhythm Makes the World Go Round: Dissociative Effects of TMS Theta Versus Alpha Entrainment of Right pTPJ on Embodied Perspective Transformations.” Brain Topography (2017): 1-4;
  • Hanslmayr, Simon, Jonas Matuschek, and Marie-Christin Fellner. “Entrainment of prefrontal beta oscillations induces an endogenous echo and impairs memory formation.” Current Biology 24.8 (2014): 904-909;
  • Heideman, Simone G., Erik S. te Woerd, and Peter Praamstra. “Rhythmic entrainment of slow brain activity preceding leg movements.” Clin. Neurophysiology 126.2 (2015): 348-355;
  • Helfrich, Randolph F., et al. “Entrainment of brain oscillations by transcranial alternating current stimulation.” Current Biology 243 (2014): 333-339;
  • Henry, Molly J., et al. “Aging affects the balance of neural entrainment and top-down neural modulation in the listening brain.” Nature Communications 8 (2017): ncomms15801;
  • Horr, Ninja K., Maria Wimber, and Massimiliano Di Luca. “Perceived time and temporal structure: Neural entrainment to isochronous stimulation increases duration estimates.” Neuroimage 132 (2016): 148-156;
  • Irwin, Rosie. “Entraining Brain Oscillations to Influence Facial Perception.” (2015);
  • Kalyan, Ritu, and Bipan Kaushal. “Binaural Entrainment and Its Effects on Memory.” (2016);
  • Keitel, Anne, et al. “Auditory cortical delta-entrainment interacts with oscillatory power in multiple fronto-parietal networks.” NeuroImage 147 (2017): 32-42;
  • Keitel, Christian, Cliodhna Quigley, and Philipp Ruhnau. “Stimulus-driven brain oscillations in the alpha range: entrainment of intrinsic rhythms or frequency-following response?” J. Neuroscience 34.31 (2014): 10137-10140;
  • Koelsch, Stefan. “Music-evoked emotions: principles, brain correlates, and implications for therapy.” Annals of the New York Academy of Sciences 1337.1 (2015): 193-201;
  • Kösem, Anne, et al. “Neural entrainment reflects temporal predictions guiding speech comprehension.” the Eighth Annual Meeting of the Society for the Neurobiology of Language (SNL 2016). 2016;
  • Lee, Daniel Keewoong, Dongyeup Daniel Synn, and Daniel Chesong Lee. “Intelligent earplug system.” U.S. patent application Ser. No. 15/106,989;
  • Lefournour, Joseph, Ramaswamy Palaniappan, and Ian V. McLoughlin. “Inter-hemispheric and spectral power analyses of binaural beat effects on the brain.” Matters 2.9 (2016): e201607000001;
  • Mai, Guangting, James W. Minett, and William S-Y. Wang. “Delta, theta, beta, and gamma brain oscillations index levels of auditory sentence processing.” Neuroimage 133(2016):516-528;
  • Marconi, Pier Luigi, et al. “The phase amplitude coupling to assess brain network system integration.” Medical Measurements and Applications (MeMeA), 2016 IEEE International Symposium on. IEEE, 2016;
  • McLaren, Elgin-Skye, and Alissa N. Antle. “Exploring and Evaluating Sound for Helping Children Self-Regulate with a Brain-Computer Application.” Proceedings of the 2017 Conference on Interaction Design and Children. ACM, 2017;
  • Moisa, Marius, et al. “Brain network mechanisms underlying motor enhancement by transcranial entrainment of gamma oscillations.” J. Neuroscience 36.47 (2016): 12053-12065;
  • Molinaro, Nicola, et al. “Out-of-synchrony speech entrainment in developmental dyslexia.” Human brain mapping 37.8 (2016): 2767-2783;
  • Moseley, Ralph. “Immersive brain entrainment in virtual worlds: actualizing meditative states.” Emerging Trends and Advanced Technologies for Computational Intelligence. Springer International Publishing, 2016. 315-346;
  • Neuling, Toralf, et al. “Friends, not foes: magnetoencephalography as a tool to uncover brain dynamics during transcranial alternating current stimulation.” Neuroimage 118 (2015): 406-413;
  • Notbohm, Annika, Jurgen Kurths, and Christoph S. Herrmann. “Modification of brain oscillations via rhythmic light stimulation provides evidence for entrainment but not for superposition of event-related responses.” Frontiers in human neuroscience 10 (2016);
  • Nozaradan, S., et al. “P943: Neural entrainment to musical rhythms in the human auditory cortex, as revealed by intracerebral recordings.” Clin. Neurophysiology 125 (2014): 5299;
  • Palaniappan, Ramaswamy, et al. “Improving the feature stability and classification performance of bimodal brain and heart biometrics.” Advances in Signal Processing and Intelligent Recognition Systems. Springer, Cham, 2016.175-186;
  • Palaniappan, Ramaswamy, Somnuk Phon-Amnuaisuk, and Chikkannan Eswaran. “On the binaural brain entrainment indicating lower heart rate variability.” Int. J. Cardiol 190 (2015): 262-263;
  • Papagiannakis, G., et al. A virtual reality brainwave entrainment method for human augmentation applications. Technical Report, FORTH-ICS/TR-458, 2015;
  • Park, Hyojin, et al. “Frontal top-down signals increase coupling of auditory low-frequency oscillations to continuous speech in human listeners.” Current Biology 25.12 (2015): 1649-1653;
  • Pérez, Alejandro, Manuel Carreiras, and Jon Andoni Duñabeitia. “Brain-to-brain entrainment: EEG interbrain synchronization while speaking and listening.” Scientific Reports 7 (2017);
  • Riecke, Lars, Alexander T. Sack, and Charles E. Schroeder. “Endogenous delta/theta sound-brain phase entrainment accelerates the buildup of auditory streaming.” Current Biology 25.24 (2015): 3196-3201;
  • Spaak, Eelke, Floris P. de Lange, and Ole Jensen. “Local entrainment of alpha oscillations by visual stimuli causes cyclic modulation of perception.” J. Neuroscience 34.10(2014):3536-3544;
  • Thaut, Michael H. “The discovery of human auditory-motor entrainment and its role in the development of neurologic music therapy.” Progress in brain research 217 (2015): 253-266;
  • Thaut, Michael H., Gerald C. Mcintosh, and Volker Hoemberg. “Neurobiological foundations of neurologic music therapy: rhythmic entrainment and the motor system.” Frontiers in psychology 5 (2014);
  • Thut, G. “1030 Guiding T M S by EEG/MEG to interact with oscillatory brain activity and associated functions.” Clin. Neurophysiology 1283 (2017): e9;
  • Treviño, Guadalupe Villarreal, et al. “The Effect of Audio Visual Entrainment on Pre-Attentive Dysfunctional Processing to Stressful Events in Anxious Individuals.” Open J. Medical Psychology 3.05 (2014): 364;
  • Trost, Wiebke, et al. “Getting the beat: entrainment of brain activity by musical rhythm and pleasantness.” NeuroImage 103 (2014): 55-64;
  • Tsai, Shu-Hui, and Yue-Der Lin. “Autonomie feedback with brain entrainment.” Awareness Science and Technology and Ubi-Media Computing (iCAST-UMEDIA), 2013 International Joint Conference on. IEEE, 2013;
  • Vossen, Alexandra, Joachim Gross, and Gregor Thut. “Alpha power increase after transcranial alternating current stimulation at alpha frequency (a-tACS) reflects plastic changes rather than entrainment.” Brain Stimulation 8.3 (2015): 499-508;
  • Witkowski, Matthias, et al. “Mapping entrained brain oscillations during transcranial alternating current stimulation (tACS).” Neuroimage 140 (2016): 89-98;
  • Zlotnik, Anatoly, Raphael Nagao, and István Z. Kiss Jr-Shin Li. “Phase-selective entrainment of nonlinear oscillator ensembles.” Nature Communications 7 (2016).


The entrainment hypothesis (Thut and Miniussi, 2009; Thut et al., 2011a, 2012), suggests the possibility of inducing a particular oscillation frequency in the brain using an external oscillatory force (e.g., rTMS, but also tACS). The physiological basis of oscillatory cortical activity lies in the timing of the interacting neurons; when groups of neurons synchronize their firing activities, brain rhythms emerge, network oscillations are generated, and the basis for interactions between brain areas may develop (Buzsáki, 2006). Because of the variety of experimental protocols for brain stimulation, limits on descriptions of the actual protocols employed, and limited controls, consistency of reported studies is lacking, and extrapolability is limited. Thus, while there is various consensus in various aspects of the effects of extra cranial brain stimulation, the results achieved have a degree of uncertainty dependent on details of implementation. On the other hand, within a specific experimental protocol, it is possible to obtain statistically significant and repeatable results. This implies that feedback control might be effective to control implementation of the stimulation for a given purpose; however, studies that employ feedback control are lacking.


Different cognitive states are associated with different oscillatory patterns in the brain (Buzsáki, 2006; Canolty and Knight, 2010; Varela et al., 2001). Thut et al. (2011 b) directly tested the entrainment hypothesis by means of a concurrent EEG-TMS experiment. They first determined the individual source of the parietal-occipital alpha modulation and the individual alpha frequency (magnetoencephalography study). They then applied rTMS at the individual alpha power while recording the EEG activity at rest. The results confirmed the three predictions of the entrainment hypothesis: the induction of a specific frequency after TMS, the enhancement of oscillation during TMS stimulation due to synchronization, and a phase alignment of the induced frequency and the ongoing activity (Thut et al., 2011b).


If associative stimulation is a general principle for human neural plasticity in which the timing and strength of activation are critical factors, it is possible that synchronization within or between areas using an external force to phase/align oscillations can also favor efficient communication and associative plasticity (or alter communication). In this respect associative, cortico-cortical stimulation has been shown to enhance coherence of oscillatory activity between the stimulated areas (Plewnia et al., 2008).


In coherence resonance (Longtin, 1997), the addition of a certain amount of noise in an excitable system results in the most coherent and proficient oscillatory responses. The brain's response to external timing-embedded stimulation can result in a decrease in phase variance and an enhanced alignment (clustering) of the phase components of the ongoing EEG activity (entraining, phase resetting) that can change the signal-to-noise ratio and increase (or decrease) signal efficacy.


If one considers neuron activity within the brain as a set of loosely coupled oscillators, then the various parameters that might be controlled include the size of the region of neurons, frequency of oscillation, resonant frequency or time-constant, oscillator damping, noise, amplitude, coupling to other oscillators, and of course, external influences that may include stimulation and/or power loss. In a human brain, pharmacological intervention may be significant. For example, drugs that alter excitability, such as caffeine, neurotransmitter release and reuptake, nerve conductance, etc. can all influence operation of the neural oscillators. Likewise, sub-threshold external stimulation effects, including DC, AC and magnetic electromagnetic effects, can also influence operation of the neural oscillators.


Phase resetting or shifting can synchronize inputs and favor communication and, eventually, Hebbian plasticity (Hebb, 1949). Thus, rhythmic stimulation may induce a statistically higher degree of coherence in spiking neurons, which facilitates the induction of a specific cognitive process (or hinders that process). Here, the perspective is slightly different (coherence resonance), but the underlining mechanisms are similar to the ones described so far (stochastic resonance), and the additional key factor is the repetition at a specific rhythm of the stimulation.


In the 1970's, the British biophysicist and psychobiologist, C. Maxwell Cade, monitored the brainwave patterns of advanced meditators and 300 of his students. Here he found that the most advanced meditators have a specific brainwave pattern that was different from the rest of his students. He noted that these meditators showed high activity of alpha brainwaves accompanied by beta, theta and even delta waves that were about half the amplitude of the alpha waves. See, Cade “The Awakened Mind: Biofeedback and the Development of Higher States of Awareness” (Dell, 1979). Anna Wise extended Cade's studies, and found that extraordinary achievers which included composers, inventors, artists, athletes, dancers, scientists, mathematicians, CEO's and presidents of large corporations have brainwave patterns differ from average performers, with a specific balance between Beta, Alpha, Theta and Delta brainwaves where Alpha had the strongest amplitude. See, Anna Wise, “The High-Performance Mind: Mastering Brainwaves for Insight, Healing, and Creativity”.


Entrainment is plausible because of the characteristics of the demonstrated EEG responses to a single TMS pulse, which have a spectral composition which resemble the spontaneous oscillations of the stimulated cortex. For example, TMS of the “resting” visual (Rosanova et al., 2009) or motor cortices (Veniero et al., 2011) triggers alpha-waves, the natural frequency at the resting state of both types of cortices. With the entrainment hypothesis, the noise generation framework moves to a more complex and extended level in which noise is synchronized with on-going activity. Nevertheless, the model to explain the outcome will not change, stimulation will interact with the system, and the final result will depend on introducing or modifying the noise level. The entrainment hypothesis makes clear predictions with respect to online repetitive TMS paradigms' frequency engagement as well as the possibility of inducing phase alignment, i.e., a reset of ongoing brain oscillations via external spTMS (Thut et al., 2011a, 2012; Veniero et al., 2011). The entrainment hypothesis is superior to the localization approach in gaining knowledge about how the brain works, rather than where or when a single process occurs. TMS pulses may phase-align the natural, ongoing oscillation of the target cortex. When additional TMS pulses are delivered in synchrony with the phase-aligned oscillation (i.e., at the same frequency), further synchronized phase-alignment will occur, which will bring the oscillation of the target area in resonance with the TMS train. Thus, entrainment may be expected when TMS is frequency-tuned to the underlying brain oscillations (Veniero et al., 2011).


Binaural Beats


Binaural beats are auditory brainstem responses which originate in the superior olivary nucleus of each hemisphere. They result from the interaction of two different auditory impulses, originating in opposite ears, below 1000 Hz and which differ in frequency between one and 30 Hz. For example, if a pure tone of 400 Hz is presented to the right ear and a pure tone of 410 Hz is presented simultaneously to the left ear, an amplitude modulated standing wave of 10 Hz, the difference between the two tones, is experienced as the two wave forms mesh in and out of phase within the superior olivary nuclei. This binaural beat is not heard in the ordinary sense of the word (the human range of hearing is from 20-20,000 Hz). It is perceived as an auditory beat and theoretically can be used to entrain specific neural rhythms through the frequency-following response (FFR)—the tendency for cortical potentials to entrain to or resonate at the frequency of an external stimulus. Thus, it is theoretically possible to utilize a specific binaural-beat frequency as a consciousness management technique to entrain a specific cortical rhythm. The binaural-beat appears to be associated with an electroencephalographic (EEG) frequency-following response in the brain.


Uses of audio with embedded binaural beats that are mixed with music or various pink or background sound are diverse. They range from relaxation, meditation, stress reduction, pain management, improved sleep quality, decrease in sleep requirements, super learning, enhanced creativity and intuition, remote viewing, telepathy, and out-of-body experience and lucid dreaming. Audio embedded with binaural beats is often combined with various meditation techniques, as well as positive affirmations and visualization.


When signals of two different frequencies are presented, one to each ear, the brain detects phase differences between these signals. “Under natural circumstances a detected phase difference would provide directional information. The brain processes this anomalous information differently when these phase differences are heard with stereo headphones or speakers. A perceptual integration of the two signals takes place, producing the sensation of a third “beat” frequency. The difference between the signals waxes and wanes as the two different input frequencies mesh in and out of phase. As a result of these constantly increasing and decreasing differences, an amplitude-modulated standing wave—the binaural beat—is heard. The binaural beat is perceived as a fluctuating rhythm at the frequency of the difference between the two auditory inputs. Evidence suggests that the binaural beats are generated in the brainstem's superior olivary nucleus, the first site of contralateral integration in the auditory system. Studies also suggest that the frequency-following response originates from the inferior colliculus. This activity is conducted to the cortex where it can be recorded by scalp electrodes. Binaural beats can easily be heard at the low frequencies (<30 Hz) that are characteristic of the EEG spectrum.


Synchronized brain waves have long been associated with meditative and hypnogogic states, and audio with embedded binaural beats has the ability to induce and improve such states of consciousness. The reason for this is physiological. Each ear is “hardwired” (so to speak) to both hemispheres of the brain. Each hemisphere has its own olivary nucleus (sound-processing center) which receives signals from each ear. In keeping with this physiological structure, when a binaural beat is perceived there are actually two standing waves of equal amplitude and frequency present, one in each hemisphere. So, there are two separate standing waves entraining portions of each hemisphere to the same frequency. The binaural beats appear to contribute to the hemispheric synchronization evidenced in meditative and hypnogogic states of consciousness. Brain function is also enhanced through the increase of cross-collosal communication between the left and right hemispheres of the brain.

  • en.wikipedia.org/wiki/Beat_(acoustics)#Binaural_beats.
  • Oster, G (October 1973). “Auditory beats in the brain”. Scientific American. 229 (4): 94-102. See:
  • Lane, J. D., Kasian, S. J., Owens, J. E., & Marsh, G. R. (1998). Binaural auditory beats affect vigilance performance and mood. Physiology & behavior, 63(2), 249-252;
  • Foster, D. S. (1990). EEG and subjective correlates of alpha frequency binaural beats stimulation combined with alpha biofeedback (Doctoral dissertation, Memphis State University);
  • Kasprzak, C. (2011). Influence of binaural beats on EEG signal. Acta Physica Polonica A, 119(6A), 986-990;
  • Pratt, H., Starr, A., Michalewski, H. J., Dimitrijevic, A., Bleich, N., & Mittelman, N. (2009). Cortical evoked potentials to an auditory illusion: binaural beats. Clinical Neurophysiology, 120(8), 1514-1524;
  • Pratt, H., Starr, A., Michalewski, H. J., Dimitrijevic, A., Bleich, N., & Mittelman, N. (2010). A comparison of auditory evoked potentials to acoustic beats and to binaural beats. Hearing research, 262(1), 34-44;
  • Padmanabhan, R., Hildreth, A. J., & Laws, D. (2005). A prospective, randomised, controlled study examining binaural beat audio and pre-operative anxiety in patients undergoing general anaesthesia for day case surgery. Anaesthesia, 60(9), 874-877;
  • Reedijk, S. A., Bolders, A., & Hommel, B. (2013). The impact of binaural beats on creativity. Frontiers in human neuroscience, 7;
  • Atwater, F. H. (2001). Binaural beats and the regulation of arousal levels. Proceedings of the TANS, 11;
  • Hink, R. F., Kodera, K., Yamada, O., Kaga, K., & Suzuki, J. (1980). Binaural interaction of a beating frequency-following response. Audiology, 19(1), 36-43;
  • Gao, X., Cao, H., Ming, D., Qi, H., Wang, X., Wang, X., & Zhou, P. (2014). Analysis of EEG activity in response to binaural beats with different frequencies. International Journal of Psychophysiology, 94(3), 399-406;
  • Sung, H. C., Lee, W. L., Li, H. M., Lin, C. Y., Wu, Y. Z., Wang, J. J., & Li, T. L. (2017). Familiar Music Listening with Binaural Beats for Older People with Depressive Symptoms in Retirement Homes. Neuropsychiatry, 7(4);
  • Colzato, L. S., Barone, H., Sellaro, R., & Hommel, B. (2017). More attentional focusing through binaural beats: evidence from the global-local task. Psychological research, 81(1), 271-277;
  • Mortazavi, S. M. J., Zahraei-Moghadam, S. M., Masoumi, S., Rafati, A., Haghani, M., Mortazavi, S. A. R., & Zehtabian, M. (2017). Short Term Exposure to Binaural Beats Adversely Affects Learning and Memory in Rats. Journal of Biomedical Physics and Engineering.
  • Brain Entrainment Frequency Following Response (or FFR). See, “Stimulating the Brain with Light and Sound,” Transparent Corporation, Neuroprogrammer™ 3, www.transparentcorp.com/products/np/entrainment.php.


Isochronic Tones

  • www.livingflow.n et/isochronic-tones-work/;
  • Schulze, H. H. (1989). The perception of temporal deviations in isochronic patterns. Attention, Perception, & Psychophysics, 45(4), 291-296;
  • Oster, G. (1973). Auditory beats in the brain. Scientific American, 229(4), 94-102;
  • Huang, T. L., & Charyton, C. (2008). A comprehensive review of the psychological effects of brainwave entrainment. Alternative therapies in health and medicine, 14(5), 38;
  • Trost, W., Fruhholz, S., Schön, D., Labbé, C., Pichon, S., Grandjean, D., & Vuilleumier, P. (2014). Getting the beat: entrainment of brain activity by musical rhythm and pleasantness. NeuroImage, 103, 55-64;
  • Casciaro, F., Laterza, V., Conte, S., Pieralice, M., Federici, A., Todarello, O., . . . & Conte, E. (2013). Alpha-rhythm stimulation using brain entrainment enhances heart rate variability in subjects with reduced HRV. World Journal of Neuroscience, 3(04), 213;
  • Conte, E., Conte, S., Santacroce, N., Federici, A., Todarello, O., Orsucci, F., . . . & Laterza, V. (2013). A Fast Fourier Transform analysis of time series data of heart rate variability during alfa-rhythm stimulation in brain entrainment. NeuroQuantology, 11(3);
  • Doherty, C. (2014). A comparison of alpha brainwave entrainment, with and without musical accompaniment;
  • Moseley, R. (2015, July). Inducing targeted brain states utilizing merged reality systems. In Science and Information Conf. (SAI), 2015 (pp. 657-663). IEEE.


Isochronic Tones


Isochronic tones are regular beats of a single tone that are used alongside monaural beats and binaural beats in the process called brainwave entrainment. At its simplest level, an isochronic tone is a tone that is being turned on and off rapidly. They create sharp, distinctive pulses of sound.


Time-Frequency Analysis


Brian J. Roach and Daniel H. Mathalon, “Event-related EEG time-frequency analysis: an overview of measures and analysis of early gamma band phase locking in schizophrenia. Schizophrenia Bull. USA. 2008; 345:907-926., describes a mechanism for EEG time-frequency analysis. Fourier and wavelet transforms (and their inverse) may be performed on EEG signals.


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 4,407,299; 4,408,616; 4,421,122; 4,493,327; 4,550,736; 4,557,270; 4,579,125; 4,583,190; 4,585,011; 4,610,259; 4,649,482; 4,705,049; 4,736,307; 4,744,029; 4,776,345; 4,792,145; 4,794,533; 4,846,190; 4,862,359; 4,883,067; 4,907,597; 4,924,875; 4,940,058; 5,010,891; 5,020,540; 5,029,082; 5,083,571; 5,092,341; 5,105,354; 5,109,862; 5,218,530; 5,230,344; 5,230,346; 5,233,517; 5,241,967; 5,243,517; 5,269,315; 5,280,791; 5,287,859; 5,309,917; 5,309,923; 5,320,109; 5,339,811; 5,339,826; 5,377,100; 5,406,956; 5,406,957; 5,443,073; 5,447,166; 5,458,117; 5,474,082; 5,555,889; 5,611,350; 5,619,995; 5,632,272; 5,643,325; 5,678,561; 5,685,313; 5,692,517; 5,694,939; 5,699,808; 5,752,521; 5,755,739; 5,771,261; 5,771,897; 5,794,623; 5,795,304; 5,797,840; 5,810,737; 5,813,993; 5,827,195; 5,840,040; 5,846,189; 5,846,208; 5,853,005; 5,871,517; 5,884,626; 5,899,867; 5,916,171; 5,995,868; 6,002,952; 6,011,990; 6,016,444; 6,021,345; 6,032,072; 6,044,292; 6,050,940; 6,052,619; 6,067,462; 6,067,467; 6,070,098; 6,071,246; 6,081,735; 6,097,980; 6,097,981; 6,115,631; 6,117,075; 6,129,681; 6,155,993; 6,157,850; 6,157,857; 6,171,258; 6,195,576; 6,196,972; 6,224,549; 6,236,872; 6,287,328; 6,292,688; 6,293,904; 6,305,943; 6,306,077; 6,309,342; 6,315,736; 6,317,627; 6,325,761; 6,331,164; 6,338,713; 6,343,229; 6,358,201; 6,366,813; 6,370,423; 6,375,614; 6,377,833; 6,385,486; 6,394,963; 6,402,520; 6,475,163; 6,482,165; 6,493,577; 6,496,724; 6,511,424; 6,520,905; 6,520,921; 6,524,249; 6,527,730; 6,529,773; 6,544,170; 6,546,378; 6,547,736; 6,547,746; 6,549,804; 6,556,861; 6,565,518; 6,574,573; 6,594,524; 6,602,202; 6,616,611; 6,622,036; 6,625,485; 6,626,676; 6,650,917; 6,652,470; 6,654,632; 6,658,287; 6,678,548; 6,687,525; 6,699,194; 6,709,399; 6,726,624; 6,731,975; 6,735,467; 6,743,182; 6,745,060; 6,745,156; 6,746,409; 6,751,499; 6,768,920; 6,798,898; 6,801,803; 6,804,661; 6,816,744; 6,819,956; 6,826,426; 6,843,774; 6,865,494; 6,875,174; 6,882,881; 6,886,964; 6,915,241; 6,928,354; 6,931,274; 6,931,275; 6,981,947; 6,985,769; 6,988,056; 6,993,380; 7,011,410; 7,014,613; 7,016,722; 7,037,260; 7,043,293; 7,054,454; 7,089,927; 7,092,748; 7,099,714; 7,104,963; 7,105,824; 7,123,955; 7,128,713; 7,130,691; 7,146,218; 7,150,710; 7,150,715; 7,150,718; 7,163,512; 7,164,941; 7,177,675; 7,190,995; 7,207,948; 7,209,788; 7,215,986; 7,225,013; 7,228,169; 7,228,171; 7,231,245; 7,254,433; 7,254,439; 7,254,500; 7,267,652; 7,269,456; 7,286,871; 7,288,066; 7,297,110; 7,299,088; 7,324,845; 7,328,053; 7,333,619; 7,333,851; 7,343,198; 7,367,949; 7,373,198; 7,376,453; 7,381,185; 7,383,070; 7,392,079; 7,395,292; 7,396,333; 7,399,282; 7,403,814; 7,403,815; 7,418,290; 7,429,247; 7,450,986; 7,454,240; 7,462,151; 7,468,040; 7,469,697; 7,471,971; 7,471,978; 7,489,958; 7,489,964; 7,491,173; 7,496,393; 7,499,741; 7,499,745; 7,509,154; 7,509,161; 7,509,163; 7,510,531; 7,530,955; 7,537,568; 7,539,532; 7,539,533; 7,547,284; 7,558,622; 7,559,903; 7,570,991; 7,572,225; 7,574,007; 7,574,254; 7,593,767; 7,594,122; 7,596,535; 7,603,168; 7,604,603; 7,610,094; 7,623,912; 7,623,928; 7,625,340; 7,630,757; 7,640,055; 7,643,655; 7,647,098; 7,654,948; 7,668,579; 7,668,591; 7,672,717; 7,676,263; 7,678,061; 7,684,856; 7,697,979; 7,702,502; 7,706,871; 7,706,992; 7,711,417; 7,715,910; 7,720,530; 7,727,161; 7,729,753; 7,733,224; 7,734,334; 7,747,325; 7,751,878; 7,754,190; 7,757,690; 7,758,503; 7,764,987; 7,771,364; 7,774,052; 7,774,064; 7,778,693; 7,787,946; 7,794,406; 7,801,592; 7,801,593; 7,803,118; 7,803,119; 7,809,433; 7,811,279; 7,819,812; 7,831,302; 7,853,329; 7,860,561; 7,865,234; 7,865,235; 7,878,965; 7,879,043; 7,887,493; 7,894,890; 7,896,807; 7,899,525; 7,904,144; 7,907,994; 7,909,771; 7,918,779; 7,920,914; 7,930,035; 7,938,782; 7,938,785; 7,941,209; 7,942,824; 7,944,551; 7,962,204; 7,974,696; 7,983,741; 7,983,757; 7,986,991; 7,993,279; 7,996,075; 8,002,553; 8,005,534; 8,005,624; 8,010,347; 8,019,400; 8,019,410; 8,024,032; 8,025,404; 8,032,209; 8,033,996; 8,036,728; 8,036,736; 8,041,136; 8,046,041; 8,046,042; 8,065,011; 8,066,637; 8,066,647; 8,068,904; 8,073,534; 8,075,499; 8,079,953; 8,082,031; 8,086,294; 8,089,283; 8,095,210; 8,103,333; 8,108,036; 8,108,039; 8,114,021; 8,121,673; 8,126,528; 8,128,572; 8,131,354; 8,133,172; 8,137,269; 8,137,270; 8,145,310; 8,152,732; 8,155,736; 8,160,689; 8,172,766; 8,177,726; 8,177,727; 8,180,420; 8,180,601; 8,185,207; 8,187,201; 8,190,227; 8,190,249; 8,190,251; 8,197,395; 8,197,437; 8,200,319; 8,204,583; 8,211,035; 8,214,007; 8,224,433; 8,236,005; 8,239,014; 8,241,213; 8,244,340; 8,244,475; 8,249,698; 8,271,077; 8,280,502; 8,280,503; 8,280,514; 8,285,368; 8,290,575; 8,295,914; 8,296,108; 8,298,140; 8,301,232; 8,301,233; 8,306,610; 8,311,622; 8,314,707; 8,315,970; 8,320,649; 8,323,188; 8,323,189; 8,323,204; 8,328,718; 8,332,017; 8,332,024; 8,335,561; 8,337,404; 8,340,752; 8,340,753; 8,343,026; 8,346,342; 8,346,349; 8,352,023; 8,353,837; 8,354,881; 8,356,594; 8,359,080; 8,364,226; 8,364,254; 8,364,255; 8,369,940; 8,374,690; 8,374,703; 8,380,296; 8,382,667; 8,386,244; 8,391,966; 8,396,546; 8,396,557; 8,401,624; 8,401,626; 8,403,848; 8,425,415; 8,425,583; 8,428,696; 8,437,843; 8,437,844; 8,442,626; 8,449,471; 8,452,544; 8,454,555; 8,461,988; 8,463,007; 8,463,349; 8,463,370; 8,465,408; 8,467,877; 8,473,024; 8,473,044; 8,473,306; 8,475,354; 8,475,368; 8,475,387; 8,478,389; 8,478,394; 8,478,402; 8,480,554; 8,484,270; 8,494,829; 8,498,697; 8,500,282; 8,500,636; 8,509,885; 8,509,904; 8,512,221; 8,512,240; 8,515,535; 8,519,853; 8,521,284; 8,525,673; 8,525,687; 8,527,435; 8,531,291; 8,538,512; 8,538,514; 8,538,705; 8,542,900; 8,543,199; 8,543,219; 8,545,416; 8,545,436; 8,554,311; 8,554,325; 8,560,034; 8,560,073; 8,562,525; 8,562,526; 8,562,527; 8,562,951; 8,568,329; 8,571,642; 8,585,568; 8,588,933; 8,591,419; 8,591,498; 8,597,193; 8,600,502; 8,606,351; 8,606,356; 8,606,360; 8,620,419; 8,628,480; 8,630,699; 8,632,465; 8,632,750; 8,641,632; 8,644,914; 8,644,921; 8,647,278; 8,649,866; 8,652,038; 8,655,817; 8,657,756; 8,660,799; 8,666,467; 8,670,603; 8,672,852; 8,680,991; 8,684,900; 8,684,922; 8,684,926; 8,688,209; 8,690,748; 8,693,756; 8,694,087; 8,694,089; 8,694,107; 8,700,137; 8,700,141; 8,700,142; 8,706,205; 8,706,206; 8,706,207; 8,708,903; 8,712,507; 8,712,513; 8,725,238; 8,725,243; 8,725,311; 8,725,669; 8,727,978; 8,728,001; 8,738,121; 8,744,563; 8,747,313; 8,747,336; 8,750,971; 8,750,974; 8,750,992; 8,755,854; 8,755,856; 8,755,868; 8,755,869; 8,755,871; 8,761,866; 8,761,869; 8,764,651; 8,764,652; 8,764,653; 8,768,447; 8,771,194; 8,775,340; 8,781,193; 8,781,563; 8,781,595; 8,781,597; 8,784,322; 8,786,624; 8,790,255; 8,790,272; 8,792,974; 8,798,735; 8,798,736; 8,801,620; 8,21,408; 8,25,149; 8,825,428; 8,27,917; 8,831,705; 8,838,226; 8,838,227; 8,843,199; 8,843,210; 8,849,390; 8,849,392; 8,849,681; 8,852,100; 8,852,103; 8,855,758; 8,858,440; 8,858,449; 8,862,196; 8,862,210; 8,862,581; 8,868,148; 8,868,163; 8,868,172; 8,868,174; 8,868,175; 8,870,737; 8,880,207; 8,880,576; 8,886,299; 8,888,672; 8,888,673; 8,888,702; 8,888,708; 8,898,037; 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RE38476; RE38749; RE46189; 20010049480; 20010051774; 20020035338; 20020055675; 20020059159; 20020077536; 20020082513; 20020085174; 20020091319; 20020091335; 20020099295; 20020099306; 20020103512; 20020107454; 20020112732; 20020117176; 20020128544; 20020138013; 20020151771; 20020177882; 20020182574; 20020183644; 20020193670; 20030001098; 20030009078; 20030023183; 20030028121; 20030032888; 20030035301; 20030036689; 20030046018; 20030055355; 20030070685; 20030093004; 20030093129; 20030100844; 20030120172; 20030130709; 20030135128; 20030139681; 20030144601; 20030149678; 20030158466; 20030158496; 20030158587; 20030160622; 20030167019; 20030171658; 20030171685; 20030176804; 20030181821; 20030185408; 20030195429; 20030216654; 20030225340; 20030229291; 20030236458; 20040002635; 20040006265; 20040006376; 20040010203; 20040039268; 20040059203; 20040059241; 20040064020; 20040064066; 20040068164; 20040068199; 20040073098; 20040073129; 20040077967; 20040079372; 20040082862; 20040082876; 20040097802; 20040116784; 20040116791; 20040116798; 20040116825; 20040117098; 20040143170; 20040144925; 20040152995; 20040158300; 20040167418; 20040181162; 20040193068; 20040199482; 20040204636; 20040204637; 20040204659; 20040210146; 20040220494; 20040220782; 20040225179; 20040230105; 20040243017; 20040254493; 20040260169; 20050007091; 20050010116; 20050018858; 20050025704; 20050033154; 20050033174; 20050038354; 20050043774; 20050075568; 20050080349; 20050080828; 20050085744; 20050096517; 20050113713; 20050119586; 20050124848; 20050124863; 20050135102; 20050137494; 20050148893; 20050148894; 20050148895; 20050149123; 20050182456; 20050197590; 20050209517; 20050216071; 20050251055; 20050256385; 20050256418; 20050267362; 20050273017; 20050277813; 20050277912; 20060004298; 20060009704; 20060015034; 20060041201; 20060047187; 20060047216; 20060047324; 20060058590; 20060074334; 20060082727; 20060084877; 20060089541; 20060089549; 20060094968; 20060100530; 20060102171; 20060111644; 20060116556; 20060135880; 20060149144; 20060153396; 20060155206; 20060155207; 20060161071; 20060161075; 20060161218; 20060167370; 20060167722; 20060173364; 20060184059; 20060189880; 20060189882; 20060200016; 20060200034; 20060200035; 20060204532; 20060206033; 20060217609; 20060233390; 20060235315; 20060235324; 20060241562; 20060241718; 20060251303; 20060258896; 20060258950; 20060265022; 20060276695; 20070007454; 20070016095; 20070016264; 20070021673; 20070021675; 20070032733; 20070032737; 20070038382; 20070060830; 20070060831; 20070066914; 20070083128; 20070093721; 20070100246; 20070100251; 20070100666; 20070129647; 20070135724; 20070135728; 20070142862; 20070142873; 20070149860; 20070161919; 20070162086; 20070167694; 20070167853; 20070167858; 20070167991; 20070173733; 20070179396; 20070191688; 20070191691; 20070191697; 20070197930; 20070203448; 20070208212; 20070208269; 20070213786; 20070225581; 20070225674; 20070225932; 20070249918; 20070249952; 20070255135; 20070260151; 20070265508; 20070265533; 20070273504; 20070276270; 20070276278; 20070276279; 20070276609; 20070291832; 20080001600; 20080001735; 20080004514; 20080004904; 20080009685; 20080009772; 20080013747; 20080021332; 20080021336; 20080021340; 20080021342; 20080033266; 20080036752; 20080045823; 20080045844; 20080051669; 20080051858; 20080058668; 20080074307; 20080077010; 20080077015; 20080082018; 20080097197; 20080119716; 20080119747; 20080119900; 20080125669; 20080139953; 20080140403; 20080154111; 20080167535; 20080167540; 20080167569; 20080177195; 20080177196; 20080177197; 20080188765; 20080195166; 20080200831; 20080208072; 20080208073; 20080214902; 20080221400; 20080221472; 20080221969; 20080228100; 20080242521; 20080243014; 20080243017; 20080243021; 20080249430; 20080255469; 20080257349; 20080260212; 20080262367; 20080262371; 20080275327; 20080294019; 20080294063; 20080319326; 20080319505; 20090005675; 20090009284; 20090018429; 20090024007; 20090030476; 20090043221; 20090048530; 20090054788; 20090062660; 20090062670; 20090062676; 20090062679; 20090062680; 20090062696; 20090076339; 20090076399; 20090076400; 20090076407; 20090082689; 20090082690; 20090083071; 20090088658; 20090094305; 20090112281; 20090118636; 20090124869; 20090124921; 20090124922; 20090124923; 20090137915; 20090137923; 20090149148; 20090156954; 20090156956; 20090157662; 20090171232; 20090171240; 20090177090; 20090177108; 20090179642; 20090182211; 20090192394; 20090198144; 20090198145; 20090204015; 20090209835; 20090216091; 20090216146; 20090227876; 20090227877; 20090227882; 20090227889; 20090240119; 20090247893; 20090247894; 20090264785; 20090264952; 20090275853; 20090287107; 20090292180; 20090297000; 20090306534; 20090312663; 20090312664; 20090312808; 20090312817; 20090316925; 20090318779; 20090323049; 20090326353; 20100010364; 20100023089; 20100030073; 20100036211; 20100036276; 20100041962; 20100042011; 20100043795; 20100049069; 20100049075; 20100049482; 20100056939; 20100069762; 20100069775; 20100076333; 20100076338; 20100079292; 20100087900; 20100094103; 20100094152; 20100094155; 20100099954; 20100106044; 20100114813; 20100130869; 20100137728; 20100137937; 20100143256; 20100152621; 20100160737; 20100174161; 20100179447; 20100185113; 20100191124; 20100191139; 20100191305; 20100195770; 20100198098; 20100198101; 20100204614; 20100204748; 20100204750; 20100217100; 20100217146; 20100217348; 20100222694; 20100224188; 20100234705; 20100234752; 20100234753; 20100245093; 20100249627; 20100249635; 20100258126; 20100261977; 20100262377; 20100268055; 20100280403; 20100286549; 20100286747; 20100292752; 20100293115; 20100298735; 20100303101; 20100312188; 20100318025; 20100324441; 20100331649; 20100331715; 20110004115; 20110009715; 20110009729; 20110009752; 20110015501; 20110015536; 20110028802; 20110028859; 20110034822; 20110038515; 20110040202; 20110046473; 20110054279; 20110054345; 20110066005; 20110066041; 20110066042; 20110066053; 20110077538; 20110082381; 20110087125; 20110092834; 20110092839; 20110098583; 20110105859; 20110105915; 20110105938; 20110106206; 20110112379; 20110112381; 20110112426; 20110112427; 20110115624; 20110118536; 20110118618; 20110118619; 20110119212; 20110125046; 20110125048; 20110125238; 20110130675; 20110144520; 20110152710; 20110160607; 20110160608; 20110160795; 20110162645; 20110178441; 20110178581; 20110181422; 20110184650; 20110190600; 20110196693; 20110208539; 20110218453; 20110218950; 20110224569; 20110224570; 20110224602; 20110245709; 20110251583; 20110251985; 20110257517; 20110263995; 20110270117; 20110270579; 20110282234; 20110288424; 20110288431; 20110295142; 20110295143; 20110295338; 20110301436; 20110301439; 20110301441; 20110301448; 20110301486; 20110301487; 20110307029; 20110307079; 20110313308; 20110313760; 20110319724; 20120004561; 20120004564; 20120004749; 20120010536; 20120016218; 20120016252; 20120022336; 20120022350; 20120022351; 20120022365; 20120022384; 20120022392; 20120022844; 20120029320; 20120029378; 20120029379; 20120035431; 20120035433; 20120035765; 20120041330; 20120046711; 20120053433; 20120053491; 20120059273; 20120065536; 20120078115; 20120083700; 20120083701; 20120088987; 20120088992; 20120089004; 20120092156; 20120092157; 20120095352; 20120095357; 20120100514; 20120101387; 20120101401; 20120101402; 20120101430; 20120108999; 20120116235; 20120123232; 20120123290; 20120125337; 20120136242; 20120136605; 20120143074; 20120143075; 20120149997; 20120150545; 20120157963; 20120159656; 20120165624; 20120165631; 20120172682; 20120172689; 20120172743; 20120191000; 20120197092; 20120197153; 20120203087; 20120203130; 20120203131; 20120203133; 20120203725; 20120209126; 20120209136; 20120209139; 20120220843; 20120220889; 20120221310; 20120226334; 20120238890; 20120242501; 20120245464; 20120245481; 20120253141; 20120253219; 20120253249; 20120265080; 20120271190; 20120277545; 20120277548; 20120277816; 20120296182; 20120296569; 20120302842; 20120302845; 20120302856; 20120302894; 20120310100; 20120310105; 20120321759; 20120323132; 20120330109; 20130006124; 20130009783; 20130011819; 20130012786; 20130012787; 20130012788; 20130012789; 20130012790; 20130012802; 20130012830; 20130013327; 20130023783; 20130030257; 20130035579; 20130039498; 20130041235; 20130046151; 20130046193; 20130046715; 20130060110; 20130060125; 20130066392; 20130066394; 20130066395; 20130069780; 20130070929; 20130072807; 20130076885; 20130079606; 20130079621; 20130079647; 20130079656; 20130079657; 20130080127; 20130080489; 20130095459; 20130096391; 20130096393; 20130096394; 20130096408; 20130096441; 20130096839; 20130096840; 20130102833; 20130102897; 20130109995; 20130109996; 20130116520; 20130116561; 20130116588; 20130118494; 20130123584; 20130127708; 20130130799; 20130137936; 20130137938; 20130138002; 20130144106; 20130144107; 20130144108; 20130144183; 20130150650; 20130150651; 20130150659; 20130159041; 20130165812; 20130172686; 20130172691; 20130172716; 20130172763; 20130172767; 20130172772; 20130172774; 20130178718; 20130182860; 20130184552; 20130184558; 20130184603; 20130188854; 20130190577; 20130190642; 20130197321; 20130197322; 20130197328; 20130197339; 20130204150; 20130211224; 20130211276; 20130211291; 20130217982; 20130218043; 20130218053; 20130218233; 20130221961; 20130225940; 20130225992; 20130231574; 20130231580; 20130231947; 20130238049; 20130238050; 20130238063; 20130245422; 20130245486; 20130245711; 20130245712; 20130266163; 20130267760; 20130267866; 20130267928; 20130274580; 20130274625; 20130275159; 20130281811; 20130282339; 20130289401; 20130289413; 20130289417; 20130289424; 20130289433; 20130295016; 20130300573; 20130303828; 20130303934; 20130304153; 20130310660; 20130310909; 20130324880; 20130338449; 20130338459; 20130344465; 20130345522; 20130345523; 20140005988; 20140012061; 20140012110; 20140012133; 20140012153; 20140018792; 20140019165; 20140023999; 20140025396; 20140025397; 20140038147; 20140046208; 20140051044; 20140051960; 20140051961; 20140052213; 20140055284; 20140058241; 20140066739; 20140066763; 20140070958; 20140072127; 20140072130; 20140073863; 20140073864; 20140073866; 20140073870; 20140073875; 20140073876; 20140073877; 20140073878; 20140073898; 20140073948; 20140073949; 20140073951; 20140073953; 20140073954; 20140073955; 20140073956; 20140073960; 20140073961; 20140073963; 20140073965; 20140073966; 20140073967; 20140073968; 20140073974; 20140073975; 20140074060; 20140074179; 20140074180; 20140077946; 20140081114; 20140081115; 20140094720; 20140098981; 20140100467; 20140104059; 20140105436; 20140107464; 20140107519; 20140107525; 20140114165; 20140114205; 20140121446; 20140121476; 20140121554; 20140128762; 20140128764; 20140135879; 20140136585; 20140140567; 20140143064; 20140148723; 20140152673; 20140155706; 20140155714; 20140155730; 20140156000; 20140163328; 20140163330; 20140163331; 20140163332; 20140163333; 20140163335; 20140163336; 20140163337; 20140163385; 20140163409; 20140163425; 20140163897; 20140171820; 20140175261; 20140176944; 20140179980; 20140180088; 20140180092; 20140180093; 20140180094; 20140180095; 20140180096; 20140180097; 20140180099; 20140180100; 20140180112; 20140180113; 20140180145; 20140180153; 20140180160; 20140180161; 20140180176; 20140180177; 20140180597; 20140187994; 20140188006; 20140188770; 20140194702; 20140194758; 20140194759; 20140194768; 20140194769; 20140194780; 20140194793; 20140203797; 20140213937; 20140214330; 20140228651; 20140228702; 20140232516; 20140235965; 20140236039; 20140236077; 20140237073; 20140243614; 20140243621; 20140243628; 20140243694; 20140249429; 20140257073; 20140257147; 20140266696; 20140266787; 20140275886; 20140275889; 20140275891; 20140276013; 20140276014; 20140276090; 20140276123; 20140276130; 20140276181; 20140276183; 20140279746; 20140288381; 20140288614; 20140288953; 20140289172; 20140296724; 20140303453; 20140303454; 20140303508; 20140309943; 20140313303; 20140316217; 20140316221; 20140316230; 20140316235; 20140316278; 20140323900; 20140324118; 20140330102; 20140330157; 20140330159; 20140330334; 20140330404; 20140336473; 20140347491; 20140350431; 20140350436; 20140358025; 20140364721; 20140364746; 20140369537; 20140371544; 20140371599; 20140378809; 20140378810; 20140379620; 20150003698; 20150003699; 20150005592; 20150005594; 20150005640; 20150005644; 20150005660; 20150005680; 20150006186; 20150016618; 20150018758; 20150025351; 20150025422; 20150032017; 20150038804; 20150038869; 20150039110; 20150042477; 20150045686; 20150051663; 20150057512; 20150065839; 20150073237; 20150073306; 20150080671; 20150080746; 20150087931; 20150088024; 20150092949; 20150093729; 20150099941; 20150099962; 20150103360; 20150105631; 20150105641; 20150105837; 20150112222; 20150112409; 20150119652; 20150119743; 20150119746; 20150126821; 20150126845; 20150126848; 20150126873; 20150134264; 20150137988; 20150141529; 20150141789; 20150141794; 20150153477; 20150157235; 20150157266; 20150164349; 20150164362; 20150164375; 20150164404; 20150181840; 20150182417; 20150190070; 20150190085; 20150190636; 20150190637; 20150196213; 20150199010; 20150201879; 20150202447; 20150203822; 20150208940; 20150208975; 20150213191; 20150216436; 20150216468; 20150217082; 20150220486; 20150223743; 20150227702; 20150230750; 20150231408; 20150238106; 20150238112; 20150238137; 20150245800; 20150247921; 20150250393; 20150250401; 20150250415; 20150257645; 20150257673; 20150257674; 20150257700; 20150257712; 20150265164; 20150269825; 20150272465; 20150282730; 20150282755; 20150282760; 20150290420; 20150290453; 20150290454; 20150297106; 20150297141; 20150304101; 20150305685; 20150309563; 20150313496; 20150313535; 20150327813; 20150327837; 20150335292; 20150342478; 20150342493; 20150351655; 20150351701; 20150359441; 20150359450; 20150359452; 20150359467; 20150359486; 20150359492; 20150366497; 20150366504; 20150366516; 20150366518; 20150374285; 20150374292; 20150374300; 20150380009; 20160000348; 20160000354; 20160007915; 20160007918; 20160012749; 20160015281; 20160015289; 20160022141; 20160022156; 20160022164; 20160022167; 20160022206; 20160027293; 20160029917; 20160029918; 20160029946; 20160029950; 20160029965; 20160030702; 20160038037; 20160038038; 20160038049; 20160038091; 20160045150; 20160045756; 20160051161; 20160051162; 20160051187; 20160051195; 20160055415; 20160058301; 20160066788; 20160067494; 20160073886; 20160074661; 20160081577; 20160081616; 20160087603; 20160089031; 20160100769; 20160101260; 20160106331; 20160106344; 20160112022; 20160112684; 20160113539; 20160113545; 20160113567; 20160113587; 20160119726; 20160120433; 20160120434; 20160120464; 20160120480; 20160128596; 20160132654; 20160135691; 20160135727; 20160135754; 20160140834; 20160143554; 20160143560; 20160143594; 20160148531; 20160150988; 20160151014; 20160151018; 20160151628; 20160157742; 20160157828; 20160162652; 20160165852; 20160165853; 20160166169; 20160166197; 20160166199; 20160166208; 20160174099; 20160174863; 20160178392; 20160183828; 20160183861; 20160191517; 20160192841; 20160192842; 20160192847; 20160192879; 20160196758; 20160198963; 20160198966; 20160202755; 20160206877; 20160206880; 20160213276; 20160213314; 20160220133; 20160220134; 20160220136; 20160220166; 20160220836; 20160220837; 20160224757; 20160228019; 20160228029; 20160228059; 20160228705; 20160232811; 20160235324; 20160235351; 20160235352; 20160239084; 20160242659; 20160242690; 20160242699; 20160248434; 20160249841; 20160256063; 20160256112; 20160256118; 20160259905; 20160262664; 20160262685; 20160262695; 20160262703; 20160278651; 20160278697; 20160278713; 20160282941; 20160287120; 20160287157; 20160287162; 20160287166; 20160287871; 20160296157; 20160302683; 20160302704; 20160302709; 20160302720; 20160302737; 20160303402; 20160310031; 20160310070; 20160317056; 20160324465; 20160331264; 20160338634; 20160338644; 20160338798; 20160346542; 20160354003; 20160354027; 20160360965; 20160360970; 20160361021; 20160361041; 20160367204; 20160374581; 20160374618; 20170000404; 20170001016; 20170007165; 20170007173; 20170014037; 20170014083; 20170020434; 20170020447; 20170027467; 20170032098; 20170035392; 20170042430; 20170042469; 20170042475; 20170053513; 20170055839; 20170055898; 20170055913; 20170065199; 20170065218; 20170065229; 20170071495; 20170071523; 20170071529; 20170071532; 20170071537; 20170071546; 20170071551; 20170071552; 20170079538; 20170079596; 20170086672; 20170086695; 20170091567; 20170095721; 20170105647; 20170112379; 20170112427; 20170120066; 20170127946; 20170132816; 20170135597; 20170135604; 20170135626; 20170135629; 20170135631; 20170135633; 20170143231; 20170143249; 20170143255; 20170143257; 20170143259; 20170143266; 20170143267; 20170143268; 20170143273; 20170143280; 20170143282; 20170143960; 20170143963; 20170146386; 20170146387; 20170146390; 20170146391; 20170147754; 20170148240; 20170150896; 20170150916; 20170156593; 20170156606; 20170156655; 20170164878; 20170164901; 20170172414; 20170172501; 20170172520; 20170173262; 20170177023; 20170181693; 20170185149; 20170188865; 20170188872; 20170188947; 20170188992; 20170189691; 20170196497; 20170202474; 20170202518; 20170203154; 20170209053; and 20170209083.


There are many approaches to time-frequency decomposition of EEG data, including the short-term Fourier transform (STFT), (Gabor D. Theory of Communication. J. Inst. Electr. Engrs. 1946; 93:429-457) continuous (Daubechies I. Ten Lectures on Wavelets. Philadelphia, Pa.: Society for Industrial and Applied Mathematics; 1992357. 21. Combes J M, Grossmann A, Tchamitchian P. Wavelets: Time-Frequency Methods and Phase Space-Proceedings of the International Conference; Dec. 14-18, 1987; Marseille, France) or discrete (Mallat S G. A theory for multiresolution signal decomposition: the wavelet representation. IEEE Trans Pattern Anal Mach Intell. 1989; 11:674-693) wavelet transforms, Hilbert transform (Lyons R G. Understanding Digital Signal Processing. 2nd ed. Upper Saddle River, N.J.: Prentice Hall PTR; 2004:688), and matching pursuits (Mallat S, Zhang Z. Matching pursuits with time-frequency dictionaries. IEEE Trans. Signal Proc. 1993; 41(12):3397-3415). Prototype analysis systems may be implemented using, for example, MatLab with the Wavelet Toolbox, www.mathworks.com/products/wavelet.html.


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 6,196,972; 6,338,713; 6,442,421; 6,507,754; 6,524,249; 6,547,736; 6,616,611; 6,816,744; 6,865,494; 6,915,241; 6,936,012; 6,996,261; 7,043,293; 7,054,454; 7,079,977; 7,128,713; 7,146,211; 7,149,572; 7,164,941; 7,209,788; 7,254,439; 7,280,867; 7,282,030; 7,321,837; 7,330,032; 7,333,619; 7,381,185; 7,537,568; 7,559,903; 7,565,193; 7,567,693; 7,604,603; 7,624,293; 7,640,055; 7,715,919; 7,725,174; 7,729,755; 7,751,878; 7,778,693; 7,794,406; 7,797,040; 7,801,592; 7,803,118; 7,803,119; 7,879,043; 7,896,807; 7,899,524; 7,917,206; 7,933,646; 7,937,138; 7,976,465; 8,014,847; 8,033,996; 8,073,534; 8,095,210; 8,137,269; 8,137,270; 8,175,696; 8,177,724; 8,177,726; 8,180,601; 8,187,181; 8,197,437; 8,233,965; 8,236,005; 8,244,341; 8,248,069; 8,249,698; 8,280,514; 8,295,914; 8,326,433; 8,335,664; 8,346,342; 8,355,768; 8,386,312; 8,386,313; 8,392,250; 8,392,253; 8,392,254; 8,392,255; 8,396,542; 8,406,841; 8,406,862; 8,412,655; 8,428,703; 8,428,704; 8,463,374; 8,464,288; 8,475,387; 8,483,815; 8,494,610; 8,494,829; 8,494,905; 8,498,699; 8,509,881; 8,533,042; 8,548,786; 8,571,629; 8,579,786; 8,591,419; 8,606,360; 8,628,480; 8,655,428; 8,666,478; 8,682,422; 8,706,183; 8,706,205; 8,718,747; 8,725,238; 8,738,136; 8,747,382; 8,755,877; 8,761,869; 8,762,202; 8,768,449; 8,781,796; 8,790,255; 8,790,272; 8,821,408; 8,825,149; 8,831,731; 8,843,210; 8,849,392; 8,849,632; 8,855,773; 8,858,440; 8,862,210; 8,862,581; 8,903,479; 8,918,178; 8,934,965; 8,951,190; 8,954,139; 8,955,010; 8,958,868; 8,983,628; 8,983,629; 8,989,835; 9,020,789; 9,026,217; 9,031,644; 9,050,470; 9,060,671; 9,070,492; 9,072,832; 9,072,905; 9,078,584; 9,084,896; 9,095,295; 9,101,276; 9,107,595; 9,116,835; 9,125,574; 9,149,719; 9,155,487; 9,192,309; 9,198,621; 9,204,835; 9,211,417; 9,215,978; 9,232,910; 9,232,984; 9,238,142; 9,242,067; 9,247,911; 9,248,286; 9,254,383; 9,277,871; 9,277,873; 9,282,934; 9,289,603; 9,302,110; 9,307,944; 9,308,372; 9,320,450; 9,336,535; 9,357,941; 9,375,151; 9,375,171; 9,375,571; 9,403,038; 9,415,219; 9,427,581; 9,443,141; 9,451,886; 9,454,646; 9,462,956; 9,462,975; 9,468,541; 9,471,978; 9,480,402; 9,492,084; 9,504,410; 9,522,278; 9,533,113; 9,545,285; 9,560,984; 9,563,740; 9,615,749; 9,616,166; 9,622,672; 9,622,676; 9,622,702; 9,622,703; 9,623,240; 9,636,019; 9,649,036; 9,659,229; 9,668,694; 9,681,814; 9,681,820; 9,682,232; 9,713,428; 20020035338; 20020091319; 20020095099; 20020103428; 20020103429; 20020193670; 20030032889; 20030046018; 20030093129; 20030160622; 20030185408; 20030216654; 20040039268; 20040049484; 20040092809; 20040133119; 20040133120; 20040133390; 20040138536; 20040138580; 20040138711; 20040152958; 20040158119; 20050010091; 20050018858; 20050033174; 20050075568; 20050085744; 20050119547; 20050148893; 20050148894; 20050148895; 20050154290; 20050167588; 20050240087; 20050245796; 20050267343; 20050267344; 20050283053; 20050283090; 20060020184; 20060036152; 20060036153; 20060074290; 20060078183; 20060135879; 20060153396; 20060155495; 20060161384; 20060173364; 20060200013; 20060217816; 20060233390; 20060281980; 20070016095; 20070066915; 20070100278; 20070179395; 20070179734; 20070191704; 20070209669; 20070225932; 20070255122; 20070255135; 20070260151; 20070265508; 20070287896; 20080021345; 20080033508; 20080064934; 20080074307; 20080077015; 20080091118; 20080097197; 20080119716; 20080177196; 20080221401; 20080221441; 20080243014; 20080243017; 20080255949; 20080262367; 20090005667; 20090033333; 20090036791; 20090054801; 20090062676; 20090177144; 20090220425; 20090221930; 20090270758; 20090281448; 20090287271; 20090287272; 20090287273; 20090287467; 20090299169; 20090306534; 20090312646; 20090318794; 20090322331; 20100030073; 20100036211; 20100049276; 20100068751; 20100069739; 20100094152; 20100099975; 20100106041; 20100198090; 20100204604; 20100204748; 20100249638; 20100280372; 20100331976; 20110004115; 20110015515; 20110015539; 20110040713; 20110066041; 20110066042; 20110074396; 20110077538; 20110092834; 20110092839; 20110098583; 20110160543; 20110172725; 20110178441; 20110184305; 20110191350; 20110218950; 20110257519; 20110270074; 20110282230; 20110288431; 20110295143; 20110301441; 20110313268; 20110313487; 20120004518; 20120004561; 20120021394; 20120022343; 20120029378; 20120041279; 20120046535; 20120053473; 20120053476; 20120053478; 20120053479; 20120083708; 20120108918; 20120108997; 20120143038; 20120145152; 20120150545; 20120157804; 20120159656; 20120172682; 20120184826; 20120197153; 20120209139; 20120253261; 20120265267; 20120271151; 20120271376; 20120289869; 20120310105; 20120321759; 20130012804; 20130041235; 20130060125; 20130066392; 20130066395; 20130072775; 20130079621; 20130102897; 20130116520; 20130123607; 20130127708; 20130131438; 20130131461; 20130165804; 20130167360; 20130172716; 20130172772; 20130178733; 20130184597; 20130204122; 20130211238; 20130223709; 20130226261; 20130237874; 20130238049; 20130238050; 20130245416; 20130245424; 20130245485; 20130245486; 20130245711; 20130245712; 20130261490; 20130274562; 20130289364; 20130295016; 20130310422; 20130310909; 20130317380; 20130338518; 20130338803; 20140039279; 20140057232; 20140058218; 20140058528; 20140074179; 20140074180; 20140094710; 20140094720; 20140107521; 20140142654; 20140148657; 20140148716; 20140148726; 20140180153; 20140180160; 20140187901; 20140228702; 20140243647; 20140243714; 20140257128; 20140275807; 20140276130; 20140276187; 20140303454; 20140303508; 20140309614; 20140316217; 20140316248; 20140324118; 20140330334; 20140330335; 20140330336; 20140330404; 20140335489; 20140350634; 20140350864; 20150005646; 20150005660; 20150011907; 20150018665; 20150018699; 20150018702; 20150025422; 20150038869; 20150073294; 20150073306; 20150073505; 20150080671; 20150080695; 20150099962; 20150126821; 20150151142; 20150164431; 20150190070; 20150190636; 20150190637; 20150196213; 20150196249; 20150213191; 20150216439; 20150245800; 20150248470; 20150248615; 20150272652; 20150297106; 20150297893; 20150305686; 20150313498; 20150366482; 20150379370; 20160000348; 20160007899; 20160022167; 20160022168; 20160022207; 20160027423; 20160029965; 20160038042; 20160038043; 20160045128; 20160051812; 20160058304; 20160066838; 20160107309; 20160113587; 20160120428; 20160120432; 20160120437; 20160120457; 20160128596; 20160128597; 20160135754; 20160143594; 20160144175; 20160151628; 20160157742; 20160157828; 20160174863; 20160174907; 20160176053; 20160183881; 20160184029; 20160198973; 20160206380; 20160213261; 20160213317; 20160220850; 20160228028; 20160228702; 20160235324; 20160239966; 20160239968; 20160242645; 20160242665; 20160242669; 20160242690; 20160249841; 20160250355; 20160256063; 20160256105; 20160262664; 20160278653; 20160278713; 20160287117; 20160287162; 20160287169; 20160287869; 20160303402; 20160331264; 20160331307; 20160345895; 20160345911; 20160346542; 20160361041; 20160361546; 20160367186; 20160367198; 20170031440; 20170031441; 20170039706; 20170042444; 20170045601; 20170071521; 20170079588; 20170079589; 20170091418; 20170113046; 20170120041; 20170128015; 20170135594; 20170135626; 20170136240; 20170165020; 20170172446; 20170173326; 20170188870; 20170188905; 20170188916; 20170188922; and 20170196519.


Single instruction, multiple data processors, such as graphic processing units including the nVidia CUDA environment or AMD Firepro high-performance computing environment are known, and may be employed for general purpose computing, finding particular application in data matrix transformations.


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 5,273,038; 5,503,149; 6,240,308; 6,272,370; 6,298,259; 6,370,414; 6,385,479; 6,490,472; 6,556,695; 6,697,660; 6,801,648; 6,907,280; 6,996,261; 7,092,748; 7,254,500; 7,338,455; 7,346,382; 7,490,085; 7,497,828; 7,539,528; 7,565,193; 7,567,693; 7,577,472; 7,597,665; 7,627,370; 7,680,526; 7,729,755; 7,809,434; 7,840,257; 7,860,548; 7,872,235; 7,899,524; 7,904,134; 7,904,139; 7,907,998; 7,983,740; 7,983,741; 8,000,773; 8,014,847; 8,069,125; 8,233,682; 8,233,965; 8,235,907; 8,248,069; 8,356,004; 8,379,952; 8,406,838; 8,423,125; 8,445,851; 8,553,956; 8,586,932; 8,606,349; 8,615,479; 8,644,910; 8,679,009; 8,696,722; 8,712,512; 8,718,747; 8,761,866; 8,781,557; 8,814,923; 8,821,376; 8,834,546; 8,852,103; 8,870,737; 8,936,630; 8,951,189; 8,951,192; 8,958,882; 8,983,155; 9,005,126; 9,020,586; 9,022,936; 9,028,412; 9,033,884; 9,042,958; 9,078,584; 9,101,279; 9,135,400; 9,144,392; 9,149,255; 9,155,521; 9,167,970; 9,179,854; 9,179,858; 9,198,637; 9,204,835; 9,208,558; 9,211,077; 9,213,076; 9,235,685; 9,242,067; 9,247,924; 9,268,014; 9,268,015; 9,271,651; 9,271,674; 9,275,191; 9,292,920; 9,307,925; 9,322,895; 9,326,742; 9,330,206; 9,368,265; 9,395,425; 9,402,558; 9,414,776; 9,436,989; 9,451,883; 9,451,899; 9,468,541; 9,471,978; 9,480,402; 9,480,425; 9,486,168; 9,592,389; 9,615,789; 9,626,756; 9,672,302; 9,672,617; 9,682,232; 20020033454; 20020035317; 20020037095; 20020042563; 20020058867; 20020103428; 20020103429; 20030018277; 20030093004; 20030128801; 20040082862; 20040092809; 20040096395; 20040116791; 20040116798; 20040122787; 20040122790; 20040166536; 20040215082; 20050007091; 20050020918; 20050033154; 20050079636; 20050119547; 20050154290; 20050222639; 20050240253; 20050283053; 20060036152; 20060036153; 20060052706; 20060058683; 20060074290; 20060078183; 20060084858; 20060149160; 20060161218; 20060241382; 20060241718; 20070191704; 20070239059; 20080001600; 20080009772; 20080033291; 20080039737; 20080042067; 20080097235; 20080097785; 20080128626; 20080154126; 20080221441; 20080228077; 20080228239; 20080230702; 20080230705; 20080249430; 20080262327; 20080275340; 20090012387; 20090018407; 20090022825; 20090024050; 20090062660; 20090078875; 20090118610; 20090156907; 20090156955; 20090157323; 20090157481; 20090157482; 20090157625; 20090157751; 20090157813; 20090163777; 20090164131; 20090164132; 20090171164; 20090172540; 20090179642; 20090209831; 20090221930; 20090246138; 20090299169; 20090304582; 20090306532; 20090306534; 20090312808; 20090312817; 20090318773; 20090318794; 20090322331; 20090326604; 20100021378; 20100036233; 20100041949; 20100042011; 20100049482; 20100069739; 20100069777; 20100082506; 20100113959; 20100249573; 20110015515; 20110015539; 20110028827; 20110077503; 20110118536; 20110125077; 20110125078; 20110129129; 20110160543; 20110161011; 20110172509; 20110172553; 20110178359; 20110190846; 20110218405; 20110224571; 20110230738; 20110257519; 20110263962; 20110263968; 20110270074; 20110288400; 20110301448; 20110306845; 20110306846; 20110313274; 20120021394; 20120022343; 20120035433; 20120053483; 20120163689; 20120165904; 20120215114; 20120219195; 20120219507; 20120245474; 20120253261; 20120253434; 20120289854; 20120310107; 20120316793; 20130012804; 20130060125; 20130063550; 20130085678; 20130096408; 20130110616; 20130116561; 20130123607; 20130131438; 20130131461; 20130178693; 20130178733; 20130184558; 20130211238; 20130221961; 20130245424; 20130274586; 20130289385; 20130289386; 20130303934; 20140058528; 20140066763; 20140119621; 20140151563; 20140155730; 20140163368; 20140171757; 20140180088; 20140180092; 20140180093; 20140180094; 20140180095; 20140180096; 20140180097; 20140180099; 20140180100; 20140180112; 20140180113; 20140180176; 20140180177; 20140184550; 20140193336; 20140200414; 20140243614; 20140257047; 20140275807; 20140303486; 20140315169; 20140316248; 20140323849; 20140335489; 20140343397; 20140343399; 20140343408; 20140364721; 20140378830; 20150011866; 20150038812; 20150051663; 20150099959; 20150112409; 20150119658; 20150119689; 20150148700; 20150150473; 20150196800; 20150200046; 20150219732; 20150223905; 20150227702; 20150247921; 20150248615; 20150253410; 20150289779; 20150290453; 20150290454; 20150313540; 20150317796; 20150324692; 20150366482; 20150375006; 20160005320; 20160027342; 20160029965; 20160051161; 20160051162; 20160055304; 20160058304; 20160058392; 20160066838; 20160103487; 20160120437; 20160120457; 20160143541; 20160157742; 20160184029; 20160196393; 20160228702; 20160231401; 20160239966; 20160239968; 20160260216; 20160267809; 20160270723; 20160302720; 20160303397; 20160317077; 20160345911; 20170027539; 20170039706; 20170045601; 20170061034; 20170085855; 20170091418; 20170112403; 20170113046; 20170120041; 20170160360; 20170164861; 20170169714; 20170172527; and 20170202475.


Statistical analysis may be presented in a form that permits parallelization, which can be efficiently implemented using various parallel processors, a common form of which is a SIMD (single instruction, multiple data) processor, found in typical graphics processors (GPUs).


See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 8,406,890; 8,509,879; 8,542,916; 8,852,103; 8,934,986; 9,022,936; 9,028,412; 9,031,653; 9,033,884; 9,037,530; 9,055,974; 9,149,255; 9,155,521; 9,198,637; 9,247,924; 9,268,014; 9,268,015; 9,367,131; 9,4147,80; 9,420,970; 9,430,615; 9,442,525; 9,444,998; 9,445,763; 9,462,956; 9,474,481; 9,489,854; 9,504,420; 9,510,790; 9,519,981; 9,526,906; 9,538,948; 9,585,581; 9,622,672; 9,641,665; 9,652,626; 9,684,335; 9,687,187; 9,693,684; 9,693,724; 9,706,963; 9,712,736; 20090118622; 20100098289; 20110066041; 20110066042; 20110098583; 20110301441; 20120130204; 20120265271; 20120321759; 20130060158; 20130113816; 20130131438; 20130184786; 20140031889; 20140031903; 20140039975; 20140114889; 20140226131; 20140279341; 20140296733; 20140303424; 20140313303; 20140315169; 20140316235; 20140364721; 20140378810; 20150003698; 20150003699; 20150005640; 20150005644; 20150006186; 20150029087; 20150033245; 20150033258; 20150033259; 20150033262; 20150033266; 20150081226; 20150088093; 20150093729; 20150105701; 20150112899; 20150126845; 20150150122; 20150190062; 20150190070; 20150190077; 20150190094; 20150192776; 20150196213; 20150196800; 20150199010; 20150241916; 20150242608; 20150272496; 20150272510; 20150282705; 20150282749; 20150289217; 20150297109; 20150305689; 20150335295; 20150351655; 20150366482; 20160027342; 20160029896; 20160058366; 20160058376; 20160058673; 20160060926; 20160065724; 20160065840; 20160077547; 20160081625; 20160103487; 20160104006; 20160109959; 20160113517; 20160120048; 20160120428; 20160120457; 20160125228; 20160157773; 20160157828; 20160183812; 20160191517; 20160193499; 20160196185; 20160196635; 20160206241; 20160213317; 20160228064; 20160235341; 20160235359; 20160249857; 20160249864; 20160256086; 20160262680; 20160262685; 20160270656; 20160278672; 20160282113; 20160287142; 20160306942; 20160310071; 20160317056; 20160324445; 20160324457; 20160342241; 20160360100; 20160361027; 20160366462; 20160367138; 20160367195; 20160374616; 20160378608; 20160378965; 20170000324; 20170000325; 20170000326; 20170000329; 20170000330; 20170000331; 20170000332; 20170000333; 20170000334; 20170000335; 20170000337; 20170000340; 20170000341; 20170000342; 20170000343; 20170000345; 20170000454; 20170000683; 20170001032; 20170007111; 20170007115; 20170007116; 20170007122; 20170007123; 20170007182; 20170007450; 20170007799; 20170007843; 20170010469; 20170010470; 20170013562; 20170017083; 20170020627; 20170027521; 20170028563; 20170031440; 20170032221; 20170035309; 20170035317; 20170041699; 20170042485; 20170046052; 20170065349; 20170086695; 20170086727; 20170090475; 20170103440; 20170112446; 20170113056; 20170128006; 20170143249; 20170143442; 20170156593; 20170156606; 20170164893; 20170171441; 20170172499; 20170173262; 20170185714; 20170188933; 20170196503; 20170205259; 20170206913; and 20170214786.


Artificial neural networks have been employed to analyze EEG signals.

  • See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 9,443,141; 20110218950; 20150248167; 20150248764; 20150248765; 20150310862; 20150331929; 20150338915; 20160026913; 20160062459; 20160085302; 20160125572; 20160247064; 20160274660; 20170053665; 20170069306; 20170173262; and 20170206691.
  • See also: Amari, S., Natural gradient works efficiently in learning, Neural Computation 10.251-276,1998.
  • Amari S., Cichocki, A. & Yang, H. H., A new learning algorithm for blind signal separation. In: Advances in Neural Information Processing Systems 8, MIT Press, 1996.
  • Bandettini P A, Wong E C, Hinks R S, Tikofsky R S, Hyde J S, Time course EPI of human brain function during task activation. Magn Reson Med 25:390-7, 1992.
  • Bell A. J. & Sejnowski T. J. An information-maximization approach to blind separation and blind deconvolution. Neural Comput 7:1129-59, 1995.
  • Bell, A. J. & Sejnowski, T. J., Learning the higher-order structure of a natural sound, Network: Computation in Neural Systems 7,1996b.
  • Bench U, Frith C D, Grasby P M, Friston K J, Paulesu E, Frackowiak R S, Dolan R J, Investigations of the functional anatomy of attention using the Stroop test. Neuropsychologia 31:907-22,1993.
  • Boynton G M, Engel S A, Glover G H, Heeger D J, Linear systems analysis of functional magnetic resonance imaging in human V1. J Neurosci 16:4207-21., 1996.
  • Bringer, Julien, Hervé Chabanne, and Bruno Kindarji. “Error-tolerant searchable encryption.” In Communications, 2009. ICC′09. IEEE International Conference on, pp. 1-6. IEEE, 2009.
  • Buckner, R. L, Bandettini, P. A., O'Craven, K M, Savoy, R. L., Petersen, S. E., Raichle, M. E. & Rosen, B. R., Proc Natl Acad Sci USA 93, 14878-83, 1996.
  • Cardoso, J-F. & Laheld, B., Equivalent adaptive source separation, IEEE Trans. Signal Proc., in press.
  • Chapman, R. M. & McCrary, J. W., E P component identification and measurement by principal components analysis. Brain Lang. 27, 288-301, 1995.
  • Cichocki A., Unbehauen R., & Rummert E., Robust learning algorithm for blind separation of signals, Electronics Letters 30, 1386-1387, 1994.
  • Comon P, Independent component analysis, A new concept? Signal Processing 36:11-20, 1994.
  • Cover, T. M. & Thomas, J. A., Elements of Information Theory John Wiley, 1991.
  • Cox, R. W., AFNI: software for analysis and visualization of functional magnetic resonance neuroimages. Comput Biomed Res 29:162-73, 1996.
  • Cox, R. W. & Hyde J. S. Software tools for analysis and visualization of fMRI data, NMR in Biomedicine, in press.
  • Dale, A. M. & Sereno, M. I., Improved localization of cortical activity by combining EEG and MEG with MRI cortical surface reconstruction—a linear approach. J. Cogn. Neurosci. 5:162-176, 1993.
  • Friston K. J., Modes or models: A critique on independent component analysis for fMRI. Trends in Cognitive Sciences, in press.
  • Friston K. J., Commentary and opinion: II. Statistical parametric mapping: ontology and current issues. J Cereb Blood Flow Metab 15.361-70, 1995.
  • Friston K. J., Statistical Parametric Mapping and Other Analyses of Functional Imaging Data. In: A. W. Toga, J. C. Mazziotta eds., Brain Mapping, The Methods. San Diego: Academic Press, 1996.363-396,1995.
  • Friston K J, Frith C D, Liddle P F, Frackowiak R S, Functional connectivity: the principal-component analysis of large (PET) data sets. J Cereb Blood Flow Metab 135-14, 1993.
  • Friston K J, Holmes A P, Worsley K J, Poline J P, Frith C D, and Frackowiak R. S. J., Statistical Parametric Maps in Functional Imaging: A General Linear Approach, Human Brain Mapping 2:189-210, 1995.
  • Friston K J, Williams 5, Howard R, Frackowiak R S and Turner R, Movement-related effects in fMRI time-series. Magn Reson Med 35346-55, 1996.
  • Galambos, R. and S. Makeig, “Dynamic changes in steady-state potentials,” in: Dynamics of Sensory and Cognitive Processing of the Brain, ed. E. Basar Springer, pp. 178-199, 1987.
  • Galambos, R., S. Makeig, and P. Talmachoff, A 40 Hz auditory potential recorded from the human scalp, Proc Natl Acad Sci USA 78(4):2643-2647, 1981.
  • Galil, Zvi, Stuart Haber, and Moti Yung. “Cryptographic computation: Secure fault-tolerant protocols and the public-key model.” In Conference on the Theory and Application of Cryptographic Techniques, pp. 135-155. Springer, Berlin, Heidelberg, 1987.
  • George J S, Aine C J, Mosher J C, Schmidt D M, Ranken D M, Schlitt H A, Wood C C, Lewine J D, Sanders J A, Belliveau J W. Mapping function in the human brain with magnetoencephalography, anatomical magnetic resonance imaging, and functional magnetic resonance imaging. J Clin Neurophysiol 12:406-31, 1995.
  • Ives, J. R., Warach 5, Schmitt F, Edelman R R and Schomer D L. Monitoring the patient's EEG during echo planar MRI, Electroencephalogr Clin Neurophysiol, 87: 417-420, 1993.
  • Jackson, J. E., A User's Guide to Principal Components. New York: John Wiley & Sons, Inc., 1991.
  • Jokeit, H. and Makeig, S., Different event-related patterns of gamma-band power in brain waves of fast- and slow-reacting subjects, Proc. Nat. Acad. Sci USA 91:6339-6343, 1994.
  • Juels, An, and Madhu Sudan. “A fuzzy vault scheme.” Designs, Codes and Cryptography 38, no. 2 (2006): 237-257.
  • Jueptner, M., K. M. Stephan, C. D. Frith, D. J. Brooks, R. S. J. Frackowiak & R. E. Passingham, Anatomy of Motor Learning. I. Frontal Cortex and Attention. J. Neurophysiology 77:1313-1324, 1977.
  • Jung, T-P., Humphries, C., Lee, T-W., Makeig, S., McKeown, M., Iragui, V. and Sejnowski, T. J., “Extended ICA removes artifacts from electroencephalographic recordings,” In: Advances in Neural Information Processing Systems 10: MIT Press, Cambridge, Mass., in press.
  • Jung, T-P., Humphries, C., Lee, T-W., McKeown, M. J., Iragui, V., Makeig, S. & Sejnowski, T. J., Removing electroencephalographic artifacts by blind source separation, submitted-a.
  • Jung, T-P., S. Makeig, M. Stensmo & T. Sejnowski, Estimating Alertness from the EEG Power Spectrum, IEEE Transactions on Biomedical Engineering, 44(1), 60-69, 1997.
  • Jung, T-P., Makeig, S., Westerfield, M., Townsend, J., Courchesne, E. and Sejnowski, T. J., Analysis and visualization of single-trial event-related potentials, submitted-b.
  • Jutten, C. & Herault, J., Blind separation of sources, part I: an adaptive algorithm based on neuromimetic architecture. Signal Processing 24,1-10, 1991.
  • Karhumen, J., Oja, E., Wang, L., Vigario, R. & Joutsenalo, J., A class of neural networks for independent component analysis, IEEE Trans. Neural Networks, in press.
  • Kwong K. K., Functional magnetic resonance imaging with echo planar imaging. Magn Reson Q 11:1-20, 1995.
  • Kwong K. K., Belliveau J W, Chesler D A, Goldberg I E, Weisskoff R M, Poncelet B P, Kennedy D N, Hoppel B E, Cohen M S, Turner R, et al., Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation. Proc Natl Acad Sci USA 89:5675-9, 1992.
  • Lee, T.-W., Girolami, M., and Sejnowski, T. J., Independent component analysis using an extended infomax algorithm for mixed Sub-gaussian and Super-gaussian sources, Neural Computation, submitted for publication.
  • Lewicki, Michael S., and Sejnowski, Terence J., Learning nonlinear overcomplete representations for efficient coding, Eds. M. Keams, M. Jordan, and S. Solla, Advances in Neural Information Processing Systems 10, in press.
  • Linsker, R., Local synaptic learning rules suffice to maximise mutual information in a linear network. Neural Computation 4, 691-702, 1992.
  • Liu A K, Belliveau J W, Dale A M. Spatiotemporal imaging of human brain activity using functional MRI-constrained magnetoencephalography data: Monte Carlo simulations. Proc Natl Acad Sci USA 95:8945-50, 1998
  • Manoach D S, Schlaug G, Siewert B, Darby D G, Bly B M, Benfield A, Edelman R R, Warach 5, Prefrontal cortex fMRI signal changes are correlated with working memory load. Neuroreport 8545-9, 1997.
  • McCarthy, G., Luby, M., Gore, J. and Goldman-Rakic, P., Infrequent events transiently activate human prefrontal and parietal cortex as measured by functional MRI. J. Neurophysiology 77:1630-1634, 1997.
  • McKeown, M., Makeig, S., Brown, G., Jung, T-P., Kindermann, S., Bell, Iragui, V. and Sejnowski, T. J., Blind separation of functional magnetic resonance imaging (fMRI) data, Human Brain Mapping, 6:160, 18, 1998a.
  • McKeown, M J., Humphries, C., Achermann, P., Borbely, A. A. and Sejnowski, T. J., A new method for detecting state changes in the EEG: exploratory application to sleep data. J. Sleep Res. 7 suppl. 1: 48-56, 1998b.
  • McKeown, M. J., Tzyy-Ping Jung, Scott Makeig, Greg Brown, Sandra S. Kindermann, Te-Won Lee and Terrence J. Sejnowski, Spatially independent activity patterns in functional magnetic resonance imaging data during the Stroop color-naming task, Proc. Natl. Acad. Sci USA, 95:803-810, 1998c.
  • McKeown, M J. and Sejnowski, T. J., Independent component analysis of fMRI data: examining the assumptions. Human Brain Mapping 6368-372, 1998d.
  • Makeig, S. Auditory event-related dynamics of the EEG spectrum and effects of exposure to tones, Electroencephalogr Clin Neurophysiol, 86:283-293, 1993.
  • Makeig, S. Toolbox for independent component analysis of psychophysiological data, [World Wide Web publication] www.cnl.salk.edu/˜scott/ica.html, 1997.
  • Makeig, S. and Galambos, R., The CERP: Event-related perturbations in steady-state responses, in: Brain Dynamics Progress and Perspectives, (pp. 375-400), ed. E. Basar and T. H. Bullock, 1989.
  • Makeig, S. and Inlow, M., Lapses in alertness: coherence of fluctuations in performance and the EEG spectrum, Electroencephalogr clin Neurophysiol, 86:23-35, 1993.
  • Makeig, S. and Jung, T-P., Changes in alertness are a principal component of variance in the EEG spectrum, NeuroReport 7:213-216, 1995.
  • Makeig, S. and T-P. Jung, Tonic, phasic, and transient EEG correlates of auditory awareness during drowsiness, Cognitive Brain Research 4:15-25, 1996.
  • Makeig, S., Bell, A. J., Jung, T-P. and Sejnowski, T. J., “Independent component analysis of electroencephalographic data,” In: D. Touretzky, M. Mozer and M. Hasselmo (Eds). Advances in Neural Information Processing Systems 8:145-151 MIT Press, Cambridge, Mass., 1996.
  • Makeig, S., Jung, T-P, and Sejnowski, T. J., “Using feedforward neural networks to monitor alertness from changes in EEG correlation and coherence,” In: D. Touretzky, M. Mozer & M. Hasselmo(Eds). Advances in Neural Information Processing Systems 8:931-937 MIT Press, Cambridge, Mass., 1996.
  • Makeig, S., T-P. Jung, D. Ghahremani, A. J. Bell & T. J. Sejnowski, Blind separation of auditory event-related brain responses into independent components. Proc. Natl. Acad. Sci. USA, 94:10979-10984, 1997.
  • Makeig, S., Westerfield, M., Jung, T-P., Covington, J., Townsend, J., Sejnowski, T. J. and Courchesne, E., Independent components of the late positive event-related potential in a visual spatial attention task, submitted.
  • Mitra P P, Ogawa S, Hu X, Ugurbil K, The nature of spatiotemporal changes in cerebral hemodynamics as manifested in functional magnetic resonance imaging. Magn Reson Med.37:511-8, 1997.
  • Nobre A C, Sebestyen G N, Gitelman D R, Mesulam M M, Frackowiak R S, Frith C D, Functional localization of the system for visuospatial attention using positron emission tomography. Brain 120:515-33, 1997.
  • Nunez, P. L., Electric Fields of the Brain. New York: Oxford, 1981.
  • Ogawa S, Tank D W, Menon R, Ellermann J M, Kim S G, Merkle H, Ugurbil K, Intrinsic signal changes accompanying sensory stimulation: functional brain mapping with magnetic resonance imaging. Proc Natl Acad Sci USA 89:951-5,1992.
  • Pearmutter, B. and Parra, L. C. Maximum likelihood blind source separation: a context-sensitive generalization of ICA. In: M. C. Mozer, M. I. Jordan and T. Petsche (Eds.), Advances in Neural Information Processing Systems 9:613-619 MIT Press, Cambridge, Mass., 1996.
  • Sakai K, Hikosaka O, Miyauchi S, Takino R, Sasaki Y, Putz B. Transition of brain activation from frontal to parietal areas in visuomotor sequence learning. J Neurosci 18:1827-40, 1998.
  • Sahai, Amit, and Brent Waters. “Fuzzy identity-based encryption.” In Annual International Conference on the Theory and Applications of Cryptographic Techniques, pp. 457-473. Springer, Berlin, Heidelberg, 2005.
  • Scherg, M. & Von Cramon, D., Evoked dipole source potentials of the human auditory cortex. Electroencephalogr. Clin. Neurophysiol. 65:344-601, 1986.
  • Tallon-Baudry, C., Bertrand, O., Delpuech, C., & Pernier, J., Stimulus Specificity of Phase-Locked and Non-Phase-Locked 40 Hz Visual Responses in Human. J. Neurosci. 16: 4240-4249, 1996.
  • Thaker, Darshan D., Diana Franklin, John Oliver, Susmit Biswas, Derek Lockhart, Tzvetan Metodi, and Frederic T. Chong. “Characterization of error-tolerant applications when protecting control data.” In Workload Characterization, 2006 IEEE International Symposium on, pp. 142-149. IEEE, 2006.
  • Tulving E, Markowitsch H J, Craik F E, Habib R, Houle S, Novelty and familiarity activations in PET studies of memory encoding and retrieval. Cereb Cortex 6:71-9, 1996.
  • Warach, S., J. R. Ives, G. Schaug, M. R. Patel, D. G. Darby, V. Thangaraj, R. R. Edelman and D. L. Schomer, EEG-triggered echo-planar functional MRI in epilepsy, Neurology 47: 89-93, 1996.


Principal Component Analysis


Principal component analysis (PCA) is a statistical procedure that uses an orthogonal transformation to convert a set of observations of possibly correlated variables into a set of values of linearly uncorrelated variables called principal components. If there are n observations with p variables, then the number of distinct principal components is min(n−1,p). This transformation is defined in such a way that the first principal component has the largest possible variance (that is, accounts for as much of the variability in the data as possible), and each succeeding component in turn has the highest variance possible under the constraint that it is orthogonal to the preceding components. The resulting vectors are an uncorrelated orthogonal basis set. PCA is sensitive to the relative scaling of the original variables. PCA is the simplest of the true eigenvector-based multivariate analyses. Often, its operation can be thought of as revealing the internal structure of the data in a way that best explains the variance in the data. If a multivariate dataset is visualized as a set of coordinates in a high-dimensional data space (1 axis per variable), PCA can supply the user with a lower-dimensional picture, a projection of this object when viewed from its most informative viewpoint. This is done by using only the first few principal components so that the dimensionality of the transformed data is reduced. PCA is closely related to factor analysis. Factor analysis typically incorporates more domain specific assumptions about the underlying structure and solves eigenvectors of a slightly different matrix. PCA is also related to canonical correlation analysis (CCA). CCA defines coordinate systems that optimally describe the cross-covariance between two datasets while PCA defines a new orthogonal coordinate system that optimally describes variance in a single dataset. See, en.wikipedia.org/wiki/Principal_component_analysis.


A general model for confirmatory factor analysis is expressed as x=α+Λξ+ε. The covariance matrix is expressed as E[(x−μ)(x−μ)′]=ΛΦΛ+Θ. If residual covariance matrix Θ=0 and correlation matrix among latent factors Φ=I, then factor analysis is equivalent to principal component analysis and the resulting covariance matrix is simplified to Σ=ΛΛ′. When there are p number of variables and all p components (or factors) are extracted, this covariance matrix can alternatively be expressed into Σ=DΛD′, or Σ=λDAD′, where D=n×p orthogonal matrix of eigenvectors, and Λ=λΛ, p×p matrix of eigenvalues, where λ is a scalar and A is a diagonal matrix whose elements are proportional to the eigenvalues of Σ. The following three components determine the geometric features of the observed data: λ parameterizes the volume of the observation, D indicates the orientation, and A represents the shape of the observation.


When population heterogeneity is explicitly hypothesized as in model-based cluster analysis, the observed covariance matrix is decomposed into the following general form ΣkkDkAk DkT,


where λk parameterizes the volume of the kth cluster, Dk indicates the orientation of that cluster, and Ak represents the shape of that cluster. The subscript k indicates that each component (or cluster) can have different volume, shape, and orientation.


Assume a random vector X, taking values in custom characterm, has a mean and covariance matrix of μX and ΣX, respectively. λ12> . . . >λm>0 are ordered eigenvalues of ΣX, such that the i-th eigenvalue of ΣX means the i-th largest of them. Similarly, a vector αi is the i-th eigenvector of ΣX when it corresponds to the i-th eigenvalue of ΣX. To derive the form of principal components (PCs), consider the optimization problem of maximizing var[α1TX]=α1TΣXα1, subject to α1Tα1=1. The Lagrange multiplier method is used to solve this question.












L


(


α
1

,

ϕ
1


)


=



α
1
T





X



α
1



+


ϕ
1



(



α
1
T



α
1


-
1

)













L




α
1



=



2




X



α
1



+

2


ϕ
1



α
1



=


0




X



α
1



=




-

ϕ
1




α
1




var


[


α
1
T


X

]



=



-

ϕ
1




α
1
T



α
1


=

-


ϕ
1

.










Because −ϕ1 is the eigenvalue of ΣX, with α1 being the corresponding normalized eigenvector, var[α1TX] is maximized by choosing α1 to be the first eigenvector of ΣX. In this case, z11TX is named the first PC of X, α1t the vector of coefficients for z1, and var(z1)=λ1.


To find the second PC, z22TX, we need to maximize var[α2TX]=α2TΣXα2 subject to z2 being uncorrelated with z1. Because cov(α1TX, α2TX)=0 ⇒α1TΣXα2=0⇒α1Tα2=0, this problem is equivalently set as maximizing α2TΣXα2, subject to α1Tα2=0, and α2Tα2=1. We still make use of the Lagrange multiplier method.







L


(


α
2

,

ϕ
1

,

ϕ
2


)


=



α
2
T





X



α
2



+


ϕ
1



α
1
T



a
2


+


ϕ
2



(



α
2
T



α
2


-
1

)












L




α
2



=



2




X



α
2



+


ϕ
1



α
1


+

2






ϕ
2



α
2



=


0



α
1
T



(


2




X



α
2



+


ϕ
1



α
1


+

2






ϕ
2



α
2



)



=


0


ϕ
1


=


0




X



α
2



=




-

ϕ
2




α
2





α
2
T





X



α
2




=

-


ϕ
2

.











Because −ϕ2 is the eigenvalue of ΣX, with α2 being the corresponding normalized eigenvector, var[α2TX] is maximized by choosing α2 to be the second eigenvector of ΣX. In this case, z22TX is named the second PC of X, α2 is the vector of coefficients for z2, and var(z2)=λ2. Continuing in this way, it can be shown that the i-th PC ziiTX is constructed by selecting αi to be the i-th eigenvector of ΣX, and has variance of λi. The key result in regards to PCA is that the principal components are the only set of linear functions of original data that are uncorrelated and have orthogonal vectors of coefficients.


For any positive integer p≤m, let B=[β1, β2, . . . , βp] be an real m×p matrix with orthonormal columns, i.e., βiTβjij, and Y=BTX. Then the trace of covariance matrix of Y is maximized by taking B=[α1, α2, . . . , αp], where αi is the i-th eigenvector of ΣX. Because ΣX is symmetric with all distinct eigenvalues, so {α1, α2, . . . , αm} is an orthonormal basis with αi being the i-th eigenvector of ΣX, and we can represent the columns of B as








β
i

=




j
=
1

m




c
ji



α
j




,





i=1, . . . , p, So we have B=PC, where P=[α1, . . . , αm], C={cij} is an m×P matrix. Then, PTΣXP=Λ, with Λ being a diagonal matrix whose k-th diagonal element is λk, and the covariance matrix of Y is,

ΣY=BTΣXB=CTPTΣXPC=CTΛC=λ1c1c1T+ . . . +λmcmcmT

where ciT is the i-th row of C. So,







trace


(


Y

)


=





i
=
1

m




λ
i



trace


(


c
i



c
i
T


)




=





i
=
1

m




λ
i



trace


(


c
i
T



c
i


)




=





i
=
1

m




λ
i



c
i
T



c
i



=




i
=
1

m




(




j
=
1

p



c
ij
2


)




λ
i

.










Because CTC=BTPPTB=BTB=I, so








trace
(


C
T


C

)

=





i
=
1

m






j
=
1

p



c
ij
2



=
p


,





and the columns of C are orthonormal. By the Gram-Schmidt method, C can expand to D, such that D has its columns as an orthonormal basis of custom characterm and contains C as its first P columns. D is square shape, thus being an orthogonal matrix and having its rows as another orthonormal basis of custom characterm. One row of C is a part of one row of D, so











j
=
1

p



c
ij
2



1

,





i=1, . . . , m. Considering the constraints











j
=
1

p



c
ij
2



1

,





i
=
1

m






j
=
1

p



c
ij
2



=
p






and the objective









i
=
1

m




(




j
=
1

p



c
ij
2


)




λ
i

.







We derive that trace(ΣY) is maximized if










j
=
1

p



c
ij
2


=
1





for i=1, . . . , p, and










j
=
1

p



c
ij
2


=
0





for i=p+1, . . . , m. When B=[α1, α2, . . . , αp], straightforward calculation yields that C is an all-zero matrix except cii=1, i=1, . . . , p. This fulfills the maximization condition. Actually, by taking B=[γ1, γ2, . . . , γp], where {γ1, γ2, . . . , γp} is any orthonormal basis of the subspace of span {α1, α2, . . . , αp}, the maximization condition is also satisfied, yielding the same trace of covariance matrix of Y.


Suppose that we wish to approximate the random vector X by its projection onto a subspace spanned by columns of B, where B=[β1, β2, . . . , βp] is a real m×p matrix with orthonormal columns, i.e., βiTβjij. If σi2 is the residual variance for each component of X, then









i
=
1

m



σ
i
2






is minimized if B=[α1, α2, . . . , αp],where {α1, α2, . . . , αp} are the first p eigenvectors of ΣX. In other words, the trace of covariance matrix of X−BBTX is minimized if B=[α1, α2, . . . , αp]. When E(X)=0, which is a commonly applied preprocessing step in data analysis methods, this property is saying that E∥X−BBTX∥2 is minimized if B=[α1, α2, . . . , αp].


The projection of a random vector X onto a subspace spanned by columns of B is {circumflex over (X)}=BBTX. Then the residual vector is ε=X−BBTX, which has a covariance matrix

Σε=(I−BBTX(I−BBT).Then,










i
=
1

m



σ
i
2


=


trace


(


ɛ

)


=


trace


(




X



-



X



BB
T




-


BB
T





X




+

BB
T






X



BB
T






)


.






Also, we know:

trace(ΣXBBT)=trace(BBTΣX)=trace(BTΣXB)
trace(BBTΣXBBT)=trace(BTΣXBBTB)=trace(BTΣXB).

The last equation comes from the fact that B has orthonormal columns. So,










i
=
1

m



σ
i
2


=


trace


(


X

)


-


trace


(


B
T





X


B


)


.






To minimize










i
=
1

m



σ
i
2


,





it suffices to maximize trace(BTΣXB) This can be done by choosing B=[α1, α2, . . . , αp], where {α1, α2, . . . , α9} are the first p eigenvectors of ΣX, as above.


See, Pietro Amenta, Luigi D'Ambra, “Generalized Constrained Principal Component Analysis with External Information,” (2000). We assume that data on K sets of explanatory variables and S criterion variables of n statistical units are collected in matrices Xk (k=1, . . . , K) and Ys (s=1, . . . , S) of orders (n×p1), . . . , (n×pK) and (n×q1), . . . , (n×qs) respectively. We suppose, without loss of generality, identity matrices for the metrics of the spaces of variables of Xk and Ys with Dn=diag(1/n), weight matrix of statistical units. We assume, moreover, that Xk's and Ys's are centered as to the weights Dn.


Let X=[X1| . . . |XK] and Y=[Y1∥ . . . ∥YS], respectively, be K and S matrices column linked of orders (n×Σkpk) and (n×Σsqs). Let be, also, WY=YY′ while we denote vk the coefficients vector (pk,1) of the linear combination for each Xk such that zk=Xkvk. Let Ck be the matrix of dimension pk×m (m≤pk), associated to the external information explanatory variables of set k.


Generalized CPCA (GCPCA) (Amenta, D'Ambra, 1999) with external information consists in seeking for K coefficients vectors vk (or, in same way, K linear combinations zk) subject to the restriction C′kvk=0 simultaneously, such that:









{




max





i
=
1

K






j
=
1

K







Y




X
i



v
i


,


Y




X
j



v
j













with





the





constraints













k
=
1

K







X
k



v
k




2


=
1










k
=
1

K




C
k




v
k



=
0












(
1
)








or, in equivalent way,






{





max







v




(


A



A

)



v






with





the





constaints











v



Bv

=
1








C



v

=
0













or






{




max






f




B

-
0.5




A




AB

-
0.5



f






with





the





constaints











f



f

=
1








C



v

=
0















where A=Y′X, B=diag(X′1X1, . . . ,X′KXK) C″=[C′1| . . . |C′k] v′=(v1′| . . . |vk′) and f=B0.5v, with








A



A

=


[





X
1




YY




X
1









X
1




YY




X
K



















X
K




YY




X
1









X
k




YY




X
k





]

.





The constrained maximum problem turns out to be an extension of criterion supΣk∥zk=1ΣiΣkcustom characterzi,zkcustom character (Sabatier, 1993) with more sets of criterion variables with external information. The solution of this constrained maximum problem leads to solve the eigen-equation

(PX−PXB−1C)WYg=λp


where g=Xv, PX−PXB−1Ck=1K(PXk−PXkX′kXk)−1Ck) is the oblique projector operator associated to the direct sum decomposition custom charactern
custom character=Im(PX−PXB−1C){dot over (⊕)}Im(PC){dot over (⊕)}Ker(PX)


with PXk=Xk(Xk′, Xk)−1 X′k and PC=C(C″B−1C)−1C″B−1 respectively, I and B−1 orthogonal projector operators onto the subspaces spanned by the columns of matrices Xk and C. Furthermore, PXB−1C=XB−1C(C′B−1C)−1C′B−1 X′ is the orthogonal projector operator onto the subspace spanned the columns of the matrix XB−1C. Starting from the relation

(PXk−PXk(X′kXk)−1Ck)WYg=λXkvk


(which is obtained from the expression (I−PC)X′WYg=λBv) the coefficients vectors vk and the linear combinations zk=Xk vk maximizing (1) can be given by the relations,







v
k

=


1
λ




(


X
k




X
k


)


-
1




(

I
-

P

C
k



)



X
k




W
Y


Xv





and









z
k

=


1
λ



(


P

X
k


-

P




X
k



(


X
k




X
k


)



-
1




C
k




)



W
Y


Xv


,





respectively.


The solution eigenvector g can be written, as sum of the linear combinations zk: g=ΣkXkvk. Notice that the eigenvalues associated to the eigen-system are, according to the Sturm theorem, lower or equal than those of GCPCA eigen-system: Σk=1KPXkWYg=λg.

  • Amenta P., D'Ambra L. (1994) Analisi non Simmetrica delle Corrispondenze Multiple con Vincoli Lineari. Atti S.I.S. XXXVII Sanremo, Aprile 1994.
  • Amenta P., D'Ambra L. (1996) L′Analisi in Componenti Principali in rapporto ad un sottospazio di riferimento con informazioni esteme, Quademi del D.M.Q.T.E., Università di Pescara, n. 18.
  • Amenta P., D'Ambra L (1999) Generalized Constrained Principal Component Analysis. Atti Riunione Scientifica del Gruppo di Classificazione dell′IFCS su “Classificazione e Analisi dei Dati”, Roma.
  • D'Ambra L., Lauro N.C. (1982) Analisi in componenti principali in rapporto ad un sottospazio di riferimento, Rivista di Statistica Applicata, n.1, vol. 15.
  • D'Ambra L., Sabatier R., Amenta P. (1998) Analisi fattoriale delle matrici a tre vie: sintesi e nuovi approcci, (invited lecture) Atti XXXIX Riunione SIS.


Huon de Kermadec F., Durand J. F., Sabatier R. (1996) Comparaison de méthodes de régression pour l′étude des liens entre données hédoniques, in Third Sensometrics Meeting, E.N.T.I.A.A., Nantes.

  • Huon de Kermadec F., Durand J. F., Sabatier R. (1997) Comparison between linear and nonlinear PLS methods to explain overall liking from sensory characteristics, Food Quality and Preference, 8, n. 5/6.
  • Kiers H. A. L. (1991) Hierarchical relations among three way methods Psychometrika, 56.
  • Kvalheim O. M. (1988) A partial least squares approach to interpretative analysis of multivariate analysis, Chemometrics and Intelligent Laboratory System, 3.
  • MacFie H. J. H, Thomson D. M. H. (1988) Preference mapping and multidimensional scaling methods, in: Sensory Analysis of Foods. Elsevier Applied Science, London.
  • Sabatier R. (1993) Criteres et contraintes pour I′ordination simultanée de K tableaux, Biométrie et Environement, Masson, 332.
  • Schlich P. (1995) Preference mapping: relating consumer preferences to sensory or instrumental measurements, in: Bioflavour, INRA, Dijon.
  • Wold S., Geladi P., Esbensen K., Ohman J. (1987) Multi-way principal components and PLS-analysis, J. of Chemometrics, vol. 1.


Spatial Principal Component Analysis


Let J (t, i; α, s) be the current density in voxel i, as estimated by LORETA, in condition α at t time-frames after stimulus onset for subject s. Let area:Voxel→fBA be a function, which assigns to each voxel i ∈ Voxel the corresponding fBA b∈fBA. In a first pre-processing step, we calculate for each subject s the value of the current density averaged over each Fba










x


(

t
,

b
;
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)


=


1

N
b







i

b




J


(

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;
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)








(
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)







where Nb is the number of voxels in the fBA b, in condition α for subject s.


In the second analysis stage, the mean current density x(t,b;α,s) from each fBA b, for every subject s and condition α, was subjected to spatial PCA analysis of the correlation matrix and varimax rotation


In the present study the spatial PCA uses the above-defined fBAs as variables sampled along the time epoch for which EEG has been sampled (0-1000 ms; 512 time-frames), and the inverse solution was estimated. Spatial matrices (each matrix was sized b×t=36×512 elements) for every subject and condition were collected, and subjected to PCA analyses, including the calculation of the covariance matrix; eigenvalue decomposition and varimax rotation, in order to maximize factor loadings. In other words, in the spatial PCA analysis we approximate the mean current density for each subject in each condition as











x


(


t
;
α

,
s

)






x
0



(

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,
s

)


+



k





c
k



(
t
)





x
k



(

α
,
s

)






,




(
2
)







where here x(r,α,s)∈R36 is a vector, which denotes the time-dependent activation of the fBAs, x0(α,s) is their mean activation, and xk(α,s) and ck are the principal components and their corresponding coefficients (factor loadings) as computed using the principal component analysis.


See, download.lww.com/wolterskluwer.com/WNR_1_12010_03_22_ARZY_1_SDC1.doc.


Nonlinear Dimensionality Reduction


High-dimensional data, meaning data that requires more than two or three dimensions to represent, can be difficult to interpret. One approach to simplification is to assume that the data of interest lie on an embedded non-linear manifold within the higher-dimensional space. If the manifold is of low enough dimension, the data can be visualized in the low-dimensional space. Non-linear methods can be broadly classified into two groups: those that provide a mapping (either from the high-dimensional space to the low-dimensional embedding or vice versa), and those that just give a visualization. In the context of machine learning, mapping methods may be viewed as a preliminary feature extraction step, after which pattern recognition algorithms are applied. Typically, those that just give a visualization are based on proximity data—that is, distance measurements. Related Linear Decomposition Methods include Independent component analysis (IA), Principal component analysis (PCA) (also called Karhunen-Loéve transform—KLT), Singular value decomposition (SVD), and Factor analysis.


The self-organizing map (SOM, also called Kohonen map) and its probabilistic variant generative topographic mapping (GTM) use a point representation in the embedded space to form a latent variable model based on a non-linear mapping from the embedded space to the high-dimensional space. These techniques are related to work on density networks, which also are based around the same probabilistic model.


Principal curves and manifolds give the natural geometric framework for nonlinear dimensionality reduction and extend the geometric interpretation of PCA by explicitly constructing an embedded manifold, and by encoding using standard geometric projection onto the manifold. How to define the “simplicity” of the manifold is problem-dependent, however, it is commonly measured by the intrinsic dimensionality and/or the smoothness of the manifold. Usually, the principal manifold is defined as a solution to an optimization problem. The objective function includes a quality of data approximation and some penalty terms for the bending of the manifold. The popular initial approximations are generated by linear PCA, Kohonen's SOM or autoencoders. The elastic map method provides the expectation-maximization algorithm for principal manifold learning with minimization of quadratic energy functional at the “maximization” step.


An autoencoder is a feed-forward neural network which is trained to approximate the identity function. That is, it is trained to map from a vector of values to the same vector. When used for dimensionality reduction purposes, one of the hidden layers in the network is limited to contain only a small number of network units. Thus, the network must learn to encode the vector into a small number of dimensions and then decode it back into the original space. Thus, the first half of the network is a model which maps from high to low-dimensional space, and the second half maps from low to high-dimensional space. Although the idea of autoencoders is quite old, training of deep autoencoders has only recently become possible through the use of restricted Boltzmann machines and stacked denoising autoencoders. Related to autoencoders is the NeuroScale algorithm, which uses stress functions inspired by multidimensional scaling and Sammon mappings (see below) to learn a non-linear mapping from the high-dimensional to the embedded space. The mappings in NeuroScale are based on radial basis function networks.


Gaussian process latent variable models (GPLVM) are probabilistic dimensionality reduction methods that use Gaussian Processes (GPs) to find a lower dimensional non-linear embedding of high dimensional data. They are an extension of the Probabilistic formulation of PCA. The model is defined probabilistically and the latent variables are then marginalized and parameters are obtained by maximizing the likelihood. Like kernel PCA they use a kernel function to form a nonlinear mapping (in the form of a Gaussian process). However, in the GPLVM the mapping is from the embedded(latent) space to the data space (like density networks and GTM) whereas in kernel PCA it is in the opposite direction. It was originally proposed for visualization of high dimensional data but has been extended to construct a shared manifold model between two observation spaces. GPLVM and its many variants have been proposed specially for human motion modeling, e.g., back constrained GPLVM, GP dynamic model (GPDM), balanced GPDM (B-GPDM) and topologically constrained GPDM. To capture the coupling effect of the pose and gait manifolds in the gait analysis, a multi-layer joint gait-pose manifolds was proposed.


Curvilinear component analysis (CCA) looks for the configuration of points in the output space that preserves original distances as much as possible while focusing on small distances in the output space (conversely to Sammon's mapping which focus on small distances in original space). It should be noticed that CCA, as an iterative learning algorithm, actually starts with focus on large distances (like the Sammon algorithm), then gradually change focus to small distances. The small distance information will overwrite the large distance information, if comprises between the two have to be made. The stress function of CCA is related to a sum of right Bregman divergences. Curvilinear distance analysis (CDA) trains a self-organizing neural network to fit the manifold and seeks to preserve geodesic distances in its embedding. It is based on Curvilinear Component Analysis (which extended Sammon's mapping), but uses geodesic distances instead. Diffeomorphic Dimensionality Reduction or Diffeomap learns a smooth diffeomorphic mapping which transports the data onto a lower-dimensional linear subspace. The method solves for a smooth time indexed vector field such that flows along the field which start at the data points will end at a lower-dimensional linear subspace, thereby attempting to preserve pairwise differences under both the forward and inverse mapping.


Perhaps the most widely used algorithm for manifold learning is Kernel principal component analysis (kernel PCA). It is a combination of Principal component analysis and the kernel trick. PCA begins by computing the covariance matrix of the M×n Matrix X. It then projects the data onto the first k eigenvectors of that matrix. By comparison, KPCA begins by computing the covariance matrix of the data after being transformed into a higher-dimensional space. It then projects the transformed data onto the first k eigenvectors of that matrix, just like PCA. It uses the kernel trick to factor away much of the computation, such that the entire process can be performed without actually computing ϕ(x). Of course ϕ must be chosen such that it has a known corresponding kernel.


Laplacian Eigenmaps, (also known as Local Linear Eigenmaps, LLE) are special cases of kernel PCA, performed by constructing a data-dependent kernel matrix. KPCA has an internal model, so it can be used to map points onto its embedding that were not available at training time. Laplacian Eigenmaps uses spectral techniques to perform dimensionality reduction. This technique relies on the basic assumption that the data lies in a low-dimensional manifold in a high-dimensional space. This algorithm cannot embed out of sample points, but techniques based on Reproducing kernel Hilbert space regularization exist for adding this capability. Such techniques can be applied to other nonlinear dimensionality reduction algorithms as well. Traditional techniques like principal component analysis do not consider the intrinsic geometry of the data. Laplacian eigenmaps builds a graph from neighborhood information of the data set. Each data point serves as a node on the graph and connectivity between nodes is governed by the proximity of neighboring points (using e.g. the k-nearest neighbor algorithm). The graph thus generated can be considered as a discrete approximation of the low-dimensional manifold in the high-dimensional space. Minimization of a cost function based on the graph ensures that points close to each other on the manifold are mapped close to each other in the low-dimensional space, preserving local distances. The eigenfunctions of the Laplace-Beltrami operator on the manifold serve as the embedding dimensions, since under mild conditions this operator has a countable spectrum that is a basis for square integrable functions on the manifold (compare to Fourier series on the unit circle manifold). Attempts to place Laplacian eigenmaps on solid theoretical ground have met with some success, as under certain nonrestrictive assumptions, the graph Laplacian matrix has been shown to converge to the Laplace-Beltrami operator as the number of points goes to infinity. In classification applications, low dimension manifolds can be used to model data classes which can be defined from sets of observed instances. Each observed instance can be described by two independent factors termed ‘content’ and ‘style’, where ‘content’ is the invariant factor related to the essence of the class and ‘style’ expresses variations in that class between instances. Unfortunately, Laplacian Eigenmaps may fail to produce a coherent representation of a class of interest when training data consist of instances varying significantly in terms of style. In the case of classes which are represented by multivariate sequences, Structural Laplacian Eigenmaps has been proposed to overcome this issue by adding additional constraints within the Laplacian Eigenmaps neighborhood information graph to better reflect the intrinsic structure of the class. More specifically, the graph is used to encode both the sequential structure of the multivariate sequences and, to minimize stylistic variations, proximity between data points of different sequences or even within a sequence, if it contains repetitions. Using dynamic time warping, proximity is detected by finding correspondences between and within sections of the multivariate sequences that exhibit high similarity.


Like LLE, Hessian LLE is also based on sparse matrix techniques. It tends to yield results of a much higher quality than LLE. Unfortunately, it has a very costly computational complexity, so it is not well-suited for heavily sampled manifolds. It has no internal model. Modified LLE (MLLE) is another LLE variant which uses multiple weights in each neighborhood to address the local weight matrix conditioning problem which leads to distortions in LLE maps. MLLE produces robust projections similar to Hessian LLE, but without the significant additional computational cost.


Manifold alignment takes advantage of the assumption that disparate data sets produced by similar generating processes will share a similar underlying manifold representation. By learning projections from each original space to the shared manifold, correspondences are recovered and knowledge from one domain can be transferred to another. Most manifold alignment techniques consider only two data sets, but the concept extends to arbitrarily many initial data sets. Diffusion maps leverages the relationship between heat diffusion and a random walk (Markov Chain); an analogy is drawn between the diffusion operator on a manifold and a Markov transition matrix operating on functions defined on the graph whose nodes were sampled from the manifold. Relational perspective map is a multidimensional scaling algorithm. The algorithm finds a configuration of data points on a manifold by simulating a multi-particle dynamic system on a closed manifold, where data points are mapped to particles and distances (or dissimilarity) between data points represent a repulsive force. As the manifold gradually grows in size the multi-particle system cools down gradually and converges to a configuration that reflects the distance information of the data points. Local tangent space alignment (LTSA) is based on the intuition that when a manifold is correctly unfolded, all of the tangent hyperplanes to the manifold will become aligned. It begins by computing the k-nearest neighbors of every point. It computes the tangent space at every point by computing the d-first principal components in each local neighborhood. It then optimizes to find an embedding that aligns the tangent spaces. Local Multidimensional Scaling performs multidimensional scaling in local regions, and then uses convex optimization to fit all the pieces together.


Maximum Variance Unfolding was formerly known as Semidefinite Embedding. The intuition for this algorithm is that when a manifold is properly unfolded, the variance over the points is maximized. This algorithm also begins by finding the k-nearest neighbors of every point. It then seeks to solve the problem of maximizing the distance between all non-neighboring points, constrained such that the distances between neighboring points are preserved. Nonlinear PCA (NLPCA) uses backpropagation to train a multi-layer perceptron (MLP) to fit to a manifold. Unlike typical MLP training, which only updates the weights, NLPCA updates both the weights and the inputs. That is, both the weights and inputs are treated as latent values. After training, the latent inputs are a low-dimensional representation of the observed vectors, and the MLP maps from that low-dimensional representation to the high-dimensional observation space. Manifold Sculpting uses graduated optimization to find an embedding. Like other algorithms, it computes the k-nearest neighbors and tries to seek an embedding that preserves relationships in local neighborhoods. It slowly scales variance out of higher dimensions, while simultaneously adjusting points in lower dimensions to preserve those relationships.


Ruffini (2015) discusses Multichannel transcranial current stimulation (tCS) systems that offer the possibility of EEG-guided optimized, non-invasive brain stimulation. A tCS electric field realistic brain model is used to create a forward “lead-field” matrix and, from that, an EEG inverter is employed for cortical mapping. Starting from EEG, 2D cortical surface dipole fields are defined that could produce the observed EEG electrode voltages.


Schestatsky et al. (2017) discuss transcranial direct current stimulation (tDCS), which stimulates through the scalp with a constant electric current that induces shifts in neuronal membrane excitability, resulting in secondary changes in cortical activity. Although tDCS has most of its neuromodulatory effects on the underlying cortex, tOCS effects can also be observed in distant neural networks. Concomitant EEG monitoring of the effects of tOCS can provide valuable information on the mechanisms of tCS. EEG findings can be an important surrogate marker for the effects of tOCS and thus can be used to optimize its parameters. This combined EEG-tDCS system can also be used for preventive treatment of neurological conditions characterized by abnormal peaks of cortical excitability, such as seizures. Such a system would be the basis of a non-invasive closed-loop device. tDCS and EEG can be used concurrently.

  • Albert, Jacobo, Sara López-Martin, Josh Antonio Hinojosa, and Luis Carretie. “Spatiotemporal characterization of response inhibition.” Neuroimage 76 (2013): 272-281.
  • Arzouan Y, Goldstein A, Faust M. Brainwaves are stethoscopes: ERP correlates of novel metaphor comprehension. Brain Res 2007; 1160: 69-81.
  • Arzouan Y, Goldstein A, Faust M. Dynamics of hemispheric activity during metaphor comprehension: electrophysiological measures. NeuroImage 2007; 36: 222-231.
  • Arzy, Shahar, Yossi Arzouan, Esther Adi-Japha, Sorin Solomon, and Olaf Blanke. “The ‘intrinsic’system in the human cortex and self-projection: a data driven analysis.” Neuroreport 21, no. 8 (2010): 569-574.
  • Bao, Xuecai, Jinli Wang, and Jianfeng Hu. “Method of individual identification based on electroencephalogram analysis.” In New Trends in Information and Service Science, 2009. NISS'09. International Conference on, pp. 390-393. IEEE, 2009.
  • Bhattacharya, Joydeep. “Complexity analysis of spontaneous EEG.” Acta neurobiologiae experimentalis 60, no. 4 (2000): 495-502.
  • Chapman R M, McCrary J W. E P component identification and measurement by principal components analysis. Brain and cognition 1995; 27: 288-310.
  • Clementz, Brett A., Stefanie K. Barber, and Jacqueline R. Dzau. “Knowledge of stimulus repetition affects the magnitude and spatial distribution of low-frequency event-related brain potentials.” Audiology and Neurotology 7, no. 5 (2002): 303-314.
  • Dien J, Frishkoff G A, Cerbone A, Tucker D M. Parametric analysis of event-related potentials in semantic comprehension: evidence for parallel brain mechanisms. Brain research 2003; 15:137-153.
  • Dien J, Frishkoff G A. Principal components analysis of event-related potential datasets. In: Handy T (ed). Event-Related Potentials: A Methods Handbook. Cambridge, Mass MIT Press; 2004.
  • Elbert, T. “Illrd Congress of the Spanish Society of Psychophysiology.” Journal of Psychophysiology 17 (2003): 39-53.
  • Groppe, David M., Scott Makeig, Marta Kutas, and S. Diego. “Independent component analysis of event-related potentials.” Cognitive science online 6, no. 1 (2008): 1-44.
  • Have, Mid-Ventrolateral Prefrontal Cortex. “Heschl's Gyms, Posterior Superior Temporal Gyrus.” J Neurophysiol 97 (2007): 2075-2082.
  • Hinojosa, J. A., J. Albert, S. López-Martin, and L. Carreti. “Temporospatial analysis of explicit and implicit processing of negative content during word comprehension.” Brain and cognition 87 (2014): 109-121.
  • Jarchi, Delaram, Saeid Sanei, Jose C. Principe, and Bahador Makkiabadi. “A new spatiotemporal filtering method for single-trial estimation of correlated ERP subcomponents.” IEEE Transactions on Biomedical Engineering 58, no. 1 (2011): 132-143.
  • John, Erwin Roy. “A field theory of consciousness.” Consciousness and cognition 10, no. 2 (2001): 184-213.
  • Johnson, Mark H., Michelle de Haan, Andrew Oliver, Warwick Smith, Haralambos Hatzakis, Leslie A. Tucker, and Gergely Csibra. “Recording and analyzing high-density event-related potentials with infants using the Geodesic Sensor Net.” Developmental Neuropsychology 19, no. 3 (2001): 295-323.
  • Jung, Tzyy-Ping, and Scott Makeig. “Mining Electroencephalographic Data Using Independent Component Analysis.” EEG Journal (2003).
  • Kashyap, Rajan. “Improved localization of neural sources and dynamical causal modelling of latency-corrected event related brain potentials and applications to face recognition and priming.” (2015).
  • Klawohn, Julia, Anja Riesel, Rosa Grutzmann, Norbert Kathmann, and Tanja Endrass. “Performance monitoring in obsessive-compulsive disorder: A temporo-spatial principal component analysis.” Cognitive, Affective, & Behavioral Neuroscience 14, no. 3 (2014): 983-995.
  • Lister, Jennifer J., Nathan D. Maxfield, and Gabriel J. Pitt. “Cortical evoked response to gaps in noise: within-channel and across-channel conditions.” Ear and hearing 28, no. 6 (2007): 862.
  • Maess, Burkhard, Angela D. Friederici, Markus Damian, Antje S. Meyer, and Willem J M Levelt. “Semantic category interference in overt picture naming: Sharpening current density localization by PCA.” Journal of cognitive neuroscience 14, no. 3 (2002): 455-462.
  • Makeig, Scott, Marissa Westerfield, Jeanne Townsend, Tzyy-Ping Jung, Eric Courchesne, and Terrence J. Sejnowski. “Functionally independent components of early event-related potentials in a visual spatial attention task.” Philosophical Transactions of the Royal Society B: Biological Sciences 354, no. 1387 (1999): 1135-1144.
  • Matsuda, Izumi, Hiroshi Nittono, Akihisa Hirota, Tokihiro Ogawa, and Noriyoshi Takasawa. “Event-related brain potentials during the standard autonomic-based concealed information test.” International Journal of Psychophysiology 74, no.1 (2009): 58-68.
  • Mazaheri, Ali, and Terence W. Picton. “EEG spectral dynamics during discrimination of auditory and visual targets.” Cognitive Brain Research 24, no.1 (2005): 81-96.
  • Pirmoradi, Mona, Boutheina Jemel, Anne Gallagher, Julie Tremblay, Fabien D′Hondt, Dang Khoa Nguyen, Renée Béland, and Maryse Lassonde. “Verbal memory and verbal fluency tasks used for language localization and lateralization during magnetoencephalography.” Epilepsy research 119 (2016): 1-9.
  • Potts G F, Dien J, Hartry-Speiser A L, McDougal L M, Tucker D M. Dense sensor array topography of the event-related potential to task-relevant auditory stimuli. Electroencephalography and clinical neurophysiology 1998; 106: 444-456.
  • Rosier F, Manzey D. Principal components and varimax-rotated components in event-related potential research: some remarks on their interpretation. Biological psychology 1981; 13: 3-26.
  • Ruchkin D S, McCalley M G, Glaser E M. Event related potentials and time estimation. Psychophysiology 1977; 14: 451-455.
  • Schroder, Hans S., James E. Glazer, Ken P. Bennett, Tim P. Moran, and Jason S. Moser. “Suppression of error-preceding brain activity explains exaggerated error monitoring in females with worry.” Biological psychology 122 (2017): 33-41.
  • Spencer K M, Dien J, Donchin E. Spatiotemporal analysis of the late ERP responses to deviant stimuli. Psychophysiology 2001; 38: 343-358.
  • Squires K C, Squires N K, Hillyard S A. Decision-related cortical potentials during an auditory signal detection task with cued observation intervals. Journal of experimental psychology 1975; 1: 268-279.
  • van Boxtel A, Boelhouwer A J, Bos A R. Optimal EMG signal bandwidth and interelectrode distance for the recording of acoustic, electrocutaneous, and photic blink reflexes. Psychophysiology 1998; 35: 690-697.
  • Veen, Vincent van, and Cameron S. Carter. “The timing of action-monitoring processes in the anterior cingulate cortex.” Journal of cognitive neuroscience 14, no. 4 (2002): 593-602.
  • Wackermann, Jiri. “Towards a quantitative characterisation of functional states of the brain: from the non-linear methodology to the global linear description.” International Journal of Psychophysiology 34, no. 1 (1999): 65-80.


EEG analysis approaches have emerged, in which event-related changes in EEG dynamics in single event-related data records are analyzed. See Allen D. Malony et al., Computational Neuroinformatics for Integrated Electromagnetic Neuroimaging and Analysis, PAR-99-138. Pfurtscheller, reported a method for quantifying the average transient suppression of alpha band (circa 10-Hz) activity following stimulation. Event-related desynchronization (ERD, spectral amplitude decreases), and event-related synchronization (ERS, spectral amplitude increases) are observed in a variety of narrow frequency bands (4-40 Hz) which are systematically dependent on task and cognitive state variables as well as on stimulus parameters. Makeig (1993) was reported event-related changes in the full EEG spectrum, yielding a 2-D time/frequency measure he called the event-related spectral perturbation (ERSP). This method avoided problems associated with analysis of a priori narrow frequency bands, since bands of interest for the analysis could be based on significant features of the complete time/frequency transform. Rappelsburger et al. introduced event-related coherence (ERCOH). A wide variety of other signal processing measures have been tested for use on EEG and/or MEG data, including dimensionality measures based on chaos theory and the bispectrum. Use of neural networks has also been proposed for EEG pattern recognition applied to clinical and practical problems, though usually these methods have not been employed with an aim of explicitly modeling the neurodynamics involved. Neurodynamics is the mobilization of the nervous system as an approach to physical treatment. The method relies on influencing pain and other neural physiology via mechanical treatment of neural tissues and the non-neural structures surrounding the nervous system. The body presents the nervous system with a mechanical interface via the musculoskeletal system. With movement, the musculoskeletal system exerts non-uniform stresses and movement in neural tissues, depending on the local anatomical and mechanical characteristics and the pattern of body movement. This activates an array of mechanical and physiological responses in neural tissues. These responses include neural sliding, pressurization, elongation, tension and changes in intraneural microcirculation, axonal transport and impulse traffic.


The availability of and interest in larger and larger numbers of EEG (and MEG) channels led immediately to the question of how to combine data from different channels. Donchin advocated the use of linear factor analysis methods based on principal component analysis (PCA) for this purpose. Temporal PCA assumes that the time course of activation of each derived component is the same in all data conditions. Because this is unreasonable for many data sets, spatial PCA (usually followed by a component rotation procedure such as Varimax or Promax) is of potentially greater interest. To this end, several variants of PCA have been proposed for ERP decomposition.


Bell and Sejnowski published an iterative algorithm based on information theory for decomposing linearly mixed signals into temporally independent by minimizing their mutual information. First approaches to blind source separation minimized third and fourth-order correlations among the observed variables and achieved limited success in simulations. A generalized approach uses a simple neural network algorithm that used joint information maximization or ‘infomax’ as a training criterion. By using a compressive nonlinearity to transform the data and then following the entropy gradient of the resulting mixtures, ten recorded voice and music sound sources were unmixed. A similar approach was used for performing blind deconvolution, and the ‘infomax’ method was used for decomposition of visual scenes.


The first applications of blind decomposition to biomedical time series analysis applied the infomax independent component analysis (ICA) algorithm to decomposition of EEG and event-related potential (ERP) data and reported the use of ICA to monitor alertness. This separated artifacts, and EEG data into constituent components defined by spatial stability and temporal independence. ICA can also be used to remove artifacts from continuous or event-related (single-trial) EEG data prior to averaging. Vigario et al. (1997), using a different ICA algorithm, supported the use of ICA for identifying artifacts in MEG data. Meanwhile, widespread interest in ICA has led to multiple applications to biomedical data as well as to other fields (Jung et al., 2000b). Most relevant to EEG/MEG analysis, ICA is effective in separating functionally independent components of functional magnetic resonance imaging (fMRI) data


Since the publication of the original infomax ICA algorithm, several extensions have been proposed. Incorporation of a ‘natural gradient’ term avoided matrix inversions, greatly speeding the convergence of the algorithm and making it practical for use with personal computers on large data EEG and fMRI data sets. An initial ‘sphering’ step further increased the reliability of convergence of the algorithm. The original algorithm assumed that sources have ‘sparse’ (super-Gaussian) distributions of activation values. This restriction has recently been relaxed in an ‘extended-ICA’ algorithm that allows both super-Gaussian and sub-Gaussian sources to be identified. A number of variant ICA algorithms have appeared in the signal processing literature. In general, these make more specific assumptions about the temporal or spatial structure of the components to be separated, and typically are more computationally intensive than the infomax algorithm.


Since individual electrodes (or magnetic sensors) each record a mixture of brain and non-brain sources, spectral measures are difficult to interpret and compare across scalp channels. For example, an increase in coherence between two electrode signals may reflect the activation of a strong brain source projecting to both electrodes, or the deactivation of a brain generator projecting mainly to one of the electrodes. If independent components of the EEG (or MEG) data can be considered to measure activity within functionally distinct brain networks, however, event-related coherence between independent components may reveal transient, event-related changes in their coupling and decoupling (at one or more EEG/MEG frequencies). ERCOH analysis has been applied to independent EEG components in a selective attention task.


SUMMARY OF THE INVENTION

In other embodiments, the processing of the brain activity patterns does not seek to classify or characterize it, but rather to filter and transform the information to a form suitable for control of the stimulation of the second subject. In particular, according to this embodiment, the subtleties that are not yet reliably classified in traditional brain activity pattern analysis are respected. For example, it is understood that all brain activity is reflected in synaptic currents and other neural modulation and, therefore, theoretically, conscious and subconscious information is, in theory, accessible through brain activity pattern analysis. Since the available processing technology generally fails to distinguish a large number of different brain activity patterns, that available processing technology, is necessarily deficient, but improving. However, just because a computational algorithm is unavailable to extract the information, does not mean that the information is absent. Therefore, this embodiment employs relatively raw brain activity pattern data, such as filtered or unfiltered EEGs, to control the stimulation of the second subject, without a full comprehension or understanding of exactly what information of significance is present. In one embodiment, brainwaves are recorded and “played back” to another subject, similar to recoding and playing back music. Such recording-playback may be digital or analog. Typically, the stimulation may include a low dimensionality stimulus, such as stereo-optic, binaural, isotonic tones, tactile, or other sensory stimulation, operating bilaterally, and with control over frequency and phase and/or waveform and/or transcranial stimulation such as TES, tDCS, HD-tDCS, tACS, or TMS. A plurality of different types of stimulation may be applied concurrently, e.g., visual, auditory, other sensory, magnetic, electrical.


Likewise, a present lack of understanding of the essential characteristics of the signal components in the brain activity patterns does not prevent their acquisition, storage, communication, and processing (to some extent). The stimulation may be direct, i.e., a visual, auditory, or tactile stimulus corresponding to the brain activity pattern, or a derivative or feedback control based on the second subject's brain activity pattern.


To address the foregoing problems, in whole or in part, and/or other problems that may have been observed by persons skilled in the art, the present disclosure provides methods, processes, systems, apparatus, instruments, and/or devices, as described by way of example in implementations set forth below.


While mental states are typically considered internal to the individual, and subjective, in fact, such states are common across individuals and have determinable physiological and electrophysiological population characteristics. Further, mental states may be externally changed or induced in a manner that bypasses the normal cognitive processes. In some cases, the triggers for the mental state are subjective, and therefore the particular subject-dependent sensory or excitation scheme required to induce a particular state will differ. For example, olfactory stimulation can have different effects on different people, based on differences in history of exposure, social and cultural norms, and the like. On the other hand, some mental state response triggers are normative, for example “tear jerker” media.


Mental states are represented in brainwave patterns, and in normal humans, the brainwave patterns and metabolic (e.g. blood flow, oxygen consumption, etc.) follow prototypical patterns. Therefore, by monitoring brainwave patterns in an individual, a state or series of mental states in that person may be determined or estimated. However, the brainwave patterns may be interrelated with context, other activity, and past history. Further, while prototypical patterns may be observed, there are also individual variations in the patterns. The brainwave patterns may include characteristic spatial and temporal patterns indicative of mental state. The brainwave signals of a person may be processed to extract these patterns, which, for example, may be represented as hemispheric signals within a frequency range of 3-100 Hz. These signals may then be synthesized or modulated into one or more stimulation signals, which are then employed to induce a corresponding mental state into a recipient, in a manner seeking to achieve a similar brainwave pattern from the source. The brainwave pattern to be introduced need not be newly acquired for each case. Rather, signals may be acquired from one or more individuals, to obtain an exemplar for various respective mental state. Once determined, the processed signal representation may be stored in a non-volatile memory for later use. However, in cases of complex interaction between a mental state and a context or content or activity, it may be appropriate to derived the signals from a single individual whose context or content-environment or activity is appropriate for the circumstances. Further, in some cases, a single mental state, emotion or mood is not described or fully characterized, and therefore acquiring signals from a source is an efficient exercise.


With a library of target brainwave patterns, a system and method is provided in which a target subject may be immersed in a presentation, which includes not only multimedia content, but also a series of defined mental states, emotional states or moods that accompany the multimedia content. In this way, the multimedia presentation becomes fully immersive. The stimulus in this case may be provided through a headset, such as a virtual reality or augmented reality headset. This headset is provided with a stereoscopic display, binaural audio, and a set of EEG and transcranial stimulatory electrodes. These electrodes (if provided) typically deliver a subthreshold signal, which is not painful, which is typically an AC signal which corresponds to the desired frequency, phase, and spatial location of the desired target pattern. The electrodes may also be used to counteract undesired signals, by destructively interfering with them while concurrently imposing the desired patterns. The headset may also generate visual and/or auditory signals which correspond to the desired state. For example, the auditory signals may induce binaural beats, which cause brainwave entrainment. The visual signals may include intensity fluctuations or other modulation patterns, especially those which are subliminal, that are also adapted to cause brainwave entrainment or induction of a desired brainwave pattern.


The headset preferably includes EEG electrodes for receiving feedback from the user. That is, the stimulatory system seeks to achieve a mental state, emotion or mood response from the user. The EEG electrodes permit determination of whether that state is achieved, and if not, what the current state is. It may be that achieving a desired brainwave pattern is state dependent, and therefore that characteristics of the stimulus to achieve a desired state depend on the starting state of the subject. Other ways of determining mental state, emotion, or mood include analysis of facial expression, electromyography (EMG) analysis of facial muscles, explicit user feedback, etc.


An authoring system is provided which permits a content designer to determine what mental states are desired, and then encode those states into media, which is then interpreted by a media reproduction system in order to generate appropriate stimuli. As noted above, the stimuli may be audio, visual, multimedia, other senses, or electrical or magnetic brain stimulation, and therefore a VR headset with transcranial electrical or magnetic stimulation is not required. Further, in some embodiments, the patterns may be directly encoded into the audiovisual content, subliminally encoded.


In some cases, the target mental state may be derived from an expert, actor or professional exemplar. The states may be read based on facial expressions, EMG, EEG, or other means, from the actor or exemplar. For example, a prototype exemplar engages in an activity that triggers a response, such as viewing the Grand Canyon or artworks within the Louvre. The responses of the exemplar are then recorded or represented, and preferably brainwave patterns recorded that represent the responses. A representation of the same experience is then presented to the target, with a goal of the target also experiencing the same experience as the exemplar. This is typically a voluntary and disclosed process, so the target will seek to willingly comply with the desired experiences. In some cases, the use of the technology is not disclosed to the target, for example in advertising presentations or billboards. In order for an actor to serve as the exemplar, the emotions achieved by that person must be authentic. However, so-called “method actors” do authentically achieve the emotions they convey. However, in some cases, for example where facial expressions are used as the indicator of mental state, an actor can present desired facial expressions with inauthentic mental states. The act of making a face corresponding to an emotion often achieves the targeted mental state.


In order to calibrate the system, the brain pattern of a person may be measured while in the desired state. The brain patterns acquired for calibration or feedback need not be of the same quality, or precision, or data depth, and indeed may represent responses rather than primary indicia. That is, there may be some asymmetry in the system, between the brainwave patterns representative of a mental state, and the stimulus patterns appropriate for inducing the brain state.


The present invention generally relates to achieving a mental state in a subject by conveying to the brain of the subject patterns of brainwaves. These brainwaves may be artificial or synthetic, or derived from the brain of a second subject (e.g., a person experiencing an authentic experience or engaged in an activity). Typically, the wave patterns of the second subject are derived while the second subject is experiencing an authentic experience.


A special case is where the first and second subjects are the same individual. For example, brainwave patterns are recorded while a subject is in a particular mental state. That same pattern may assist in achieving the same mental state at another time. Thus, there may be a time delay between acquisition of the brainwave information from the second subject, and exposing the first subject to corresponding stimulation. The signals may be recorded and transmitted.


The temporal pattern may be conveyed or induced non-invasively via light (visible or infrared), sound (or ultrasound), transcranial direct or alternating current stimulation (tDCS or tACS), transcranial magnetic stimulation (TMS), Deep transcranial magnetic stimulation (Deep TMS, or dTMS), Repetitive Transcranial Magnetic Stimulation (rTMS) olfactory stimulation, tactile stimulation, or any other means capable of conveying frequency patterns. In a preferred embodiment, normal human senses are employed to stimulate the subject, such as light, sound, smell and touch. Combinations of stimuli may be employed. In some cases, the stimulus or combination is innate, and therefore largely pan-subject. In other cases, response to a context is learned, and therefore subject-specific. Therefore, feedback from the subject may be appropriate to determine the triggers and stimuli appropriate to achieve a mental state.


This technology may be advantageously used to enhance mental response to a stimulus or context. Still another aspect provides for a change in the mental state. The technology may be used in humans or animals.


The present technology may employ an event-correlated EEG time and/or frequency analysis performed on neuronal activity patterns. In a time-analysis, the signal is analyzed temporally and spatially, generally looking for changes with respect to time and space. In a frequency analysis, over an epoch of analysis, the data, which is typically a time-sequence of samples, is transformed, using e.g., a Fourier transform (FT, or one implementation, the Fast Fourier Transform, FFT), into a frequency domain representation, and the frequencies present during the epoch are analyzed. The window of analysis may be rolling, and so the frequency analysis may be continuous. In a hybrid time-frequency analysis, for example, a wavelet analysis, the data during the epoch is transformed using a “wavelet transform”, e.g., the Discrete Wavelet Transform (DWT) or continuous wavelet transform (CWT), which has the ability to construct a time-frequency representation of a signal that offers very good time and frequency localization. Changes in transformed data over time and space may be analyzed. In general, the spatial aspect of the brainwave analysis is anatomically modelled. In most cases, anatomy is considered universal, but in some cases, there are significant differences. For example, brain injury, psychiatric disease, age, race, native language, training, sex, handedness, and other factors may lead to distinct spatial arrangement of brain function, and therefore when transferring mood from one individual to another, it is preferred to normalize the brain anatomy of both individuals by experiencing roughly the same experiences, and measuring spatial parameters of the EEG or MEG. Note that spatial organization of the brain is highly persistent, absent injury or disease, and therefore this need only be performed infrequently. However, since electrode placement may be inexact, a spatial calibration may be performed after electrode placement.


Different aspects of EEG magnitude and phase relationships may be captured, to reveal details of the neuronal activity. The “time-frequency analysis” reveals the brain's parallel processing of information, with oscillations at various frequencies within various regions of the brain reflecting multiple neural processes co-occurring and interacting. See, Lisman J, Buzsaki G. A neural coding scheme formed by the combined function of gamma and theta oscillations. Schizophr Bull. Jun. 16, 2008; doi:10.1093/schbul/sbn060. Such a time-frequency analysis may take the form of a wavelet transform analysis. This may be used to assist in integrative and dynamically adaptive information processing. Of course, the transform may be essentially lossless and may be performed in any convenient information domain representation. These EEG-based data analyses reveal the frequency-specific neuronal oscillations and their synchronization in brain functions ranging from sensory processing to higher-order cognition. Therefore, these patterns may be selectively analyzed, for transfer to or induction in, a subject.


A statistical clustering analysis may be performed in high dimension space to isolate or segment regions which act as signal sources, and to characterize the coupling between various regions. This analysis may also be used to establish signal types within each brain region, and decision boundaries characterizing transitions between different signal types. These transitions may be state dependent, and therefore the transitions may be detected based on a temporal analysis, rather than merely a concurrent oscillator state.


The various measures make use of the magnitude and/or phase angle information derived from the complex data extracted from the EEG during spectral decomposition and/or temporal/spatial/spectral analysis. Some measures estimate the magnitude or phase consistency of the EEG within one channel across trials, whereas others estimate the consistency of the magnitude or phase differences between channels across trials. Beyond these two families of calculations, there are also measures that examine the coupling between frequencies, within trials and recording sites. Of course, in the realm of time-frequency analysis, many types of relationships can be examined beyond those already mentioned.


These sensory processing specific neuronal oscillations, e.g., brainwave patterns, e.g., of a subject (a “source”) or to a person trained (for example, an actor trained in “the method”) to create a desired state, and can be stored on a tangible medium and/or can be simultaneously conveyed to a recipient making use of the brain's frequency following response nature. See, Galbraith, Gary C., Darlene M. Olfman, and Todd M. Huffman. “Selective attention affects human brain stem frequency-following response.” Neuroreport 14, no. 5 (2003): 735-738, journals.lww.com/neuroreport/Abstract/2003/04150/Selective_attention_affects_human_brain_stem.15.aspx.


Of course, in some cases, one or more components of the stimulation of the target subject (recipient) may be represented as abstract or semantically defined signals, and, more generally, the processing of the signals to define the stimulation will involve high level modulation or transformation between the source signal received from the first subject (donor) or plurality of donors, to define the target signal for stimulation of the second subject (recipient).


Preferably, each component represents a subset of the neural correlates reflecting brain activity that have a high autocorrelation in space and time, or in a hybrid representation such as wavelet. These may be separated by optimal filtering (e.g., spatial PCA), once the characteristics of the signal are known, and bearing in mind that the signal is accompanied by a modulation pattern, and that the two components themselves may have some weak coupling and interaction.


For example, if the first subject (donor) is listening to music, there will be significant components of the neural correlates that are synchronized with the particular music. On the other hand, the music per se may not be part of the desired stimulation of the target subject (recipient). Further, the target subject (recipient) may be in a different acoustic environment, and it may be appropriate to modify the residual signal dependent on the acoustic environment of the recipient, so that the stimulation is appropriate for achieving the desired effect, and does not represent phantoms, distractions, or irrelevant or inappropriate content. In order to perform signal processing, it is convenient to store the signals or a partially processed representation, though a complete real-time signal processing chain may be implemented.


The stimulation may be one or more stimulus applied to the second subject (trainee or recipient), which may be an electrical or magnetic transcranial stimulation (tDCS, HD-tDCS, tACS, osc-tDCS, or TMS), sensory stimulation (e.g., visual, auditory, or tactile), mechanical stimulation, ultrasonic stimulation, etc., and controlled with respect to waveform, frequency, phase, intensity/amplitude, duration, or controlled via feedback, self-reported effect by the second subject, manual classification by third parties, automated analysis of brain activity, behavior, physiological parameters, etc. of the second subject (recipient).


Typically, the first and the second subjects are spatially remote from each other and may be temporally remote as well. In some cases, the first and second subject are the same subject (human or animal), temporally displaced. In other cases, the first and the second subject are spatially proximate to each other. These different embodiments differ principally in the transfer of the signal from at least one first subject (donor) to the second subject (recipient). However, when the first and the second subjects share a common environment, the signal processing of the neural correlates and, especially of real-time feedback of neural correlates from the second subject, may involve interactive algorithms with the neural correlates of the first subject.


According to another embodiment, the first and second subjects are each subject to stimulation. In one particularly interesting embodiment, the first subject and the second subject communicate with each other in real-time, with the first subject receiving stimulation based on the second subject, and the second subject receiving feedback based on the first subject. This can lead to synchronization of neural correlates (e.g., neuronal oscillations, or brainwaves). The neural correlates may be neuronal oscillations resulting in brainwaves that are detectable as, for example, EEG, qEEG, or MEG signals. Traditionally, these signals are found to have dominant frequencies, which may be determined by various analyses, such as spectral analysis, wavelet analysis, or principal component analysis (PCA), for example. One embodiment provides that the modulation pattern of a brainwave of at least one first subject (donor) is determined independent of the dominant frequency of the brainwave (though, typically, within the same class of brainwaves), and this modulation imposed on a brainwave corresponding to the dominant frequency of the second subject (recipient). That is, once the second subject achieves that same brainwave pattern as the first subject (which may be achieved by means other than electromagnetic, mechanical, or sensory stimulation), the modulation pattern of the first subject is imposed as a way of guiding the brain state of the second subject.


According to another embodiment, the second subject (recipient) is stimulated with a stimulation signal, which faithfully represents the frequency composition of a defined component of the neural correlates of at least one first subject (donor). The defined component may be determined based on a principal component analysis, independent component analysis (ICI), eigenvector-based multivariable analysis, factor analysis, canonical correlation analysis (CCA), nonlinear dimensionality reduction (NLDR), or related technique.


The stimulation may be performed, for example, by using a TES device, such as a tDCS device, a high-definition tDCS device, an osc-tDCS device, a pulse-tDCS (“electrosleep”) device, an osc-tDCS, a tACS device, a CES device, a TMS device, rTMS device, a deep TMS device, a light source, or a sound source configured to modulate the dominant frequency on respectively the light signal or the sound signal. The stimulus may be a light signal, a sonic signal (sound), an electric signal, a magnetic field, olfactory or a tactile stimulation. The current signal may be a pulse signal or an oscillating signal. The stimulus may be applied via a cranial electric stimulation (CES), a transcranial electric stimulation (TES), a deep electric stimulation, a transcranial magnetic stimulation (TMS), a deep magnetic stimulation, a light stimulation, a sound stimulation, a tactile stimulation, or an olfactory stimulation. An auditory stimulus may be, for example, binaural beats or isochronic tones.


The technology also provides a processor configured to process the neural correlates of brain state from the first subject (donor), and to produce or define a stimulation pattern for the second subject (recipient) selectively dependent on a waveform pattern of the neural correlates from the first subject. The processor may also perform a PCA, a spatial PCA, an independent component analysis (IA), eigenvalue decomposition, eigenvector-based multivariate analyses, factor analysis, an autoencoder neural network with a linear hidden layer, linear discriminant analysis, network component analysis, nonlinear dimensionality reduction (NLDR), or another statistical method of data analysis.


A signal is presented to a second apparatus, configured to stimulate the second subject (recipient), which may be an open loop stimulation dependent on a non-feedback-controlled algorithm, or a closed loop feedback dependent algorithm. The second apparatus produces a stimulation intended to induce in the second subject (recipient) the desired brain state, e.g., representing the same brain state as was present in the first subject (donor).


A typically process performed on the neural correlates is a filtering to remove noise. In some embodiments, noise filters may be provided, for example, at 50 Hz, 60 Hz, 100 Hz, 120 Hz, and additional overtones (e.g., tertiary and higher harmonics). The stimulator associated with the second subject (recipient) would typically perform decoding, decompression, decryption, inverse transformation, modulation, etc.


Alternately, an authentic wave or hash thereof may be authenticated via a blockchain, and thus authenticatable by an immutable record. In some cases, it is possible to use the stored encrypted signal in its encrypted form, without decryption.


Due to different brain sizes, and other anatomical, morphological, and/or physiological differences, dominant frequencies associated with the same brain state may be different in different subjects. Consequently, it may not be optimal to forcefully impose on the recipient the frequency of the donor that may or may not precisely correspond to the recipient's frequency associated with the same brain state. Accordingly, in some embodiments, the donor's frequency may be used to start the process of inducing the desired brain state in a recipient. As some point, when the recipient is close to achieving the desired brain state, the stimulation is either stopped or replaced with neurofeedback allowing the brain of the recipient to find its own optimal frequency associated with the desired brain state.


In one embodiment, the feedback signal from the second subject may be correspondingly encoded as per the source signal, and the error between the two minimized. According to one embodiment, the processor may perform a noise reduction distinct from a frequency-band filtering. According to one embodiment, the neural correlates are transformed into a sparse matrix, and in the transform domain, components having a high probability of representing noise are masked, while components having a high probability of representing signal are preserved. That is, in some cases, the components that represent modulation that are important may not be known a priori. However, dependent on their effect in inducing the desired response in the second subject (recipient), the “important” components may be identified, and the remainder filtered or suppressed. The transformed signal may then be inverse-transformed and used as a basis for a stimulation signal.


According to another embodiment, a method of brain state modification, e.g., brain entrainment, is provided, comprising: ascertaining a brain state in a plurality of first subjects (donors); acquiring brain waves of the plurality of first subjects (donors), e.g., using one of EEG and MEG, to create a dataset containing brain waves corresponding to different brain states. The database may be encoded with a classification of brain states, activities, environment, or stimulus patterns, applied to the plurality of first subjects, and the database may include acquired brainwaves across a large number of brain states, activities, environment, or stimulus patterns, for example. In many cases, the database records will reflect a characteristic or dominate frequency of the respective brainwaves.


The record(s) thus retrieved are used to define a stimulation pattern for the second subject (recipient). As a relatively trivial example, a female recipient could be stimulated principally based on records from female donors. Similarly, a child recipient of a certain age could be stimulated principally based on the records from children donors of a similar age. Likewise, various demographic, personality, and/or physiological parameters may be matched to ensure a high degree of correspondence to between the source and target subjects. In the target subject, a guided or genetic algorithm may be employed to select modification parameters from the various components of the signal, which best achieve the desired target state based on feedback from the target subject.


Of course, a more nuanced approach is to process the entirety of the database and stimulate the second subject based on a global brainwave-stimulus model, though this is not required, and also, the underlying basis for the model may prove unreliable or inaccurate. In fact, it may be preferred to derive a stimulus waveform from only a single first subject (donor), in order to preserve micro-modulation aspects of the signal, which, as discussed above, have not been fully characterized. However, the selection of the donor(s) need not be static and can change frequently. The selection of donor records may be based on population statistics of other users of the records, i.e., whether or not the record had the expected effect, filtering donors whose response pattern correlates highest with a given recipient, etc. The selection of donor records may also be based on feedback patterns from the recipient.


The process of stimulation typically seeks to target a desired brain state in the recipient, which is automatically or semi-automatically determined or manually entered. In one embodiment, the records are used to define a modulation waveform of a synthesized carrier or set of carriers, and the process may include a frequency domain multiplexed multi-subcarrier signal (which is not necessarily orthogonal). A plurality of stimuli may be applied concurrently, through the different subchannels and/or though different stimulator electrodes, electric current stimulators, magnetic field generators, mechanical stimulators, sensory stimulators, etc. The stimulus may be applied to achieve brain entrainment (i.e., synchronization) of the second subject (recipient) with one or more first subjects (donors). If the plurality of donors are mutually entrained, then each will have a corresponding brainwave pattern dependent on the basis of brainwave entrainment. This link between donors may be helpful in determining compatibility between a respective donor and the recipient. For example, characteristic patterns in the entrained brainwaves may be determined, even for different target brain states, and the characteristic patterns may be correlated to find relatively close matches and to exclude relatively poor matches.


This technology may also provide a basis for a social network, dating site, employment, mission (e.g., space or military), or vocational testing, or other interpersonal environments, wherein people may be matched with each other based on entrainment characteristics. For example, people who efficiently entrain with each other may have better compatibility and, therefore, better marriage, work, or social relationships than those who do not. The entrainment effect need not be limited to learning or training, and may arise across any context.


As discussed above, the plurality of first subjects (donors) may have their respective brainwave patterns stored in separate database records. Data from a plurality of first subjects (donors) is used to train the neural network, which is then accessed by inputting the target stage and/or feedback information, and which outputs a stimulation pattern or parameters for controlling a stimulator(s). When multiple first subject (donors) form the basis for the stimulation pattern, it is preferred that the neural network output parameters of the stimulation, derived from and comprising features of the brainwave patterns or other neural correlates of brain state from the plurality of first subject (donors), which are then used to control a stimulator which, for example, generates its own carrier wave(s) which are then modulated based on the output of the neural network. A trained neural network need not periodically retrieve records, and therefore may operate in a more time-continuous manner, rather than the more segmented scheme of record-based control.


In any of the feedback dependent methods, the brainwave patterns or other neural correlates of brain states may be processed by a neural network, to produce an output that guides or controls the stimulation. The stimulation, is, for example, at least one of a light signal, a sound signal, an electric signal, a magnetic field, an olfactory signal, a chemical signal, and a vibration or mechanical stimulus. The process may employ a relational database of brain states and brainwave patterns, e.g., frequencies/neural correlate waveform patterns associated with the respective brain states. The relational database may comprise a first table, the first table further comprising a plurality of data records of brainwave patterns, and a second table, the second table comprising a plurality of brain states, each of the brain states being linked to at least one brainwave pattern. Data related to brain states and brainwave patterns associated with the brain states are stored in the relational database and maintained. The relational database is accessed by receiving queries for selected (existing or desired) brain states, and data records are returned representing the associated brainwave pattern. The brainwave pattern retrieved from the relational database may then be used for modulating a stimulator seeking to produce an effect selectively dependent on the desired brain state.


A further aspect of the technology provides a computer apparatus for creating and maintaining a relational database of brain states and frequencies associated with the brain state. The computer apparatus may comprise a non-volatile memory for storing a relational database of brain states and neural correlates of brain activity associated with the brain states, the database comprising a first table comprising a plurality of data records of neural correlates of brain activity associated with the brain states, and a second table comprising a plurality of brain states, each of the brain states being linked to one or more records in the first table; a processor coupled with the non-volatile memory, and being configured to process relational database queries, which are then used for searching the database; RAM coupled with the processor and the non-volatile memory for temporary holding database queries and data records retrieved from the relational database; and an IO interface configured to receive database queries and deliver data records retrieved from the relational database. A structured query language (SQL) or alternate to SQL (e.g., noSQL) database may also be used to store and retrieve records. A relational database described above maintained and operated by a general-purpose computer, improves the operations of the general-purpose computer by making searches of specific brain states and brainwaves associated therewith more efficient thereby, inter alia, reducing the demand on computing power.


A further aspect of the technology provides a method of brain entrainment comprising: ascertaining a brain state in at least one first subject (donor), recording brainwaves of said at least one first subject (donor) using at least one channel of EEG and/or MEG; storing the recorded brainwaves in a physical memory device, retrieving the brain waves from the memory device, applying a stimulus signal comprising a brainwave pattern derived from at least one-channel of the EEG and/or MEG to a second subject (recipient) via transcranial electrical and/or magnetic stimulation, whereby the brain state desired by the second subject (recipient) is achieved. The stimulation may be of the same dimension (number of channels) as the EEG or MEG, or a different number of channels, typically reduced. For example, the EEG or MEG may comprise 64,128 or 256 channels, while the transcranial stimulator may have 32 or fewer channels. The placement of electrodes used for transcranial stimulation may be approximately the same as the placement of electrodes used in recording of EEG or MEG to preserve the topology of the recorded signals and, possibly, use these signals for spatial modulation.


One of the advantages of transforming the data is the ability to select a transform that separates the information of interest represented in the raw data, from noise or other information. Some transforms preserve the spatial and state transition history, and may be used for a more global analysis. Another advantage of a transform is that it can present the information of interest in a form where relatively simple linear or statistical functions of low order may be applied. In some cases, it is desired to perform an inverse transform on the data. For example, if the raw data includes noise, such as 50 or 60 Hz interference, a frequency transform may be performed, followed by a narrow band filtering of the interference and its higher order intermodulation products. An inverse transform may be performed to return the data to its time-domain representation for further processing. (In the case of simple filtering, a finite impulse response (FIR) or infinite impulse response (IIR) filter could be employed). In other cases, the analysis is continued in the transformed domain.


Transforms may be part of an efficient algorithm to compress data for storage or analysis, by making the representation of the information of interest consume fewer bits of information (if in digital form) and/or allow it to be communication using lower bandwidth. Typically, compression algorithms will not be lossless, and as a result, the compression is irreversible with respect to truncated information.


Typically, the transformation(s) and filtering of the signal are conducted using traditional computer logic, according to defined algorithms. The intermediate stages may be stored and analyzed. However, in some cases, neural networks or deep neural networks may be used, convolutional neural network architectures, or even analog signal processing. According to one set of embodiments, the transforms (if any) and analysis are implemented in a parallel processing environment. Such as using an SIMD processor such as a GPU (or GPGPU). Algorithms implemented in such systems are characterized by an avoidance of data-dependent branch instructions, with many threads concurrently executing the same instructions.


EEG signals are analyzed to determine the location (e.g., voxel or brain region) from which an electrical activity pattern is emitted, and the wave pattern characterized. The spatial processing of the EEG signals will typically precede the content analysis, since noise and artifacts may be useful for spatial resolution. Further, the signal from one brain region will typically be noise or interference in the signal analysis from another brain region; so the spatial analysis may represent part of the comprehension analysis. The spatial analysis is typically in the form of a geometrically and/or anatomically-constrained statistical model, employing all of the raw inputs in parallel. For example, where the input data is transcutaneous electroencephalogram information, from 32 EEG electrodes, the 32 input channels, sampled at e.g., 500 sps, 1 ksps or 2 ksps, are processed in a four or higher dimensional matrix, to permit mapping of locations and communication of impulses over time, space and state.


The matrix processing may be performed in a standard computing environment, e.g., an i7-7920HQ, i7-8700K, or i9-7980XE processor, under the Windows 10 operating system, executing Matlab (Mathworks, Woburn Mass.) software platform. Alternately, the matrix processing may be performed in a computer cluster or grid or cloud computing environment. The processing may also employ parallel processing, in either a distributed and loosely coupled environment, or asynchronous environment. One preferred embodiment employs a single instruction, multiple data processors, such as a graphics processing unit such as the nVidia CUDA environment or AMD Firepro high-performance computing environment.


Artificial intelligence (AI) and machine learning methods, such as artificial neural networks, deep neural networks, etc., may be implemented to extract the signals of interest. Neural networks act as an optimized statistical classifier and may have arbitrary complexity. A so-called deep neural network having multiple hidden layers may be employed. The processing is typically dependent on labeled training data, such as EEG data, or various processed, transformed, or classified representations of the EEG data. The label represents the emotion, mood, context, or state of the subject during acquisition. In order to handle the continuous stream of data represented by the EEG, a recurrent neural network architecture may be implemented. Depending preprocessing before the neural network, formal implementations of recurrence may be avoided. A four or more dimensional data matrix may be derived from the traditional spatial-temporal processing of the EEG and fed to a neural network. Since the time parameter is represented in the input data, a neural network temporal memory is not required, though this architecture may require a larger number of inputs. Principal component analysis (PCA, en.wikipedia.org/wiki/Principal_component_analysis), spatial PCA (arxiv.org/pdf/1501.03221v3.pdf, adegenetr-forge.r-project.org/files/tutorial-spca.pdf, www.ncbi.nlm.nih.gov/pubmed/1510870); and clustering analysis may also be employed (en.wikipedia.org/wiki/Cluster_analysis, see U.S. Pat. Nos. 9,336,302, 9,607,023 and cited references).


In general, a neural network of this type of implementation will, in operation, be able to receive unlabeled EEG data, and produce the output signals representative of the predicted or estimated task, performance, context, or state of the subject during acquisition of the unclassified EEG. Of course, statistical classifiers may be used rather than neural networks.


The analyzed EEG, either by conventional processing, neural network processing, or both, serves two purposes. First, it permits one to deduce which areas of the brain are subject to which kinds of electrical activity under which conditions. Second, it permits feedback during training of a trainee (assuming proper spatial and anatomical correlates between the trainer and trainee), to help the system achieve the desired state, or as may be appropriate, desired series of states and/or state transitions. According to one aspect of the technology, the applied stimulation is dependent on a measured starting state or status (which may represent a complex context and history dependent matrix of parameters), and therefore the target represents a desired complex vector change. Therefore, this aspect of the technology seeks to understand a complex time-space-brain activity associated with an activity or task in a trainer, and to seek a corresponding complex time-space-brain activity associated with the same activity or task in a trainee, such that the complex time-space-brain activity state in the trainer is distinct from the corresponding state sought to be achieved in the trainee. This permits transfer of training paradigms from qualitatively different persons, in different contexts, and, to some extent, to achieve a different result.


The conditions of data acquisition from the trainer will include both task data, and sensory-stimulation data. That is, a preferred application of the system is to acquire EEG data from a trainer or skilled individual, which will then be used to transfer learning, or more likely, learning readiness states, to a naïve trainee. The goal for the trainee is to produce a set of stimulation parameters that will achieve, in the trainee, the corresponding neural activity resulting in the EEG state of the trainer at the time of or preceding the learning of a skill or a task, or performance of the task.


It is noted that EEG is not the only neural or brain activity or state data that may be acquired, and of course any and all such data may be included within the scope of the technology, and therefore EEG is a representative example only of the types of data that may be used. Other types include fMRI, magnetoencephalogram, motor neuron activity, PET, etc.


While mapping the stimulus-response patterns distinct from the task is not required in the trainer, it is advantageous to do so, because the trainer may be available for an extended period, the stimulus of the trainee may influence the neural activity patterns, and it is likely that the trainer will have correlated stimulus-response neural activity patterns with the trainee(s). It should be noted that the foregoing has suggested that the trainer is a single individual, while in practice, the trainer may be a population of trainers or skilled individuals. The analysis and processing of brain activity data may, therefore, be adaptive, both for each respective individual and for the population as a whole.


For example, the system may determine that not all human subjects have common stimulus-response brain activity correlates, and therefore that the population needs to be segregated and clustered. If the differences may be normalized, then a normalization matrix or other correction may be employed. On the other hand, if the differences do not permit feasible normalization, the population(s) may be segmented, with different trainers for the different segments. For example, in some tasks, male brains have different activity patterns and capabilities than female brains. This, coupled with anatomical differences between the sexes, implies that the system may provide gender-specific implementations. Similarly, age differences may provide a rational and scientific basis for segmentation of the population. However, depending on the size of the information base and matrices required, and some other factors, each system may be provided with substantially all parameters required for the whole population, with a user-specific implementation based on a user profile or initial setup, calibration, and system training session.


According to one aspect of the present invention, a source subject is instrumented with sensors to determine localized brain activity during experiencing an event. The objective is to identify regions of the brain involved in processing this response.


The sensors will typically seek to determine neuron firing patterns and brain region excitation patterns, which can be detected by implanted electrodes, transcutaneous electroencephalograms, magnetoencephalograms, fMRI, and other technologies. Where appropriate, transcutaneous EEG is preferred, since this is non-invasive and relatively simple.


The source is observed with the sensors in a quiet state, a state in which he or she is experiencing an event, and various control states in which the source is at rest or engaged in different activities resulting in different states. The data may be obtained for a sufficiently long period of time and over repeated trials to determine the effect of duration. The data may also be a population statistical result, and need not be derived from only a single individual at a single time.


The sensor data is then processed using a 40 (or higher) model to determine the characteristic location-dependent pattern of brain activity over time associated with the state of interest. Where the data is derived from a population with various degrees of arousal, the model maintains this arousal state variable dimension.


A recipient is then prepared for receipt of the mental state. The mental state of the recipient may be assessed. This can include responses to a questionnaire, sell-assessment, or other psychological assessment method. Further, the transcutaneous EEG (or other brain activity data) of the recipient may be obtained, to determine the starting state for the recipient, as well as activity during experiencing the desired mental state.


In addition, a set of stimuli, such as visual patterns, acoustic patterns, vestibular, smell, taste, touch (light touch, deep touch, proprioception, stretch, hot, cold, pain, pleasure, electric stimulation, acupuncture, etc.), vagus nerve (e.g., parasympathetic), are imposed on the subject, optionally over a range of baseline brain states, to acquire data defining the effect of individual and various combinations of sensory stimulation on the brain state of the recipient. Population data may also be used for this aspect.


The data from the source or population of sources (see above) may then be processed in conjunction with the recipient or population of recipient data, to extract information defining the optimal sensory stimulation over time of the recipient to achieve the desired brain state resulting in the desired mental state.


In general, for populations of sources and recipients, the data processing task is immense. However, the statistical analysis will generally be of a form that permits parallelization of mathematical transforms for processing the data, which can be efficiently implemented using various parallel processors, a common form of which is a SIMD (single instruction, multiple data) processor, found in typical graphics processors (GPUs). Because of the cost-efficiency of GPUs, it is referred to implement the analysis using efficient parallelizable algorithms, even if the computational complexity is nominally greater than a CISC-type processor implementation.


During stimulation of the recipient, the EEG pattern may be monitored to determine if the desired state is achieved through the sensory stimulation. A closed loop feedback control system may be implemented to modify the stimulation seeking to achieve the target. An evolving genetic algorithm may be used to develop a user model, which relates the mental state, arousal and valence, sensory stimulation, and brain activity patterns, both to optimize the current session of stimulation and learning, as well as to facilitate future sessions, where the mental states of the recipient have further enhanced, and to permit use of the system for a range of mental states.


The stimulus may comprise a chemical messenger or stimulus to alter the subject's level of consciousness or otherwise alter brain chemistry or functioning. The chemical may comprise a hormone or endocrine analog molecule, (such as adrenocorticotropic hormone [ACTH] (4-11)), a stimulant (such as cocaine, caffeine, nicotine, phenethylamines), a psychoactive drug, psychotropic or hallucinogenic substance (a chemical substance that alters brain function, resulting in temporary changes in perception, mood, consciousness and behavior such as pleasantness (e.g. euphoria) or advantageousness (e.g., increased alertness).


While typically, controlled or “illegal” substances are to be avoided, in some cases, these may be appropriate for use. For example, various drugs may alter the state of the brain to enhance or selectively enhance the effect of the stimulation. Such drugs include stimulants (e.g., cocaine, methylphenidate (Ritalin), ephedrine, phenylpropanolamine, amphetamines), narcotics/opiates (opium, morphine, heroin, methadone, oxymorphine, oxycodone, codeine, fentanyl), hallucinogens (lysergic acid diethylamide (LSD), PCP, MDMA (ecstasy), mescaline, psilocybin, magic mushroom (Psilocybe cubensis), Amanita muscaria mushroom, marijuana/cannabis), Salvia divinorum, diphenhydramine (Benadryl), flexeril, tobacco, nicotine, bupropion (Zyban), opiate antagonists, depressants, gamma aminobutyric acid (GABA) agonists or antagonists, NMDA receptor agonists or antagonists, depressants (e.g., alcohol, Xanax; Valium; Halcion; Librium; other benzodiazepines, Ativan; Klonopin; Amytal; Nembutal; Seconal; Phenobarbital, other barbiturates), psychedelics, disassociatives, and deliriants (e.g., a special class of acetykholine-inhibitor hallucinogen). For example, Carhart-Harris showed using fMRI that LSD and psilocybin caused synchronisation of different parts of the brain that normally work separately by making neurons fire simultaneously. This effect can be used to induce synchronization of various regions of the brain to heighten the mental state.


It is noted that a large number of substances, natural and artificial, can alter mood or arousal and, as a result, may impact emotions or non-target mental states. Typically, such substances will cross the blood-brain barrier, and exert a psychtropic effect. Often, however, this may not be necessary or appropriate. For example, a painful stimulus can alter mood, without acting as a psychtropic drug; on the other hand, a narcotic can also alter mood by dulling emotions. Further, sensory stimulation can induce mood and/or emotional changes, such as smells, sights, sounds, various types of touch and proprioception sensation, balance and vestibular stimulation, etc. Therefore, peripherally acting substances that alter sensory perception or stimulation may be relevant to mood. Likewise, pharmacopsychtropic drugs may alter alertness, perceptiveness, memory, and attention, which may be relevant to task-specific mental state control.


The skill may comprise a mental skill, e.g., cognitive, alertness, concentration, attention, focusing, memorization, visualization, relaxation, meditation, speedreading, creative skill, “whole-brain-thinking”, analytical, reasoning, problem-solving, critical thinking, intuitive, leadership, learning, speedreading, patience, balancing, perception, linguistic or language, language comprehension, quantitative, “fluid intelligence”, pain management, skill of maintaining positive attitude, a foreign language, musical, musical composition, writing, poetry composition, mathematical, science, art, visual art, rhetorical, emotional control, empathy, compassion, motivational skill, people, computational, science skill, or an inventorship skill. See, U.S. Pub. App. Nos. and U.S. Pat. Nos. 6,435,878, 5,911,581, and 20090069707. The mental state may be associated with learning or performing. The skill may comprise a motor skill, e.g., fine motor, muscular coordination, walking, running, jumping, swimming, dancing, gymnastics, yoga; an athletic or sports, massage skill, martial arts or fighting, shooting, self-defense; speech, singing, playing a musical instrument, penmanship, calligraphy, drawing, painting, visual, auditory, olfactory, game-playing, gambling, sculptor's, craftsman, massage, or assembly skill. Where a skill is to be enhanced, and an emotion to be achieved (or suppresed), concurrently, the stimulus to the recipient may be combined in such a way as to achieve the result. In some cases, the component is universal, while in others, it is subjective. Therefore, the combination ny require adaptation based on the recipient characteristics.


The technology may be embodied in apparatuses for acquiring the brain activity information from the source, processing the brain activity information to reveal a target brain activity state and a set of stimuli, which seek to achieve that state in a recipient, and generating stimuli for the recipient to achieve and maintain the target brain activity state over a period of time and potential state transitions. The generated stimuli may be feedback controlled. A general-purpose computer may be used for the processing of the information, a microprocessor, a FPGA, an ASIC, a system-on-a-chip, or a specialized system, which employs a customized configuration to efficiently achieve the information transformations required. Typically, the source and recipient act asynchronously, with the brain activity of the source recorded and later processed. However, real-time processing and brain activity transfer are also possible. In the case of a general purpose programmable processor implementation or portions of the technology, computer instructions may be stored on a nontransient computer readable medium. Typically, the system will have special-purpose components, such as a transcranial stimulator, or a modified audio and/or display system, and therefore the system will not be a general purpose system. Further, even in a general purpose system the operation per se is enhanced according to the present technology.


It is an object of the present invention to provide a method of facilitating a process of learning a skill, comprising: determining a neuronal activity pattern of a first subject skilled in the skill, while engaged in an activity involving the skill; processing the neuronal activity pattern of the first subject with at least one microprocessor; and subjecting a second subject learning the skill to a neurostimulation having at least one stimulus dependent on the processed neuronal activity pattern of the first subject.


The at least one stimulus may be selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a cranial electrotherapy stimulation (CES), a transcranial electric stimulation (TES), transcranial magnetic stimulation (TMS), and a deep brain stimulation (DBS).


The at least one stimulus may comprise at least one of a sensory excitation, a peripheral excitation, a transcranial excitation, a sensible stimulation of a sensory input, an insensible stimulation of a sensory input, a visual stimulus, an electromagnetic wave stimulus, an auditory stimulus, a tactile stimulus, a proprioceptive stimulus, a somatosensory stimulus, a pressure, a cranial nerve stimulus, a gustatory stimulus, an olfactory stimulus, a pain stimulus, and a thermal stimulus.


The at least one stimulus may comprise at least one of a transcranial alternating current stimulation (tACS), transcranial random noise stimulation (tRNS), transcranial pulsed current stimulation (tPCS), spinal cord stimulation (SCS), transcranial pulsed ultrasound (TPU), pulsed electromagnetic field (PEMF), a cochlear implant stimulus, deep brain stimulation (DBS), electrical stimulation of the retina, a pacemaker, a stimulation microelectrode array, vagus nerve stimulation (VNS), electrical brain stimulation (EBS), and focal brain stimulation (FBS).


The method may further comprise determining a neuronal baseline activity of the first subject, while not engaged in the skill. The neurostimulation may be is at least one of a visual excitation, an auditory excitation; a transcranial Direct Current Stimulation (tDCS), an oscillating transcranial Direct Current Stimulation (osc-tDCS), a High-Definition transcranial Direct Current Stimulation (HD-tDCS), a transcranial Alternating Current Stimulation (tACS), a high-frequency repetitive transcranial magnetic stimulation (HF-rTMS), a low-frequency repetitive transcranial magnetic stimulation (LF-rTMS), a deep transcranial electric stimulation (deep TES), and a deep transcranial magnetic stimulation (deep TMS).


The neuronal activity pattern may be obtained by at least one of electroencephalography (EEG), low-resolution brain electromagnetic tomography, magnetoencephalography, positron emission tomography (PET) scan, and functional magnetic resonance (fMRI) imaging.


The neurostimulation may be adapted to cause a brainwave entrainment of the second subject with the first subject.


The skill may comprise at least one of a mental, motor, musical instrument playing, singing, dancing, sports, martial arts, speech, mathematical, calligraphical, drawing, painting, massage, assembly, walking, running, swimming, yoga, fighting, shooting, self-defense, olfactory, and muscular coordination skill.


The method may further comprise controlling said at least one stimulus to synchronize brain activity patterns of the first subject while engaged in an activity involving the skill and the second subject.


It is also an object to provide an apparatus for facilitating a skill learning process, comprising at least one automated processor, configured to process information derived from a brain wave pattern of a first subject while engaged in a task, and in dependence thereon, define a neural stimulus pattern representing a modulation of a waveform of at least one stimulus of a stimulation device for stimulation of a second subject, effective to improve at least one of learning, performance, and appreciation of the task by the second subject receiving stimulation with the neural stimulus pattern; and to at least one of store and output the defined neural stimulus pattern. The apparatus may further comprise the stimulation device, configured to subject the second subject to the neural stimulus pattern.


It is a further object to provide a method of facilitating a process of learning a skill, comprising: a step for determining a neuronal activity pattern of a first subject skilled in the skill, while engaged in an activity involving the skill; a step for processing the neuronal activity pattern of the first subject; and a step for subjecting a second subject learning the skill to a neurostimulation having at least one stimulus dependent on the processed neuronal activity pattern of the first subject, said steps being implemented employing the structures and elements disclosed herein.


It is a still further object to provide an apparatus for facilitating a skill learning process, comprising: means for processing information derived from a brain wave pattern of a first subject while engaged in a task, and in dependence thereon, define a neural stimulus pattern representing a modulation of a waveform of at least one stimulus for stimulation of a second subject, effective to improve at least one of learning, performance, and appreciation of the task by the second subject receiving stimulation with the neural stimulus pattern; and at least one of output means for outputting the defined neural stimulus pattern; memory means for storing the defined neural stimulus pattern; and stimulus means for stimulating the second subject according to the defined neural stimulus pattern, said means corresponding to the structures and elements disclosed herein.


The neural stimulus pattern may comprise at least one stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation. The neural stimulus pattern may be responsive to a brain wave pattern of the second subject prior to application of the stimulation of the second subject. The neural stimulus pattern may be adaptive to a brain wave pattern of the second subject subsequent to initiation of the stimulation of the second subject.


The at least one processor may be configured to monitor the spatial brain activity pattern over time of the second subject after commencement of the application of the stimulus pattern, and to adapt the stimulus pattern based on feedback dependent on the monitored spatial brain activity pattern over time of the second subject. The at least one processor may be configured to determine neuronal activity patterns selectively associated with the task by analysis of a spatial brain activity pattern over time of the first subject while engaged in the task. The at least one processor may be configured to determine neuronal activity patterns which represent readiness for training in the task by analysis of a spatial brain activity pattern over time of the first subject prior to engaging in the task. The at least one processor may be configured to define the neural stimulus pattern by analysis of a spatial brain activity pattern over time of the second subject, and translate the determined spatial brain activity pattern over time of the first subject which represent readiness for training in the task, to define the neural stimulus pattern for the second subject to achieve a spatial brain activity pattern over time in the second subject corresponding to readiness for training in the task.


The system may store a computer-implemented brain activity model in a memory, wherein the at least one processor is configured to further define the neural stimulus pattern in dependence on the brain activity model.


It is a further object to provide a non-transitory computer-readable medium, storing therein instructions for a programmable processor to automatically perform a process, comprising: synchronizing brain activity data of a first subject with at least one event involving the first subject; analyzing the brain activity data to determine a selective change in the brain activity data over time corresponding to the event; and determine a stimulation pattern adapted to induce a brain activity in a second subject having a correspondence to the brain activity data associated with the event. The stimulation pattern may be determined based on at least a brain activity model. The process may store data describing a temporal pattern extracted from the brain activity of the first subject, the stored temporal pattern being adapted for modulation of a signal usable as the stimulation pattern for the second subject, to facilitate learning relating to the event by the second subject. The at least one event may involve a cognitive skill or a motor skill, for example.


The programmable processor may execute instructions ro control a stimulation of the second subject with the determined stimulation pattern to induce the brain activity in the second subject having the correspondence to the brain activity data associated with the event.


It is an object of the present invention to provide a system and method for facilitating a skill-learning process, comprising: determining a neuronal activity pattern, of a skilled subject while engaged in a respective skill; processing the determined neuronal activity pattern with at least one automated processor; and subjecting a subject training in the respective skill to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed electromagnetic determined neuronal activity pattern.


It is yet another object of the present invention to provide a system and method for facilitating a skill or information-learning process, comprising: determining a neuronal activity pattern of a skilled subject with the knowledge of a respective skill or information while engaged in learning this skill or information; processing the determined neuronal activity pattern with at least one automated processor; and subjecting a subject learning the respective skill or information to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed electromagnetic determined neuronal activity pattern.


It is still another object of the present invention to provide a system and method for improving performance of an activity, comprising: determining a neuronal activity pattern, of a skilled subject with mastery of a respective activity while engaged in performing the respective activity; processing the determined neuronal activity pattern with at least one automated processor; and subjecting a subject performing the respective activity to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed electromagnetic determined neuronal activity pattern.


It is also an object of the present invention to provide an apparatus for facilitating a skill learning process, comprising: an input, configured to receive data representing a neuronal activity pattern of a skilled subject while engaged in a respective skill; at least one automated processor, configured to process the determined neuronal activity pattern, to determine neuronal activity patterns selectively associated with successful learning of the skill; and a stimulator, configured to subject a subject training in the respective skill to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed determined neuronal activity pattern.


It is further an object of the present invention to provide an apparatus for facilitating a skill or information learning process, comprising: an input, configured to receive data representing a neuronal activity pattern of a skilled subject while engaged in a respective skill or learning information; at least one automated processor, configured to process the determined neuronal activity pattern, to determine neuronal activity patterns selectively associated with successful learning of the skill or information; and a stimulator, configured to subject a subject training in the respective skill or learning the information to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed determined neuronal activity pattern.


It is also an object of the present invention to provide an apparatus for improving a performance of an activity, comprising: an input, configured to receive data representing a neuronal activity pattern of a skilled subject while engaged in the performance of an activity; at least one automated processor, configured to process the determined neuronal activity pattern, to determine neuronal activity patterns selectively associated with effective performance of the respective activity; and a stimulator, configured to subject a less-experienced subject performing the respective activity to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed determined neuronal activity pattern.


It is a further object of the present invention to provide a system for influencing a brain electrical activity pattern of a subject during training in a task, comprising: an input, configured to determine a target brain activity state for the subject, dependent on the task; at least one processor, configured to generate a stimulation pattern profile adapted to achieve the target brain activity state for the subject, dependent on the task; and a stimulator, configured to output at least one stimulus, proximate to the subject, dependent on the generated stimulation pattern profile.


It is yet a further object of the present invention to provide a system for influencing a brain electrical activity pattern of a subject during learning new information, comprising: an input, configured to determine a target brain activity state for the subject, dependent on the nature of the respective information; at least one processor, configured to generate a stimulation pattern profile adapted to achieve the target brain activity state for the subject, dependent on the task; and a stimulator, configured to output at least one stimulus, proximate to the subject, dependent on the generated stimulation pattern profile.


It is still a further object of the present invention to provide a system for influencing a brain electrical activity pattern of a subject during performing of an activity, comprising: an input, configured to determine a target brain activity state for the subject, dependent on the activity; at least one processor, configured to generate a stimulation pattern profile adapted to achieve the target brain activity state for the subject, dependent on the activity; and a stimulator, configured to output at least one stimulus, proximate to the subject, dependent on the generated stimulation pattern profile.


It is a still further object of the present invention to provide a system for determining a target brain activity state for a subject, dependent on a task, comprising: a first monitor, configured to acquire a brain activity of a first subject during performance of a task; at least one first processor, configured to analyze a spatial brain activity state over time of the first subject; and determine spatial brain activity states of the first subject, which represent readiness for training in the task; a second monitor, configured to acquire a brain activity of a second subject during performance of a variety of activities, under a variety of stimuli; and at least one second processor, configured to: analyze a spatial brain activity state over time of the second subject; and translate the determined spatial brain activity states of the first subject which represent readiness for training in the task, into a stimulus pattern for the second subject to achieve a spatial brain activity state in the second subject corresponding to readiness for training in the task.


It is a still further object of the present invention to provide a system for determining a target brain activity state for a subject, dependent on a physical activity, comprising: a first monitor, configured to acquire a brain activity of a first subject during performance of a physical activity; at least one first processor, configured to analyze a spatial brain activity state over time of the first subject; and determine spatial brain activity states of the first subject, which represent readiness for training in the task; a second monitor, configured to acquire a brain activity of a second subject during performance of a variety of activities, under a variety of stimuli; and at least one second processor, configured to: analyze a spatial brain activity state over time of the second subject; and translate the determined spatial brain activity states of the first subject which represent readiness for training in the task, into a stimulus pattern for the second subject to achieve a spatial brain activity state in the second subject corresponding to optimal physical activity.


It is a further object to provide a method of teaching a task to a first subject, the method comprising: recording a second subject's brainwaves EEG while at rest; having the second subject perform said task; recording the second subject's brainwaves EEG while performing said task; extracting a predominant temporal pattern associated with said task from the recorded brainwaves by comparing them with the brainwaves at rest; encoding said temporal pattern as a digital code stored in a tangible media; and using said digital code to modulate the temporal pattern on a signal perceptible to the first subject while said first subject is learning said one if a mental and a motor skill, whereby said light signal stimulates in the second subject brain waves having said temporal pattern to accelerate learning of said task.


It is still a further object to provide a method of enhancing performance of a task of a first subject, the method comprising: recording a second subject's brainwaves EEG while at rest; having the second subject perform said task; recording the second subject's brainwaves EEG while performing said task; extracting a predominant temporal pattern associated with said task from the recorded brainwaves by comparing them with the brainwaves at rest; encoding said temporal pattern as a digital code stored in a tangible media; and using said digital code to modulate the temporal pattern on a signal perceptible to the first subject while said first subject is performing said task, whereby said light signal stimulates in the second subject brain waves having said temporal pattern to enhance the performance of said task.


A still further object provides a method of assisted reading a new text by a first subject, the method comprising: recording a second subject's brainwaves EEG while at rest, wherein the second subject is knowledgeable in the subject matter of the text; having the second subject read the text; recording the second subject's brainwaves EEG while reading the text; extracting a predominant temporal pattern associated with reading the text from the recorded brainwaves by comparing them with the brainwaves at rest; encoding said temporal pattern as a digital code stored in a tangible media; and using said digital code to modulate the temporal pattern on a signal perceptible to the first subject while the first subject is reading, whereby said signal stimulates in the first subject brain waves having said temporal pattern to accelerate reading, comprehension, and retention of the text.


It is another object to provide a computer readable medium, storing therein non-transitory instructions for a programmable processor to perform a process, comprising the computer-implemented steps: synchronizing brain activity data of a subject with at least one event involving the subject; analyzing the brain activity data to determine a selective change in the brain activity data corresponding to a timing of the event; and determine a stimulation pattern adapted to induce a brain activity having a correspondence to the brain activity data associated with the event, based on at least a brain activity model.


The at least one of a sensory excitation, peripheral excitation, and transcranial excitation may be generated based on a digital code. The subjecting of the subject training in the respective skill to the sensory excitation increases a learning rate of the skill in the training subject. Similarly, the subjecting of the subject learning the respective new information to the sensory excitation increases a learning rate of the new information in the learning subject. Likewise, the subjecting of the subject engaged in the respective physical activity to the sensory excitation improves the performance of the respective physical activity in the subject engages in the respective activity.


The method may further comprise determining a neuronal baseline activity of the skilled subject while not engaged in the skill, a neuronal baseline activity of the subject training in the respective skill while not engaged in the skill, a neuronal activity of the skilled subject while engaged in the respective skill, and/or a neuronal activity of the subject training in the respective skill while engaged in the skill.


The method may further comprise determining a neuronal baseline activity of the skilled subject while not engaged in the learning of new information, a neuronal baseline activity of the subject learning respective information while not engaged in the learning, a neuronal activity of the skilled subject while engaged in the learning, and/or a neuronal activity of the subject learning respective information while engaged in the learning.


The method may further comprise determining a neuronal baseline activity of the skilled subject while not engaged in the physical activity, a neuronal baseline activity of the less-experienced subject to be engaged in a physical activity while not engaged in the physical activity, a neuronal activity of the skilled subject while engaged in the respective physical activity, and/or a neuronal activity of the less-experienced subject while engaging in the respective physical activity.


The skilled subject may be at the same level of training as the trainee, or one or more stages advanced beyond the training of the trainee.


The representation of the processed the determined neuronal activity pattern may be stored in memory. The storage could be on a tangible medium as an analog or digital representation. It is possible to store the representation in a data storage and access system either for a permanent backup or further processing the respective representation. The storage can also be in a cloud storage and/or processing system.


The neuronal activity pattern may be obtained by electroencephalography, magnetoencephalography, MRI, fMRI, PET, low-resolution brain electromagnetic tomography, or other electrical or non-electrical means.


The neuronal activity pattern may be obtained by at least one implanted central nervous system (cerebral, spinal) or peripheral nervous system electrode. An implanted neuronal electrode can be either within the peripheral nervous system or the central nervous system (brain, spinal cord). The recording device could be portable or stationary. Either with or without onboard electronics such as signal transmitters and/or amplifiers, etc. The at least one implanted electrode can consist of a microelectrode array featuring more than one recording site. Its main purpose can be for stimulation and/or recoding.


The neuronal activity pattern may be obtained by at least a galvanic skin response. Galvanic skin response or resistance is often also referred as electrodermal activity (EDA), psychogalvanic reflex (PGR), skin conductance response (SCR), sympathetic skin response (SSR) and skin conductance level (SCL) and is the property of the human body that causes continuous variation in the electrical characteristics of the skin.


The stimulus may comprise a sensory excitation. The sensory excitation may by either sensible or insensible. It may be either peripheral or transcranial. It may consist of at least one of a visual, an auditory, a tactile, a proprioceptive, a somatosensory, a cranial nerve, a gustatory, an olfactory, a pain, a compression and a thermal stimulus or a combination of aforesaid. It can, for example, consist of light flashes either within ambient light or aimed at the subject's eyes, 2D or 3D picture noise, modulation of intensity, within the focus of the subjects eye the visual field or within peripheral sight. The stimulus may comprise a peripheral excitation, a transcranial excitation, a sensible stimulation of a sensory input, an insensible stimulation of a sensory input, a visual stimulus, an auditory stimulus, a tactile stimulus, a proprioceptive stimulus, a somatosensory stimulus, a cranial nerve stimulus, a gustatory stimulus, an olfactory stimulus, a pain stimulus, an electric stimulus, a magnetic stimulus, or a thermal stimulus. The stimulus may comprise transcranial magnetic stimulation (TMS), cranial electrotherapy stimulation (CES), transcranial direct current stimulation (tDCS), comprise transcranial alternating current stimulation (tACS), transcranial random noise stimulation (tRNS), comprise transcranial pulsed current stimulation (tPCS), pulsed electromagnetic field (PEMF), or noninvasive or invasive deep brain stimulation (DBS), for example. The stimulus may comprise transcranial pulsed ultrasound (TPU). The stimulus may comprise a cochlear implant stimulus, spinal cord stimulation (SCS) or a vagus nerve stimulation (VNS), or other direct or indirect cranial or peripheral nerve stimulus. The stimulus may comprise or achieve brainwave entrainment. The stimulus may comprise electrical stimulation of the retina, a pacemaker, a stimulation microelectrode array, electrical brain stimulation (EBS), focal brain stimulation (FBS), light, sound, vibrations, an electromagnetic wave. The light stimulus may be emitted by at least one of a light bulb, a light emitting diode (LED), and a laser. The signal may be one of a light ray, a sound wave, and an electromagnetic wave. The signal may be a light signal projected onto the first subject by one of a smart bulb generating ambient light, at least one LED position near the eyes of the first subject and laser generating low-intensity pulses.


It is another object to provide a method of teaching one of a mental skill and a motor skill to a first subject, the method comprising: recording a second subject's brainwaves EEG while at rest; having the second subject perform said one of a mental skill and a motor skill; recording the second subject's brainwaves EEG while performing said one of a mental skill and a motor skill; extracting a predominant temporal pattern associated with said one of a mental skill and a motor skill from the recorded brainwaves by comparing them with the brainwaves at rest; encoding said temporal pattern as a digital code stored in a tangible media; and using said digital code to modulate the temporal pattern on a signal perceptible to the first subject while the first subject is learning said one if a mental and a motor skill, whereby said light signal stimulates in the first subject brain waves having said temporal pattern to accelerate learning of said one if a mental skill and a motor skill.


It is a further object to provide a high-definition transcranial alternating current stimultion (HD-tACS) stimultion of a trainee, having a stimulation frequency, amplitude pattern, spatial pattern, dependent on an existing set of states in the target, and a set of brainwave patterns from a trainor engaged in an activity, adapted to improve the learning or performance of the trainee.


It is yet another object of the present invention to provide a system and method for facilitating a skill-learning process, comprising: determining a neuronal activity pattern, of a skilled subject while engaged in a respective skill; processing the determined neuronal activity pattern with at least one automated processor; and subjecting a subject training in the respective skill to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed electromagnetic determined neuronal activity pattern while the subject is subjected to tES, a psychedelic and/or other pharmaceutical agents.


It is a still further object to provide a method of facilitating a skill learning process, comprising: determining a neuronal activity pattern of a skilled subject while engaged in a respective skill; processing the determined neuronal activity pattern with at least one automated processor; subjecting a subject training in the respective skill to one of transcranial electric stimulation (tES) and magnetic brain stimulation; and subjecting a subject training in the respective skill to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed determined neuronal activity pattern. The transcranial electric stimulation (tES) may be one of transcranial direct current stimulation (tDCS), transcranial alternative current stimulation (tACS), and high-definition transcranial alternative current stimulation (tES).


Another object provides a method of facilitating a skill learning process, comprising: determining a neuronal activity pattern of a skilled subject while engaged in a respective skill; processing the determined neuronal activity pattern with at least one automated processor; subjecting a subject training in the respective skill to one of a pharmaceutical agent and a psychedelic agent; and subjecting a subject training in the respective skill to a stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation, dependent on the processed determined neuronal activity pattern.


The present invention generally relates to enhancing emotional response by a subject in connection with the received information by conveying to the brain of the subject temporal patterns of brainwaves of a second subject who had experienced such emotional response, said temporal pattern being provided non-invasively via light, sound, transcranial direct current stimulation (tDCS), transcranial alternating current stimulation (tDAS) or HD-tACS, transcranial magnetic stimulation (TMS) or other means capable of conveying frequency patterns.


The transmission of the brain waves can be accomplished through direct electrical contact with the electrodes implanted in the brain or remotely employing light, sound, electromagnetic waves and other non-invasive techniques. Light, sound, or electromagnetic fields may be used to remotely convey the temporal pattern of prerecorded brainwaves to a subject by modulating the encoded temporal frequency on the light, sound or electromagnetic filed signal to which the subject is exposed.


Every activity, mental or motor, and emotion is associated with unique brainwaves having specific spatial and temporal patterns, i.e., a characteristic frequency or a characteristic distribution of frequencies over time and space. Such waves can be read and recorded by several known techniques, including electroencephalography (EEG), magnetoencephalography (MEG), exact low-resolution brain electromagnetic tomography (eLORETA), sensory evoked potentials (SEP), fMRI, functional near-infrared spectroscopy (fNIRS), etc. The cerebral cortex is composed of neurons that are interconnected in networks. Cortical neurons constantly send and receive nerve impulses-electrical activity-even during sleep. The electrical or magnetic activity measured by an EEG or MEG (or another device) device reflects the intrinsic activity of neurons in the cerebral cortex and the information sent to it by subcortical structures and the sense receptors.


It has been observed that “playing back the brainwaves” to another animal or person by providing decoded temporal pattern through transcranial direct current stimulation (tDCS), transcranial alternating current stimulation (tACS), high definition transcranial alternating current stimulation (HD-tDCS), transcranial magnetic stimulation (TMS), or through electrodes implanted in the brain allows the recipient to achieve the mental state at hand or to increase a speed of achievement. For example, if the brain waves of a mouse navigated a familiar maze are decoded (by EEG or via implanted electrodes), playing this temporal pattern to another mouse unfamiliar with this maze will allow it to learn to navigate this maze faster.


Similarly, recording brainwaves associated with a specific response of one subject and later “playing back” this response to another subject will induce a similar response in the second subject. More generally, when one animal assumes a mental state, parts of the brain will have characteristic activity patterns. Further, by “artificially” inducing the same pattern in another animal, the other animal will have the same mental state, or more easily be induced into that state. The pattern of interest may reside deep in the brain, and thus be overwhelmed in an EEG signal by cortical potentials and patterns. However, techniques other than surface electrode EEG may be used to determine and spatially discriminate deep brain activity, e.g., from the limbic system. For example, various types of magnetic sensors may sense deep brain activity. See, e.g., 9,618,591; 9,261,573; 8,618,799; and 8,593,141.


In some cases, EEGs dominated by cortical excitation patterns may be employed to sense the mental state, since the cortical patterns may correlate with lower-level brain activity. Note that the determination of a state representation of a mental state need not be performed each time the system is used; rather, once the brain spatial and temporal activity patterns and synchronization states associated with a particular mental states are determined, those patterns may be used for multiple targets and over time.


Similarly, while the goal is, for example, to trigger the target to assume the same brain activity patterns are the exemplar, this can be achieved in various ways, and these methods of inducing the desired patterns need not be invasive. Further, user feedback, especially in the case of a human transferee, may be used to tune the process. Finally, using the various senses, especially sight, sound, vestibular, touch, proprioception, taste, smell, vagus afferent, other cranial nerve afferent, etc. can be used to trigger high level mental activity, that in a particular subject achieves the desired metal state, emotion or mood.


Thus, in an experimental subject, which may include laboratory scale and/or invasive monitoring, a set of brain electrical activity patterns that correspond to particular emotions or mental states is determined. Preferably, these are also correlated with surface EEG findings. For the transferee, a stimulation system is provided that is non-hazardous and non-invasive. For example, audiovisual stimulation may be exclusively used. A set of EEG electrodes is provided to measure brain activity, and an adaptive or genetic algorithm scheme is provided to optimize the audiovisual presentation, seeking to induce in the transferee the target pattern found in the experimental subject. After the stimulation patterns, which may be path dependent, are determined, it is likely that these patterns will be persistent, though over longer time periods, there may be some desensitization to the stimulation pattern(s). In some cases, audiovisual stimulation is insufficient, and TMS or other electromagnetic stimulation (superthreshold, or preferably subthreshold) is employed to assist in achieving the desired state and maintaining it for the desired period.


The transmission of the brain waves can be accomplished through direct electrical contact with the electrodes implanted in the brain or remotely employing light, sound, electromagnetic waves and other non-invasive techniques. Light, sound or invisible electromagnetic fields may be used to remotely convey the temporal pattern of prerecorded brainwaves to a subject, by modulating the encoded temporal frequency on the light, sound or electromagnetic filed signal to which the subject is exposed. Employing light, sound or electromagnetic field to remotely convey the temporal pattern of brainwaves (which may be prerecorded) to a subject by modulating the encoded temporal frequency on the light, sound or electromagnetic filed signal to which the subject is exposed.


When a group of neurons fires simultaneously, the activity appears as a brainwave. Different brainwave-frequencies are linked to different mental states in the brain.


A desired metal state may be induced in a target individual (e.g., human, animal), by providing selective stimulation according to a temporal pattern, wherein the temporal pattern is correlated with an EEG pattern of the target when in the desired mental state, or represents a transition which represents an intermediate toward achieving the desired mental state. The temporal pattern may be targeted to a discrete spatial region within the brain, either by a physical arrangement of a stimulator, or natural neural pathways through which the stimulation (or its result) passes.


The EEG pattern may be derived from another individual or individuals, the same individual at a different time, or an in vivo animal model of the desired metal state. The method may therefore replicate a mental state of a first subject in a second subject. The mental state typically is not a state of consciousness or an idea, but rather a subconscious (in a technical sense) state, representing an emotion, readiness, receptivity, or other state, often independent of particular thoughts or ideas. In essence, a mental state of the first subject (a “trainer” or “donor” who is in a desired mental state) is captured by recording neural correlates of the mental state, e.g., as expressed by brain activity patterns, such as EEG or MEG signals. The neural correlates of the first subject, either as direct or recorded representations, may then be used to control a stimulation of the second subject (a “trainee” or “recipient”), seeking to induce the same brain activity patterns in the second subject (recipient/trainee) as were present in the first subject (donor/trainer) to assist the second subject (recipient/trainee) to attain the desired mental state that had been attained by the donor/trainer. In an alternative embodiment, the signals from the first subject (donor/trainer) being in the first mental state are employed to prevent the second subject (recipient/trainee) from achieving a second mental state, wherein the second mental state is an undesirable one.


The source brain wave pattern may be acquired through multichannel EEG or MEG, from a human in the desired brain state. A computational model of the brain state is difficult to create. However, such a model is not required according to the present technology. Rather, the signals may be processed by a statistical process (e.g., PCA or a related technology), or a statistically trained process (e.g., a neural network). The processed signals preferably retain information regarding signal source special location, frequency, and phase. In stimulating the recipient's brain, the source may be modified to account for brain size differences, electrode locations, etc. Therefore, the preserved characteristics are normalized spatial characteristics, frequency, phase, and modulation patterns.


The normalization may be based on feedback from the target subject, for example based on a comparison of a present state of the target subject and a corresponding state of the source subject, or other comparison of known states between the target and source. Typically, the excitation electrodes in the target subject do not correspond to the feedback electrodes or the electrodes on the source subject. Therefore, an additional type of normalization is required, which may also be based on a statistical or statistically trained algorithm.


According to one embodiment, the stimulation of the second subject is associated with a feedback process, to verify that the second subject has appropriately responded to the stimulation, e.g., has a predefined similarity to the mental state as the first subject, has a mental state with a predefined difference from the first subject, or has a desire change from a baseline mental state. Advantageously, the stimulation may be adaptive to the feedback. In some cases, the feedback may be functional, i.e., not based on brain activity per se, or neural correlates of mental state, but rather physical, psychological, or behavioral effects that may be reported or observed.


The feedback typically is provided to a computational model-based controller for the stimulator, which alters stimulation parameters to optimize the stimulation in dependence on a brain and brain state model applicable to the target.


For example, it is believed that brainwaves represent a form of resonance, where ensembles of neurons interact in a coordinated fashion as a set of coupled or intercting oscillators. The frequency of the wave is related to neural responsivity to neurotransmitters, distances along neural pathways, diffusion limitations, etc., and perhaps pacemaker neurons or neural pathways. That is, the same mental state may be represented by different frequencies in two different individuals, based on differences in the size of their brains, neuromodulators present, physiological differences, etc. These differences may be measured in microseconds or less, resulting in fractional changes in frequency. However, if the stimulus is different from the natural or resonant frequency of the target process, the result may be different from that expected. Therefore, the model-based controller can determine the parameters of neural transmission and ensemble characteristics, vis-à-vis stimulation, and resynthesize the stimulus wave to match the correct waveform, with the optimization of the waveform adaptively determined. This may not be as simple as speeding up or slowing down playback of the signal, as different elements of the various waveforms representing neural correlates of mental state may have different relative differences between subjects. Therefore, according to one set of embodiments, the stimulator autocalibrates for the target, based on a correspondence (error) of a measured response to the stimulation and the desired mental state sought by the stimulation. In cases where the results are chaotic or unpredictable based on existing data, a genetic algorithm may be employed to explore the range of stimulation parameters, and determine the response of the target. In some cases, the target has an abnormal or unexpected response to stimulation based on a model maintained within the system. In this case, when the deviance from the expected response is identified, the system may seek to new model, such as from a model repository that may be on-line, such as through the Internet. If the models are predictable, a translation may be provided between an applicable model of a source or trainer, and the applicable model of the target, to account for differences. In some cases, the desired mental state is relatively universal, such as sleep and awake. In this case, the brain response model may be a statistical model, rather than a neural network or deep neural network type implementation.


Thus, in one embodiment, a hybrid approach is provided, with use of donor-derived brainwaves, on one hand, which may be extracted from the brain activity readings (e.g., EEG or MEG) of the first at least one subject (donor), preferably processed by principal component analysis, or spatial principal component analysis, autocorrelation, or other statistical processing technique (clustering, PCA, etc.) or statistically trained technique (backpropagation of errors, etc.) that separates components of brain activity, which can then be modified or modulated based on high-level parameters, e.g., abstractions. See, ml4a.github.io/ml4a/how_neural_networks_are_trained/. Thus, the stimulator may be programmed to induce a series of brain states defined by name or as a sequence of“abstract” semantic labels, icons, or other representations, each corresponding to a technical brain state or sequence of sub-states. The sequence may be automatically defined, based on biology and the system training, and thus relieve the programmer of low-level tasks. However, in a general case, the present technology maintains use of components or subcomponents of the donor's brain activity readings, e.g., EEG or MEG, and does not seek to characterize or abstract them to a semantic level.


According to the present technology, a neural network system or statistical classifier may be employed to characterize the brain wave activity and/or other data from a subject. In addition to the classification or abstraction, a reliability parameter is presented, which predicts the accuracy of the output. Where the accuracy is high, a model-based stimulator may be provided to select and/or parameterize the model, and generate a stimulus for a target subject. Where the accuracy is low, a filtered representation of the signal may be used to control the stimulator, bypassing the model(s). The advantage of this hybrid scheme is that when the model-based stimulator is employed, many different parameters may be explicitly controlled independent of the source subject. On the other hand, where the data processing fails to yield a highly useful prediction of the correct model-based stimulator parameters, the model itself may be avoided, in favor of a direct stimulation type system.


Of course, in some cases, one or more components of the stimulation of the target subject may be represented as abstract or semantically defined signals, and more generally the processing of the signals to define the stimulation will involve high level modulation or transformation between the source signal received from the first subject, to define the target signal for stimulation of the second subject.


Preferably, each component represents a subset of the neural correlates reflecting brain activity that have a high spatial autocorrelation in space and time, or in a hybrid representation such as wavelet. For example, one signal may represent a modulated 10.2 Hz signal, while another signal represents a superposed modulated 15.7 Hz signal, with respectively different spatial origins. These may be separated by optimal filtering, once the spatial and temporal characteristics of the signal are known, and bearing in mind that the signal is accompanied by a modulation pattern, and that the two components themselves may have some weak coupling and interaction.


In some cases, the base frequency, modulation, coupling, noise, phase jitter, or other characteristic of the signal may be substituted. For example, if the first subject is listening to music, there will be significant components of the neural correlates that are synchronized with the particular music. On the other hand, the music per se may not be part of the desired stimulation of the target subject. Therefore, through signal analysis and decomposition, the components of the signal from the first subject, which have a high temporal correlation with the music, may be extracted or suppressed from the resulting signal. Further, the target subject may be in a different acoustic environment, and it may be appropriate to modify the residual signal dependent on the acoustic environment of the target subject, so that the stimulation is appropriate for achieving the desired effect, and does not represent phantoms, distractions, or irrelevant or inappropriate content. In order to perform processing, it is convenient to store the signals or a partially processed representation, though a complete real-time signal processing chain may be implemented. Such a real-time signal processing chain is generally characterized in that the average size of a buffer remains constant, i.e., the lag between output and input is relatively constant, bearing in mind that there may be periodicity to the processing.


The mental state of the first subject may be identified, and the neural correlates of brain activity captured. The second subject is subject to stimulation based on the captured neural correlates and the identified mental state. The mental state may be represented as a semantic variable, within a limited classification space. The mental state identification need not be through analysis of the neural correlates signal, and may be a volitional self-identification by the first subject, a manual classification by third parties, or an automated determination. The identified mental state is useful, for example, because it represents a target toward (or against) which the second subject can be steered.


The stimulation may be one or more inputs to the second subject, which may be an electrical or magnetic transcranial stimulation, sensors stimulation, mechanical stimulation, ultrasonic stimulation, etc., and controlled with respect to waveform, intensity/amplitude, duration, feedback, self-reported effect by the second subject, manual classification by third parties, automated analysis of brain activity, behavior, physiological parameters, etc. of the second subject.


The process may be used to induce in the target subject neural correlates of the desired mental state, which are derived from a different time for the same person, or a different person at the same or a different time. For example, one seeks to induce the neural correlates of the first subject in a desired mental state in a second subject, through the use of stimulation parameters comprising a waveform over a period of time derived from the neural correlates of mental state of the first subject.


The first and second subjects may be spatially remote from each other, and may be temporally remote as well. In some cases, the first and second subject are the same animal (e.g., human), temporally displaced. In other cases, the first and second subject are spatially proximate to each other. In some cases, neural correlates of a desired mental state are derived from a mammal having a simpler brain, which are then extrapolated to a human brain. (Animal brain stimulation is also possible, for example to enhance training and performance). When the first and second subjects share a common environment, the signal processing of the neural correlates, and especially of real-time feedback of neural correlates from the second subject may involve interactive algorithms with the neural correlates of the first subject.


The first and second subjects may each be subject to stimulators. The first subject and the second subject may communicate with each other in real-time, with the first subject receiving stimulation based on the second subject, and the second subject receiving feedback based on the first subject. This can lead to synchronization of mental state between the two subjects. However, the first subject need not receive stimulation based on real-time signals from the second subject, as the stimulation may derive from a third subject, or the first or second subjects at different points in time.


The neural correlates may be, for example, EEG, qEEG, or MEG signals. Traditionally, these signals are found to have dominant frequencies, which may be determined by various analyses. One embodiment provides that the modulation pattern of a brainwave of the first subject is determined independent of the dominant frequency of the brainwave (though typically within the same class of brainwaves), and this modulation imposed on a wave corresponding to the dominant frequency of the second subject. That is, once the second subject achieves that same brainwave pattern as the first subject (which may be achieved by means other than electromagnetic, mechanical, or sensors stimulation), the modulation pattern of the first subject is imposed as a way of guiding the mental state of the second subject.


The second subject may be stimulated with a stimulation signal which faithfully represents the frequency composition of a defined component of the neural correlates of the first subject.


The stimulation may be performed, for example, by using a tDCS device, a high-definition tDCS device, a tACS device, a TMS device, a deep TMS device, and a source of one of a light signal and a sound signal configured to modulate the dominant frequency on the one of a light signal and a sound signal. The stimulus may be at least one of a light signal, a sound signal, an electric signal, and a magnetic field. The electric signal may be a direct current signal or an alternating current signal. The stimulus may be a transcranial electric stimulation, a transcranial magnetic stimulation, a deep magnetic stimulation, a light stimulation, or a sound stimulation. A visual stimulus may be ambient light or a direct light. An auditory stimulus may be binaural beats or isochronic tones.


The technology may also provide a processor configured to process the neural correlates of mental state from the first subject, and to produce or define a stimulation pattern for the second subject selectively dependent on a waveform pattern of the neural correlates from the first subject. Typically, the processor performs signal analysis and calculates at least a dominant frequency of the brainwaves of the first subject, and preferably also spatial and phase patterns within the brain of the first subject.


A signal is presented to a second apparatus, configured to stimulate the second subject, which may be an open loop stimulation dependent on a non-feedback controlled algorithm, or a closed loop feedback dependent algorithm. In other cases, analog processing is employed in part or in whole, wherein the algorithm comprises an analog signal processing chain. The second apparatus receives information from the processor (first apparatus), typically comprising a representation of a portion of a waveform represented in the neural correlates. The second apparatus produces a stimulation intended to induce in the second subject the desired mental state, e.g., representing the same mental state as was present in the first subject.


A typical process performed on the neural correlates is a filtering to remove noise. For example, notch filters may be provided at 50 Hz, 60 Hz, 100 Hz, 120 Hz, and additional overtones. Other environmental signals may also be filtered in a frequency-selective or waveform-selective (temporal) manner. Higher level filtering may also be employed, as is known in the art. The neural correlates, after noise filtering, may be encoded, compressed (lossy or losslessly), encrypted, or otherwise processed or transformed. The stimulator associated with the second subject would typically perform decoding, decompression, decryption, inverse transformation, etc.


Information security and copy protection technology, similar to that employed for audio signals, may be employed to protect the neural correlate signals from copying or content analysis before use. In some cases, it is possible to use the stored encrypted signal in its encrypted for, without decryption. For example, with an asymmetric encryption scheme, which supports distance determination. See U.S. Pat. No. 7,269,277; Sahai and Waters (2005) Annual International Conference on the Theory and Applications of Cryptographic Techniques, pp. 457-473. Springer, Berlin, Heidelberg; Bringer et al. (2009) IEEE International Conference on Communications, pp. 1-6; Juels and Sudan (2006) Designs, Codes and Cryptography 2:237-257; Thaker et al. (2006) IEEE International Conference on Workload Characterization, pp. 142-149; Galil et al. (1987) Conference on the Theory and Application of Cryptographic Techniques, pp. 135-155.


Because the system may act intrusively, it may be desirable to authenticate the stimulator or parameters employed by the stimulator before use. For example, the stimulator and parameters it employs may be authenticated by a distributed ledger, e.g., a blockchain. On the other hand, in a closed system, digital signatures and other hierarchical authentication schemes may be employed. Permissions to perform certain processes may be defined according to smart contracts, which automated permissions (i.e., cryptographic authorization) provided from a blockchain or distributed ledger system. Of course, centralized management may also be employed.


In practice, the feedback signal from the second subject may be correspondingly encoded as per the source signal, and the error between the two minimized. In such an algorithm, the signal sought to be authenticated is typically brought within an error tolerance of the encrypted signal before usable feedback is available. One way to accomplish this is to provide a predetermined range of acceptable authenticatable signals which are then encoded, such that an authentication occurs when the putative signal matches any of the predetermined range. In the case of the neural correlates, a large set of digital hash patterns may be provided representing different signals as hash patterns. The net result is relatively weakened encryption, but the cryptographic strength may still be sufficiently high to abate the risks.


The processor may perform a noise reduction distinct from a frequency-band filtering. The neural correlates may be transformed into a sparse matrix, and in the transform domain, components representing high probability noise are masked, while components representing high probability signal are preserved. The distinction may be optimized or adaptive. That is, in some cases, the components which represent modulation that are important may not be known a priori. However, dependent on their effect in inducing the desired response in the second subject, the “important” components may be identified, and the remainder filtered or suppressed. The transformed signal may then be inverse-transformed, and used as a basis for a stimulation signal.


A mental state modification, e.g., brain entrainment, may be provided, which ascertains a mental state in a plurality of first subjects; acquires brain waves of the plurality of first subjects, e.g., using one of EEG and MEG, to create a dataset containing representing brain waves of the plurality of first subjects. The database may be encoded with a classification of mental state, activities, environment, or stimulus patterns, applied to the plurality of first subjects, and the database may include acquired brain waves across a large number of mental states, activities, environment, or stimulus patterns, for example. In many cases, the database records will reflect a characteristic or dominate frequency of the respective brain waves. As discussed above, the trainer or first subject is a convenient source of the stimulation parameters, but is not the sole available source. The database may be accessed according to its indexing, e.g., mental states, activities, environment, or stimulus patterns, for example, and a stimulation pattern for a second subject defined based on the database records of one or more subjects.


The record(s) thus retrieved are used to define a stimulation pattern for the second subject. The selection of records, and their use, may be dependent on the second subject and/or feedback from the second subject. As a relatively trivial example, a female second subject could be stimulated principally dependent on records from female first subjects. Of course, a more nuanced approach is to process the entirety of the database and stimulate the second subject based on a global brain wave-stimulus model, though this is not required, and also, the underlying basis for the model may prove unreliable or inaccurate. In fact, it may be preferred to derive a stimulus waveform from only a single first subject, in order to preserve micro-modulation aspects of the signal, which as discussed above have not been fully characterized. However, the selection of the first subject(s) need not be static, and can change frequently. The selection of first subject records may be based on population statistics of other users of the records (i.e., collaborative filtering, i.e., whose response pattern do I correlate highest with? etc.). The selection of first subject records may also be based on feedback patterns from the second user.


The process of stimulation may seek to target a desired mental state in the second subject, which is automatically or semi-automatically determined of manually entered. That target then represents a part of the query against the database to select the desired record(s). The selection of records may be a dynamic process, and reselection of records may be feedback dependent.


The records may be used to define a modulation waveform of a synthesized carrier or set of carriers, and the process may include a frequency domain multiplexed multi-subcarrier signal (which is not necessarily orthogonal). A plurality of stimuli may be applied concurrently, through the suffered subchannels and/or though different stimulator electrodes, magnetic field generators, mechanical stimulators, sensory stimulators, etc. The stimuli for the different subchannels or modalities need not be derived from the same records.


The stimulus may be applied to achieve the desired mental state, e.g., brain entrainment of the second subject with one or more first subjects. Brain entrainment is not the only possible outcome of this process. If the plurality of first subjects are mutually entrained, then each will have a corresponding brain wave pattern dependent on the basis of brainwave entrainment. This link between first subject may be helpful in determining compatibility between a respective first subject and the second subject. For example, characteristic patterns in the entrained brainwaves may be determined, even for different target mental states, and the characteristic patterns correlated to find relatively close matches and to exclude relatively poor matches.


This technology may also provide a basis for a social network, dating site, employment or vocational testing, or other interpersonal environments, wherein people may be matched with each other based on entrainment characteristics. For example, people who efficiently entrain with each other may have better social relationships than those who do not. Thus, rather than seeking to match people based on personality profiles, the match could be made based on an ability of each party to efficiently entrain the brainwave pattern of the other party. This enhances non-verbal communication, and assists in achieving corresponding states during activities. This can be assessed by monitoring neural responses of each individual to video, and also by providing a test stimulation based on the other party's brainwave correlates of mental state, to see whether coupling is efficiently achieved. On the other hand, the technology could be used to assist in entrainment when natural coupling is inefficient, or to block coupling where the coupling is undesirable. An example of the latter is hostility; when two people are entrained in a hostile environment, emotional escalation ensures. However, if the entrainment is attenuated, undesired escalation may be impeded.


As discussed above, the plurality of first subjects may have their respective brain wave patterns stored in association with separate database records. However, they may also be combined into a more global model. One such model is a neural network or deep neural network. Typically, such a network would have recurrent features. Data from a plurality of first subjects is used to train the neural network, which is then accessed by inputting the target state and/or feedback information, and which outputs a stimulation pattern or parameters for controlling a stimulator. When multiple first subjects form the basis for the stimulation pattern, it is preferred that the neural network output parameters of the stimulation, derived from and comprising features of the brain wave patterns or other neural correlates of mental state from the plurality of first subjects, which are then used to control a stimulator which, for example, generates its own carrier wave(s) which are then modulated based on the output of the neural network. The neural network need not periodically retrieve records, and therefore may operate in a more time-continuous manner, rather than the more segmented scheme of record-based control.


In any of the feedback dependent methods, the brainwave patterns or other neural correlates of mental state may be processed by a neural network, to produce an output that guides or controls the stimulation. The stimulation, is, for example, at least one of a light (visual) signal, a sound signal, an electric signal, a magnetic field, and a vibration or mechanical stimulus, or other sensory input. The fields may be static or dynamically varying.


The process may employ a relational database of mental states and brainwave patterns, e.g., frequencies/neural correlate waveform patterns associated with the respective mental states. The relational database may comprise a first table, the first table further comprising a plurality of data records of brainwave patterns, and a second table, the second table comprising a plurality of mental states, each of the mental states being linked to at least one brainwave pattern. Data related to mental states and brainwave patterns associated with the mental states are stored in the relational database and maintained. The relational database is accessed by receiving queries for selected mental states, and data records are returned representing the associated brainwave pattern. The brainwave pattern retrieved from the relational database may then be used for modulating a stimulator seeking to produce an effect selectively dependent on the mental state at issue.


A computer apparatus may be provided for creating and maintaining a relational database of mental states and frequencies associated with the mental states, the computer apparatus comprising: a non-volatile memory for storing a relational database of mental states and neural correlates of brain activity associated with the mental states, the database comprising a first table, the first table further comprising a plurality of data records of neural correlates of brain activity associated with the mental states, and a second table, the second table comprising a plurality of mental states, each of the mental states being linked to one or more records in the first table; a processor coupled with the non-volatile memory, configured to process relational database queries, which are then used for searching the database; RAM coupled with the processor and the non-volatile memory for temporary holding database queries and data records retrieved from the relational database; and an I/O interface configured to receive database queries and deliver data records retrieved from the relational database. A SQL or noSQL database may also be used to store and retrieve records.


A further aspect of the technology provides a method of brain entrainment comprising: ascertaining a mental state in a first subject; recording brain waves of the plurality of subjects using at least one channel one of EEG and MEG; storing the recorded brain waves in a physical memory device; retrieving the brain waves from the memory device; applying a stimulus signal comprising a brainwave pattern derived from at least one-channel one of the EEG and MEG to a second subject via transcranial stimulation, whereby the mental state desired by the second subject is achieved. The stimulation may be of the same order (number of channels) as the EEG or MEG, or a different number of channels, typically reduced. For example, the EEG or MEG may comprise 128 or 256 channels, while the transcranial stimulator may have 8 or fewer channels. Sensory stimulation of various modalities and patterns may accompany the transcranial stimulation.


The at least one channel may be less than six channels and the placement of electrodes used for transcranial stimulation may be approximately the same as the placement of electrodes used in recording of said one of EEG and MEG.


The present technology may be responsive to chronobiology, and in particular to the subjective sense of time. For a subject, this may be determined volitionally subjectively, but also automatically, for example by judging attention span, using e.g., eye movements, and analyzing persistence of brainwave patterns or other physiological parameters after a discrete stimulus. Further, time-constants of the brain, reflected by delays and phase may also be analyzed. Further, the contingent negative variation (CNV) preceding a volitional act may be used, both to determine (or measure) conscious action timing, and also the time relationships between thought and action more generally.


Typically, brainwave activity is measured with a large number of EEG electrodes, which each receive signals from a small area on the scalp, or in the case of a MEG, by a number of sensitive magnetic field detectors, which are responsive to local field differences. Typically, the brainwave capture is performed in a relatively high number of spatial dimensions, e.g., corresponding to the number of sensors. It is often unfeasible to process the brainwave signals to create a source model, given that the brainwaves are created by billions of neurons, connected through axons, which have long distances. Further, the neurons are generally non-linear, and interconnected. However, a source model is not required.


Various types of artificial intelligence techniques may be exploited to analyze the neural correlates of a brain state represented in the brain activity data of both the first subject (donor) (or plurality of donors) and the second subject (recipient). The algorithm or implementation need not be the same, though in some cases, it is useful to conform the approach of the source processing and feedback processing so that the feedback does not achieve or seek a suboptimal target brain state. However, given the possible differences in conditions, resources, equipment, and purpose, there is no necessary coordination of these processes. The artificial intelligence may take the form of neural networks or deep neural networks, though rule/expert-based systems, hybrids, and more classical statistical analysis may be used. In a typical case, an artificial intelligence process will have at least one aspect, which is non-linear in its output response to an input signal, and thus at least the principle of linear superposition is violated. Such systems tend to permit discrimination, since a decision and the process of decision-making are, ultimately, non-linear. An artificially intelligent system requires a base of experience or information upon which to train. This can be a supervised (external labels applied to data), unsupervised (self-discrimination of classes), or semi-supervised (a portion of the data is externally labelled).


A self-learning or genetic algorithm may be used to tune the system, including both or either the signal processing at the donor system and the recipient system. In a genetic algorithm feedback-dependent self-learning system, the responsivity of a subject, e.g., the target, to various kinds of stimuli may be determined over a stimulus space. This stimulation may be in the context of use, with a specific target brain state provided, or unconstrained. The stimulator may operate using a library of stimulus patterns, or seek to generate synthetic patterns or modifications of patterns. Over a period of time, the system will learn to map a desired brain state to optimal context-dependent parameters of the stimulus pattern.


In some cases it may be appropriate to administer a drug or pharmacological agent, such as melatonin, hypnotic or soporific drug, a sedative (e.g., barbiturates, benzodiazepines, nonbenzodiazepine hypnotics, orexin antagonists, antihistamines, general anesthetics, cannabis and other herbal sedatives, methaqualone and analogues, muscle relaxants, opioids) that assists in achieving the target brain state, and for emotional states and/or dreams, this may include certain psychotropic drugs, such as epinephrine, norepinephrine reuptake inhibitors, serotonin reuptake inhibitors, peptide endocrine hormones, such as oxytocin, ACTH fragments, insulin, etc. Combining a drug with stimulation may reduce the required dose of the drug and the associated side effects of the drug.


The technology may be used to modify or alter a mental state (e.g., from sleep to waking and vice versa) in a subject. Typically, the starting mental state, brain state, or brainwave pattern is assessed, such as by EEG, MEG, observation, stimulus-response amplitude and/or delay, or the like. Of particular interest in uncontrolled environments are automated mental state assessments, which do not rely on human observation or EEG signals, and rather may be acquired through MEG (e.g., SQID, optically-pumped magnetometer), EMG, MMG (magnetomyogram), mechanical (e.g., accelerometer, gyroscope, etc.), data from physiological sensors (e.g., AKG, heartrate, respiration rate, temperature, galvanic skim potential, etc.), or automated camera sensors.


For example, cortical stimulus-response pathways and reflexes may be exercised automatically, to determine their characteristics on a generally continuous basis. These characteristics may include, for example, a delay between stimulus and the observed central (e.g., EEG) or peripheral response (e.g., EMG, limb accelerometer, video). Typically, the same modality will be used to assess the pre-stimulation state, stimulus response, and post-stimulation state, though this is not a limitation.


In order to change the mental state, a stimulus is applied in a way designed to alter the mental state in a desired manner. A state transition table, or algorithm, may be employed to optimize the transition from a starting mental state to a desired mental state. The stimulus may be provided in an open loop (predetermined stimulus protocol) or closed loop (feedback adapted stimulus protocol), based on observed changes in a monitored variable.


Advantageously, a characteristic delay between application of stimulus and determination of response varies with the brain or mental state. For example, some mental states may lead to increased delay or greater variability in delay, while others may lead to decreased or lower variability. Further, some states may lead to attenuation of response, while others may lead to exaggerated response. In addition, different mental states can be associated with qualitatively different responses. Typically, the mere assessment of the brain or mental state should not itself alter the state, though in some cases the assessment and transition influence may be combined. For example, in seeking to assist in achieving a deep sleep state, excitation that disturbs sleep is contraindicated.


In cases where a brainwave pattern is itself determined by EEG (which may be limited to relatively controlled environments), brainwaves representing that pattern represent coherent firing of an ensemble of neurons, defining a phase. One way to change the state is to advance or retard the triggering of the neuronal excitation, which can be a direct or indirect excitation or inhibition, caused, for example, by electrical, magnetic, mechanical, or sensory stimulation. This stimulation may be time-synchronized with the detected (e.g., by EEG) brainwaves, for example with a phase lead or lag with respect to the detected pattern. Further, the excitation can steer the brainwave signal by continually advancing to a desired state, which through the continual phase rotation represents a different frequency. After the desired new state is achieved, the stimulus may cease, or be maintained in a phase-locked manner to hold the desired state.


A predictive model may be used to determine the current mental state, optimal transition to a desired mental state, when the subject has achieved the desired mental state, and how to maintain the desired mental state. The desired mental state itself may represent a dynamic sequence (e.g., stage 1⇒stage 2⇒stage 3, etc.), such that the subject's mental state is held for a desired period in a defined condition. Accordingly, the stimulus may be time-synchronized with respect to the measured brainwave pattern.


Direct measurement or determination of brainwaves or their phase relationships is not necessarily required. Rather, the system may determine tremor or reflex patterns. Typically, the reflex patterns of interest involve central pathways, and more preferably brain reflex pathways, and not spinal cord mediated reflexes, which are less dependent on instantaneous brain state. The central reflex patterns can reflect a time delay between stimulation and motor response, an amplitude of motor response, a distribution of response through various afferent pathways, variability of response, tremor or other modulation of motor activity, etc. Combinations of these characteristics may be employed, and different subsets may be employed at different times or to reflect different states. Similar to evoked potentials, the stimulus may be any sense, especially sight, sound, touch/proprioception/pain/etc., though the other senses, such as taste, smell, balance, etc., may also be exercised. A direct electrical or magnetic excitation is also possible. As discussed, the response may be determined through EEG, MEG, or peripheral afferent pathways.


Normalization of brain activity information may be spatial and/or temporal. For example, the EEG electrodes between sessions or for different subject may be in different locations, leading to a distortion of the multichannel spatial arrangement. Further, head size and shape of different individuals is different, and this needs to be normalized and/or encoded as well. The size and shape of the head/skull and/or brain, may also lead to temporal differences in the signals, such as characteristic time delays, resonant or characteristic frequencies, etc.


One way to account for these effects is through use of a time-space transform, such as a wavelet-type transform. It is noted that, in a corresponding way that statistical processes are subject to frequency decomposition analysis through Fourier transforms, they are also subject to time-frequency decomposition through wavelet transforms. Typically, the wavelet transform is a discrete wavelet transform (DWT), though more complex and less regular transforms may be employed. As discussed above, principal component analysis (PCA) and spatial PCA may be used to analyze signals, presuming linearity (linear superposition) and statistical independence of components. However, these presumptions technically do not apply to brainwave data, and practically, one would normally expect interaction between brain wave components (non-independence) and lack of linearity (since “neural networks” by their nature are non-linear), defeating use of PCA or spatial PCA unmodified.


However, a field of nonlinear dimensionality reduction provides various techniques to permit corresponding analyses under presumptions of non-linearity and non-independence. See,

  • en.wikipedia.org/wiki/Nonlinear_dimensionality_reduction,
  • www.image.ucar.edu/pub/toyIV/monahan_5_16.pdf (An Introduction to Nonlinear Principal Component Analysis, Adam Monahan),
  • Barros, Allan Kardec, and Andrzej Cichocki. “Extraction of specific signals with temporal structure.” Neural computation 13, no. 9 (2001): 1995-2003.;
  • Crainiceanu, Ciprian M., Ana-Maria Staicu, Shubankar Ray, and Naresh Punjabi. “Statistical inference on the difference in the means of two correlated functional processes: an application to sleep EEG power spectra.” Johns Hopkins University, Dept. of Biostatistics Working Papers (2011): 225.;
  • Ewald, Arne. “Novel multivariate data analysis techniques to determine functionally connected networks within the brain from EEG or MEG data.” (2014).;
  • Friston, Karl J. “Basic concepts and overview.” SPMcourse, Short course;
  • Friston, Karl J., Andrew P. Holmes, Keith J. Worsley, J-P. Poline, Chris D. Frith, and Richard S J Frackowiak. “Statistical parametric maps in functional imaging: a general linear approach.” Human brain mapping 2, no. 4 (1994): 189-210.;
  • Friston, Karl, “Nonlinear PCA: characterizing interactions between modes of brain activity” (www.fil.ion.ucl.ac.uk/˜karl/Nonlinear %20PCA.pdf, 2000),
  • Howard et al., “Distinct Variation Pattern Discovery Using Alternating Nonlinear Principal Component Analysis”, IEEE Trans Neural Network Learn Syst. 2018 January; 29(1):156-166. doi: 10.1109/TNNLS.2016.2616145. Epub 2016 Oct. 26 (www.ncbi.nlm.nih.gov/pubmed/27810837); Hyvärinen, Aapo, and Patrik Hoyer. “Emergence of phase- and shift-invariant features by decomposition of natural images into independent feature subspaces.” Neural computation 12, no. 7 (2000): 1705-1720.;
  • Jolliffe, I. T., “Principal Component Analysis, Second Edition”, Springer 2002, cda.psych.uiuc.edu/statistical_learning_course/Jolliffe %201.%2Principal %2Component %20Anaylsis%20(2ed., Springer, 2002) (518s)_MVsα_.pdf,
  • Jutten, Christian, and Massoud Babaie-Zadeh. “Source separation: Principles, current advances and applications.” IAR Annu Meet Nancy Fr 110 (2006).;
  • Kohl, Florian. “Blind separation of dependent source signals for MEG sensory stimulation experiments.” (2013).;
  • Konar, Amit, and Aruna Chakraborty. Emotion recognition: A pattern analysis approach. John Wiley & Sons, 2014.;
  • Lee, Soo-Young. “Blind source separation and independent component analysis: A review.” Neural Information Processing-Letters and Reviews 6, no. 1 (2005): 1-57.;
  • Nonlinear PCA (www.comp.nus.edu.sg/˜cs5240/lecture/nonlinear-pca.pdf),
  • Nonlinear PCA toolbox for MATLAB (www.nlpca.org),
  • Nonlinear Principal Component Analysis: Neural Network Models and Applications (pdfs.semanticsch olar.org/9d31/23542031a227d2f4c4602066cf8ebceaeb7a.pdf),
  • Nonlinear Principal Components Analysis: Introduction and Application (openaccess.leidenuniv.nl/bitstream/handle/1887/12386/Chapter2.pdf?sequence=10, 2007),
  • Onken, Arno, Jian K. Liu, P P Chamanthi R. Karunasekara, loannis Delis, Tim Gollisch, and Stefano Panzeri. “Using matrix and tensor factorizations for the single-trial analysis of population spike trains.” PLoS computational biology 12, no.11 (2016): e1005189.;
  • Parida, Shantipriya, Satchidananda Dehuri, and Sung-Bae Cho. “Machine Learning Approaches for Cognitive State Classification and Brain Activity Prediction: A Survey.” Current Bioinformatics 10, no. 4 (2015): 344-359.;
  • Sapienza, La. “Blind Source Separation in real-world environments: new algorithms, applications and implementations Separazione cieca di sorgenti in ambienti reali: nuovi algoritmi, applicazioni e.”;
  • Saproo, Sameer, Victor Shih, David C. Jangraw, and Paul Sajda. “Neural mechanisms underlying catastrophic failure in human-machine interaction during aerial navigation.” Journal of neural engineering 13, no. 6 (2016): 066005.;
  • Stone, James V. “Blind source separation using temporal predictability.” Neural computation 13, no. 7 (2001): 1559-1574.;
  • Tressoldi, Patrizio, Luciano Pederzoli, Marco Bilucaglia, Patrizio Caini, Pasquale Fedele, Alessandro Ferrini, Simone Melloni, Diana Richeldi, Florentina Richeldi, and Agostino Accardo. “Brain-to-Brain (Mind-to-Mind) Interaction at Distance: A Confirmatory Study.” (2014). f1000researchdata.s3.amazonaws.com/manuscripts/5914/5adbf847-787a-4fc1-ac04-2e1 cd61ca972_4336_-_patrizio_tressoldi_v3.pdf? doi=10.12688/f1000research.43363;
  • Tsiaparas, Nikolaos N. “Wavelet analysis in coherence estimation of electroencephalographic signals in children for the detection of dyslexia-related abnormalities.” PhD diss., 2006.
  • Valente, Giancarlo. “Separazione cieca di sorgenti in ambienti reali: nuovi algoritmi, applicazioni e implementazioni.” (2006).;
  • Wahlund, Björn, Wlodzimierz Klonowski, Pawel Stepien, Robert Stepien, Tatjana von Rosen, and Dietrich von Rosen. “EEG data, fractal dimension and multivariate statistics.” Journal of Computer Science and Engineering 3, no. 1 (2010): 10-14.;
  • Wang, Yan, Matthew T. Sutherland, Lori L. Sanfratello, and Akaysha C. Tang. “Single-trial classification of ERPS using second-order blind identification (SOBI).” In Machine Learning and Cybernetics, 2004. Proceedings of 2004 International Conference on, vol. 7, pp. 4246-4251. IEEE, 2004.;
  • Yu, Xianchuan, Dan Hu, and Jindong Xu. Blind source separation: theory and applications. John Wiley & Sons, 2013.;


Therefore, statistical approaches are available for separating EEG signals from other signals, and for analyzing components of EEG signals themselves. According to the present invention, various components that might be considered noise in other contexts, e.g., according to prior technologies, such as a modulation pattern of a brainwave, are preserved. Likewise, interactions and characteristic delays between significant brainwave events are preserved. This information may be stored either integrated with the brainwave pattern in which it occurs, or as a separated modulation pattern that can then be recombined with an unmodulated brainwave pattern to approximate the original subject.


According to the present technology, lossy “perceptual” encoding (i.e., functionally optimized with respect to subjective response) of the brainwaves may be employed to process, store and communicate the brainwave information. In a testing scenario, the “perceptual” features may be tested, so that important information is preserved over information that does not strongly correspond to the effective signal. Thus, while one might not know a priori which components represent useful information, a genetic algorithm may empirically determine which features or data reduction algorithms or parameter sets optimize retention of useful information vs. information efficiency. It is noted that subjects may differ in their response to signal components, and therefore the “perceptual” encoding may be subjective with respect to the recipient. On the other hand, different donors may have different information patterns, and therefore each donor may also require individual processing. As a result, pairs of donor and recipient may require optimization, to ensure accurate and efficient communication of the relevant information. According to the present invention, sleep/wake mental states and their corresponding patterns are sought to be transferred. In the recipient, these patterns have characteristic brainwave patterns. Thus, the donor may be used, under a variety of alternate processing schemes, to stimulate the recipient, and the sleep/wake response of the recipient determined based on objective criteria, such as resulting brainwave patterns or expert observer reports, or subjective criteria, such as recipient self-reporting, survey or feedback. Thus, after a training period, an optimized processing of the donor, which may include filtering, dominant frequency resynthesis, feature extraction, etc., may be employed, which is optimized for both donor and recipient. In other cases, the donor characteristics may be sufficiently normalized, that only recipient characteristics need be compensated. In a trivial case, there is only one exemplar donor, and the signal is oversampled and losslessly recorded, leaving only recipient variation as a significant factor.


Because dominant frequencies tend to have low information content (as compared to the modulation of these frequencies and interrelation of various sources within the brain), one efficient way to encode the main frequencies is by location, frequency, phase, and amplitude. The modulation of a wave may also be represented as a set of parameters. By decomposing the brainwaves according to functional attributes, it becomes possible, during stimulation, to modify the sequence of “events” from the donor, so that the recipient need not experience the same events, in the same order, and in the same duration, as the donor. Rather, a high-level control may select states, dwell times, and transitions between states, based on classified patterns of the donor brainwaves. The extraction and analysis of the brainwaves of the donors, and response of the recipient, may be performed using statistical processes, such as principle components analysis (PCA), independent component analysis (ICA), and related techniques; clustering, classification, dimensionality reduction and related techniques; neural networks and other known technologies. These algorithms may be implemented on general purpose CPUs, array processors such as GPUs, and other technologies.


In practice, a brainwave pattern of the first subject may be analyzed by a PCA technique that respects the non-linearity and non-independence of the brainwave signals, to extract the major cyclic components, their respective modulation patterns, and their respective interrelation. The major cyclic components may be resynthesized by a waveform synthesizer, and thus may be efficiently coded. Further, a waveform synthesizer may modify frequencies or relationships of components from the donor based on normalization and recipient characteristic parameters. For example, the brain of the second subject (recipient) may have characteristic classified brainwave frequencies 3% lower than the donor (or each type of wave may be separately parameterized), and therefore the resynthesis may take this difference into account. The modulation patterns and interrelations may then be reimposed onto the resynthesized patterns. The normalization of the modulation patterns and interrelations may be distinct from the underlying major cyclic components, and this correction may also be made, and the normalized modulation patterns and interrelations included in the resynthesis. If the temporal modifications are not equal, the modulation patterns and interrelations may be decimated or interpolated to provide a correct continuous time sequence of the stimulator. The stimulator may include one or more stimulation channels, which may be implemented as electrical, magnetic, auditory, visual, tactile, or other stimulus, and/or combinations.


The stimulator is preferably feedback controlled. The feedback may relate to the brainwave pattern of the recipient, and/or context or ancillary biometric basis. For example, if the second subject (recipient) begins to awaken from sleep, which differs from the first subject (donor) sleep pattern, then the stimulator may resynchronize based on this finding. That is, the stimulator control will enter a mode corresponding to the actual state of the recipient, and seek to guide the recipient to a desired state from a current state, using the available range and set of stimulation parameters. The feedback may also be used to tune the stimulator, to minimize error from a predicted or desired state of the recipient subject based on the prior and current stimulation.


The control for the stimulator is preferably adaptive, and may employ a genetic algorithm to improve performance over time. For example, if there are multiple first subjects (donors), the second subject (recipient) may be matched with those donors from whose brainwave signals (or algorithmically modified versions thereof) the predicted response in the recipient is best, and distinguished from those donors from whose brainwave signals the predicted response in the recipient subject poorly corresponds. Similarly, if the donors have brainwave patterns determined over a range of time and context and stored in a database, the selection of alternates from the database may be optimized to ensure best correspondence of the recipient subject to the desired response.


It is noted that a resynthesizer-based stimulator is not required, if a signal pattern from a donor is available that properly corresponds to the recipient and permits a sufficiently low error between the desired response and the actual response. For example, if a donor and a recipient are the same subject at different times, a large database may be unnecessary, and the stimulation signal may be a minimally processed recording of the same subject at an earlier time. Likewise, in some cases, a deviation is tolerable, and an exemplar signal may be emitted, with relatively slow periodic correction. For example, a sleep signal may be derived from a single subject, and replayed with a periodicity of 90 minutes or 180 minutes, such as a light or sound signal, which may be useful in a dormitory setting, where individual feedback is unavailable or unhelpful.


In some cases, it is useful to provide a stimulator and feedback-based controller on the donor. This will better match the conditions of the donor and recipient, and further allow determination of not only the brainwave pattern of the donor, but also responsivity of the donor to the feedback. One difference between the donors and the recipients is that in the donor, the natural sleep pattern is sought to be maintained and not interrupted. Thus, the adaptive multi-subject database may include data records from all subject, whether selected ab initio as a useful exemplar or not. Therefore, the issue is whether a predictable and useful response can be induced in the recipient from the database record, and if so, that record may be employed. If the record would produce an unpredictable result, or a non-useful result, the use of that record should be avoided. The predictability and usefulness of the responses may be determined by a genetic algorithm, or other parameter-space searching technology.





BRIEF DESCRIPTION OF THE DRAWINGS

The detailed description is described with reference to the accompanying figures. In the figures, the left-most digit(s) of a reference number identifies the figure in which the reference number first appears. The use of the same reference number in different figures indicates similar or identical items.



FIG. 1 shows the electric activity of a neuron contributing to a brainwave.



FIG. 2 shows transmission of an electrical signal generated by a neuron through the skull, skin and other tissue to be detectable by an electrode transmitting this signal to EEG amplifier.



FIG. 3 shows an illustration of a typical EEG setup with a subject wearing a cup with electrodes connected to the EEG machine, which is, in turn, connected to a computer screen displaying the EEG.



FIG. 4 shows a typical EEG reading.



FIG. 5 shows one second of a typical EEG signal.



FIG. 6 shows main brainwave patterns.



FIG. 7 shows a flowchart according to one embodiment of the invention.



FIG. 8 shows a flowchart according to one embodiment of the invention.



FIG. 9 shows a flowchart according to one embodiment of the invention.



FIG. 10 shows a flowchart according to one embodiment of the invention.



FIG. 11 shows a flowchart according to one embodiment of the invention.



FIG. 12 shows a flowchart according to one embodiment of the invention.



FIG. 13 shows a flowchart according to one embodiment of the invention.



FIG. 14 shows a schematic representation of an apparatus according to one embodiment of the invention.



FIG. 15 shows brainwave real-time BOLD (Blood Oxygen Level Dependent) studies acquired with synchronized stimuli.



FIG. 16 shows Brain Entrainment Frequency Following Response (or FFR).



FIG. 17 shows brainwave entrainment before and after synchronization.



FIG. 18 shows brainwaves during inefficient problem solving and stress.



FIGS. 19 and 20 show how binaural beats work.



FIG. 21 shows Functional Magnetic Resonance Imaging (fMRI)



FIG. 22 shows a photo of a brain forming a new idea.



FIG. 23 shows 3D T2 CUBE (SPACE/VISTA) FLAIR & DSI tractography



FIG. 24 shows an EEG tracing.



FIG. 25 shows a flowchart according to one embodiment of the invention.



FIG. 26 shows a flowchart according to one embodiment of the invention.



FIG. 27 shows a flowchart according to one embodiment of the invention.



FIG. 28 shows a flowchart according to one embodiment of the invention.





DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention generally relates to enhancing emotional response by a subject in connection with the received information by conveying to the brain of the subject temporal patterns of brainwaves of a second subject who had experienced such emotional response, said temporal pattern being provided non-invasively via light, sound, transcranial direct current stimulation (tDCS), transcranial alternating current stimulation (tDAS) or HD-tACS, transcranial magnetic stimulation (TMS) or other means capable of conveying frequency patterns.


The transmission of the brain waves can be accomplished through direct electrical contact with the electrodes implanted in the brain or remotely employing light, sound, electromagnetic waves and other non-invasive techniques. Light, sound, or electromagnetic fields may be used to remotely convey the temporal pattern of prerecorded brainwaves to a subject by modulating the encoded temporal frequency on the light, sound or electromagnetic filed signal to which the subject is exposed.


Every activity, mental or motor, every emotion is associated with unique brainwaves having specific spatial and temporal patterns, i.e., a characteristic frequency or a characteristic distribution of frequencies over time and space. Such waves can be read and recorded by several known techniques, including electroencephalography (EEG), magnetoencephalography (MEG), exact low-resolution brain electromagnetic tomography (eLORETA), sensory evoked potentials (SEP), fMRI, functional near-infrared spectroscopy (fNIRS), etc. The cerebral cortex is composed of neurons that are interconnected in networks. Cortical neurons constantly send and receive nerve impulses-electrical activity-even during sleep. The electrical or magnetic activity measured by an EEG or MEG (or another device) device reflects the intrinsic activity of neurons in the cerebral cortex and the information sent to it by subcortical structures and the sense receptors.


An EEG electrode will mainly detect the neuronal activity in the brain region just beneath it. However, the electrodes receive the activity from thousands of neurons. One square millimeter of cortex surface, for example, has more than 100,000 neurons. It is only when the input to a region is synchronized with electrical activity occurring at the same time that simple periodic waveforms in the EEG become distinguishable. The temporal pattern associated with specific brainwaves can be digitized and encoded a non-transient memory.


“Playing back the brainwaves” to another animal or person by providing decoded temporal pattern through tDCS, tACS, HD-tACS, TMS, or through electrodes implanted in the brain, allows the recipient to learn the task at hand faster. For example, if the brain waves of a mouse navigated a familiar maze are decoded (by EEG or via implanted electrodes), playing this temporal pattern to another mouse unfamiliar with this maze will allow it to learn to navigate this maze faster.


Employing light, sound or electromagnetic field to remotely convey the temporal pattern of brainwaves (which may be prerecorded) to a subject by modulating the encoded temporal frequency on the light, sound or electromagnetic filed signal to which the subject is exposed.


When a group of neurons fires simultaneously, the activity appears as a brainwave. Different brainwave-frequencies are linked to different tasks in the brain.



FIG. 1 shows the electric activity of a neuron contributing to a brainwave.



FIG. 2 shows transmission of an electrical signal generated by a neuron through the skull, skin and other tissue to be detectable by an electrode transmitting this signal to EEG amplifier.



FIG. 3 shows an illustration of a typical EEG setup with a subject wearing a cup with electrodes connected to the EEG machine, which is, in turn, connected to a computer screen displaying the EEG. FIG. 4 shows a typical EEG reading. FIG. 5 shows one second of a typical EEG signal. FIG. 6 shows main brainwave patterns.



FIG. 7 shows a flowchart according to one embodiment of the invention. Brainwaves from a subject engaged in a task are recorded. Brainwaves associated with the task are identified. A temporal pattern in the brainwave associated with the task is decoded. The decoded temporal pattern is used to modulate the frequency of at least one stimulus. The temporal pattern is transmitted to the second subject by exposing the second subject to said at least one stimulus.



FIG. 8 shows a flowchart according to one embodiment of the invention. Brainwaves in a subject at rest and engaged in a task are recorded, and a brainwave characteristic associated with the task is separated by comparing with the brainwaves at rest. A temporal pattern in the brainwave associated with the task is decoded and stored. The stored code is used to modulate the temporal pattern on a stimulus, which is transmitted to the second subject by exposing the second subject to the stimulus.



FIG. 9 shows a flowchart according to one embodiment of the invention. Brainwaves in a subject engaged in a task are recorded, and a Fourier Transform analysis performed. A temporal pattern in the brainwave associated with the task is then decoded and stored. The stored code is then used to modulate the temporal pattern on a stimulus, which is transmitted to the second subject by exposing the second subject to the stimulus.



FIG. 10 shows a flowchart according to one embodiment of the invention. Brainwaves in a plurality of subjects engaged in a respective task are recorded. A neural network is trained on the recorded brainwaves associated with the task. After the neural network is defined, brainwaves in a first subject engaged in the task are recorded. The neural network is used to recognize brainwaves associated with the task. A temporal pattern in the brainwaves associated with the task is decoded and stored. The code is used to modulate the temporal pattern on a stimulus. Brainwaves associated with the task in a second subject are induced by exposing the second subject to the stimulus



FIG. 11 shows a flowchart according to one embodiment of the invention. Brainwaves in a subject both at rest and engaged in a task are recorded. A brainwave pattern associated with the task is separated by comparing with the brainwaves at rest. For example, a filter or optimal filter may be designed to distinguish between the patterns. A temporal pattern in the brainwave associated with the task is decoded, and stored in software code, which is then used to modulate the temporal pattern of light, which is transmitted to the second subject, by exposing the second subject to the source of the light.



FIG. 12 shows a flowchart according to one embodiment of the invention. Brainwaves in a subject at rest and engaged in a task are recoded. A brainwave pattern associated with the task is separated by comparing with the brainwaves at rest. A temporal pattern in the brainwave associated with the task is decoded and stored as a temporal pattern in software code. The software code is used to modulate the temporal pattern on a sound signal. The temporal pattern is transmitted to the second subject by exposing the second subject to the sound signal.



FIG. 13 shows a flowchart according to one embodiment of the invention. Brainwaves in a subject engaged in a task are recorded, and brainwaves selectively associated with the task are identified. A pattern, e.g., a temporal pattern, in the brainwave associated with the task, is decoded and used to entrain the brainwaves of the second subject.



FIG. 14 shows a schematic representation of an apparatus according to one embodiment of the invention.



FIG. 15 shows brainwave real time BOLD (Blood Oxygen Level Dependent) fMRI studies acquired with synchronized stimuli.



FIG. 16 shows Brain Entrainment Frequency Following Response (or FFR). See, “Stimulating the Brain with Light and Sound,” Transparent Corporation, Neuroprogrammer™ 3, www.transparentcorp.com/products/np/entrainment.php.



FIG. 17 shows brainwave entrainment before and after synchronization. See, Understanding Brainwaves to Expand our Consciousness, fractalenlightenment.com/14794/spirituality/understanding-brainwaves-to-expand-our-consciousness



FIG. 18 shows brainwaves during inefficient problem solving and stress.



FIGS. 19 and 20 show how binaural beats work. Binaural beats are perceived when two different pure-tone sine waves, both with frequencies lower than 1500 Hz, with less than a 40 Hz difference between them, are presented to a listener dichotically (one through each ear). See, for example, if a 530 Hz pure tone is presented to a subject's right ear, while a 520 Hz pure tone is presented to the subject's left ear, the listener will perceive the auditory illusion of a third tone, in addition to the two pure-tones presented to each ear. The third sound is called a binaural beat, and in this example would have a perceived pitch correlating to a frequency of 10 Hz, that being the difference between the 530 Hz and 520 Hz pure tones presented to each ear. Binaural-beat perception originates in the inferior colliculus of the midbrain and the superior olivary complex of the brainstem, where auditory signals from each ear are integrated and precipitate electrical impulses along neural pathways through the reticular formation up the midbrain to the thalamus, auditory cortex, and other cortical regions. “Auditory beats in the brain.” . . . . FIG. 21 shows Functional Magnetic Resonance Imaging (fMRI)



FIG. 22 shows a photo of a brain forming a new idea.



FIG. 23 shows 3D T2 CUBE (SPACE/VISTA) FLAIR & DSI tractography.



FIG. 24 shows The EEG activities for a healthy subject during a working memory task.



FIG. 25 shows a flowchart according to one embodiment of the invention. Brainwaves in a subject engaged in a task are recorded. Brainwaves associated with the task are identified. A temporal pattern in the brainwave associated with the task is extracted. First and second dynamic audio stimuli are generated, whose frequency differential corresponds to the temporal pattern. Binaural beats are provided using the first and the second audio stimuli to stereo headphones worn by the second subject to entrain the brainwaves of the second subject.



FIG. 25 shows a flowchart according to one embodiment of the invention. Brainwaves of a subject engaged in a task are recorded, and brainwaves associated with the task identified. A pattern in the brainwave associated with the task is identified, having a temporal variation. Two dynamic audio stimuli whose frequency differential corresponds to the temporal variation are generated, and applied as a set of binaural bits to the second subject, to entrain the brainwaves of the second subject.



FIG. 26 shows a flowchart according to one embodiment of the invention. Brainwaves of a subject engaged in a task are recorded, and brainwaves associated with the task identified. A pattern in the brainwave associated with the task is identified, having a temporal variation. A series of isochronic tones whose frequency differential corresponds to the temporal variation is generated and applied as a set of stimuli to the second subject, to entrain the brainwaves of the second subject.



FIG. 27 shows a flowchart according to one embodiment of the invention. Brainwaves of a subject engaged in a task are recorded, and brainwaves associated with the task identified. A pattern in the brainwave associated with the task is identified, having a temporal variation. Two dynamic light stimuli whose frequency differential corresponds to the temporal variation are generated, and applied as a set of stimuli to the second subject, wherein each eye sees only one light stimuli, to entrain the brainwaves of the second subject.



FIG. 28 shows a flowchart according to one embodiment of the invention. Brainwaves of a subject engaged in a task are recorded, and brainwaves associated with the task identified. A pattern in the brainwave associated with the task is identified, having a temporal variation. Two dynamic electric stimuli whose frequency differential corresponds to the temporal variation are generated, and applied as transcranial stimulation to the second subject, wherein each electric signal is applied to the opposite side of the subject's head, to entrain the brainwaves of the second subject.


Example 1

We record EEG of a concert pianist while the pianist is playing a particular piece (e.g., Beethoven sonata); then decode the dynamic spatial and/or temporal patterns of the EEG and encode them in software. If a music student wants to learn this particular Beethoven sonata, we use the software with an encoded dynamic temporal pattern to drive “smart bulbs” or another source of light while the student is learning to play this piece from the music sheet. The result is accelerated learning. See FIG. 1.


Example 2

We record EEG of a martial art master while performing a particular move (say Karate or Kong Fu), decode the dynamic spatial and temporal patterns of the EEG and encode them in software. If a karate student wants to learn this particular move, we use the software with an encoded temporal pattern to drive smart bulbs or another source of light while the student is practicing this move. The result is accelerated learning. FIG. 2 represents an embodiment of the invention as applied to learning a drawing task, which is representative of various motor skills.


Example 3

A person is reading a book, and during the course of the reading, brain activity, including electrical or magnetic activity, and optionally other measurements, as acquired. The data is processed to determine the frequency and phase, and dynamic changes of brainwave activity, as well as the spatial location of emission. Based on a brain model, a set of non-invasive stimuli, which may include any and all senses, magnetic nerve or brain stimulation, ultrasound, etc., is devised for a subject who is to read or learn the same book. The subject is provided with the book to read, and the stimuli are presented to the subject synchronized with the progress through the book. Typically, the book is presented to the subject through an electronic reader device, such as a computer or computing pad, to assist in synchronization. The same electronic reader device may produce the temporal pattern of stimulation across the various stimulus modalities. The result is speed reading and improved comprehension and retention of the information.


Other examples of skill domains that may be facilitated include learning foreign languages, math, sports or specialized skills.


The method of the present invention can be used to accelerate learning of new information, new subjects or fine motor skills.


In this description, several preferred embodiments were discussed. Persons skilled in the art will, undoubtedly, have other ideas as to how the systems and methods described herein may be used. It is understood that this broad invention is not limited to the embodiments discussed herein. Rather, the invention is limited only by the following claims.


The aspects of the invention are intended to be separable and may be implemented in combination, sub-combination, and with various permutations of embodiments. Therefore, the various disclosure herein, including that which is represented by acknowledged prior art, may be combined, sub-combined and permuted in accordance with the teachings hereof, without departing from the spirit and scope of the invention.


All references and information sources cited herein are expressly incorporated herein by reference in their entirety.


Hereinafter, embodiments of the present disclosure will be described in detail with reference to the accompanying drawings so that the present disclosure may be readily implemented by those skilled in the art. However, it is to be noted that the present disclosure is not limited to the embodiments but can be embodied in various other ways. In drawings, parts irrelevant to the description are omitted for the simplicity of explanation, and like reference numerals denote like parts through the whole document.


Through the whole document, the term “connected to” or “coupled to” that is used to designate a connection or coupling of one element to another element includes both a case that an element is “directly connected or coupled to” another element and a case that an element is “electronically connected or coupled to” another element via still another element. Further, it is to be understood that the term “comprises or includes” and/or “comprising or including” used in the document means that one or more other components, steps, operation and/or existence or addition of elements are not excluded in addition to the described components, steps, operation and/or elements unless context dictates otherwise.


Through the whole document, the term “unit” or “module” includes a unit implemented by hardware or software and a unit implemented by both of them. One unit may be implemented by two or more pieces of hardware, and two or more units may be implemented by one piece of hardware.


Other devices, apparatus, systems, methods, features and advantages of the invention will be or will become apparent to one with skill in the art upon examination of the following figures and detailed description. It is intended that all such additional systems, methods, features and advantages be included within this description, be within the scope of the invention, and be protected by the accompanying claims.

Claims
  • 1. A method of facilitating a process of learning a skill, comprising: determining brain wave electrical activity patterns of a first subject skilled in the skill, the brain wave electrical activity patterns being selectively associated with a cognitive state representing a readiness for training in a physical activity involving the skill;processing the brain wave electrical activity patterns of the first subject with at least one microprocessor, to determine the cognitive state representing the readiness for training in the skill;subjecting a second subject, while learning to perform the physical activity involving the skill, to a neurostimulation having at least one stimulus selectively dependent on the processed brain wave electrical activity patterns of the first subject, the neurostimulation being adapted to induce in the second subject a spatial brain activity pattern over time corresponding to the cognitive state representing the readiness for training in the skill;determining spatial brain wave electrical activity patterns of the second subject over time while subject to the neurostimulation; andadaptively controlling said neurostimulation to which the second subject is subjected, dependent on the determined spatial brain wave electrical activity patterns of the second subject over time, to alter a timing of said neurostimulation to synchronize an electrical phase of the processed brain wave electrical activity patterns of the first subject with the determined brain wave electrical activity patterns of the second subject while engaged in an activity involving the skill.
  • 2. The method according to claim 1, wherein said at least one stimulus is selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a cranial electrotherapy stimulation (CES), a transcranial electric stimulation (TES), transcranial magnetic stimulation (TMS), and a deep brain stimulation (DBS).
  • 3. The method according to claim 1, further comprising determining a neuronal baseline activity of the first subject, while not engaged in the skill.
  • 4. The method according to claim 1, wherein the neurostimulation is a visual excitation.
  • 5. The method according to claim 1, wherein the processing comprises performing a hybrid time-frequency domain transform on the brain wave electrical activity patterns of the first subject.
  • 6. The method according to claim 1, wherein the neurostimulation is further dependent on a concurrent state of the second subject.
  • 7. The method according to claim 1, further comprising determining brain wave electrical activity patterns of the second subject, wherein the neurostimulation is synchronized with the determined brain wave electrical activity patterns of the second subject.
  • 8. The method according to claim 1, wherein said brain wave electrical activity patterns are obtained by at least one of electroencephalography (EEG), low-resolution brain electromagnetic tomography, and magnetoencephalography.
  • 9. The method according to claim 1, wherein the neurostimulation is an auditory excitation.
  • 10. The method according to claim 1, wherein the brain wave electrical activity patterns are determined over time and space, and the processing comprises performing a transform from a time and space domain on a representation of the brain wave electrical activity patterns.
  • 11. The method according to claim 1, wherein the neurostimulation is adapted to cause a brainwave entrainment of the second subject with the first subject.
  • 12. The method according to claim 1, wherein the skill comprises at least one of a mental, motor, musical instrument playing, singing, dancing, sports, martial arts, speech, mathematical, calligraphical, drawing, painting, massage, assembly, walking, running, swimming, yoga, fighting, shooting, self-defense, olfactory, and muscular coordination skill.
  • 13. An apparatus for facilitating a skill learning process, comprising at least one automated processor, configured to: process information derived from brain wave patterns representing electrical activity of the brain of a first subject while engaged in a skill to determine a cognitive state corresponding to a readiness of the first subject for training in the skill, and in dependence thereon, define a neural stimulus pattern, the neural stimulus pattern representing a modulation of a waveform of at least one stimulus of a stimulation device for stimulation of a second subject during performance of the skill, adapted to induce the cognitive state corresponding to readiness for training in the skill in the second subject and effective to improve at least one of learning and performance of the skill by the second subject receiving stimulation with the neural stimulus pattern;at least one of store and output the defined neural stimulus pattern;determine spatial brain wave electrical activity patterns of the second subject over time while subject to the neural stimulus pattern; andcontrol said at least one stimulus selectively dependent on the determined spatial brain wave electrical activity patterns of the second subject over time to adaptively modify the at least one stimulus to synchronize an electrical phase of a representation of the brain wave electrical activity patterns of the first subject while engaged in an activity involving the skill in the at least one stimulus, with the determined spatial brain wave electrical activity patterns of the second subject over time.
  • 14. The apparatus according to claim 13, further comprising the stimulation device, configured to subject the second subject to the neural stimulus pattern adapted to induce the cognitive state corresponding to the readiness for training in the skill in the second subject.
  • 15. The apparatus according to claim 13, wherein the neural stimulus pattern comprises at least one stimulus selected from the group consisting of one or more of a sensory excitation, a peripheral excitation, a transcranial excitation, and a deep brain stimulation.
  • 16. The apparatus according to claim 13, wherein the neural stimulus pattern is responsive to at least a brain wave pattern representing electrical activity of the brain of the second subject prior to application of the stimulation of the second subject.
  • 17. The apparatus according to claim 13, wherein the neural stimulus pattern is adaptive to at least a brain wave pattern representing electrical activity of the brain of the second subject subsequent to initiation of the stimulation of the second subject.
  • 18. The apparatus system according to claim 13, wherein the brain wave patterns representing electrical activity of the brain of the first subject are obtained by a device comprising at least 19 electrodes.
  • 19. The apparatus according to claim 13, wherein the at least one processor is further configured to: determine brain wave patterns selectively associated with the skill and the cognitive state corresponding to the readiness for training in the skill, by analysis of spatial brain wave electrical activity patterns over time of the first subject while preparing for and while being engaged in the skill, anddetermine brain wave patterns of the second subject corresponding to the determined brain wave patterns selectively associated with the skill and the cognitive state corresponding to the readiness for training in the skill of the first subject.
  • 20. The apparatus according to claim 13, wherein the at least one processor comprises at least one single-instruction multiple-data (SIMD) type processor, and is further configured to determine brain wave patterns which represent the cognitive state corresponding to the readiness for training in the skill by analysis of a spatial brain activity pattern over time of the first subject prior to engaging in the skill,the analysis comprising at least one of a statistical analysis and machine learning of the spatial brain activity pattern over time with the at least one single-instruction multiple-data (SIMD) type processor.
  • 21. The apparatus according to claim 20, wherein the at least one processor is further configured to define the neural stimulus pattern by analysis of a spatial brain wave activity pattern over time of the second subject, and translate the determined spatial brain activity pattern over time of the first subject which represent the cognitive state representing the readiness for training in the skill according to at least one transform of the spatial brain wave activity pattern over time of the second subject from a space-time domain, to define the neural stimulus pattern for the second subject to achieve a spatial brain activity pattern over time in the second subject corresponding to the cognitive state representing the readiness for training in the skill.
  • 22. The apparatus according to claim 13, further comprising a memory configured to store a brain wave pattern model, wherein the at least one processor is configured to further define the neural stimulus pattern in dependence on the stored brain activity model.
  • 23. A non-transitory computer-readable medium, storing therein instructions for a programmable processor to automatically perform a process, comprising: instructions for synchronizing brain wave electrical activity data of a first subject with at least one physical activity event involving the first subject;instructions for analyzing the brain wave electrical activity data of the first subject to determine brain activity data over time corresponding to cognitive state representing a readiness for training in the physical activity event;instructions for analyzing the brain activity data to determine a selective change in the brain activity data over time corresponding to the performance of the physical activity event;instructions for determining a stimulation pattern adapted to induce a brain wave electrical activity in a second subject having a correspondence to the brain wave electrical activity data associated with the cognitive state representing the readiness for training in the physical activity event, followed by performance of the physical activity event;instructions for monitoring a spatial brain wave electrical activity in the second subject over time after commencement of the application of the stimulation pattern; andinstructions for adaptively controlling the stimulation pattern dependent on the monitored brain wave electrical activity in the second subject over time, to synchronize an electrical phase timing of a representation of the brain wave electrical activity data of the first subject during performance of the physical activity event in the stimulation pattern with the determined brain wave electrical activity of the second subject.
  • 24. The non-transitory computer-readable medium according to claim 23, further comprising instructions for determining the stimulation pattern further based on at least a brain wave electrical activity model.
  • 25. The non-transitory computer-readable medium according to claim 23, further comprising: instructions for storing data describing a spatial and temporal pattern extracted from the brain wave electrical activity of the first subject, the stored spatial and temporal pattern being adapted for modulation of at least one signal usable as the stimulation pattern for the second subject, to facilitate learning relating to performance of the physical activity event by the second subject after achieving the cognitive state representing the readiness of the second subject for training relating to performance of the physical activity event is achieved in the second subject.
  • 26. The non-transitory computer-readable medium according to claim 23, wherein the physical activity event involves performance of an artistic skill.
  • 27. The non-transitory computer-readable medium according to claim 23, wherein the physical activity event involves performance of a motor skill.
  • 28. The non-transitory computer-readable medium according to claim 23, further comprising: instructions for stimulating the second subject with the determined stimulation pattern to induce the brain activity in the second subject having the correspondence to the brain activity data associated with achieving the cognitive state representing the readiness for training related to performance of the physical activity event, followed by performance of the physical activity event.
  • 29. A method of facilitating a process of learning a physical motor skill, comprising: determining a brain wave electrical activity pattern of a first subject skilled in the physical motor skill comprising a cognitive state representing a readiness for training in the physical motor skill, and while engaged in an activity involving the physical motor skill;processing the brain wave electrical activity pattern of the first subject;subjecting the second subject learning the physical motor skill to a neurostimulation after said processing, comprising a sequence of stimuli selectively dependent on the processed brain wave electrical activity pattern of the first subject, to initially induce in the second subject the brain wave electrical activity pattern corresponding to the cognitive state representing the readiness for training in the physical motor skill, and subsequently the brain wave electrical activity pattern corresponding to a cognitive state representing performance of the activity involving the physical motor skill;controlling said neurostimulation of the second subject, selectively dependent on a concurrent spatial brain wave electrical activity of the second subject over time, to adaptively synchronize an electrical phase of a representation of the brain wave electrical activity patterns of the first subject while engaged in performance of the activity involving the physical motor skill represented in the neurostimulation, with the concurrent brain wave electrical activity patterns of the second subject.
  • 30. An apparatus for facilitating a skill learning process, comprising: means for processing information derived from an electromagnetic brain wave pattern of a first subject while preparing to perform a task involving the skill, comprising a brain wave pattern corresponding to a cognitive state of readiness for training in the task, and subsequently a cognitive state while engaged in performance of the task, and selectively in dependence thereon, define a neural stimulus pattern sequence representing a modulation of a waveform of at least one stimulus for stimulation of a second subject, effective to generate the cognitive state of readiness for training in the task, to improve readiness for training in performance of the task, and subsequently at least one of learning and performance of the task by the second subject receiving stimulation with the neural stimulus pattern;means for controlling the neural stimulus pattern sequence delivered to the second subject, to adaptively synchronize an electrical phase of a representation of the brain wave patterns of the first subject while engaged in the at least one of learning and performance of the task, selectively dependent on concurrent spatial brain wave patterns of the second subject, with the concurrent brain wave patterns of the second subject over time;means for monitoring a spatial brain wave pattern over time of the second subject after commencement of the application of the neural stimulus pattern, and to adapt the neural stimulus pattern based on feedback dependent on the monitored spatial brain wave pattern over time of the second subject; andat least one of:at output port configured to present the defined neural stimulus pattern;a memory configured to store the defined neural stimulus pattern; anda stimulator configured to stimulate the second subject according to the defined neural stimulus pattern.
CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a non-provisional of, and claims benefit of priority from, U.S. Provisional Patent Application No. 62/594,452, filed Dec. 4, 2017, the entirety of which is expressly incorporated herein by reference.

US Referenced Citations (6822)
Number Name Date Kind
3951134 Malech Apr 1976 A
4172014 Sequeira, Jr. et al. Oct 1979 A
4296756 Dunning et al. Oct 1981 A
4367527 Desjacques Jan 1983 A
4407299 Culver Oct 1983 A
4408616 Duffy et al. Oct 1983 A
4421122 Duffy Dec 1983 A
4437064 Overton, Jr. et al. Mar 1984 A
4493327 Bergelson et al. Jan 1985 A
4550736 Broughton et al. Nov 1985 A
4557270 John Dec 1985 A
4562540 Devaney Dec 1985 A
4579125 Strobl et al. Apr 1986 A
4583190 Salb Apr 1986 A
4585011 Broughton et al. Apr 1986 A
4591787 Hoenig May 1986 A
4594662 Devaney Jun 1986 A
4610259 Cohen et al. Sep 1986 A
4613817 Hoenig Sep 1986 A
4649482 Raviv et al. Mar 1987 A
4689559 Hastings et al. Aug 1987 A
4693000 Hoenig Sep 1987 A
4700135 Hoenig Oct 1987 A
4705049 John Nov 1987 A
4733180 Hoenig et al. Mar 1988 A
4736307 Salb Apr 1988 A
4736751 Gevins et al. Apr 1988 A
4744029 Raviv et al. May 1988 A
4749946 Hoenig Jun 1988 A
4753246 Freeman Jun 1988 A
4761611 Hoenig Aug 1988 A
4776345 Cohen et al. Oct 1988 A
4792145 Eisenberg et al. Dec 1988 A
4794533 Cohen Dec 1988 A
4801882 Daalmans Jan 1989 A
4846190 John Jul 1989 A
4862359 Trivedi et al. Aug 1989 A
4883067 Knispel et al. Nov 1989 A
4907597 Chamoun Mar 1990 A
4913152 Ko et al. Apr 1990 A
4924875 Chamoun May 1990 A
4937525 Daalmans Jun 1990 A
4940058 Taff et al. Jul 1990 A
4947480 Lewis Aug 1990 A
4949725 Raviv et al. Aug 1990 A
4951674 Zanakis et al. Aug 1990 A
4974602 Abraham-Fuchs et al. Dec 1990 A
4977505 Pelizzari et al. Dec 1990 A
4982157 Seifert Jan 1991 A
4983912 Roehrlein et al. Jan 1991 A
4996479 Hoenig Feb 1991 A
5008622 Overton, Jr. et al. Apr 1991 A
5010891 Chamoun Apr 1991 A
5012190 Dossel Apr 1991 A
5020538 Morgan et al. Jun 1991 A
5020540 Chamoun Jun 1991 A
5027817 John Jul 1991 A
5029082 Shen et al. Jul 1991 A
5059814 Mead et al. Oct 1991 A
5061680 Paulson et al. Oct 1991 A
5069218 Ikeda Dec 1991 A
5070399 Martel Dec 1991 A
5083571 Prichep Jan 1992 A
5088497 Ikeda Feb 1992 A
5092341 Kelen Mar 1992 A
5092835 Schurig et al. Mar 1992 A
5095270 Ludeke Mar 1992 A
5105354 Nishimura Apr 1992 A
5109862 Kelen et al. May 1992 A
5118606 Lynch et al. Jun 1992 A
5126315 Nishino et al. Jun 1992 A
RE34015 Duffy Aug 1992 E
5136687 Edelman et al. Aug 1992 A
5158932 Hinshaw et al. Oct 1992 A
5159703 Lowery Oct 1992 A
5159928 Keppel Nov 1992 A
5166614 Yokosawa et al. Nov 1992 A
5187327 Ohta et al. Feb 1993 A
5198977 Salb Mar 1993 A
5213338 Brotz May 1993 A
5215086 Terry, Jr. et al. Jun 1993 A
5218530 Jastrzebski et al. Jun 1993 A
5224203 Skeirik Jun 1993 A
5230344 Ozdamar et al. Jul 1993 A
5230346 Leuchter et al. Jul 1993 A
5231988 Wernicke et al. Aug 1993 A
5233517 Jindra Aug 1993 A
5241967 Yasushi et al. Sep 1993 A
5243281 Ahonen et al. Sep 1993 A
5243517 Schmidt et al. Sep 1993 A
5263488 Van Veen et al. Nov 1993 A
5265611 Hoenig et al. Nov 1993 A
5269315 Leuchter et al. Dec 1993 A
5269325 Robinson et al. Dec 1993 A
5273038 Beavin Dec 1993 A
5280791 Lavie Jan 1994 A
5282474 Valdes Sosa et al. Feb 1994 A
5283523 Uhl et al. Feb 1994 A
5287859 John Feb 1994 A
5291888 Tucker Mar 1994 A
5293187 Knapp et al. Mar 1994 A
5299569 Wernicke et al. Apr 1994 A
5303705 Nenov Apr 1994 A
5306228 Rubins Apr 1994 A
5307807 Valdes Sosa et al. May 1994 A
5309095 Ahonen et al. May 1994 A
5309917 Wang et al. May 1994 A
5309923 Leuchter et al. May 1994 A
5311129 Ludwig et al. May 1994 A
5320109 Chamoun et al. Jun 1994 A
5323777 Ahonen et al. Jun 1994 A
5325862 Lewis et al. Jul 1994 A
5326745 Nishino et al. Jul 1994 A
5331970 Gevins et al. Jul 1994 A
5335657 Terry, Jr. et al. Aug 1994 A
5339811 Ohta et al. Aug 1994 A
5339826 Schmidt et al. Aug 1994 A
5343871 Bittman et al. Sep 1994 A
5356368 Monroe Oct 1994 A
5359363 Kuban et al. Oct 1994 A
5377100 Pope et al. Dec 1994 A
5384588 Martin et al. Jan 1995 A
5406956 Farwell Apr 1995 A
5406957 Tansey Apr 1995 A
5409445 Rubins Apr 1995 A
5417211 Abraham-Fuchs et al. May 1995 A
5418512 Ohta et al. May 1995 A
5422689 Knapp et al. Jun 1995 A
5442289 Dilorio et al. Aug 1995 A
5443073 Wang et al. Aug 1995 A
5447154 Cinquin et al. Sep 1995 A
5447166 Gevins Sep 1995 A
5458117 Chamoun et al. Oct 1995 A
5458142 Farmer et al. Oct 1995 A
5459536 Shalon et al. Oct 1995 A
5461699 Arbabi et al. Oct 1995 A
5469057 Robinson Nov 1995 A
5474082 Junker Dec 1995 A
5476438 Edrich et al. Dec 1995 A
5491492 Knapp et al. Feb 1996 A
5496798 Sakai et al. Mar 1996 A
5503149 Beavin Apr 1996 A
5513649 Gevins et al. May 1996 A
5515301 Corby, Jr. et al. May 1996 A
5522863 Spano et al. Jun 1996 A
5546943 Gould Aug 1996 A
5552375 Nishino et al. Sep 1996 A
5555889 Karagueuzian et al. Sep 1996 A
5568816 Gevins et al. Oct 1996 A
5571150 Wernicke et al. Nov 1996 A
5579241 Corby, Jr. et al. Nov 1996 A
5594849 Kuc et al. Jan 1997 A
5600243 Colclough Feb 1997 A
5601081 Tomita et al. Feb 1997 A
5611350 John Mar 1997 A
5617856 Tamura et al. Apr 1997 A
5619995 Lobodzinski Apr 1997 A
5622168 Keusch et al. Apr 1997 A
5626145 Clapp et al. May 1997 A
5632272 Diab et al. May 1997 A
5640493 Skeirik Jun 1997 A
5643325 Karagueuzian et al. Jul 1997 A
5649061 Smyth Jul 1997 A
5650726 Gasnier et al. Jul 1997 A
5656937 Cantor Aug 1997 A
5662109 Hutson Sep 1997 A
5671740 Tomita et al. Sep 1997 A
5678561 Karagueuzian et al. Oct 1997 A
5682889 Tomita et al. Nov 1997 A
5685313 Mayevsky Nov 1997 A
5692517 Junker Dec 1997 A
5694939 Cowings Dec 1997 A
5699808 John Dec 1997 A
5701909 Amir et al. Dec 1997 A
5706402 Bell Jan 1998 A
5706811 Takeda et al. Jan 1998 A
5711305 Swanson et al. Jan 1998 A
5715821 Faupel Feb 1998 A
5719561 Gonzales Feb 1998 A
5720619 Fisslinger Feb 1998 A
5722418 Bro Mar 1998 A
5724987 Gevins et al. Mar 1998 A
5729046 Nishino et al. Mar 1998 A
5730146 Itil et al. Mar 1998 A
5736543 Rogers et al. Apr 1998 A
5737485 Flanagan et al. Apr 1998 A
5740812 Cowan Apr 1998 A
5742748 Sever, Jr. Apr 1998 A
5743854 Dobson et al. Apr 1998 A
5743860 Hively et al. Apr 1998 A
5747492 Lynch et al. May 1998 A
5752514 Okamura et al. May 1998 A
5752521 Dardik May 1998 A
5752911 Canedo et al. May 1998 A
5755227 Tomita et al. May 1998 A
5755739 Sun et al. May 1998 A
5761332 Wischmann et al. Jun 1998 A
5762611 Lewis et al. Jun 1998 A
5767043 Cantor et al. Jun 1998 A
5771261 Anbar Jun 1998 A
5771893 Kassai et al. Jun 1998 A
5771894 Richards et al. Jun 1998 A
5771897 Zufrin Jun 1998 A
5791342 Woodard Aug 1998 A
5794623 Forbes Aug 1998 A
5795304 Sun et al. Aug 1998 A
5797840 Akselrod et al. Aug 1998 A
5797853 Musha et al. Aug 1998 A
5810737 Dardik Sep 1998 A
5813993 Kaplan et al. Sep 1998 A
5815413 Hively et al. Sep 1998 A
5816247 Maynard Oct 1998 A
5825830 Kopf Oct 1998 A
5827195 Lander Oct 1998 A
5840040 Altschuler et al. Nov 1998 A
5842986 Avrin et al. Dec 1998 A
5845639 Hochman et al. Dec 1998 A
5846189 Pincus Dec 1998 A
5846208 Pichlmayr et al. Dec 1998 A
5853005 Scanlon Dec 1998 A
5857978 Hively et al. Jan 1999 A
5859533 Gasnier et al. Jan 1999 A
5871517 Abrams et al. Feb 1999 A
5877801 Martin et al. Mar 1999 A
5884626 Kuroda et al. Mar 1999 A
5885976 Sandyk Mar 1999 A
5891131 Rajan et al. Apr 1999 A
5899867 Collura May 1999 A
5911581 Reynolds et al. Jun 1999 A
5916171 Mayevsky Jun 1999 A
5921245 O'Donnell, Jr. Jul 1999 A
5928272 Adkins et al. Jul 1999 A
5938598 Takeda et al. Aug 1999 A
5938688 Schiff Aug 1999 A
5954662 Swanson et al. Sep 1999 A
5970499 Smith et al. Oct 1999 A
5971923 Finger Oct 1999 A
5983129 Cowan et al. Nov 1999 A
5995868 Dorfmeister et al. Nov 1999 A
5999856 Kennedy Dec 1999 A
6002254 Kassai et al. Dec 1999 A
6002952 Diab et al. Dec 1999 A
6011990 Schultz et al. Jan 2000 A
6011991 Mardirossian Jan 2000 A
6016444 John Jan 2000 A
6021345 Karagueuzian et al. Feb 2000 A
6023161 Dantsker et al. Feb 2000 A
6026173 Svenson et al. Feb 2000 A
6032072 Greenwald et al. Feb 2000 A
6042548 Giuffre Mar 2000 A
6044292 Heyrend et al. Mar 2000 A
6050940 Braun et al. Apr 2000 A
6050962 Kramer et al. Apr 2000 A
6052619 John Apr 2000 A
6053739 Stewart et al. Apr 2000 A
6057846 Sever, Jr. May 2000 A
6066084 Edrich et al. May 2000 A
6067462 Diab et al. May 2000 A
6067467 John May 2000 A
6069369 Nishino et al. May 2000 A
6070098 Moore-Ede et al. May 2000 A
6071246 Sturzebecher et al. Jun 2000 A
6080164 Oshio et al. Jun 2000 A
6081735 Diab et al. Jun 2000 A
6088611 Lauterbur et al. Jul 2000 A
6092058 Smyth Jul 2000 A
6097980 Monastra et al. Aug 2000 A
6097981 Freer Aug 2000 A
6099319 Zaltman et al. Aug 2000 A
6104956 Naritoku et al. Aug 2000 A
6115631 Heyrend et al. Sep 2000 A
6117075 Barnea Sep 2000 A
6129681 Kuroda et al. Oct 2000 A
6132724 Blum Oct 2000 A
6144872 Graetz Nov 2000 A
6149586 Elkind Nov 2000 A
6154026 Dantsker et al. Nov 2000 A
6155966 Parker Dec 2000 A
6155993 Scott Dec 2000 A
6157850 Diab et al. Dec 2000 A
6157857 Dimpfel Dec 2000 A
6161031 Hochman et al. Dec 2000 A
6167298 Levin Dec 2000 A
6167311 Rezai Dec 2000 A
6171239 Humphrey Jan 2001 B1
6171258 Karakasoglu et al. Jan 2001 B1
6182013 Malinverno et al. Jan 2001 B1
6188924 Swanson et al. Feb 2001 B1
6195576 John Feb 2001 B1
6196972 Moehring Mar 2001 B1
6205359 Boveja Mar 2001 B1
6208902 Boveja Mar 2001 B1
6224549 Drongelen May 2001 B1
6226418 Miller et al. May 2001 B1
6230037 Tsukada et al. May 2001 B1
6236872 Diab et al. May 2001 B1
6239145 Utsumi et al. May 2001 B1
6240308 Hardy et al. May 2001 B1
6241686 Balkin et al. Jun 2001 B1
6248126 Lesser et al. Jun 2001 B1
6259399 Krasner Jul 2001 B1
6263189 Reagor Jul 2001 B1
6266453 Hibbard et al. Jul 2001 B1
6269270 Boveja Jul 2001 B1
6272370 Gillies et al. Aug 2001 B1
6280393 Granger et al. Aug 2001 B1
6287328 Snyder et al. Sep 2001 B1
6290638 Canedo et al. Sep 2001 B1
6292688 Patton Sep 2001 B1
6293904 Blazey et al. Sep 2001 B1
6294917 Nichols Sep 2001 B1
6298259 Kucharczyk et al. Oct 2001 B1
6305943 Pougatchev et al. Oct 2001 B1
6306077 Prabhu et al. Oct 2001 B1
6309342 Blazey et al. Oct 2001 B1
6309361 Thornton Oct 2001 B1
6315736 Tsutsumi et al. Nov 2001 B1
6317627 Ennen et al. Nov 2001 B1
6319205 Goor et al. Nov 2001 B1
6322515 Goor et al. Nov 2001 B1
6325475 Hayes et al. Dec 2001 B1
6325761 Jay Dec 2001 B1
6331164 Shaw et al. Dec 2001 B1
6332087 Svenson et al. Dec 2001 B1
6338713 Chamoun et al. Jan 2002 B1
6339725 Naritoku et al. Jan 2002 B1
6341236 Osorio et al. Jan 2002 B1
6343229 Siebler et al. Jan 2002 B1
6354087 Nakahara et al. Mar 2002 B1
6354299 Fischell et al. Mar 2002 B1
6356079 Mizoguchi et al. Mar 2002 B1
6356781 Lee et al. Mar 2002 B1
6356788 Boveja Mar 2002 B2
6358201 Childre et al. Mar 2002 B1
6364845 Duffy et al. Apr 2002 B1
6366813 DiLorenzo Apr 2002 B1
6366814 Boveja et al. Apr 2002 B1
6370414 Robinson Apr 2002 B1
6370423 Guerrero et al. Apr 2002 B1
6374131 Tomita et al. Apr 2002 B1
6375614 Braun et al. Apr 2002 B1
6377833 Albert Apr 2002 B1
6385479 Sibbitt et al. May 2002 B1
6385486 John et al. May 2002 B1
6390979 Njemanze May 2002 B1
6393363 Wilt et al. May 2002 B1
6394963 Blazey et al. May 2002 B1
6402520 Freer Jun 2002 B1
6402689 Scarantino et al. Jun 2002 B1
6408107 Miller et al. Jun 2002 B1
6418344 Rezai et al. Jul 2002 B1
6419629 Balkin et al. Jul 2002 B1
6427086 Fischell et al. Jul 2002 B1
6428490 Kramer et al. Aug 2002 B1
6430443 Karell Aug 2002 B1
6435878 Reynolds et al. Aug 2002 B1
6442421 Le Van Quyen et al. Aug 2002 B1
6442948 Takeda Sep 2002 B1
6466816 Granger et al. Oct 2002 B2
6470220 Kraus, Jr. et al. Oct 2002 B1
6475163 Smits et al. Nov 2002 B1
6482165 Patton et al. Nov 2002 B1
6487441 Swanson et al. Nov 2002 B1
6488617 Katz Dec 2002 B1
6490472 Li et al. Dec 2002 B1
6493577 Williams Dec 2002 B1
6496724 Levendowski et al. Dec 2002 B1
6497658 Roizen et al. Dec 2002 B2
6497699 Ludvig et al. Dec 2002 B1
6503085 Elkind Jan 2003 B1
6507754 Le Van Quyen et al. Jan 2003 B2
6510340 Jordan Jan 2003 B1
6511424 Moore-Ede et al. Jan 2003 B1
6516246 Derakhshan Feb 2003 B2
6520905 Surve et al. Feb 2003 B1
6520921 Patton et al. Feb 2003 B1
6522906 Salisbury, Jr. et al. Feb 2003 B1
6524249 Moehring et al. Feb 2003 B2
6526297 Merilainen Feb 2003 B1
6526415 Smith et al. Feb 2003 B2
6527715 Balkin et al. Mar 2003 B2
6527730 Blazey et al. Mar 2003 B2
6529759 Tucker et al. Mar 2003 B1
6529773 Dewan Mar 2003 B1
6530884 Balkin et al. Mar 2003 B2
6534986 Nichols Mar 2003 B2
6538436 Simola et al. Mar 2003 B1
6539245 Tsukada et al. Mar 2003 B2
6539263 Schiff et al. Mar 2003 B1
6544170 Kajihara et al. Apr 2003 B1
6546378 Cook Apr 2003 B1
6547736 Moehring et al. Apr 2003 B1
6547746 Marino Apr 2003 B1
6549804 Osorio et al. Apr 2003 B1
6551243 Bocionek et al. Apr 2003 B2
6553252 Balkin et al. Apr 2003 B2
6556695 Packer et al. Apr 2003 B1
6556861 Prichep Apr 2003 B1
6556868 Naritoku et al. Apr 2003 B2
6557558 Tajima et al. May 2003 B1
6560486 Osorio et al. May 2003 B1
6565518 Blazey et al. May 2003 B2
6574573 Asano Jun 2003 B1
6587727 Osorio et al. Jul 2003 B2
6587729 O'Loughlin et al. Jul 2003 B2
6591132 Gotman et al. Jul 2003 B2
6591137 Fischell et al. Jul 2003 B1
6594524 Esteller et al. Jul 2003 B2
6597954 Pless et al. Jul 2003 B1
6602202 John et al. Aug 2003 B2
6603502 Martin et al. Aug 2003 B2
6609030 Rezai et al. Aug 2003 B1
6611698 Yamashita et al. Aug 2003 B1
6615158 Wenzel et al. Sep 2003 B2
6616611 Moehring Sep 2003 B1
6622036 Suffin Sep 2003 B1
6622047 Barrett et al. Sep 2003 B2
6625485 Levendowski et al. Sep 2003 B2
6626676 Freer Sep 2003 B2
6633686 Bakircioglu et al. Oct 2003 B1
6644976 Kullok et al. Nov 2003 B2
6648822 Hamamoto et al. Nov 2003 B2
6648880 Chauvet et al. Nov 2003 B2
6650917 Diab et al. Nov 2003 B2
6652458 Blazey et al. Nov 2003 B2
6652470 Patton et al. Nov 2003 B2
6654632 Lange et al. Nov 2003 B2
6654729 Hickman et al. Nov 2003 B1
6656137 Tyldsley et al. Dec 2003 B1
6658287 Litt et al. Dec 2003 B1
6663571 Njemanze Dec 2003 B1
6665552 Yokosawa et al. Dec 2003 B2
6665553 Kandori et al. Dec 2003 B2
6665562 Gluckman et al. Dec 2003 B2
6671555 Gielen et al. Dec 2003 B2
6671556 Osorio et al. Dec 2003 B2
6678548 Echauz et al. Jan 2004 B1
6684098 Oshio et al. Jan 2004 B2
6684105 Cohen et al. Jan 2004 B2
6687525 Llinas et al. Feb 2004 B2
6695761 Oschman et al. Feb 2004 B2
6697660 Robinson Feb 2004 B1
RE38476 Diab et al. Mar 2004 E
6699194 Diab et al. Mar 2004 B1
6701173 Nowinski et al. Mar 2004 B2
6703838 Conti Mar 2004 B2
6708051 Durousseau Mar 2004 B1
6708064 Rezai Mar 2004 B2
6708184 Smith et al. Mar 2004 B2
6709399 Shen et al. Mar 2004 B1
6725080 Melkent et al. Apr 2004 B2
6726624 Keirsbilck et al. Apr 2004 B2
6728424 Zhu et al. Apr 2004 B1
6728564 Lahteenmaki Apr 2004 B2
6731975 Viertio-Oja et al. May 2004 B1
6735460 Tsukada et al. May 2004 B2
6735467 Wilson May 2004 B2
6735475 Whitehurst et al. May 2004 B1
6740032 Balkin et al. May 2004 B2
6743167 Balkin et al. Jun 2004 B2
6743182 Miller et al. Jun 2004 B2
6745060 Diab et al. Jun 2004 B2
6745156 Cook Jun 2004 B2
6746409 Keirsbilck et al. Jun 2004 B2
6751499 Lange et al. Jun 2004 B2
6758813 Meadows Jul 2004 B2
6768920 Lange et al. Jul 2004 B2
6773400 Njemanze Aug 2004 B2
6774929 Kopp Aug 2004 B1
6775405 Zhu Aug 2004 B1
6782292 Whitehurst Aug 2004 B2
6785409 Suri Aug 2004 B1
6788975 Whitehurst et al. Sep 2004 B1
6791331 Conti Sep 2004 B2
6795724 Hogan Sep 2004 B2
6798898 Fedorovskaya et al. Sep 2004 B1
6801648 Cheng Oct 2004 B2
6801803 Viertio-Oja Oct 2004 B2
6804558 Haller et al. Oct 2004 B2
6804661 Cook Oct 2004 B2
6815949 Kandori et al. Nov 2004 B2
6816744 Garfield et al. Nov 2004 B2
6819956 DiLorenzo Nov 2004 B2
6826426 Lange et al. Nov 2004 B2
6843774 Foust et al. Jan 2005 B2
6853186 Li Feb 2005 B2
6856830 He Feb 2005 B2
6863127 Clark et al. Mar 2005 B2
6865494 Duensing et al. Mar 2005 B2
6873872 Gluckman et al. Mar 2005 B2
6875174 Braun et al. Apr 2005 B2
6876196 Taulu et al. Apr 2005 B1
6879859 Boveja Apr 2005 B1
6882881 Lesser et al. Apr 2005 B1
6885192 Clarke et al. Apr 2005 B2
6885886 Bauch et al. Apr 2005 B2
6886964 Gardiner et al. May 2005 B2
6893407 Brooks et al. May 2005 B1
6896655 Patton et al. May 2005 B2
RE38749 Dardik Jun 2005 E
6907280 Becerra et al. Jun 2005 B2
6915241 Kohlmorgen et al. Jul 2005 B2
6920357 Osorio et al. Jul 2005 B2
6926921 Stasiak et al. Aug 2005 B2
6928354 Ryu et al. Aug 2005 B2
6931274 Williams Aug 2005 B2
6931275 Collura Aug 2005 B2
6936012 Wells Aug 2005 B2
6947790 Gevins et al. Sep 2005 B2
6950697 Jordan Sep 2005 B2
6950698 Sarkela et al. Sep 2005 B2
6959215 Gliner et al. Oct 2005 B2
6961618 Osorio et al. Nov 2005 B2
6963770 Scarantino et al. Nov 2005 B2
6963771 Scarantino et al. Nov 2005 B2
6978179 Flagg et al. Dec 2005 B1
6980863 van Venrooij et al. Dec 2005 B2
6981947 Melker Jan 2006 B2
6983184 Price Jan 2006 B2
6983264 Shimizu Jan 2006 B2
6985769 Jordan Jan 2006 B2
6988056 Cook Jan 2006 B2
6990377 Gliner et al. Jan 2006 B2
6993380 Modarres Jan 2006 B1
6996261 deCharms Feb 2006 B2
6996549 Zhang et al. Feb 2006 B2
7003352 Whitehurst Feb 2006 B1
7006872 Gielen et al. Feb 2006 B2
7010340 Scarantino et al. Mar 2006 B2
7010351 Firlik et al. Mar 2006 B2
7011410 Bolger et al. Mar 2006 B2
7011814 Suddarth et al. Mar 2006 B2
7014613 John et al. Mar 2006 B2
7016722 Prichep Mar 2006 B2
7022083 Tanaka et al. Apr 2006 B2
7023206 Viehland et al. Apr 2006 B2
7024247 Gliner et al. Apr 2006 B2
7030617 Conti Apr 2006 B2
7035686 Hogan Apr 2006 B2
7037260 Keirsbilck et al. May 2006 B2
7038450 Romalis et al. May 2006 B2
7039266 Doty May 2006 B1
7039547 Wilson May 2006 B2
7043293 Baura May 2006 B1
7053610 Clarke et al. May 2006 B2
7054454 Causevic et al. May 2006 B2
7062391 Wilson Jun 2006 B2
7063535 Stamm et al. Jun 2006 B2
7070571 Kramer et al. Jul 2006 B2
7079977 Osorio et al. Jul 2006 B2
7089927 John et al. Aug 2006 B2
7092748 Valdes Sosa et al. Aug 2006 B2
7099714 Houben Aug 2006 B2
7104947 Riehl Sep 2006 B2
7104963 Melker et al. Sep 2006 B2
7105824 Stoddart et al. Sep 2006 B2
7107090 Salisbury, Jr. et al. Sep 2006 B2
7116102 Clarke et al. Oct 2006 B2
7117026 Shao et al. Oct 2006 B2
7119553 Yang et al. Oct 2006 B2
7120486 Leuthardt et al. Oct 2006 B2
7123955 Gao et al. Oct 2006 B1
7127100 Wenzel et al. Oct 2006 B2
7128713 Moehring et al. Oct 2006 B2
7130673 Tolvanen-Laakso et al. Oct 2006 B2
7130675 Ewing et al. Oct 2006 B2
7130691 Falci Oct 2006 B2
7145333 Romalis et al. Dec 2006 B2
7146211 Frei et al. Dec 2006 B2
7146217 Firlik et al. Dec 2006 B2
7146218 Esteller et al. Dec 2006 B2
7149572 Frei et al. Dec 2006 B2
7149773 Haller et al. Dec 2006 B2
7150710 Haber et al. Dec 2006 B2
7150715 Collura et al. Dec 2006 B2
7150717 Katura et al. Dec 2006 B2
7150718 Okada et al. Dec 2006 B2
7151961 Whitehurst et al. Dec 2006 B1
7155279 Whitehurst et al. Dec 2006 B2
7163512 Childre et al. Jan 2007 B1
7164941 Misczynski et al. Jan 2007 B2
7167751 Whitehurst et al. Jan 2007 B1
7170294 Kasevich Jan 2007 B2
7171252 Scarantino et al. Jan 2007 B1
7171339 Repucci et al. Jan 2007 B2
7174206 Frei et al. Feb 2007 B2
7176680 Veryaskin Feb 2007 B1
7177675 Suffin et al. Feb 2007 B2
7177678 Osorio et al. Feb 2007 B1
7181505 Haller et al. Feb 2007 B2
7183381 Varadhachary et al. Feb 2007 B2
7184837 Goetz Feb 2007 B2
7186209 Jacobson et al. Mar 2007 B2
7187169 Clarke et al. Mar 2007 B2
7190826 Russell et al. Mar 2007 B2
7190995 Chervin et al. Mar 2007 B2
7193413 Kandori et al. Mar 2007 B2
7196514 Li Mar 2007 B2
7197352 Gott et al. Mar 2007 B2
7199708 Terauchi et al. Apr 2007 B2
7203548 Whitehurst et al. Apr 2007 B2
7207948 Coyle Apr 2007 B2
7209787 DiLorenzo Apr 2007 B2
7209788 Nicolelis et al. Apr 2007 B2
7212851 Donoghue et al. May 2007 B2
7215986 Diab et al. May 2007 B2
7215994 Huiku May 2007 B2
7218104 Clarke et al. May 2007 B2
7221981 Gliner May 2007 B2
7222964 Gotze et al. May 2007 B2
7224282 Terauchi et al. May 2007 B2
7225013 Geva et al. May 2007 B2
7228167 Kara et al. Jun 2007 B2
7228169 Viertio-Oja et al. Jun 2007 B2
7228171 Lesser et al. Jun 2007 B2
7228178 Carroll et al. Jun 2007 B2
7231245 Greenwald et al. Jun 2007 B2
7231254 DiLorenzo Jun 2007 B2
7236830 Gliner Jun 2007 B2
7236831 Firlik et al. Jun 2007 B2
7239731 Semenov et al. Jul 2007 B1
7239926 Goetz Jul 2007 B2
7242983 Frei et al. Jul 2007 B2
7242984 DiLorenzo Jul 2007 B2
7252090 Goetz Aug 2007 B2
7254433 Diab et al. Aug 2007 B2
7254439 Misczynski et al. Aug 2007 B2
7254500 Makeig et al. Aug 2007 B2
7257439 Llinas Aug 2007 B2
7258659 Anninou et al. Aug 2007 B2
7260430 Wu et al. Aug 2007 B2
7267644 Thomas et al. Sep 2007 B2
7267652 Coyle et al. Sep 2007 B2
7269455 Pineda Sep 2007 B2
7269456 Collura Sep 2007 B2
7269516 Brunner et al. Sep 2007 B2
7276916 Hammer Oct 2007 B2
7277758 DiLorenzo Oct 2007 B2
7278966 Hjelt et al. Oct 2007 B2
7280861 Thomas et al. Oct 2007 B2
7280867 Frei et al. Oct 2007 B2
7280870 Nurmikko et al. Oct 2007 B2
7282030 Frei et al. Oct 2007 B2
7283861 Bystritsky Oct 2007 B2
7286871 Cohen Oct 2007 B2
7288066 Drew Oct 2007 B2
7292890 Whitehurst et al. Nov 2007 B2
7295019 Yang et al. Nov 2007 B2
7297110 Goyal et al. Nov 2007 B2
7299088 Thakor et al. Nov 2007 B1
7299096 Balzer et al. Nov 2007 B2
7302298 Lowry et al. Nov 2007 B2
7305268 Gliner et al. Dec 2007 B2
7309315 Kullok et al. Dec 2007 B2
7313442 Velasco et al. Dec 2007 B2
7321837 Osorio et al. Jan 2008 B2
7324845 Mietus et al. Jan 2008 B2
7324851 DiLorenzo Jan 2008 B1
7328053 Diab et al. Feb 2008 B1
7330032 Donnangelo Feb 2008 B2
7333619 Causevic et al. Feb 2008 B2
7333851 Echauz et al. Feb 2008 B2
7334892 Goodall et al. Feb 2008 B2
7338171 Hsieh et al. Mar 2008 B2
7338455 White et al. Mar 2008 B2
7340125 Doty Mar 2008 B1
7340289 Kandori et al. Mar 2008 B2
7343198 Behbehani et al. Mar 2008 B2
7346382 McIntyre et al. Mar 2008 B2
7346395 Lozano et al. Mar 2008 B2
7353064 Gliner et al. Apr 2008 B2
7353065 Morrell Apr 2008 B2
7355597 Laidlaw et al. Apr 2008 B2
7359837 Drew Apr 2008 B2
7363164 Little et al. Apr 2008 B2
7366571 Armstrong Apr 2008 B2
7367807 Pennebaker May 2008 B1
7367949 Korhonen et al. May 2008 B2
7369896 Gesotti May 2008 B2
7371365 Poduslo et al. May 2008 B2
7373198 Bibian et al. May 2008 B2
7376453 Diab et al. May 2008 B1
7376459 Rosenfeld May 2008 B2
7378056 Black May 2008 B2
7381185 Zhirnov et al. Jun 2008 B2
7383070 Diab et al. Jun 2008 B2
7383237 Zhang et al. Jun 2008 B2
7386347 Chung et al. Jun 2008 B2
7389144 Osorio et al. Jun 2008 B1
7392079 Donoghue et al. Jun 2008 B2
7394246 Chieh et al. Jul 2008 B2
7395292 Johnson Jul 2008 B2
7396333 Stahmann et al. Jul 2008 B2
7399282 John et al. Jul 2008 B2
7400984 Kandori et al. Jul 2008 B2
7403809 Tsukada et al. Jul 2008 B2
7403814 Cox et al. Jul 2008 B2
7403815 Katz et al. Jul 2008 B2
7403820 DiLorenzo Jul 2008 B2
7407485 Huiku Aug 2008 B2
7409321 Repucci et al. Aug 2008 B2
7418290 Devlin et al. Aug 2008 B2
7420033 Varadhachary et al. Sep 2008 B2
7422555 Zabara Sep 2008 B2
7429247 Okada et al. Sep 2008 B2
7437196 Wyler et al. Oct 2008 B2
7440789 Hannula et al. Oct 2008 B2
7440806 Whitehurst et al. Oct 2008 B1
7444184 Boveja et al. Oct 2008 B2
7450986 Nguyen et al. Nov 2008 B2
7453263 Kim et al. Nov 2008 B2
7454240 Diab et al. Nov 2008 B2
7454243 Silberstein Nov 2008 B2
7454245 Armstrong et al. Nov 2008 B2
7454387 Abercrombie et al. Nov 2008 B2
7457653 Fujimaki Nov 2008 B2
7457665 Osorio et al. Nov 2008 B1
7461045 Chaovalitwongse et al. Dec 2008 B1
7462151 Childre et al. Dec 2008 B2
7462155 England Dec 2008 B2
7463024 Simola et al. Dec 2008 B2
7463142 Lindsay Dec 2008 B2
7463927 Chaouat Dec 2008 B1
7466132 Clarke et al. Dec 2008 B2
7468040 Hartley et al. Dec 2008 B2
7468350 Gong et al. Dec 2008 B2
7469697 Lee et al. Dec 2008 B2
7471971 Diab et al. Dec 2008 B2
7471978 John et al. Dec 2008 B2
7478108 Townsend et al. Jan 2009 B2
7482298 Nepela Jan 2009 B2
7483747 Gliner et al. Jan 2009 B2
7486986 Osorio et al. Feb 2009 B1
7488294 Torch Feb 2009 B2
7489958 Diab et al. Feb 2009 B2
7489964 Suffin et al. Feb 2009 B2
7490085 Walker et al. Feb 2009 B2
7491173 Heim Feb 2009 B2
7493171 Whitehurst et al. Feb 2009 B1
7493172 Whitehurst et al. Feb 2009 B2
7496393 Diab et al. Feb 2009 B2
7497828 Wilk et al. Mar 2009 B1
7499741 Diab et al. Mar 2009 B2
7499745 Littrup et al. Mar 2009 B2
7499752 Maschino et al. Mar 2009 B2
7499894 Marom et al. Mar 2009 B2
7502720 Taulu Mar 2009 B2
7509154 Diab et al. Mar 2009 B2
7509161 Viertio-Oja Mar 2009 B2
7509163 Luo et al. Mar 2009 B1
7510531 Lee et al. Mar 2009 B2
7510699 Black et al. Mar 2009 B2
7515054 Torch Apr 2009 B2
7530955 Diab et al. May 2009 B2
7537568 Moehring May 2009 B2
7539528 Xiong et al. May 2009 B2
7539532 Tran May 2009 B2
7539533 Tran May 2009 B2
7539543 Schiff et al. May 2009 B2
7547284 Brainard, II Jun 2009 B2
7553810 Gong et al. Jun 2009 B2
7558622 Tran Jul 2009 B2
7559903 Moussavi et al. Jul 2009 B2
7561918 Armstrong et al. Jul 2009 B2
7565193 Laken Jul 2009 B2
7565199 Sheffield et al. Jul 2009 B2
7565200 Wyler et al. Jul 2009 B2
7565809 Takeda Jul 2009 B2
7567693 deCharms Jul 2009 B2
7570054 Lin Aug 2009 B1
7570991 Milgramm et al. Aug 2009 B2
7572225 Stahmann et al. Aug 2009 B2
7573264 Xu et al. Aug 2009 B2
7573268 Volegov et al. Aug 2009 B2
7574007 Shaw et al. Aug 2009 B2
7574254 Milgramm et al. Aug 2009 B2
7577472 Li et al. Aug 2009 B2
7577481 Firlik et al. Aug 2009 B2
7580798 Brunner et al. Aug 2009 B2
7582062 Magill et al. Sep 2009 B2
7583857 Xu et al. Sep 2009 B2
7593767 Modarres Sep 2009 B1
7594122 Milgramm et al. Sep 2009 B2
7594889 St. Ores et al. Sep 2009 B2
7596535 de Voir et al. Sep 2009 B2
7597665 Wilk et al. Oct 2009 B2
7603168 Bibian et al. Oct 2009 B2
7603174 De Ridder Oct 2009 B2
7604603 Sackner et al. Oct 2009 B2
7606405 Sawyer et al. Oct 2009 B2
7608579 Gong et al. Oct 2009 B2
7610083 Drew et al. Oct 2009 B2
7610094 Stahmann et al. Oct 2009 B2
7610096 McDonald, III Oct 2009 B2
7610100 Jaax et al. Oct 2009 B2
7613502 Yamamoto et al. Nov 2009 B2
7613519 De Ridder Nov 2009 B2
7613520 De Ridder Nov 2009 B2
7617002 Goetz Nov 2009 B2
7618381 Krebs et al. Nov 2009 B2
7620455 Maschino Nov 2009 B2
7620456 Gliner et al. Nov 2009 B2
7623912 Akselrod et al. Nov 2009 B2
7623927 Rezai Nov 2009 B2
7623928 DiLorenzo Nov 2009 B2
7624293 Osorio et al. Nov 2009 B2
7625340 Sarkela Dec 2009 B2
7627370 Marks Dec 2009 B2
7629889 Sachanandani et al. Dec 2009 B2
7630757 Dorfmeister et al. Dec 2009 B2
7634317 Ben-David et al. Dec 2009 B2
7640055 Geva et al. Dec 2009 B2
7643655 Liang et al. Jan 2010 B2
7643881 Armstrong Jan 2010 B2
7647097 Flaherty et al. Jan 2010 B2
7647098 Prichep Jan 2010 B2
7648498 Hempel Jan 2010 B2
7649351 Kajola et al. Jan 2010 B2
7653433 Lozano et al. Jan 2010 B2
7654948 Kaplan et al. Feb 2010 B2
7657316 Jaax et al. Feb 2010 B2
7668579 Lynn Feb 2010 B2
7668591 Lee et al. Feb 2010 B2
7670838 Deisseroth et al. Mar 2010 B2
7672707 Takeda Mar 2010 B2
7672717 Zikov et al. Mar 2010 B1
7672730 Firlik et al. Mar 2010 B2
7676263 Harris et al. Mar 2010 B2
7678047 Shiomi et al. Mar 2010 B2
7678061 Lee et al. Mar 2010 B2
7678767 Gong et al. Mar 2010 B2
7680526 McIntyre et al. Mar 2010 B2
7680540 Jensen et al. Mar 2010 B2
7684856 Virtanen et al. Mar 2010 B2
7684858 He et al. Mar 2010 B2
7684866 Fowler et al. Mar 2010 B2
7684867 Jaax et al. Mar 2010 B2
7697979 Martinerie et al. Apr 2010 B2
7702387 Stevenson et al. Apr 2010 B2
7702502 Ricci et al. Apr 2010 B2
7706871 Devlin et al. Apr 2010 B2
7706992 Ricci et al. Apr 2010 B2
7711417 John et al. May 2010 B2
7711432 Thimineur et al. May 2010 B2
7714936 Martin et al. May 2010 B1
7715894 Dunseath et al. May 2010 B2
7715910 Hargrove et al. May 2010 B2
7715919 Osorio et al. May 2010 B2
7720519 Ruohonen May 2010 B2
7720530 Causevic May 2010 B2
7725174 Kern et al. May 2010 B2
7725192 Eskandar et al. May 2010 B2
7727161 Coyle et al. Jun 2010 B2
7729740 Kraus, Jr. et al. Jun 2010 B2
7729753 Kremliovsky et al. Jun 2010 B2
7729755 Laken Jun 2010 B2
7729773 Sloan Jun 2010 B2
7733224 Tran Jun 2010 B2
7733973 Moriya et al. Jun 2010 B2
7734334 Mietus et al. Jun 2010 B2
7734340 De Ridder Jun 2010 B2
7734355 Cohen et al. Jun 2010 B2
7736382 Webb et al. Jun 2010 B2
7737687 Na et al. Jun 2010 B2
7738683 Cahill et al. Jun 2010 B2
7740592 Graham et al. Jun 2010 B2
7742820 Wyler et al. Jun 2010 B2
7746979 Dilmanian et al. Jun 2010 B2
7747318 John et al. Jun 2010 B2
7747325 Dilorenzo Jun 2010 B2
7747326 Velasco et al. Jun 2010 B2
7747551 Snyder Jun 2010 B2
7749155 Anderson et al. Jul 2010 B1
7751877 Flaherty et al. Jul 2010 B2
7751878 Merkle et al. Jul 2010 B1
7753836 Peterchev Jul 2010 B2
7754190 Suffin Jul 2010 B2
7756564 Matsui et al. Jul 2010 B2
7756568 Scarantino et al. Jul 2010 B2
7756584 Sheffield et al. Jul 2010 B2
7757690 Stahmann et al. Jul 2010 B2
7758503 Lynn et al. Jul 2010 B2
7763588 van Praag et al. Jul 2010 B2
7764987 Dorr et al. Jul 2010 B2
7765088 Drew Jul 2010 B2
7766827 Balkin et al. Aug 2010 B2
7769424 Sato Aug 2010 B2
7769431 Scarantino et al. Aug 2010 B2
7769461 Whitehurst et al. Aug 2010 B2
7769464 Gerber et al. Aug 2010 B2
7771341 Rogers Aug 2010 B2
7771364 Arbel et al. Aug 2010 B2
7774052 Burton et al. Aug 2010 B2
7774064 Meyer et al. Aug 2010 B2
7775993 Heruth et al. Aug 2010 B2
7778490 Quist Aug 2010 B2
7778692 Scarantino et al. Aug 2010 B2
7778693 Barbour et al. Aug 2010 B2
7783362 Whitehurst et al. Aug 2010 B2
7787937 Scarantino et al. Aug 2010 B2
7787946 Stahmann et al. Aug 2010 B2
7792575 Fujimaki et al. Sep 2010 B2
7794403 Schaafsma Sep 2010 B2
7794406 Reisfeld et al. Sep 2010 B2
7797040 Pesaran et al. Sep 2010 B2
7800493 Terauchi et al. Sep 2010 B2
7801591 Shusterman Sep 2010 B1
7801592 Shan et al. Sep 2010 B2
7801593 Behbehani et al. Sep 2010 B2
7801601 Maschino et al. Sep 2010 B2
7801686 Hyde et al. Sep 2010 B2
7803118 Reisfeld et al. Sep 2010 B2
7803119 Reisfeld Sep 2010 B2
7804441 DeChiaro, Jr. Sep 2010 B1
7805203 Ben-David et al. Sep 2010 B2
7809433 Keenan Oct 2010 B2
7809434 Kofol et al. Oct 2010 B2
7811279 John Oct 2010 B2
7819794 Becker Oct 2010 B2
7819812 John et al. Oct 2010 B2
7822481 Gerber et al. Oct 2010 B2
D627476 Gaw et al. Nov 2010 S
7829562 Shamloo et al. Nov 2010 B2
7831302 Thomas Nov 2010 B2
7831305 Gliner Nov 2010 B2
7834627 Sakai et al. Nov 2010 B2
7835787 Sajda et al. Nov 2010 B2
7840039 Fuchs Nov 2010 B2
7840248 Fuchs et al. Nov 2010 B2
7840250 Tucker Nov 2010 B2
7840257 Chance Nov 2010 B2
7840280 Parnis et al. Nov 2010 B2
7841986 He et al. Nov 2010 B2
7844324 Sarkela et al. Nov 2010 B2
7848803 Jaax et al. Dec 2010 B1
7852087 Wilt et al. Dec 2010 B2
7853321 Jaax et al. Dec 2010 B2
7853322 Bourget et al. Dec 2010 B2
7853323 Goetz Dec 2010 B2
7853329 DiLorenzo Dec 2010 B2
7856264 Firlik et al. Dec 2010 B2
7860548 McIntyre et al. Dec 2010 B2
7860552 Borsook et al. Dec 2010 B2
7860561 Modarres Dec 2010 B1
7860570 Whitehurst et al. Dec 2010 B2
7863272 Oksenberg et al. Jan 2011 B2
7865234 Modarres Jan 2011 B1
7865235 Le et al. Jan 2011 B2
7865244 Giftakis et al. Jan 2011 B2
7869867 Armstrong et al. Jan 2011 B2
7869884 Scott et al. Jan 2011 B2
7869885 Begnaud et al. Jan 2011 B2
7872235 Rousso et al. Jan 2011 B2
7873411 Eda et al. Jan 2011 B2
7876938 Huang et al. Jan 2011 B2
7878965 Haber et al. Feb 2011 B2
7879043 Meneghini et al. Feb 2011 B2
7881760 Matsui et al. Feb 2011 B2
7881770 Melkent et al. Feb 2011 B2
7881780 Flaherty Feb 2011 B2
7882135 Brunner et al. Feb 2011 B2
7884101 Teegarden et al. Feb 2011 B2
7887493 Stahmann et al. Feb 2011 B2
7890155 Burns et al. Feb 2011 B2
7890176 Jaax et al. Feb 2011 B2
7890185 Cohen et al. Feb 2011 B2
7891814 Harada et al. Feb 2011 B2
7892764 Xiong et al. Feb 2011 B2
7894890 Sun et al. Feb 2011 B2
7894903 John Feb 2011 B2
7895033 Joublin et al. Feb 2011 B2
7896807 Clancy et al. Mar 2011 B2
7899524 Kozel Mar 2011 B2
7899525 John et al. Mar 2011 B2
7899539 Whitehurst et al. Mar 2011 B2
7899545 John Mar 2011 B2
7901211 Pennebaker Mar 2011 B2
7904134 McIntyre et al. Mar 2011 B2
7904139 Chance Mar 2011 B2
7904144 Causevic et al. Mar 2011 B2
7904151 Ben-David et al. Mar 2011 B2
7904175 Scott et al. Mar 2011 B2
7904507 Jung et al. Mar 2011 B2
7907994 Stolarski et al. Mar 2011 B2
7907998 Arad Mar 2011 B2
7908008 Ben-David et al. Mar 2011 B2
7908009 Wyler et al. Mar 2011 B2
7909771 Meyer et al. Mar 2011 B2
7912530 Seki et al. Mar 2011 B2
7917199 Drew et al. Mar 2011 B2
7917206 Frei et al. Mar 2011 B2
7917221 Tass Mar 2011 B2
7917225 Wyler et al. Mar 2011 B2
7918779 Haber et al. Apr 2011 B2
7920914 Shieh et al. Apr 2011 B2
7920915 Mann et al. Apr 2011 B2
7920916 Johnson et al. Apr 2011 B2
7925353 Whitehurst et al. Apr 2011 B1
7929693 Terauchi et al. Apr 2011 B2
7930035 DiLorenzo Apr 2011 B2
7932225 Gong et al. Apr 2011 B2
7933645 Strychacz et al. Apr 2011 B2
7933646 Frei et al. Apr 2011 B2
7933727 Taulu et al. Apr 2011 B2
7937138 Liley May 2011 B2
7937152 Lozano May 2011 B1
7937222 Donadille et al. May 2011 B2
7938782 Stahmann et al. May 2011 B2
7938785 Aguilar et al. May 2011 B2
7941209 Hughes et al. May 2011 B2
7942824 Kayyali et al. May 2011 B1
7944551 Addison et al. May 2011 B2
7945304 Feinberg May 2011 B2
7945316 Giftakis et al. May 2011 B2
7945330 Gliner et al. May 2011 B2
7957796 Maschino Jun 2011 B2
7957797 Bourget et al. Jun 2011 B2
7957806 Stevenson et al. Jun 2011 B2
7957809 Bourget et al. Jun 2011 B2
7961922 Spence et al. Jun 2011 B2
7962204 Suffin et al. Jun 2011 B2
7962214 Byerman et al. Jun 2011 B2
7962219 Jaax et al. Jun 2011 B2
7962220 Kolafa et al. Jun 2011 B2
7970734 Townsend et al. Jun 2011 B2
7972278 Graham et al. Jul 2011 B2
7974688 Armstrong et al. Jul 2011 B2
7974693 Ben-David et al. Jul 2011 B2
7974696 DiLorenzo Jul 2011 B1
7974697 Maschino et al. Jul 2011 B2
7974701 Armstrong Jul 2011 B2
7974787 Hyde et al. Jul 2011 B2
7976465 Frei et al. Jul 2011 B2
7983740 Culver et al. Jul 2011 B2
7983741 Chance Jul 2011 B2
7983757 Miyazawa et al. Jul 2011 B2
7983762 Gliner et al. Jul 2011 B2
7986991 Prichep Jul 2011 B2
7988613 Becker Aug 2011 B2
7988969 Poduslo et al. Aug 2011 B2
7991461 Flaherty et al. Aug 2011 B2
7991477 McDonald, III Aug 2011 B2
7993279 Hartley et al. Aug 2011 B2
7996075 Korzinov et al. Aug 2011 B2
7996079 Armstrong Aug 2011 B2
8000767 Eden et al. Aug 2011 B2
8000773 Rousso et al. Aug 2011 B2
8000788 Giftakis et al. Aug 2011 B2
8000793 Libbus Aug 2011 B2
8000794 Lozano Aug 2011 B2
8000795 Lozano Aug 2011 B2
8001179 Jung et al. Aug 2011 B2
8002553 Hatlestad et al. Aug 2011 B2
8005534 Greenwald et al. Aug 2011 B2
8005624 Starr Aug 2011 B1
8005894 Jung et al. Aug 2011 B2
8010178 Seki et al. Aug 2011 B2
8010347 Ricci et al. Aug 2011 B2
8012107 Einav et al. Sep 2011 B2
8014847 Shastri et al. Sep 2011 B2
8014870 Seidman Sep 2011 B2
8016597 Becker et al. Sep 2011 B2
8019400 Diab et al. Sep 2011 B2
8019410 Bharmi et al. Sep 2011 B1
8024029 Drew et al. Sep 2011 B2
8024032 Osorio et al. Sep 2011 B1
8025404 Bolger et al. Sep 2011 B2
8027730 John Sep 2011 B2
8029553 Nemenov Oct 2011 B2
8031076 Sachanandani et al. Oct 2011 B2
8032209 He et al. Oct 2011 B2
8032229 Gerber et al. Oct 2011 B2
8032486 Townsend et al. Oct 2011 B2
8033996 Behar Oct 2011 B2
8036434 Hewett et al. Oct 2011 B2
8036728 Diab et al. Oct 2011 B2
8036736 Snyder et al. Oct 2011 B2
8036745 Ben-David et al. Oct 2011 B2
8041136 Causevic Oct 2011 B2
8041418 Giftakis et al. Oct 2011 B2
8041419 Giftakis et al. Oct 2011 B2
8046041 Diab et al. Oct 2011 B2
8046042 Diab et al. Oct 2011 B2
8046076 Whitehurst et al. Oct 2011 B2
8050768 Firlik et al. Nov 2011 B2
8055348 Heruth et al. Nov 2011 B2
8055591 Jung et al. Nov 2011 B2
8059879 Tsukimoto Nov 2011 B2
8060181 Rodriguez Ponce et al. Nov 2011 B2
8060194 Flaherty Nov 2011 B2
8064994 Pardo et al. Nov 2011 B2
8065011 Echauz et al. Nov 2011 B2
8065012 Firlik et al. Nov 2011 B2
8065017 Cornejo Cruz et al. Nov 2011 B2
8065240 Jung et al. Nov 2011 B2
8065360 Jung et al. Nov 2011 B2
8066637 Childre et al. Nov 2011 B2
8066647 Armitstead Nov 2011 B2
8068904 Sun et al. Nov 2011 B2
8068911 Giftakis et al. Nov 2011 B2
8069125 Jung et al. Nov 2011 B2
8073534 Low Dec 2011 B2
8073546 Sheffield et al. Dec 2011 B2
8073631 Wilber et al. Dec 2011 B2
8075499 Nathan et al. Dec 2011 B2
8079953 Braun et al. Dec 2011 B2
8082031 Ochs Dec 2011 B2
8082033 Rezai et al. Dec 2011 B2
8082215 Jung et al. Dec 2011 B2
8083786 Gafni et al. Dec 2011 B2
8086294 Echauz et al. Dec 2011 B2
8086296 Bystritsky Dec 2011 B2
8086563 Jung et al. Dec 2011 B2
8088057 Honeycutt et al. Jan 2012 B2
8089283 Kaplan et al. Jan 2012 B2
8090164 Bullitt et al. Jan 2012 B2
8092549 Hillis et al. Jan 2012 B2
8095209 Flaherty Jan 2012 B2
8095210 Burdick et al. Jan 2012 B2
8097926 De Graff et al. Jan 2012 B2
8099299 Sirohey et al. Jan 2012 B2
8103333 Tran Jan 2012 B2
8108033 Drew et al. Jan 2012 B2
8108036 Tran Jan 2012 B2
8108038 Giftakis et al. Jan 2012 B2
8108039 Saliga et al. Jan 2012 B2
8108042 Johnson et al. Jan 2012 B1
8112148 Giftakis et al. Feb 2012 B2
8112153 Giftakis et al. Feb 2012 B2
8114021 Robertson et al. Feb 2012 B2
8116874 Tass Feb 2012 B2
8116877 Lozano Feb 2012 B2
8116883 Williams et al. Feb 2012 B2
8121361 Ernst et al. Feb 2012 B2
8121673 Tran Feb 2012 B2
8121694 Molnar et al. Feb 2012 B2
8121695 Gliner et al. Feb 2012 B2
8126228 Fueyo et al. Feb 2012 B2
8126243 Hamada et al. Feb 2012 B2
8126528 Diab et al. Feb 2012 B2
8126542 Grey Feb 2012 B2
8126567 Gerber et al. Feb 2012 B2
8126568 Gliner Feb 2012 B2
8128572 Diab et al. Mar 2012 B2
8131354 Arad Mar 2012 B2
8131526 Neville Mar 2012 B2
8133172 Shachar et al. Mar 2012 B2
8135472 Fowler et al. Mar 2012 B2
8135957 Dinges et al. Mar 2012 B2
8137269 Sheikhzadeh-Nadjar et al. Mar 2012 B2
8137270 Keenan et al. Mar 2012 B2
8140152 John et al. Mar 2012 B2
8145295 Boyden et al. Mar 2012 B2
8145310 Dong et al. Mar 2012 B2
8148417 Teegarden et al. Apr 2012 B2
8148418 Teegarden et al. Apr 2012 B2
8150508 Craig Apr 2012 B2
8150523 Schiff et al. Apr 2012 B2
8150524 Maschino et al. Apr 2012 B2
8150796 Jung et al. Apr 2012 B2
8152732 Lynn et al. Apr 2012 B2
8155726 Seki et al. Apr 2012 B2
8155736 Sullivan et al. Apr 2012 B2
8160273 Visser et al. Apr 2012 B2
8160317 Amunts et al. Apr 2012 B2
8160680 Boyden et al. Apr 2012 B2
8160689 Jadidi Apr 2012 B2
8160696 Bendett et al. Apr 2012 B2
8165687 Cornejo Cruz et al. Apr 2012 B2
8167784 Honeycutt et al. May 2012 B1
8167826 Oohashi et al. May 2012 B2
8170315 Mistretta et al. May 2012 B2
8170347 Ancelin May 2012 B2
8172759 Bukhman May 2012 B2
8172766 Kayyali et al. May 2012 B1
8174430 DeChiaro, Jr. May 2012 B1
8175359 O'Halloran et al. May 2012 B2
8175360 Razifar et al. May 2012 B2
8175686 Utsugi et al. May 2012 B2
8175696 Liley et al. May 2012 B2
8175700 Johnson et al. May 2012 B2
8177724 Derchak et al. May 2012 B2
8177726 John May 2012 B2
8177727 Kwak May 2012 B2
8180125 Avinash et al. May 2012 B2
8180148 Cover et al. May 2012 B2
8180420 Diab et al. May 2012 B2
8180436 Boyden et al. May 2012 B2
8180601 Butson et al. May 2012 B2
8185186 Ross et al. May 2012 B2
8185207 Molnar et al. May 2012 B2
8185382 Joublin et al. May 2012 B2
8187181 Osorio et al. May 2012 B2
8187201 Lynn May 2012 B2
8188749 Wilt et al. May 2012 B2
8190227 Diab et al. May 2012 B2
8190248 Besio et al. May 2012 B2
8190249 Gharieb et al. May 2012 B1
8190251 Molnar et al. May 2012 B2
8190264 Lozano et al. May 2012 B2
8195295 Stevenson et al. Jun 2012 B2
8195298 Lozano Jun 2012 B2
8195300 Gliner et al. Jun 2012 B2
8195593 Jung et al. Jun 2012 B2
8197395 Jassemidis et al. Jun 2012 B2
8197437 Kalafut et al. Jun 2012 B2
8199982 Fueyo et al. Jun 2012 B2
8199985 Jakobsson et al. Jun 2012 B2
8200319 Pu et al. Jun 2012 B2
8200340 Skelton et al. Jun 2012 B2
8204583 Sackellares et al. Jun 2012 B2
8204603 Maschino Jun 2012 B2
8209009 Giftakis et al. Jun 2012 B2
8209018 Osorio et al. Jun 2012 B2
8209019 Giftakis et al. Jun 2012 B2
8209224 Pradeep et al. Jun 2012 B2
8211035 Melker et al. Jul 2012 B2
8212556 Schwindt et al. Jul 2012 B1
8213670 Lai Jul 2012 B2
8214007 Baker et al. Jul 2012 B2
8214035 Giftakis et al. Jul 2012 B2
8219188 Craig Jul 2012 B2
8221330 Sarkela et al. Jul 2012 B2
8222378 Masure Jul 2012 B2
8223023 Sachanandani et al. Jul 2012 B2
8224431 Drew Jul 2012 B2
8224433 Suffin et al. Jul 2012 B2
8224444 Ben-David et al. Jul 2012 B2
8224451 Jaax et al. Jul 2012 B2
8229540 Sami et al. Jul 2012 B2
8229559 Westendorp et al. Jul 2012 B2
8233682 Fessler et al. Jul 2012 B2
8233689 Razifar et al. Jul 2012 B2
8233965 Bjornerud et al. Jul 2012 B2
8233990 Goetz Jul 2012 B2
8235907 Wilk et al. Aug 2012 B2
8236005 Meneghini et al. Aug 2012 B2
8236038 Nofzinger Aug 2012 B2
8239014 Ochs Aug 2012 B2
8239028 Scott Aug 2012 B2
8239029 De Ridder Aug 2012 B2
8239030 Hagedorn et al. Aug 2012 B1
8241213 Lynn et al. Aug 2012 B2
8244340 Wu et al. Aug 2012 B2
8244341 Hinrikus et al. Aug 2012 B2
8244347 Lozano Aug 2012 B2
8244475 Aguilar et al. Aug 2012 B2
8244552 Firminger et al. Aug 2012 B2
8244553 Firminger et al. Aug 2012 B2
8248069 Buracas Aug 2012 B2
8249316 Hu et al. Aug 2012 B2
8249698 Mugler et al. Aug 2012 B2
8249718 Skelton et al. Aug 2012 B2
8249815 Taylor Aug 2012 B2
8260426 Armstrong et al. Sep 2012 B2
8262714 Hulvershorn et al. Sep 2012 B2
8263574 Schaller et al. Sep 2012 B2
8267851 Kroll Sep 2012 B1
8270814 Pradeep et al. Sep 2012 B2
8271077 Rotenberg Sep 2012 B1
8280502 Hargrove et al. Oct 2012 B2
8280503 Linderman Oct 2012 B2
8280505 Craig Oct 2012 B2
8280514 Lozano et al. Oct 2012 B2
8280517 Skelton et al. Oct 2012 B2
8285351 Johnson et al. Oct 2012 B2
8285368 Chen et al. Oct 2012 B2
8290575 Tarassenko et al. Oct 2012 B2
8290596 Wei et al. Oct 2012 B2
8295914 Kalafut et al. Oct 2012 B2
8295934 Leyde Oct 2012 B2
8295935 Okun et al. Oct 2012 B2
8296108 Tanaka Oct 2012 B2
8298078 Sutton et al. Oct 2012 B2
8298140 Beck-Nielsen et al. Oct 2012 B2
8301222 Rongen et al. Oct 2012 B2
8301232 Albert et al. Oct 2012 B2
8301233 Zhang et al. Oct 2012 B2
8301257 Hsu et al. Oct 2012 B2
8303636 Schiffer Nov 2012 B2
8304246 Cook et al. Nov 2012 B2
8305078 Savukov et al. Nov 2012 B2
8306607 Levi et al. Nov 2012 B1
8306610 Mirow Nov 2012 B2
8306627 Armstrong Nov 2012 B2
8308646 Belohlavek et al. Nov 2012 B2
8308661 Miesel et al. Nov 2012 B2
8311622 Snyder et al. Nov 2012 B2
8311747 Taylor Nov 2012 B2
8311748 Taylor et al. Nov 2012 B2
8311750 Taylor Nov 2012 B2
8313441 Dalton Nov 2012 B2
8314707 Kobetski et al. Nov 2012 B2
8315703 Lozano Nov 2012 B2
8315704 Jaax et al. Nov 2012 B2
8315710 Skelton et al. Nov 2012 B2
8315812 Taylor Nov 2012 B2
8315813 Taylor et al. Nov 2012 B2
8315814 Taylor et al. Nov 2012 B2
8315962 Horne Nov 2012 B1
8315970 Zalay et al. Nov 2012 B2
8320649 Shahaf et al. Nov 2012 B2
8321150 Taylor Nov 2012 B2
8323188 Tran Dec 2012 B2
8323189 Tran et al. Dec 2012 B2
8323204 Stahmann et al. Dec 2012 B2
8326418 Sommer et al. Dec 2012 B2
8326420 Skelton et al. Dec 2012 B2
8326433 Blum et al. Dec 2012 B2
8328718 Tran Dec 2012 B2
8332017 Tarassenko et al. Dec 2012 B2
8332024 Rapoport et al. Dec 2012 B2
8332038 Heruth et al. Dec 2012 B2
8332041 Skelton et al. Dec 2012 B2
8332191 Rosthal et al. Dec 2012 B2
8334690 Kitching et al. Dec 2012 B2
8335561 Modarres Dec 2012 B1
8335664 Eberle Dec 2012 B2
8335715 Pradeep et al. Dec 2012 B2
8335716 Pradeep et al. Dec 2012 B2
8337404 Osorio Dec 2012 B2
8340752 Cox et al. Dec 2012 B2
8340753 Hardt Dec 2012 B2
8340771 Thimineur et al. Dec 2012 B2
8343026 Gardiner et al. Jan 2013 B2
8343027 DiMino et al. Jan 2013 B1
8343066 Eagleman et al. Jan 2013 B1
8346331 Bunce et al. Jan 2013 B2
8346342 Kalafut Jan 2013 B2
8346349 Guttag et al. Jan 2013 B2
8346354 Hyde et al. Jan 2013 B2
8346365 Lozano Jan 2013 B2
8350804 Moll Jan 2013 B1
8352023 John et al. Jan 2013 B2
8352031 Rousso et al. Jan 2013 B2
8353837 John et al. Jan 2013 B2
8354438 Chez Jan 2013 B2
8354881 Denison Jan 2013 B2
8355768 Masmanidis et al. Jan 2013 B2
8356004 Jung et al. Jan 2013 B2
8356594 Ujhazy et al. Jan 2013 B2
8358818 Miga et al. Jan 2013 B2
8359080 Diab et al. Jan 2013 B2
8362780 Rosthal et al. Jan 2013 B2
8364226 Diab et al. Jan 2013 B2
8364254 Jacquin et al. Jan 2013 B2
8364255 Isenhart et al. Jan 2013 B2
8364271 De Ridder Jan 2013 B2
8364272 Goetz Jan 2013 B2
8369940 Sun et al. Feb 2013 B2
8374411 Ernst et al. Feb 2013 B2
8374412 Kimura Feb 2013 B2
8374690 Ma Feb 2013 B2
8374696 Sanchez et al. Feb 2013 B2
8374701 Hyde et al. Feb 2013 B2
8374703 Imran Feb 2013 B2
8376965 Schuette et al. Feb 2013 B2
8379947 Garg et al. Feb 2013 B2
8379952 McIntyre et al. Feb 2013 B2
8380289 Zellers et al. Feb 2013 B2
8380290 Scarantino et al. Feb 2013 B2
8380296 Lee et al. Feb 2013 B2
8380314 Panken et al. Feb 2013 B2
8380316 Hagedorn et al. Feb 2013 B2
8380658 Jung et al. Feb 2013 B2
8382667 Osorio Feb 2013 B2
8386188 Taylor et al. Feb 2013 B2
8386244 Ricci et al. Feb 2013 B2
8386312 Pradeep et al. Feb 2013 B2
8386313 Pradeep et al. Feb 2013 B2
RE44097 Wilber et al. Mar 2013 E
8388529 Fueyo et al. Mar 2013 B2
8388530 Shusterman Mar 2013 B2
8388555 Panken et al. Mar 2013 B2
8391942 Benni Mar 2013 B2
8391956 Zellers et al. Mar 2013 B2
8391966 Luo et al. Mar 2013 B2
8392250 Pradeep et al. Mar 2013 B2
8392251 Pradeep et al. Mar 2013 B2
8392253 Pradeep et al. Mar 2013 B2
8392254 Pradeep et al. Mar 2013 B2
8392255 Pradeep et al. Mar 2013 B2
8396542 Johnson et al. Mar 2013 B2
8396545 Berridge et al. Mar 2013 B2
8396546 Hirata et al. Mar 2013 B2
8396557 DiLorenzo Mar 2013 B2
8396565 Singhal et al. Mar 2013 B2
8396744 Pradeep et al. Mar 2013 B2
8398692 Deisseroth et al. Mar 2013 B2
8401624 Govari Mar 2013 B2
8401626 Mietus et al. Mar 2013 B2
8401634 Whitehurst et al. Mar 2013 B2
8401654 Foster et al. Mar 2013 B1
8401655 De Ridder Mar 2013 B2
8401666 Skelton et al. Mar 2013 B2
8403848 Mietus et al. Mar 2013 B2
8406838 Kato Mar 2013 B2
8406841 Lin et al. Mar 2013 B2
8406848 Wu et al. Mar 2013 B2
8406862 Hopenfeld Mar 2013 B2
8406890 Goetz Mar 2013 B2
8412334 Whitehurst et al. Apr 2013 B2
8412335 Gliner et al. Apr 2013 B2
8412337 Lozano Apr 2013 B2
8412338 Faltys Apr 2013 B2
8412655 Colman et al. Apr 2013 B2
8415123 Pilla et al. Apr 2013 B2
8417344 Colborn et al. Apr 2013 B2
8423118 Wenzel et al. Apr 2013 B2
8423125 Rousso et al. Apr 2013 B2
8423144 Tass et al. Apr 2013 B2
8423155 Jaax et al. Apr 2013 B1
8423297 Wilber Apr 2013 B2
8425415 Tran Apr 2013 B2
8425583 Nofzinger Apr 2013 B2
8428696 Foo Apr 2013 B2
8428703 Hopenfeld Apr 2013 B2
8428704 Johnson et al. Apr 2013 B2
8428726 Ignagni et al. Apr 2013 B2
8429225 Jung et al. Apr 2013 B2
8430805 Burnett et al. Apr 2013 B2
8430816 Avinash et al. Apr 2013 B2
8431537 Gong et al. Apr 2013 B2
8433388 Blunt et al. Apr 2013 B2
8433410 Stevenson et al. Apr 2013 B2
8433414 Gliner et al. Apr 2013 B2
8433418 DeRidder Apr 2013 B2
8435166 Burnett et al. May 2013 B2
8437843 Kayyali et al. May 2013 B1
8437844 Syed Momen et al. May 2013 B2
8437861 Skelton et al. May 2013 B2
8439845 Folkerts et al. May 2013 B2
8442626 Zavoronkovs et al. May 2013 B2
8444571 Folkerts et al. May 2013 B2
8445021 Akhtari et al. May 2013 B2
8445851 Rousso et al. May 2013 B2
8447392 Llinas May 2013 B2
8447407 Talathi et al. May 2013 B2
8447411 Skelton et al. May 2013 B2
8449471 Tran May 2013 B2
8452387 Osorio et al. May 2013 B2
8452544 Hymel May 2013 B2
8454555 Struijk et al. Jun 2013 B2
8456164 Subbarao Jun 2013 B2
8456166 DePavia et al. Jun 2013 B2
8456309 Sachanandani et al. Jun 2013 B2
8457730 Makinen Jun 2013 B2
8457746 Libbus Jun 2013 B2
8457747 Terry, Jr. Jun 2013 B2
8461988 Tran Jun 2013 B2
8463006 Prokoski Jun 2013 B2
8463007 Steinberg et al. Jun 2013 B2
8463349 Diab et al. Jun 2013 B2
8463370 Korhonen et al. Jun 2013 B2
8463374 Hudson et al. Jun 2013 B2
8463378 Tass Jun 2013 B2
8463386 Tass Jun 2013 B2
8463387 De Ridder Jun 2013 B2
8464288 Pradeep et al. Jun 2013 B2
8465408 Phillips et al. Jun 2013 B2
8467877 Imran Jun 2013 B2
8467878 Lozano et al. Jun 2013 B2
8473024 Causevic et al. Jun 2013 B2
8473044 Lee et al. Jun 2013 B2
8473306 Seely Jun 2013 B2
8473345 Pradeep et al. Jun 2013 B2
8475354 Phillips et al. Jul 2013 B2
8475368 Tran et al. Jul 2013 B2
8475371 Derchak et al. Jul 2013 B2
8475387 Derchak et al. Jul 2013 B2
8475506 Bendett et al. Jul 2013 B1
8478389 Brockway et al. Jul 2013 B1
8478394 Prichep et al. Jul 2013 B2
8478402 Wahlstrand et al. Jul 2013 B2
8478417 Drew et al. Jul 2013 B2
8478428 Cowley Jul 2013 B2
8480554 Phillips et al. Jul 2013 B2
8483795 Okada Jul 2013 B2
8483815 Liley Jul 2013 B2
8483816 Payton et al. Jul 2013 B1
8484081 Pradeep et al. Jul 2013 B2
8484270 Kurtz et al. Jul 2013 B2
8485979 Giftakis et al. Jul 2013 B2
8487760 Kangas et al. Jul 2013 B2
8489185 Kilgard et al. Jul 2013 B2
8492336 Masure Jul 2013 B2
8494610 Pradeep et al. Jul 2013 B2
8494829 Teixeira Jul 2013 B2
8494857 Pakhomov Jul 2013 B2
8494905 Pradeep et al. Jul 2013 B2
8496594 Taylor et al. Jul 2013 B2
8498697 Yong et al. Jul 2013 B2
8498699 Wells et al. Jul 2013 B2
8498708 Bentwich Jul 2013 B2
RE44408 Lindsay Aug 2013 E
8500282 Bolger et al. Aug 2013 B2
8500636 Tran Aug 2013 B2
8504150 Skelton Aug 2013 B2
8506469 Dietrich et al. Aug 2013 B2
8509879 Durkin et al. Aug 2013 B2
8509881 Thiagarajan et al. Aug 2013 B2
8509885 Snyder et al. Aug 2013 B2
8509904 Rickert et al. Aug 2013 B2
8512219 Ferren et al. Aug 2013 B2
8512221 Kaplan et al. Aug 2013 B2
8512240 Zuckerman-Stark et al. Aug 2013 B1
8515535 Hopper et al. Aug 2013 B2
8515538 Osorio et al. Aug 2013 B1
8515541 Jaax et al. Aug 2013 B1
8515549 Panken et al. Aug 2013 B2
8515550 Skelton et al. Aug 2013 B2
8517909 Honeycutt et al. Aug 2013 B2
8517912 Clare Aug 2013 B2
8519705 Savukov et al. Aug 2013 B2
8519853 Eskandarian et al. Aug 2013 B2
8520974 Fujita et al. Aug 2013 B2
8521284 Kim et al. Aug 2013 B2
8523779 Taylor et al. Sep 2013 B2
8525673 Tran Sep 2013 B2
8525687 Tran Sep 2013 B2
8527029 Okada Sep 2013 B2
8527035 Diamond Sep 2013 B2
8527435 Han et al. Sep 2013 B1
8529463 Della Santina et al. Sep 2013 B2
8531291 Tran Sep 2013 B2
8532756 Schalk et al. Sep 2013 B2
8532757 Molnar et al. Sep 2013 B2
8533042 Pradeep et al. Sep 2013 B2
8536667 de Graff et al. Sep 2013 B2
8538108 Shekhar et al. Sep 2013 B2
8538512 Bibian et al. Sep 2013 B1
8538513 Molnar et al. Sep 2013 B2
8538514 Sun et al. Sep 2013 B2
8538523 Sommer et al. Sep 2013 B2
8538536 Rezai et al. Sep 2013 B2
8538543 McIntyre et al. Sep 2013 B2
8538700 Badri et al. Sep 2013 B2
8538705 Greenwald Sep 2013 B2
8542900 Tolkowsky et al. Sep 2013 B2
8542916 Tognoli et al. Sep 2013 B2
8543189 Paitel et al. Sep 2013 B2
8543199 Snyder et al. Sep 2013 B2
8543214 Osorio et al. Sep 2013 B2
8543219 Tass Sep 2013 B2
8545378 Peterchev Oct 2013 B2
8545416 Kayyali et al. Oct 2013 B1
8545420 Einav et al. Oct 2013 B2
8545436 Robertson et al. Oct 2013 B2
8548583 Rousso et al. Oct 2013 B2
8548594 Thimineur et al. Oct 2013 B2
8548604 Whitehurst et al. Oct 2013 B2
8548786 Plenz Oct 2013 B2
8548852 Pradeep et al. Oct 2013 B2
8553956 Wu et al. Oct 2013 B2
8554311 Warner et al. Oct 2013 B2
8554325 Molnar et al. Oct 2013 B2
8559645 Corona-Strauss et al. Oct 2013 B2
8560034 Diab et al. Oct 2013 B1
8560041 Flaherty et al. Oct 2013 B2
8560073 Osorio Oct 2013 B2
8562525 Nakashima et al. Oct 2013 B2
8562526 Heneghan et al. Oct 2013 B2
8562527 Braun et al. Oct 2013 B2
8562536 Osorio et al. Oct 2013 B2
8562540 Goodall et al. Oct 2013 B2
8562548 Shimada et al. Oct 2013 B2
8562660 Peyman Oct 2013 B2
8562951 Suffin et al. Oct 2013 B2
8565606 Kim et al. Oct 2013 B2
8565864 Drew et al. Oct 2013 B2
8565867 Armstrong et al. Oct 2013 B2
8565883 Lozano Oct 2013 B2
8565886 Nelson et al. Oct 2013 B2
8568231 Solanki et al. Oct 2013 B2
8568329 Lee et al. Oct 2013 B2
8571293 Ernst et al. Oct 2013 B2
8571629 Faro et al. Oct 2013 B2
8571642 Gill et al. Oct 2013 B2
8571643 Osorio et al. Oct 2013 B2
8571653 Ben-David et al. Oct 2013 B2
8574164 Mashiach Nov 2013 B2
8574279 Schiffer Nov 2013 B2
8577103 Vija et al. Nov 2013 B2
8577464 Mashiach Nov 2013 B2
8577465 Mashiach Nov 2013 B2
8577466 Mashiach Nov 2013 B2
8577467 Mashiach et al. Nov 2013 B2
8577468 Mashiach et al. Nov 2013 B2
8577472 Mashiach et al. Nov 2013 B2
8577478 Mashiach et al. Nov 2013 B2
8579786 Osorio et al. Nov 2013 B2
8579793 Honeycutt et al. Nov 2013 B1
8579795 Martel Nov 2013 B2
8579834 Davis et al. Nov 2013 B2
8583238 Heldman et al. Nov 2013 B1
8583252 Skelton et al. Nov 2013 B2
8585568 Phillips et al. Nov 2013 B2
8586019 Satchi-Fainaro et al. Nov 2013 B2
8586932 Rousso et al. Nov 2013 B2
8587304 Budker et al. Nov 2013 B2
8588486 Virtue et al. Nov 2013 B2
8588552 Garg et al. Nov 2013 B2
8588899 Schiff Nov 2013 B2
8588929 Skelton et al. Nov 2013 B2
8588933 Floyd et al. Nov 2013 B2
8588941 Mashiach Nov 2013 B2
8589316 Lujan et al. Nov 2013 B2
8591419 Tyler Nov 2013 B2
8591498 John Nov 2013 B2
8593141 Radparvar et al. Nov 2013 B1
8593154 Ross Nov 2013 B2
8594798 Osorio et al. Nov 2013 B2
8594800 Butson et al. Nov 2013 B2
8594950 Taylor Nov 2013 B2
8597171 Altman et al. Dec 2013 B2
8597193 Grunwald et al. Dec 2013 B2
8600493 Tanner et al. Dec 2013 B2
8600502 Lovett et al. Dec 2013 B2
8600513 Aur et al. Dec 2013 B2
8600521 Armstrong et al. Dec 2013 B2
8600696 Zafiris Dec 2013 B2
8603790 Deisseroth et al. Dec 2013 B2
8606349 Rousso et al. Dec 2013 B2
8606351 Wheeler Dec 2013 B2
8606356 Lee et al. Dec 2013 B2
8606360 Butson et al. Dec 2013 B2
8606361 Gliner et al. Dec 2013 B2
8606530 Taylor Dec 2013 B2
8606592 Hyde et al. Dec 2013 B2
8612005 Rezai et al. Dec 2013 B2
8613695 Von Ohlsen et al. Dec 2013 B2
8613905 El-Agnaf Dec 2013 B2
8614254 Llinas et al. Dec 2013 B2
8614873 Beran Dec 2013 B1
8615293 Jacobson et al. Dec 2013 B2
8615309 Craig Dec 2013 B2
8615479 Jung et al. Dec 2013 B2
8615664 Jung et al. Dec 2013 B2
8618799 Radparvar et al. Dec 2013 B1
8620206 Brown et al. Dec 2013 B2
8620419 Rotenberg et al. Dec 2013 B2
8626264 Beran Jan 2014 B1
8626301 Libbus Jan 2014 B2
8628328 Palacios Jan 2014 B2
8628480 Derchak Jan 2014 B2
8630699 Baker et al. Jan 2014 B2
8630705 Mann et al. Jan 2014 B2
8630812 Taylor Jan 2014 B2
8632465 Brockway Jan 2014 B1
8632750 Suffin et al. Jan 2014 B2
8634616 Den Harder et al. Jan 2014 B2
8634922 Osorio et al. Jan 2014 B1
8635105 Pradeep et al. Jan 2014 B2
8636640 Chang Jan 2014 B2
8638950 Anderson et al. Jan 2014 B2
8641632 Quintin et al. Feb 2014 B2
8641646 Colborn Feb 2014 B2
8644754 Brown Feb 2014 B2
8644910 Rousso et al. Feb 2014 B2
8644914 Hunt Feb 2014 B2
8644921 Wilson Feb 2014 B2
8644945 Skelton et al. Feb 2014 B2
8644946 Butson et al. Feb 2014 B2
8644954 Jaax et al. Feb 2014 B2
8644957 Mashiach Feb 2014 B2
8647278 Ji et al. Feb 2014 B2
8648017 Umansky et al. Feb 2014 B2
8649845 McIntyre et al. Feb 2014 B2
8649866 Brooke Feb 2014 B2
8649871 Frei et al. Feb 2014 B2
8652038 Tran et al. Feb 2014 B2
8652187 Wells et al. Feb 2014 B2
8652189 Gafni et al. Feb 2014 B2
8655428 Pradeep et al. Feb 2014 B2
8655437 Pradeep et al. Feb 2014 B2
8655817 Hasey et al. Feb 2014 B2
8657732 Vasishta Feb 2014 B2
8657756 Stahmann et al. Feb 2014 B2
8658149 Satchi-Fainaro et al. Feb 2014 B2
8660642 Ferren et al. Feb 2014 B2
8660649 Ruffini et al. Feb 2014 B2
8660666 Craig Feb 2014 B2
8660799 Watson et al. Feb 2014 B2
8664258 Teegarden et al. Mar 2014 B2
8666099 Nielsen et al. Mar 2014 B2
8666467 Lynn et al. Mar 2014 B2
8666478 LaViolette et al. Mar 2014 B2
8666501 Kilgard et al. Mar 2014 B2
8668496 Nolen Mar 2014 B2
8670603 Tolkowsky et al. Mar 2014 B2
8672852 Gavish Mar 2014 B2
8675936 Vija et al. Mar 2014 B2
8675945 Barnhorst et al. Mar 2014 B2
8675983 Yahil Mar 2014 B2
8676324 Simon et al. Mar 2014 B2
8676325 Lindenthaler et al. Mar 2014 B2
8676330 Simon et al. Mar 2014 B2
8679009 Osorio Mar 2014 B2
8680119 Teegarden et al. Mar 2014 B2
8680991 Tran Mar 2014 B2
8682422 Hopenfeld Mar 2014 B2
8682441 De Ridder Mar 2014 B2
8682449 Simon Mar 2014 B2
8682687 Hyde et al. Mar 2014 B2
8684742 Siefert Apr 2014 B2
8684900 Tran Apr 2014 B2
8684921 Osorio Apr 2014 B2
8684922 Tran Apr 2014 B2
8684926 Arndt Apr 2014 B2
8688209 Verbitskiy Apr 2014 B2
8690748 Fu Apr 2014 B1
8693756 Tolkowsky et al. Apr 2014 B2
8693765 Mercier et al. Apr 2014 B2
8694087 Schiff Apr 2014 B2
8694089 Arad Apr 2014 B2
8694092 Ferren et al. Apr 2014 B2
8694107 Falci Apr 2014 B2
8694118 Armstrong Apr 2014 B2
8694157 Wenderow et al. Apr 2014 B2
8696722 Deisseroth et al. Apr 2014 B2
8696724 Rogers Apr 2014 B2
8698639 Fung et al. Apr 2014 B2
8700137 Albert Apr 2014 B2
8700141 Causevic Apr 2014 B2
8700142 John et al. Apr 2014 B2
8700163 Terry, Jr. et al. Apr 2014 B2
8700167 Sabel Apr 2014 B2
8700174 Skelton et al. Apr 2014 B2
8700183 Mashiach Apr 2014 B2
8703114 Satchi-Fainaro et al. Apr 2014 B2
8706183 Cui et al. Apr 2014 B2
8706205 Shahaf et al. Apr 2014 B2
8706206 Kanai et al. Apr 2014 B2
8706207 Flint Apr 2014 B2
8706237 Giftakis et al. Apr 2014 B2
8706241 Firlik et al. Apr 2014 B2
8706518 Hyde et al. Apr 2014 B2
8708903 Tran Apr 2014 B2
8708934 Skelton et al. Apr 2014 B2
8711655 Gzara et al. Apr 2014 B2
8712507 Cazares et al. Apr 2014 B2
8712512 Doidge et al. Apr 2014 B2
8712513 Modarres Apr 2014 B1
8712547 Whitehurst et al. Apr 2014 B2
8716447 Deisseroth et al. May 2014 B2
8717430 Simon et al. May 2014 B2
8718747 Bjornerud et al. May 2014 B2
8718776 Mashiach et al. May 2014 B2
8718777 Lowry et al. May 2014 B2
8718779 Whitehurst et al. May 2014 B2
8721695 Tass et al. May 2014 B2
8724871 Biagiotti et al. May 2014 B1
8725238 Liu et al. May 2014 B2
8725243 Dilorenzo et al. May 2014 B2
8725311 Breed May 2014 B1
8725668 Georgopoulos May 2014 B2
8725669 Fu May 2014 B1
8725796 Serena May 2014 B2
8727978 Tran et al. May 2014 B2
8728001 Lynn May 2014 B2
8729040 Deisseroth et al. May 2014 B2
8731650 Sajda et al. May 2014 B2
8731656 Bourget et al. May 2014 B2
8731987 Chen et al. May 2014 B2
8733290 Gerashchenko May 2014 B2
8734356 Taylor May 2014 B2
8734357 Taylor May 2014 B2
8734498 DiMauro et al. May 2014 B2
8738121 Virag et al. May 2014 B2
8738126 Craig May 2014 B2
8738136 Frei et al. May 2014 B2
8738140 De Ridder May 2014 B2
8738395 Hyde et al. May 2014 B2
8744562 Giftakis et al. Jun 2014 B2
8744563 Yoshida Jun 2014 B2
8747313 Tran et al. Jun 2014 B2
8747336 Tran Jun 2014 B2
8747382 D'Souza et al. Jun 2014 B2
8750971 Tran Jun 2014 B2
8750974 Baker et al. Jun 2014 B2
8750992 Hopper et al. Jun 2014 B2
8751008 Carlton et al. Jun 2014 B2
8751011 Skelton et al. Jun 2014 B2
8753296 Einav et al. Jun 2014 B2
8754238 Teegarden et al. Jun 2014 B2
8755854 Addison et al. Jun 2014 B2
8755856 Diab et al. Jun 2014 B2
8755868 Yazicioglu Jun 2014 B2
8755869 Zhang et al. Jun 2014 B2
8755871 Weng et al. Jun 2014 B2
8755877 Zoica Jun 2014 B2
8755901 Skelton et al. Jun 2014 B2
8756017 Hu et al. Jun 2014 B2
8758274 Sahasrabudhe et al. Jun 2014 B2
8761438 Lee et al. Jun 2014 B2
8761866 Chance Jun 2014 B2
8761868 Giftakis et al. Jun 2014 B2
8761869 Leuthardt et al. Jun 2014 B2
8761889 Wingeier et al. Jun 2014 B2
8762065 DiLorenzo Jun 2014 B2
8762202 Pradeep et al. Jun 2014 B2
8764651 Tran Jul 2014 B2
8764652 Lee et al. Jul 2014 B2
8764653 Kaminska et al. Jul 2014 B2
8764673 McCraty et al. Jul 2014 B2
8768022 Miga et al. Jul 2014 B2
8768427 Sjaaheim et al. Jul 2014 B2
8768431 Ross et al. Jul 2014 B2
8768446 Drew et al. Jul 2014 B2
8768447 Ermes et al. Jul 2014 B2
8768449 Pesaran et al. Jul 2014 B2
8768471 Colborn et al. Jul 2014 B2
8768477 Spitzer et al. Jul 2014 B2
8768718 Cazares et al. Jul 2014 B2
8771194 John et al. Jul 2014 B2
8774923 Rom Jul 2014 B2
8775340 Waxman et al. Jul 2014 B2
8781193 Steinberg et al. Jul 2014 B2
8781197 Wang et al. Jul 2014 B2
8781557 Dean et al. Jul 2014 B2
8781563 Foo Jul 2014 B2
8781595 Grevious et al. Jul 2014 B2
8781597 DiLorenzo Jul 2014 B2
8781796 Mott et al. Jul 2014 B2
8784109 Gottfried Jul 2014 B2
8784322 Kim et al. Jul 2014 B2
8785441 Teegarden et al. Jul 2014 B2
8786624 Echauz et al. Jul 2014 B2
8787637 Duchesnay et al. Jul 2014 B2
8788030 Payton et al. Jul 2014 B1
8788033 Rossi Jul 2014 B2
8788044 John Jul 2014 B2
8788055 Gerber et al. Jul 2014 B2
8788057 Stevenson et al. Jul 2014 B2
8790255 Behar Jul 2014 B2
8790272 Sackner et al. Jul 2014 B2
8790297 Bromander et al. Jul 2014 B2
8792972 Zaidel et al. Jul 2014 B2
8792974 Rothman Jul 2014 B2
8792991 Gerber et al. Jul 2014 B2
8795175 Funane et al. Aug 2014 B2
8798717 Roscher Aug 2014 B2
8798728 Drew et al. Aug 2014 B2
8798735 Bibian et al. Aug 2014 B1
8798736 Sullivan et al. Aug 2014 B2
8798773 Mashiach Aug 2014 B2
8801620 Melker et al. Aug 2014 B2
8805516 Bentwich Aug 2014 B2
8805518 King et al. Aug 2014 B2
8812126 Butson et al. Aug 2014 B2
8812237 Wilt et al. Aug 2014 B2
8812245 Taylor Aug 2014 B2
8812246 Taylor Aug 2014 B2
8814923 Nissila et al. Aug 2014 B2
8815582 Deisseroth et al. Aug 2014 B2
8821376 Tolkowsky Sep 2014 B2
8821408 Hu et al. Sep 2014 B2
8821559 DiMauro et al. Sep 2014 B2
8825149 Kraus et al. Sep 2014 B2
8825166 John Sep 2014 B2
8825167 Tass et al. Sep 2014 B2
8825428 Addison et al. Sep 2014 B2
8827912 Bukhman Sep 2014 B2
8827917 Watson et al. Sep 2014 B2
8829908 Roshtal et al. Sep 2014 B2
8831705 Dobak Sep 2014 B2
8831731 Blum et al. Sep 2014 B2
8831732 Frei et al. Sep 2014 B2
8834392 Panken et al. Sep 2014 B2
8834546 Deisseroth et al. Sep 2014 B2
8838201 Mori et al. Sep 2014 B2
8838225 Ahonen et al. Sep 2014 B2
8838226 Bibian et al. Sep 2014 B2
8838227 Causevic et al. Sep 2014 B2
8838247 Hagedorn et al. Sep 2014 B2
8843199 Kim et al. Sep 2014 B2
8843201 Heldman et al. Sep 2014 B1
8843210 Simon et al. Sep 2014 B2
8845545 Folkerts et al. Sep 2014 B2
8849390 Echauz et al. Sep 2014 B2
8849392 Lozano Sep 2014 B2
8849407 Danilov et al. Sep 2014 B1
8849409 Colborn et al. Sep 2014 B2
8849632 Sparks et al. Sep 2014 B2
8849681 Hargrove et al. Sep 2014 B2
8852073 Genereux et al. Oct 2014 B2
8852100 Osorio Oct 2014 B2
8852103 Rothberg et al. Oct 2014 B2
8855758 Rodriquez-Villegas et al. Oct 2014 B2
8855773 Kokones et al. Oct 2014 B2
8855775 Leyde Oct 2014 B2
8858440 Tyler Oct 2014 B2
8858449 Inan et al. Oct 2014 B2
8861819 Lee et al. Oct 2014 B2
8862196 Lynn Oct 2014 B2
8862210 Yazicioglu et al. Oct 2014 B2
8862236 Wolpaw et al. Oct 2014 B2
8862581 Zhang et al. Oct 2014 B2
8864310 Gross et al. Oct 2014 B2
8864806 Wells et al. Oct 2014 B2
8868148 Engelbrecht et al. Oct 2014 B2
8868163 Guttag et al. Oct 2014 B2
8868172 Leyde et al. Oct 2014 B2
8868173 Nelson et al. Oct 2014 B2
8868174 Sato et al. Oct 2014 B2
8868175 Arad Oct 2014 B2
8868177 Simon et al. Oct 2014 B2
8868189 Stevenson et al. Oct 2014 B2
8868201 Roberts et al. Oct 2014 B2
8870737 Phillips et al. Oct 2014 B2
8871797 Teegarden et al. Oct 2014 B2
8872640 Horseman Oct 2014 B2
8874205 Simon et al. Oct 2014 B2
8874218 Terry, Jr. Oct 2014 B2
8874227 Simon et al. Oct 2014 B2
8874439 Kim et al. Oct 2014 B2
8880207 Abeyratne et al. Nov 2014 B2
8880576 Ochs et al. Nov 2014 B2
8886299 Yazicioglu et al. Nov 2014 B2
8886302 Skelton et al. Nov 2014 B2
8888672 Phillips et al. Nov 2014 B2
8888673 Phillips et al. Nov 2014 B2
8888702 Osorio Nov 2014 B2
8888708 Diab et al. Nov 2014 B2
8888723 Einav Nov 2014 B2
8892207 Nelson et al. Nov 2014 B2
8893120 Pinsky et al. Nov 2014 B2
8898037 Watson et al. Nov 2014 B2
8900284 DiMauro et al. Dec 2014 B2
8902070 Kobetski et al. Dec 2014 B2
8903479 Zoicas Dec 2014 B2
8903483 Sun et al. Dec 2014 B2
8903486 Bourget et al. Dec 2014 B2
8903494 Goldwasser et al. Dec 2014 B2
8906360 Deisseroth et al. Dec 2014 B2
8907668 Okada Dec 2014 B2
8909345 Danilov et al. Dec 2014 B1
8910638 Boyden et al. Dec 2014 B2
8913810 Panin et al. Dec 2014 B2
8914100 Adachi et al. Dec 2014 B2
8914115 Giftakis et al. Dec 2014 B2
8914119 Wu et al. Dec 2014 B2
8914122 Simon et al. Dec 2014 B2
8915741 Hatlestad et al. Dec 2014 B2
8915871 Einav Dec 2014 B2
8918162 Prokoski Dec 2014 B2
8918176 Nelson et al. Dec 2014 B2
8918178 Simon et al. Dec 2014 B2
8918183 Carlton et al. Dec 2014 B2
8921320 Paul et al. Dec 2014 B2
8922376 Kangas et al. Dec 2014 B2
8922788 Addison et al. Dec 2014 B2
8923958 Gupta et al. Dec 2014 B2
8924235 Seely Dec 2014 B2
RE45336 Teegarden et al. Jan 2015 E
RE45337 Teegarden et al. Jan 2015 E
8926959 Deisseroth et al. Jan 2015 B2
8929991 Fowler et al. Jan 2015 B2
8929999 Maschiach Jan 2015 B2
8932218 Thompson Jan 2015 B1
8932227 Lynn Jan 2015 B2
8932562 Deisseroth et al. Jan 2015 B2
8933696 Nishikawa Jan 2015 B2
8934685 Avinash et al. Jan 2015 B2
8934965 Rogers et al. Jan 2015 B2
8934967 Kilgard et al. Jan 2015 B2
8934979 Moffitt Jan 2015 B2
8934986 Goetz Jan 2015 B2
8936629 Boyden et al. Jan 2015 B2
8936630 Denison et al. Jan 2015 B2
8938102 Carroll Jan 2015 B2
8938289 Einav et al. Jan 2015 B2
8938290 Wingeier et al. Jan 2015 B2
8938301 Hagedorn Jan 2015 B2
8939903 Roberts et al. Jan 2015 B2
8942777 Diab et al. Jan 2015 B2
8942813 Hagedorn et al. Jan 2015 B1
8942817 Hyde et al. Jan 2015 B2
8945006 Osorio Feb 2015 B2
8948834 Diab et al. Feb 2015 B2
8948849 Diamond et al. Feb 2015 B2
8948855 Osorio et al. Feb 2015 B2
8948860 Causevic Feb 2015 B2
8951189 Osorio Feb 2015 B2
8951190 Chmiel et al. Feb 2015 B2
8951192 Osorio Feb 2015 B2
8951203 Patangay et al. Feb 2015 B2
8954139 Hopenfeld et al. Feb 2015 B2
8954146 Hopper et al. Feb 2015 B2
8954293 Klinkenbusch Feb 2015 B2
8955010 Pradeep et al. Feb 2015 B2
8955974 Gross et al. Feb 2015 B2
8956277 Mishelevich Feb 2015 B2
8956363 Schneider et al. Feb 2015 B2
8958868 Ghovanloo et al. Feb 2015 B2
8958870 Gerber et al. Feb 2015 B2
8958882 Hagedorn Feb 2015 B1
8961187 Boers et al. Feb 2015 B2
8961385 Pilla et al. Feb 2015 B2
8961386 Phillips et al. Feb 2015 B2
8962042 Geng Feb 2015 B2
8962589 Deisseroth et al. Feb 2015 B2
8964298 Haddick et al. Feb 2015 B2
8965492 Baker et al. Feb 2015 B2
8965513 Wingeier et al. Feb 2015 B2
8965514 Bikson et al. Feb 2015 B2
8968172 Wang et al. Mar 2015 B2
8968176 Altman et al. Mar 2015 B2
8968195 Tran Mar 2015 B2
8968376 Wells et al. Mar 2015 B2
8971936 Derchak Mar 2015 B2
8972004 Simon et al. Mar 2015 B2
8972013 Maschino Mar 2015 B2
8974365 Best Mar 2015 B2
8977024 Rex et al. Mar 2015 B1
8977110 Pradeep et al. Mar 2015 B2
8977362 Saab Mar 2015 B2
8980891 Stirn et al. Mar 2015 B2
8983155 McIntyre et al. Mar 2015 B2
8983591 Leininger et al. Mar 2015 B2
8983620 Cinbis Mar 2015 B2
8983628 Simon et al. Mar 2015 B2
8983629 Simon et al. Mar 2015 B2
8985119 Webb et al. Mar 2015 B1
8986207 Li et al. Mar 2015 B2
8989835 Badower et al. Mar 2015 B2
8989836 Machon et al. Mar 2015 B2
8989863 Osorio Mar 2015 B2
8989867 Chow et al. Mar 2015 B2
8989868 Mashiach et al. Mar 2015 B2
8989871 Ollivier Mar 2015 B2
8992230 Tuchschmid et al. Mar 2015 B2
8993623 Goodenowe Mar 2015 B2
8996112 Brooke Mar 2015 B2
8996120 Calle et al. Mar 2015 B1
8998828 Reichow et al. Apr 2015 B2
9002458 Pal et al. Apr 2015 B2
9002471 Stevenson et al. Apr 2015 B2
9002477 Burnett Apr 2015 B2
9004687 Stack Apr 2015 B2
9005102 Burnett et al. Apr 2015 B2
9005126 Beach et al. Apr 2015 B2
9005649 Ho et al. Apr 2015 B2
9008367 Tolkowsky et al. Apr 2015 B2
9008754 Steinberg et al. Apr 2015 B2
9008771 Dong et al. Apr 2015 B2
9008780 Nudo et al. Apr 2015 B2
9008970 Donderici et al. Apr 2015 B2
9011329 Ferren et al. Apr 2015 B2
9014216 Lazar et al. Apr 2015 B2
9014453 Steinberg et al. Apr 2015 B2
9014804 Giftakis et al. Apr 2015 B2
9014811 Pal et al. Apr 2015 B2
9014819 Lee et al. Apr 2015 B2
9014823 Simon et al. Apr 2015 B2
9015057 Phillips et al. Apr 2015 B2
9015087 Li et al. Apr 2015 B2
9020576 Nagatani Apr 2015 B2
9020582 Osorio et al. Apr 2015 B2
9020585 John et al. Apr 2015 B2
9020586 Yamada et al. Apr 2015 B2
9020598 Simon et al. Apr 2015 B2
9020612 Danilov et al. Apr 2015 B1
9020789 Butson et al. Apr 2015 B2
9022930 Sachanandani et al. May 2015 B2
9022936 Rothberg et al. May 2015 B2
9025845 Carroll May 2015 B2
9026194 Okada May 2015 B2
9026202 Albert May 2015 B2
9026217 Kokones et al. May 2015 B2
9026218 Lozano et al. May 2015 B2
9026372 O'Donnell, Jr. et al. May 2015 B2
9028405 Tran May 2015 B2
9028412 Rothberg et al. May 2015 B2
9031644 Johnson et al. May 2015 B2
9031653 Mashiach May 2015 B2
9031655 Osorio et al. May 2015 B2
9031658 Chiao et al. May 2015 B2
9033884 Rothberg et al. May 2015 B2
9034055 Vinjamuri et al. May 2015 B2
9034911 Selvey et al. May 2015 B2
9034923 Goodenowe May 2015 B2
9035657 Zhang et al. May 2015 B2
9036844 Suhami et al. May 2015 B1
9037224 Fu May 2015 B1
9037225 Saliga et al. May 2015 B1
9037254 John May 2015 B2
9037256 Bokil May 2015 B2
9037530 Tan et al. May 2015 B2
9042074 Beran May 2015 B1
9042201 Tyler et al. May 2015 B2
9042952 Lynn et al. May 2015 B2
9042958 Karmarkar et al. May 2015 B2
9042988 DiLorenzo May 2015 B2
9043001 Simon et al. May 2015 B2
9044188 DiLorenzo et al. Jun 2015 B2
9044612 Mashiach et al. Jun 2015 B2
9050469 Osorio et al. Jun 2015 B1
9050470 Carlton et al. Jun 2015 B2
9050471 Skelton et al. Jun 2015 B2
9053516 Stempora Jun 2015 B2
9053534 Ross et al. Jun 2015 B2
9055871 Inan et al. Jun 2015 B2
9055974 Goetz Jun 2015 B2
9056195 Sabesan Jun 2015 B2
9058473 Navratil et al. Jun 2015 B2
9060671 Badower et al. Jun 2015 B2
9060683 Tran Jun 2015 B2
9060695 Peters Jun 2015 B2
9060722 Teixeira Jun 2015 B2
9060746 Weng et al. Jun 2015 B2
9061132 Zweber et al. Jun 2015 B1
9061133 Wurster et al. Jun 2015 B2
9061151 Mashiach et al. Jun 2015 B2
9061153 Lebovitz et al. Jun 2015 B1
9063183 Toda et al. Jun 2015 B2
9063643 Sparks et al. Jun 2015 B2
9064036 Hyde et al. Jun 2015 B2
9067052 Moses et al. Jun 2015 B2
9067054 Simon et al. Jun 2015 B2
9067070 Connor Jun 2015 B2
9069031 Guedes et al. Jun 2015 B2
9069097 Zhang et al. Jun 2015 B2
9070492 Yarmush et al. Jun 2015 B2
9072449 Semenov Jul 2015 B2
9072482 Sarkela et al. Jul 2015 B2
9072832 Frei et al. Jul 2015 B2
9072870 Wu et al. Jul 2015 B2
9072905 Kokones et al. Jul 2015 B2
9074976 Adolphi et al. Jul 2015 B2
9076212 Ernst et al. Jul 2015 B2
9078564 Taylor Jul 2015 B2
9078577 He et al. Jul 2015 B2
9078584 Jorge et al. Jul 2015 B2
9079039 Carlson et al. Jul 2015 B2
9079940 Deisseroth et al. Jul 2015 B2
9081488 Soederstroem Jul 2015 B2
9081882 Taylor Jul 2015 B2
9081890 An et al. Jul 2015 B2
9082169 Thomson et al. Jul 2015 B2
9084584 Weiland et al. Jul 2015 B2
9084885 Deisseroth et al. Jul 2015 B2
9084896 Kokones et al. Jul 2015 B2
9084900 Hershey et al. Jul 2015 B2
9087147 Fonte Jul 2015 B1
9089310 Isenhart et al. Jul 2015 B2
9089400 Nofzinger Jul 2015 B2
9089683 Mishelevich Jul 2015 B2
9089707 Kilgard et al. Jul 2015 B2
9089713 John Jul 2015 B2
9089719 Simon et al. Jul 2015 B2
9091785 Donderici et al. Jul 2015 B2
9092556 Amble et al. Jul 2015 B2
9092895 Ross et al. Jul 2015 B2
9095266 Fu Aug 2015 B1
9095268 Kurtz et al. Aug 2015 B2
9095295 Eagleman et al. Aug 2015 B2
9095303 Osorio Aug 2015 B2
9095314 Osorio et al. Aug 2015 B2
9095618 Satchi-Fainaro et al. Aug 2015 B2
9095713 Foster et al. Aug 2015 B2
9100758 Adachi et al. Aug 2015 B2
9101263 Jung et al. Aug 2015 B2
9101276 Georgopoulos Aug 2015 B2
9101279 Ritchey et al. Aug 2015 B2
9101690 Deisseroth et al. Aug 2015 B2
9101759 Delp et al. Aug 2015 B2
9101766 Nekhendzy Aug 2015 B2
9102717 Huang et al. Aug 2015 B2
9107586 Tran Aug 2015 B2
9107595 Smyth Aug 2015 B1
9108041 Craig Aug 2015 B2
9113777 Mittal Aug 2015 B2
9113801 DiLorenzo Aug 2015 B2
9113803 Zhang Aug 2015 B2
9113830 Galen et al. Aug 2015 B2
9116201 Shah et al. Aug 2015 B2
9116835 Smyth Aug 2015 B1
9118775 Lim et al. Aug 2015 B2
9119533 Ghaffari Sep 2015 B2
9119551 Qi et al. Sep 2015 B2
9119583 Tass Sep 2015 B2
9119597 Dripps et al. Sep 2015 B2
9119598 Engelbrecht et al. Sep 2015 B2
9121964 Lewis et al. Sep 2015 B2
9125574 Zia et al. Sep 2015 B2
9125581 Wu et al. Sep 2015 B2
9125788 Tee et al. Sep 2015 B2
9126050 Simon et al. Sep 2015 B2
9131864 Korenberg Sep 2015 B2
9133024 Phan et al. Sep 2015 B2
9133709 Huh et al. Sep 2015 B2
9135221 Shahaf et al. Sep 2015 B2
9135400 McIntyre et al. Sep 2015 B2
9138156 Wu et al. Sep 2015 B2
9138175 Ernst et al. Sep 2015 B2
9138183 McKenna et al. Sep 2015 B2
9138579 Wolpaw et al. Sep 2015 B2
9138580 Ignagni et al. Sep 2015 B2
9142145 Tuchschmid et al. Sep 2015 B2
9142185 Fateh Sep 2015 B2
9144392 Santosh et al. Sep 2015 B2
RE45766 Lindsay Oct 2015 E
9149195 Hadley Oct 2015 B2
9149197 Taylor Oct 2015 B2
9149210 Sahasrabudhe et al. Oct 2015 B2
9149214 Adachi et al. Oct 2015 B2
9149226 Jadidi Oct 2015 B2
9149255 Rothberg et al. Oct 2015 B2
9149577 Robertson et al. Oct 2015 B2
9149599 Walter et al. Oct 2015 B2
9149719 Guan et al. Oct 2015 B2
9152757 Taylor Oct 2015 B2
9155373 Allen et al. Oct 2015 B2
9155484 Baker et al. Oct 2015 B2
9155487 Linderman et al. Oct 2015 B2
9155521 Rothberg et al. Oct 2015 B2
9161715 Jung et al. Oct 2015 B2
9162051 Morrell Oct 2015 B2
9162052 Morrell Oct 2015 B2
9165472 Hagedorn et al. Oct 2015 B2
9167970 Gratton et al. Oct 2015 B2
9167974 Taylor Oct 2015 B2
9167976 Wingeier et al. Oct 2015 B2
9167977 Wingeier et al. Oct 2015 B2
9167978 Wingeier et al. Oct 2015 B2
9167979 Skidmore et al. Oct 2015 B2
9171353 Vija et al. Oct 2015 B2
9171366 Declerck et al. Oct 2015 B2
9173582 Popovic et al. Nov 2015 B2
9173609 Nelson Nov 2015 B2
9173610 Navakatikyan Nov 2015 B2
9174045 Simon et al. Nov 2015 B2
9174055 Davis et al. Nov 2015 B2
9174066 Simon et al. Nov 2015 B2
9175095 Deisseroth et al. Nov 2015 B2
9177379 Biagiotti et al. Nov 2015 B1
9177416 Sharp Nov 2015 B2
9179850 Wingeier et al. Nov 2015 B2
9179854 Doidge et al. Nov 2015 B2
9179855 Burdea et al. Nov 2015 B2
9179858 Hasson et al. Nov 2015 B2
9179875 Hua Nov 2015 B2
9179876 Ochs et al. Nov 2015 B2
9183351 Shusterman Nov 2015 B2
9186060 De Graff et al. Nov 2015 B2
9186106 Osorio Nov 2015 B2
9186503 Lindenthaler et al. Nov 2015 B2
9186510 Gliner et al. Nov 2015 B2
9187745 Deisseroth et al. Nov 2015 B2
9192300 Jung et al. Nov 2015 B2
9192309 Hopenfeld et al. Nov 2015 B1
9198563 Ferren et al. Dec 2015 B2
9198612 Fueyo et al. Dec 2015 B2
9198621 Fernstrom et al. Dec 2015 B2
9198624 Funane et al. Dec 2015 B2
9198637 Rothberg et al. Dec 2015 B2
9198707 McKay et al. Dec 2015 B2
9198733 Neal, II et al. Dec 2015 B2
9204796 Tran Dec 2015 B2
9204835 Parsey et al. Dec 2015 B2
9204838 Osorio Dec 2015 B2
9204998 Kilgard et al. Dec 2015 B2
9208430 Solari Dec 2015 B2
9208557 Pautot Dec 2015 B2
9208558 Dean et al. Dec 2015 B2
9211076 Kim Dec 2015 B2
9211077 Jung et al. Dec 2015 B2
9211212 Nofzinger et al. Dec 2015 B2
9211411 Wu et al. Dec 2015 B2
9211417 Heldman et al. Dec 2015 B2
9213074 van der Kouwe et al. Dec 2015 B2
9213076 Liu Dec 2015 B2
9215298 Schiff Dec 2015 B2
9215978 Knight et al. Dec 2015 B2
9220910 Colborn Dec 2015 B2
9220917 Boyden et al. Dec 2015 B2
9221755 Teegarden et al. Dec 2015 B2
9226672 Taylor Jan 2016 B2
9227056 Heldman et al. Jan 2016 B1
9229080 Lin Jan 2016 B2
9230065 Hasegawa et al. Jan 2016 B2
9230539 Pakhomov Jan 2016 B2
9232910 Alshaer et al. Jan 2016 B2
9232984 Guthart et al. Jan 2016 B2
9233244 Pal et al. Jan 2016 B2
9233245 Lamensdorf et al. Jan 2016 B2
9233246 Simon et al. Jan 2016 B2
9233258 Simon et al. Jan 2016 B2
9235679 Taylor Jan 2016 B2
9235685 McIntyre et al. Jan 2016 B2
9238142 Heldman et al. Jan 2016 B2
9238150 Deisseroth et al. Jan 2016 B2
9241647 Osorio et al. Jan 2016 B2
9241665 deCharms Jan 2016 B2
9242067 Shore et al. Jan 2016 B2
9242092 Simon et al. Jan 2016 B2
9247890 Turnbull et al. Feb 2016 B2
9247911 Galloway et al. Feb 2016 B2
9247924 Rothberg et al. Feb 2016 B2
9248003 Wright et al. Feb 2016 B2
9248280 Moffitt et al. Feb 2016 B2
9248286 Simon et al. Feb 2016 B2
9248288 Panken et al. Feb 2016 B2
9248290 Mashiach Feb 2016 B2
9248291 Mashiach Feb 2016 B2
9248296 Carcieri et al. Feb 2016 B2
9249200 Deisseroth et al. Feb 2016 B2
9249234 Deisseroth et al. Feb 2016 B2
9251566 Bajic Feb 2016 B1
9254097 Espy et al. Feb 2016 B2
9254099 Connor Feb 2016 B2
9254383 Simon et al. Feb 2016 B2
9254387 Blum et al. Feb 2016 B2
9256982 Sharp et al. Feb 2016 B2
9259177 Drew et al. Feb 2016 B2
9259482 Satchi-Fainaro et al. Feb 2016 B2
9259591 Brown et al. Feb 2016 B2
9261573 Radparvar et al. Feb 2016 B1
9265458 Stack Feb 2016 B2
9265660 Kilgard et al. Feb 2016 B2
9265661 Kilgard et al. Feb 2016 B2
9265662 Kilgard et al. Feb 2016 B2
9265663 Kilgard et al. Feb 2016 B2
9265931 Morrell Feb 2016 B2
9265943 Yun et al. Feb 2016 B2
9265946 Morrell Feb 2016 B2
9265965 Fox et al. Feb 2016 B2
9265974 You et al. Feb 2016 B2
9268014 Rothberg et al. Feb 2016 B2
9268015 Rothberg et al. Feb 2016 B2
9268902 Taylor et al. Feb 2016 B2
9271651 Avinash et al. Mar 2016 B2
9271657 Taylor Mar 2016 B2
9271660 Luo et al. Mar 2016 B2
9271674 Deisseroth et al. Mar 2016 B2
9271679 Cho et al. Mar 2016 B2
9272091 Skelton et al. Mar 2016 B2
9272139 Hamilton et al. Mar 2016 B2
9272145 Kilgard et al. Mar 2016 B2
9272153 Blum et al. Mar 2016 B2
9273035 Teegarden et al. Mar 2016 B2
9275191 Dean et al. Mar 2016 B2
9275451 Ben-Haim et al. Mar 2016 B2
9277871 Keenan et al. Mar 2016 B2
9277873 Sarma et al. Mar 2016 B2
9278159 Deisseroth et al. Mar 2016 B2
9278231 Vasishta Mar 2016 B2
9280784 Barnett et al. Mar 2016 B2
9282927 Hyde et al. Mar 2016 B2
9282930 Machon et al. Mar 2016 B2
9282934 Liley et al. Mar 2016 B2
9283279 Satchi-Fainaro et al. Mar 2016 B2
9283394 Whitehurst et al. Mar 2016 B2
9284353 Deisseroth et al. Mar 2016 B2
9285249 Schober et al. Mar 2016 B2
9289143 Wingeier et al. Mar 2016 B2
9289595 Floyd et al. Mar 2016 B2
9289599 Craig Mar 2016 B2
9289603 Giuffrida et al. Mar 2016 B1
9289609 Moffitt Mar 2016 B2
9292471 Fung et al. Mar 2016 B2
9292858 Marci et al. Mar 2016 B2
9292920 Dean et al. Mar 2016 B2
9295838 Starr et al. Mar 2016 B2
9296382 Fung et al. Mar 2016 B2
9302069 Tass et al. Apr 2016 B2
9302093 Mashiach Apr 2016 B2
9302103 Nirenberg Apr 2016 B1
9302109 Sabesan Apr 2016 B2
9302110 Kokones et al. Apr 2016 B2
9302114 Rossi Apr 2016 B2
9302116 Vo-Dinh et al. Apr 2016 B2
9305376 Lee et al. Apr 2016 B2
9307925 Russell et al. Apr 2016 B2
9307944 Colman et al. Apr 2016 B2
9308372 Sparks et al. Apr 2016 B2
9308392 Deisseroth et al. Apr 2016 B2
9309296 Deisseroth et al. Apr 2016 B2
9310985 Blum et al. Apr 2016 B2
9311335 Simon Apr 2016 B2
9314190 Giuffrida et al. Apr 2016 B1
9314613 Mashiach Apr 2016 B2
9314633 Osorio et al. Apr 2016 B2
9314635 Libbus Apr 2016 B2
9320449 Gu Apr 2016 B2
9320450 Badower Apr 2016 B2
9320451 Feldkamp et al. Apr 2016 B2
9320900 DiLorenzo Apr 2016 B2
9320913 Dimino et al. Apr 2016 B2
9320914 Toselli et al. Apr 2016 B2
9322895 Santosh et al. Apr 2016 B2
9326705 Derchak May 2016 B2
9326720 McLaughlin May 2016 B2
9326742 Hirschman et al. May 2016 B2
9327069 Foster et al. May 2016 B2
9327070 Skelton et al. May 2016 B2
9328107 Teegarden et al. May 2016 B2
9329758 Guzak et al. May 2016 B2
9330206 Dean et al. May 2016 B2
9330523 Sutton et al. May 2016 B2
9331841 Kim et al. May 2016 B2
9332939 Osorio May 2016 B2
9333334 Jeffery et al. May 2016 B2
9333347 Simon et al. May 2016 B2
9333350 Rise et al. May 2016 B2
9336302 Swamy May 2016 B1
9336535 Pradeep et al. May 2016 B2
9336611 Bilgic et al. May 2016 B2
9339200 Fonte May 2016 B2
9339227 D'arcy et al. May 2016 B2
9339641 Rajguru et al. May 2016 B2
9339654 Kilgard et al. May 2016 B2
9340589 Deisseroth et al. May 2016 B2
9345412 Horne May 2016 B2
9345609 Hyde et al. May 2016 B2
9345886 Kilgard et al. May 2016 B2
9345901 Peterchev May 2016 B2
9348974 Goetz May 2016 B2
9349178 Itu et al. May 2016 B1
9351640 Tran May 2016 B2
9351651 Nagasaka May 2016 B2
9352145 Whitehurst et al. May 2016 B2
9352152 Lindenthaler et al. May 2016 B2
9352156 Lane et al. May 2016 B2
9357240 Pradeep et al. May 2016 B2
9357298 Hiroe May 2016 B2
9357941 Simon Jun 2016 B2
9357949 Drew Jun 2016 B2
9357970 Clark et al. Jun 2016 B2
9358361 Hyde et al. Jun 2016 B2
9358381 Simon et al. Jun 2016 B2
9358392 Mashiach Jun 2016 B2
9358393 Lozano Jun 2016 B1
9358398 Moffitt et al. Jun 2016 B2
9359449 Deisseroth et al. Jun 2016 B2
9360472 Deisseroth et al. Jun 2016 B2
9364462 Simpson, Jr. Jun 2016 B2
9364665 Bokil et al. Jun 2016 B2
9364674 Cook et al. Jun 2016 B2
9364679 John Jun 2016 B2
9365628 Deisseroth et al. Jun 2016 B2
9367131 Klappert et al. Jun 2016 B2
9367738 Harumatsu et al. Jun 2016 B2
9368018 Kangas et al. Jun 2016 B2
9368265 Park et al. Jun 2016 B2
9370309 Ko et al. Jun 2016 B2
9370667 Schmidt Jun 2016 B2
9375145 Chin et al. Jun 2016 B2
9375151 Hopenfeld et al. Jun 2016 B1
9375171 Teixeira Jun 2016 B2
9375564 Wingeier et al. Jun 2016 B2
9375571 Errico et al. Jun 2016 B2
9375573 Dilorenzo Jun 2016 B2
9377348 Kataoka Jun 2016 B2
9377515 Kim et al. Jun 2016 B2
9380976 Stack Jul 2016 B2
9381346 Lee et al. Jul 2016 B2
9381352 Yun et al. Jul 2016 B2
9383208 Mohanty Jul 2016 B2
9387320 Wingeier et al. Jul 2016 B2
9387338 Burnett Jul 2016 B2
9390233 Fueyo et al. Jul 2016 B2
9392955 Folkerts et al. Jul 2016 B2
9393406 Ollivier Jul 2016 B2
9393418 Giuffrida et al. Jul 2016 B2
9394347 Deisseroth et al. Jul 2016 B2
9395425 Diamond et al. Jul 2016 B2
9396533 Skidmore Jul 2016 B2
9396669 Karkanias et al. Jul 2016 B2
9398873 Van Dooren et al. Jul 2016 B2
9399126 Pal et al. Jul 2016 B2
9399133 Besio Jul 2016 B2
9399134 Simon et al. Jul 2016 B2
9399144 Howard Jul 2016 B2
9401021 Biagiotti et al. Jul 2016 B1
9401033 Bajic Jul 2016 B2
9402558 John et al. Aug 2016 B2
9402994 Chow et al. Aug 2016 B2
9403000 Lyons et al. Aug 2016 B2
9403001 Simon et al. Aug 2016 B2
9403009 Mashiach Aug 2016 B2
9403010 Fried et al. Aug 2016 B2
9403038 Tyler Aug 2016 B2
9405366 Segal Aug 2016 B2
9408530 Ferren et al. Aug 2016 B2
9409013 Mashiach et al. Aug 2016 B2
9409022 Jaax et al. Aug 2016 B2
9409028 Whitehurst et al. Aug 2016 B2
9410885 Schober et al. Aug 2016 B2
9411033 He et al. Aug 2016 B2
9411935 Moffitt et al. Aug 2016 B2
9412076 Sapiro et al. Aug 2016 B2
9412233 Bagherzadeh et al. Aug 2016 B1
9414029 Miyazaki et al. Aug 2016 B2
9414749 Semenov Aug 2016 B2
9414763 Semenov Aug 2016 B2
9414764 Semenov Aug 2016 B2
9414776 Sillay et al. Aug 2016 B2
9414780 Rhoads Aug 2016 B2
9414907 Wortz et al. Aug 2016 B2
9415215 Mashiach Aug 2016 B2
9415216 Mashiach Aug 2016 B2
9415219 Simon et al. Aug 2016 B2
9415222 DiLorenzo Aug 2016 B2
9415233 Pilla et al. Aug 2016 B2
9418368 Jung et al. Aug 2016 B2
9420970 Dagum Aug 2016 B2
9421258 Deisseroth et al. Aug 2016 B2
9421372 Mashiach et al. Aug 2016 B2
9421373 DiLorenzo Aug 2016 B2
9421379 Zhu Aug 2016 B2
9424761 Tuchschmid et al. Aug 2016 B2
9427474 Satchi-Fainaro et al. Aug 2016 B2
9427581 Simon et al. Aug 2016 B2
9427585 Gliner Aug 2016 B2
9427598 Pilla et al. Aug 2016 B2
9430615 Michaelis et al. Aug 2016 B2
9432777 Lunner et al. Aug 2016 B2
9433797 Pilla et al. Sep 2016 B2
9434692 Xiong et al. Sep 2016 B2
9436989 Uber, III Sep 2016 B2
9438650 Serena Sep 2016 B2
9439150 Carlson et al. Sep 2016 B2
9440063 Ho et al. Sep 2016 B2
9440064 Wingeier et al. Sep 2016 B2
9440070 Goldwasser et al. Sep 2016 B2
9440084 Davis et al. Sep 2016 B2
9440089 Pilla et al. Sep 2016 B2
9440646 Fung et al. Sep 2016 B2
9442088 Feldkamp et al. Sep 2016 B2
9442525 Choi et al. Sep 2016 B2
9443141 Mirowski et al. Sep 2016 B2
9444998 Kim et al. Sep 2016 B2
9445713 Douglas et al. Sep 2016 B2
9445730 Snyder et al. Sep 2016 B2
9445739 Payton et al. Sep 2016 B1
9445763 Davis et al. Sep 2016 B2
9446238 Lozano Sep 2016 B2
9448289 Wang et al. Sep 2016 B2
9449147 Taylor Sep 2016 B2
9451303 Kothuri et al. Sep 2016 B2
9451734 Onuma et al. Sep 2016 B2
9451883 Gallant et al. Sep 2016 B2
9451886 Teixeira Sep 2016 B2
9451899 Ritchey et al. Sep 2016 B2
9452287 Rosenbluth et al. Sep 2016 B2
9453215 Deisseroth et al. Sep 2016 B2
9454646 Siefert Sep 2016 B2
9458208 Deisseroth et al. Oct 2016 B2
9459597 Kahn et al. Oct 2016 B2
9460400 De Bruin et al. Oct 2016 B2
9462733 Hokari Oct 2016 B2
9462956 Pandia et al. Oct 2016 B2
9462975 Sackner et al. Oct 2016 B2
9462977 Horseman Oct 2016 B2
9463327 Lempka et al. Oct 2016 B2
9468541 Contreras-Vidal et al. Oct 2016 B2
9468761 Frei et al. Oct 2016 B2
9470728 George et al. Oct 2016 B2
9471978 Chen et al. Oct 2016 B2
9472000 Dempsey et al. Oct 2016 B2
9474481 Dagum Oct 2016 B2
9474852 Lozano et al. Oct 2016 B2
9474903 Chen et al. Oct 2016 B2
9475502 Fung et al. Oct 2016 B2
RE46189 Prichep et al. Nov 2016 E
RE46209 Gong et al. Nov 2016 E
9480402 Leuthardt et al. Nov 2016 B2
9480425 Culver et al. Nov 2016 B2
9480812 Thompson Nov 2016 B1
9480841 Hershey et al. Nov 2016 B2
9480845 Harris et al. Nov 2016 B2
9480854 Von Ohlsen et al. Nov 2016 B2
9483117 Karkkainen et al. Nov 2016 B2
9483613 Fueyo et al. Nov 2016 B2
9486168 Bonmassar et al. Nov 2016 B2
9486381 Juto et al. Nov 2016 B2
9486389 Tass Nov 2016 B2
9486618 Wingeier et al. Nov 2016 B2
9486632 Saab Nov 2016 B2
9489854 Haruta et al. Nov 2016 B2
9492084 Behar et al. Nov 2016 B2
9492114 Reiman Nov 2016 B2
9492120 Horseman Nov 2016 B2
9492313 Nofzinger Nov 2016 B2
9492656 Chow et al. Nov 2016 B2
9492678 Chow Nov 2016 B2
9495684 Jung et al. Nov 2016 B2
9497017 Kim et al. Nov 2016 B1
9498134 Trobaugh et al. Nov 2016 B1
9498628 Kaemmerer et al. Nov 2016 B2
9498634 De Ridder Nov 2016 B2
9500722 Takahashi Nov 2016 B2
9501829 Carlton et al. Nov 2016 B2
9504390 Osorio Nov 2016 B2
9504410 Gal Nov 2016 B2
9504420 Davis et al. Nov 2016 B2
9504788 Hyde et al. Nov 2016 B2
9505402 Fung et al. Nov 2016 B2
9505817 Deisseroth et al. Nov 2016 B2
9510790 Kang et al. Dec 2016 B2
9513398 Wilson et al. Dec 2016 B2
9517020 Shacham-Diamand et al. Dec 2016 B2
9517031 Jung Dec 2016 B2
9517222 Goodenowe Dec 2016 B2
9519981 Sudarsky et al. Dec 2016 B2
9521958 Nagasaka et al. Dec 2016 B2
9522085 Kilgard et al. Dec 2016 B2
9522278 Heldman et al. Dec 2016 B1
9522282 Chow et al. Dec 2016 B2
9522288 Deisseroth et al. Dec 2016 B2
9526419 Derchak et al. Dec 2016 B2
9526902 Blum et al. Dec 2016 B2
9526906 Mashiach Dec 2016 B2
9526913 Vo-Dinh et al. Dec 2016 B2
9526914 Vo-Dinh et al. Dec 2016 B2
9533113 Lain et al. Jan 2017 B2
9533144 Bahmer Jan 2017 B2
9533147 Osorio Jan 2017 B2
9533148 Carcieri Jan 2017 B2
9533150 Nudo et al. Jan 2017 B2
9533151 Craig Jan 2017 B2
9534044 El-Agnaf Jan 2017 B2
9538635 Beran Jan 2017 B1
9538948 Dagum Jan 2017 B2
9538951 Osorio Jan 2017 B2
9539118 Leuthardt et al. Jan 2017 B2
9541383 Abovitz et al. Jan 2017 B2
9545221 Adhikari et al. Jan 2017 B2
9545222 Derchak et al. Jan 2017 B2
9545225 Cavuoto et al. Jan 2017 B2
9545226 Osorio Jan 2017 B2
9545285 Ghaffari et al. Jan 2017 B2
9545510 Kokones et al. Jan 2017 B2
9545515 Wolpaw et al. Jan 2017 B2
9549691 Tran Jan 2017 B2
9550064 Mashiach Jan 2017 B2
9556149 Krishnan et al. Jan 2017 B2
9556487 Umansky et al. Jan 2017 B2
9557439 Wilson et al. Jan 2017 B2
9558558 Stehle et al. Jan 2017 B2
9560458 Lunner et al. Jan 2017 B2
9560967 Hyde et al. Feb 2017 B2
9560984 Pradeep et al. Feb 2017 B2
9560986 Varcoe Feb 2017 B2
9561380 Carcieri et al. Feb 2017 B2
9562988 Wilson et al. Feb 2017 B2
9563273 Mann Feb 2017 B2
9563740 Abdelghani et al. Feb 2017 B2
9563950 Raj Feb 2017 B2
9566426 Simon et al. Feb 2017 B2
9567327 Xiong et al. Feb 2017 B2
9568564 Ma et al. Feb 2017 B2
9568635 Suhami Feb 2017 B2
9572996 Tass et al. Feb 2017 B2
9577992 Zizi et al. Feb 2017 B2
9578425 Hakansson Feb 2017 B2
9579035 Sarkela Feb 2017 B2
9579048 Rayner et al. Feb 2017 B2
9579247 Juto et al. Feb 2017 B2
9579457 Osorio Feb 2017 B2
9579506 Osorio Feb 2017 B2
9582072 Connor Feb 2017 B2
9582152 Gulaka et al. Feb 2017 B2
9582925 Durand et al. Feb 2017 B2
9584928 Laudanski et al. Feb 2017 B2
9585581 Mullins et al. Mar 2017 B1
9585723 Taylor Mar 2017 B2
9586047 Osorio et al. Mar 2017 B2
9586053 Moffitt et al. Mar 2017 B2
9588203 Zhu et al. Mar 2017 B2
9588490 Tsang Mar 2017 B2
9590986 Zizi et al. Mar 2017 B2
9592003 Osorio et al. Mar 2017 B2
9592004 DiLorenzo et al. Mar 2017 B2
9592384 Tass Mar 2017 B2
9592387 Skelton et al. Mar 2017 B2
9592389 Moffitt Mar 2017 B2
9592409 Yoo et al. Mar 2017 B2
9596224 Woods et al. Mar 2017 B2
9597493 Wingeier et al. Mar 2017 B2
9597494 Wingeier et al. Mar 2017 B2
9597501 Danilov et al. Mar 2017 B1
9597504 Danilov et al. Mar 2017 B1
9600138 Thomas et al. Mar 2017 B2
9600778 Sapiro et al. Mar 2017 B2
9604056 Starr et al. Mar 2017 B2
9604067 Kothandaraman et al. Mar 2017 B2
9604073 Deisseroth et al. Mar 2017 B2
9607023 Swamy Mar 2017 B1
9607377 Lovberg et al. Mar 2017 B2
9609453 Jabri Mar 2017 B2
9610442 Yoo et al. Apr 2017 B2
9610456 Linke et al. Apr 2017 B2
9610459 Burnett et al. Apr 2017 B2
9612295 Toda et al. Apr 2017 B2
9613184 Giftakis et al. Apr 2017 B2
9613186 Fonte Apr 2017 B2
9615746 Horseman Apr 2017 B2
9615749 Clifton et al. Apr 2017 B2
9615789 Deisseroth et al. Apr 2017 B2
9616166 Kalafut et al. Apr 2017 B2
9616227 Lindenthaler et al. Apr 2017 B2
9618591 Radparvar et al. Apr 2017 B1
9622660 Le et al. Apr 2017 B2
9622672 Yoshida et al. Apr 2017 B2
9622675 Leyde et al. Apr 2017 B2
9622676 Masmanidis et al. Apr 2017 B2
9622700 Sahasrabudhe et al. Apr 2017 B2
9622702 Badower et al. Apr 2017 B2
9622703 Badower et al. Apr 2017 B2
9623240 Simon et al. Apr 2017 B2
9623241 Wagner et al. Apr 2017 B2
9626756 Dean et al. Apr 2017 B2
9629548 Sachanandani et al. Apr 2017 B2
9629568 Hagedorn et al. Apr 2017 B2
9629976 Acton Apr 2017 B1
9630004 Rajguru et al. Apr 2017 B2
9630008 McLaughlin et al. Apr 2017 B2
9630011 Lipani Apr 2017 B2
9630029 Wurster et al. Apr 2017 B2
9636019 Hendler et al. May 2017 B2
9636185 Quaid et al. May 2017 B2
9640167 DeFranks et al. May 2017 B2
9641665 Lee et al. May 2017 B2
9642552 Hua May 2017 B2
9642553 Hokari May 2017 B2
9642554 Simola et al. May 2017 B2
9642699 Wortz et al. May 2017 B2
9643015 Moffitt et al. May 2017 B2
9643017 Carcieri et al. May 2017 B2
9643019 Higgins et al. May 2017 B2
9646248 Benvenuto et al. May 2017 B1
9649030 Gross et al. May 2017 B2
9649036 Teixeira May 2017 B2
9649439 John May 2017 B2
9649493 Mashiach May 2017 B2
9649494 Gerber et al. May 2017 B2
9649501 Best May 2017 B2
9651368 Abovitz et al. May 2017 B2
9651706 Mandviwala et al. May 2017 B2
9652626 Son et al. May 2017 B2
9652871 Han et al. May 2017 B2
9655573 Majewski et al. May 2017 B2
9655669 Palti et al. May 2017 B2
9656069 Danilov et al. May 2017 B1
9656075 Osorio May 2017 B2
9656078 Danilov et al. May 2017 B1
9656096 Pilla May 2017 B2
9659186 Pinsky et al. May 2017 B2
9659229 Clifton et al. May 2017 B2
9662049 Scarantino et al. May 2017 B2
9662069 De Graff et al. May 2017 B2
9662083 Sakaue May 2017 B2
9662490 Tracey et al. May 2017 B2
9662492 Tucker et al. May 2017 B1
9662502 Giuffrida et al. May 2017 B2
9664856 Nagasaka May 2017 B2
9665824 Chang et al. May 2017 B2
9665987 Fateh May 2017 B2
9668694 Badower Jun 2017 B2
9669185 Nofzinger Jun 2017 B2
9669239 Carpentier Jun 2017 B2
9672302 Dean et al. Jun 2017 B2
9672617 Dean et al. Jun 2017 B2
9674621 Bahmer Jun 2017 B2
9675254 Semenov Jun 2017 B2
9675255 Semenov Jun 2017 B2
9675292 Fadem Jun 2017 B2
9675794 Miller Jun 2017 B2
9675809 Chow Jun 2017 B2
9681814 Galloway et al. Jun 2017 B2
9681820 Wagner Jun 2017 B2
9682232 Shore et al. Jun 2017 B2
9682241 Hyde et al. Jun 2017 B2
9684051 Nieminen et al. Jun 2017 B2
9684335 Kim et al. Jun 2017 B2
9685600 Washington, II et al. Jun 2017 B2
9687187 Dagum Jun 2017 B2
9687562 Satchi-Fainaro et al. Jun 2017 B2
9693684 Lopez et al. Jul 2017 B2
9693724 Dagum Jul 2017 B2
9693725 Soza Jul 2017 B2
9693734 Horseman Jul 2017 B2
9694155 Panova et al. Jul 2017 B2
9694178 Ruffini et al. Jul 2017 B2
9694197 Segal Jul 2017 B2
9697330 Taylor Jul 2017 B2
9697336 Hyde et al. Jul 2017 B2
9700256 Osorio et al. Jul 2017 B2
9700716 Faltys et al. Jul 2017 B2
9700723 Sabesan Jul 2017 B2
9704205 Akutagawa et al. Jul 2017 B2
9706910 Blaha et al. Jul 2017 B1
9706925 Taylor Jul 2017 B2
9706957 Wu et al. Jul 2017 B2
9706963 Gupta et al. Jul 2017 B2
9707372 Smith Jul 2017 B2
9707390 Ahmed Jul 2017 B2
9707391 Ahmed Jul 2017 B2
9707396 Su et al. Jul 2017 B2
9710788 Horseman Jul 2017 B2
9712736 Kearns et al. Jul 2017 B2
9713428 Chon et al. Jul 2017 B2
9713433 Gadot et al. Jul 2017 B2
9713444 Severson Jul 2017 B2
9713712 Wingeier et al. Jul 2017 B2
9715032 Song et al. Jul 2017 B2
9717461 Yu et al. Aug 2017 B2
9717904 Simon et al. Aug 2017 B2
9717920 Heldman et al. Aug 2017 B1
9724517 Giftakis et al. Aug 2017 B2
9729252 Tyler et al. Aug 2017 B2
9732039 Xiong et al. Aug 2017 B2
9734589 Yu et al. Aug 2017 B2
9734601 Bresler et al. Aug 2017 B2
9734632 Thomas et al. Aug 2017 B2
9737230 Sarma et al. Aug 2017 B2
9740710 Han et al. Aug 2017 B2
9740946 Varkuti et al. Aug 2017 B2
9741114 Varkuti Aug 2017 B2
9743197 Petersen et al. Aug 2017 B2
9743835 Taylor Aug 2017 B2
9744358 Hehrmann et al. Aug 2017 B2
9763592 Le et al. Sep 2017 B2
20010003799 Boveja Jun 2001 A1
20010009975 Tsukada et al. Jul 2001 A1
20010014818 Kennedy Aug 2001 A1
20010020127 Oshio et al. Sep 2001 A1
20010021800 Balkin et al. Sep 2001 A1
20010029391 Gluckman et al. Oct 2001 A1
20010049480 John et al. Dec 2001 A1
20010051774 Littrup et al. Dec 2001 A1
20010051787 Haller et al. Dec 2001 A1
20020000808 Nichols Jan 2002 A1
20020005784 Balkin et al. Jan 2002 A1
20020006875 Mcfetridge Jan 2002 A1
20020013612 Whitehurst Jan 2002 A1
20020013613 Haller et al. Jan 2002 A1
20020016552 Granger et al. Feb 2002 A1
20020017905 Conti Feb 2002 A1
20020017994 Balkin et al. Feb 2002 A1
20020024450 Townsend et al. Feb 2002 A1
20020032375 Bauch et al. Mar 2002 A1
20020033454 Cheng et al. Mar 2002 A1
20020035317 Cheng et al. Mar 2002 A1
20020035338 Dear et al. Mar 2002 A1
20020037095 Cheng Mar 2002 A1
20020042563 Becerra et al. Apr 2002 A1
20020052539 Haller et al. May 2002 A1
20020055675 Llinas et al. May 2002 A1
20020058867 Breiter et al. May 2002 A1
20020059159 Cook May 2002 A1
20020072776 Osorio et al. Jun 2002 A1
20020072782 Osorio et al. Jun 2002 A1
20020077536 Diab et al. Jun 2002 A1
20020082513 Ennen et al. Jun 2002 A1
20020082665 Haller et al. Jun 2002 A1
20020085174 Bolger et al. Jul 2002 A1
20020087201 Firlik et al. Jul 2002 A1
20020091319 Moehring et al. Jul 2002 A1
20020091335 John et al. Jul 2002 A1
20020091419 Firlik et al. Jul 2002 A1
20020095099 Quyen et al. Jul 2002 A1
20020097332 Martin et al. Jul 2002 A1
20020099273 Bocionek et al. Jul 2002 A1
20020099295 Gil et al. Jul 2002 A1
20020099306 Shaw et al. Jul 2002 A1
20020099412 Fischell et al. Jul 2002 A1
20020099417 Naritoku et al. Jul 2002 A1
20020099418 Naritoku et al. Jul 2002 A1
20020103428 deCharms Aug 2002 A1
20020103429 deCharms Aug 2002 A1
20020103512 Echauz et al. Aug 2002 A1
20020107454 Collura et al. Aug 2002 A1
20020112732 Blazey et al. Aug 2002 A1
20020117176 Mantzaridis et al. Aug 2002 A1
20020128540 Kim et al. Sep 2002 A1
20020128544 Diab et al. Sep 2002 A1
20020128638 Chauvet et al. Sep 2002 A1
20020138013 Guerrero et al. Sep 2002 A1
20020151771 Braun et al. Oct 2002 A1
20020151939 Rezai Oct 2002 A1
20020158631 Kandori et al. Oct 2002 A1
20020173714 Tsukada et al. Nov 2002 A1
20020177882 DiLorenzo Nov 2002 A1
20020182574 Freer Dec 2002 A1
20020183607 Bauch et al. Dec 2002 A1
20020183644 Levendowski et al. Dec 2002 A1
20020188330 Gielen et al. Dec 2002 A1
20020193670 Garfield et al. Dec 2002 A1
20030001098 Stoddart et al. Jan 2003 A1
20030004429 Price Jan 2003 A1
20030009078 Fedorovskaya et al. Jan 2003 A1
20030009096 Lahteenmaki Jan 2003 A1
20030013981 Gevins et al. Jan 2003 A1
20030018277 He Jan 2003 A1
20030018278 Jordan Jan 2003 A1
20030023183 Williams Jan 2003 A1
20030023282 Barrett et al. Jan 2003 A1
20030028081 Blazey et al. Feb 2003 A1
20030028121 Blazey et al. Feb 2003 A1
20030028348 Wenzel et al. Feb 2003 A1
20030031357 Wenzel et al. Feb 2003 A1
20030032870 Farwell Feb 2003 A1
20030032888 Dewan Feb 2003 A1
20030032889 Wells Feb 2003 A1
20030035301 Gardiner et al. Feb 2003 A1
20030036689 Diab et al. Feb 2003 A1
20030040660 Jackowski et al. Feb 2003 A1
20030045914 Cohen et al. Mar 2003 A1
20030046018 Kohlmorgen et al. Mar 2003 A1
20030055355 Viertio-Oja Mar 2003 A1
20030068605 Kullok et al. Apr 2003 A1
20030070685 Patton et al. Apr 2003 A1
20030074032 Gliner Apr 2003 A1
20030081818 Fujimaki May 2003 A1
20030083596 Kramer et al. May 2003 A1
20030083716 Nicolelis et al. May 2003 A1
20030088274 Gliner et al. May 2003 A1
20030093004 Sosa et al. May 2003 A1
20030093005 Tucker May 2003 A1
20030093129 Nicolelis et al. May 2003 A1
20030097159 Schiff et al. May 2003 A1
20030097161 Firlik et al. May 2003 A1
20030100844 Miller et al. May 2003 A1
20030105408 Gotman et al. Jun 2003 A1
20030114886 Gluckman et al. Jun 2003 A1
20030120140 Bango Jun 2003 A1
20030120172 Foust et al. Jun 2003 A1
20030125786 Gliner et al. Jul 2003 A1
20030128801 Eisenberg et al. Jul 2003 A1
20030130706 Sheffield et al. Jul 2003 A1
20030130709 D. C. et al. Jul 2003 A1
20030135128 Suffin et al. Jul 2003 A1
20030139681 Melker et al. Jul 2003 A1
20030144601 Prichep Jul 2003 A1
20030149351 Nowinski et al. Aug 2003 A1
20030149678 Cook Aug 2003 A1
20030153818 Bocionek et al. Aug 2003 A1
20030158466 Lynn et al. Aug 2003 A1
20030158495 Hogan Aug 2003 A1
20030158496 Keirsbilck et al. Aug 2003 A1
20030158497 Graham et al. Aug 2003 A1
20030158587 Esteller et al. Aug 2003 A1
20030160622 Duensing et al. Aug 2003 A1
20030163027 Balkin et al. Aug 2003 A1
20030163028 Balkin et al. Aug 2003 A1
20030167019 Viertio-Oja et al. Sep 2003 A1
20030171658 Keirsbilck et al. Sep 2003 A1
20030171685 Lesser et al. Sep 2003 A1
20030171689 Millan et al. Sep 2003 A1
20030176804 Melker Sep 2003 A1
20030181791 Thomas et al. Sep 2003 A1
20030181821 Greenwald et al. Sep 2003 A1
20030181954 Rezai Sep 2003 A1
20030181955 Gielen et al. Sep 2003 A1
20030185408 Causevic et al. Oct 2003 A1
20030187359 Njemanze Oct 2003 A1
20030195429 Wilson Oct 2003 A1
20030195574 Osorio et al. Oct 2003 A1
20030199749 Lowery, Jr. et al. Oct 2003 A1
20030204135 Bystritsky Oct 2003 A1
20030216654 Xu et al. Nov 2003 A1
20030225335 Njemanze Dec 2003 A1
20030225340 Collura Dec 2003 A1
20030229291 Collura Dec 2003 A1
20030233039 Shao et al. Dec 2003 A1
20030233250 Joffe et al. Dec 2003 A1
20030234781 Laidlaw et al. Dec 2003 A1
20030236458 Hochman Dec 2003 A1
20030236557 Whitehurst et al. Dec 2003 A1
20030236558 Whitehurst et al. Dec 2003 A1
20040002635 Hargrove et al. Jan 2004 A1
20040006265 Alhussiny Jan 2004 A1
20040006376 Falci Jan 2004 A1
20040010203 Bibian et al. Jan 2004 A1
20040015204 Whitehurst et al. Jan 2004 A1
20040015205 Whitehurst et al. Jan 2004 A1
20040019257 Meadows Jan 2004 A1
20040019370 Gliner et al. Jan 2004 A1
20040024287 Patton et al. Feb 2004 A1
20040030585 Sariel Feb 2004 A1
20040034299 Kandori et al. Feb 2004 A1
20040039268 Barbour et al. Feb 2004 A1
20040049124 Kullok et al. Mar 2004 A1
20040049484 Kamba Mar 2004 A1
20040059203 Guerrero et al. Mar 2004 A1
20040059241 Suffin Mar 2004 A1
20040064020 Diab et al. Apr 2004 A1
20040064066 John et al. Apr 2004 A1
20040068164 Diab et al. Apr 2004 A1
20040068172 Nowinski et al. Apr 2004 A1
20040068199 Echauz et al. Apr 2004 A1
20040072133 Kullok et al. Apr 2004 A1
20040073098 Geva et al. Apr 2004 A1
20040073129 Caldwell et al. Apr 2004 A1
20040073273 Gluckman et al. Apr 2004 A1
20040077960 Tanaka et al. Apr 2004 A1
20040077967 Jordan Apr 2004 A1
20040078056 Zangen et al. Apr 2004 A1
20040079372 John et al. Apr 2004 A1
20040082862 Chance Apr 2004 A1
20040082876 Viertio-Oja et al. Apr 2004 A1
20040088732 Martin et al. May 2004 A1
20040092809 DeCharms May 2004 A1
20040096395 Xiong et al. May 2004 A1
20040097802 Cohen May 2004 A1
20040101146 Laitinen et al. May 2004 A1
20040116784 Gavish Jun 2004 A1
20040116791 Miyauchi Jun 2004 A1
20040116798 Cancro et al. Jun 2004 A1
20040116825 Sturzebecher Jun 2004 A1
20040117098 Ryu et al. Jun 2004 A1
20040122787 Avinash et al. Jun 2004 A1
20040122790 Walker et al. Jun 2004 A1
20040127803 Berkes et al. Jul 2004 A1
20040131998 Marom et al. Jul 2004 A1
20040133118 Llinas Jul 2004 A1
20040133119 Osorio et al. Jul 2004 A1
20040133120 Frei et al. Jul 2004 A1
20040133248 Frei et al. Jul 2004 A1
20040133390 Osorio et al. Jul 2004 A1
20040138516 Osorio et al. Jul 2004 A1
20040138517 Osorio et al. Jul 2004 A1
20040138518 Rise et al. Jul 2004 A1
20040138536 Frei et al. Jul 2004 A1
20040138580 Frei et al. Jul 2004 A1
20040138581 Frei et al. Jul 2004 A1
20040138647 Osorio et al. Jul 2004 A1
20040138711 Osorio et al. Jul 2004 A1
20040138721 Osorio et al. Jul 2004 A1
20040140811 Conti Jul 2004 A1
20040143170 DuRousseau Jul 2004 A1
20040144925 Stoddart et al. Jul 2004 A1
20040145370 Conti Jul 2004 A1
20040151368 Cruickshank et al. Aug 2004 A1
20040152958 Frei et al. Aug 2004 A1
20040152995 Cox et al. Aug 2004 A1
20040153129 Pless et al. Aug 2004 A1
20040158119 Osorio et al. Aug 2004 A1
20040158298 Gliner et al. Aug 2004 A1
20040158300 Gardiner Aug 2004 A1
20040166536 Kerkman et al. Aug 2004 A1
20040167418 Nguyen et al. Aug 2004 A1
20040172089 Whitehurst et al. Sep 2004 A1
20040172091 Rezai Sep 2004 A1
20040172094 Cohen et al. Sep 2004 A1
20040181162 Wilson Sep 2004 A1
20040184024 Katura et al. Sep 2004 A1
20040186542 van Venrooij et al. Sep 2004 A1
20040193037 Tsukada et al. Sep 2004 A1
20040193068 Burton et al. Sep 2004 A1
20040193220 Whitehurst et al. Sep 2004 A1
20040195512 Crosetto Oct 2004 A1
20040199482 Wilson Oct 2004 A1
20040204636 Diab et al. Oct 2004 A1
20040204637 Diab et al. Oct 2004 A1
20040204656 Tolvanen-Laakso et al. Oct 2004 A1
20040204659 John et al. Oct 2004 A1
20040210127 Kandori et al. Oct 2004 A1
20040210146 Diab et al. Oct 2004 A1
20040210156 Hogan Oct 2004 A1
20040215082 Chance Oct 2004 A1
20040220494 Sturzebecher Nov 2004 A1
20040220782 Cook Nov 2004 A1
20040225179 Kaplan et al. Nov 2004 A1
20040230105 Geva et al. Nov 2004 A1
20040243017 Causevic Dec 2004 A1
20040243182 Cohen et al. Dec 2004 A1
20040254493 Chervin et al. Dec 2004 A1
20040260169 Sternnickel Dec 2004 A1
20040260356 Kara et al. Dec 2004 A1
20040263162 Kandori et al. Dec 2004 A1
20040267152 Pineda Dec 2004 A1
20050004489 Sarkela et al. Jan 2005 A1
20050007091 Makeig et al. Jan 2005 A1
20050010091 Woods et al. Jan 2005 A1
20050010116 Korhonen et al. Jan 2005 A1
20050015205 Repucci et al. Jan 2005 A1
20050018858 John Jan 2005 A1
20050019734 Peled Jan 2005 A1
20050020483 Oksenberg et al. Jan 2005 A1
20050020918 Wilk et al. Jan 2005 A1
20050021105 Firlik et al. Jan 2005 A1
20050025704 Keirsbilck et al. Feb 2005 A1
20050027284 Lozano et al. Feb 2005 A1
20050032827 Oksenberg et al. Feb 2005 A1
20050033122 Balkin et al. Feb 2005 A1
20050033154 deCharms Feb 2005 A1
20050033174 Moehring et al. Feb 2005 A1
20050033379 Lozano et al. Feb 2005 A1
20050038354 Miller et al. Feb 2005 A1
20050043774 Devlin et al. Feb 2005 A1
20050049651 Whitehurst et al. Mar 2005 A1
20050059689 Oksenberg et al. Mar 2005 A1
20050059874 Fuchs et al. Mar 2005 A1
20050060001 Singhal et al. Mar 2005 A1
20050060007 Goetz Mar 2005 A1
20050060008 Goetz Mar 2005 A1
20050060009 Goetz Mar 2005 A1
20050060010 Goetz Mar 2005 A1
20050065412 Shiomi et al. Mar 2005 A1
20050065427 Magill et al. Mar 2005 A1
20050075568 Moehring Apr 2005 A1
20050079474 Lowe Apr 2005 A1
20050079636 White et al. Apr 2005 A1
20050080124 Teegarden et al. Apr 2005 A1
20050080349 Okada et al. Apr 2005 A1
20050080828 Johnson Apr 2005 A1
20050085744 Beverina et al. Apr 2005 A1
20050096311 Suffin et al. May 2005 A1
20050096517 Diab et al. May 2005 A1
20050106713 Phan et al. May 2005 A1
20050107654 Riehl May 2005 A1
20050113713 Foust et al. May 2005 A1
20050118286 Suffin et al. Jun 2005 A1
20050119547 Shastri et al. Jun 2005 A1
20050119586 Coyle et al. Jun 2005 A1
20050124848 Holzner Jun 2005 A1
20050124851 Patton et al. Jun 2005 A1
20050124863 Cook Jun 2005 A1
20050131311 Leuthardt et al. Jun 2005 A1
20050135102 Gardiner et al. Jun 2005 A1
20050136002 Fossheim et al. Jun 2005 A1
20050137494 Viertio-Oja Jun 2005 A1
20050137645 Voipio et al. Jun 2005 A1
20050144042 Joffe et al. Jun 2005 A1
20050148828 Lindsay Jul 2005 A1
20050148893 Misczynski et al. Jul 2005 A1
20050148894 Misczynski et al. Jul 2005 A1
20050148895 Misczynski et al. Jul 2005 A1
20050149123 Lesser et al. Jul 2005 A1
20050149157 Hunter et al. Jul 2005 A1
20050153268 Junkin Jul 2005 A1
20050154290 Langleben Jul 2005 A1
20050154419 Whitehurst et al. Jul 2005 A1
20050154425 Boveja et al. Jul 2005 A1
20050154426 Boveja et al. Jul 2005 A1
20050156602 Conti Jul 2005 A1
20050159670 Sneddon Jul 2005 A1
20050159671 Sneddon Jul 2005 A1
20050165458 Boveja et al. Jul 2005 A1
20050167588 Donnangelo Aug 2005 A1
20050171410 Hjelt et al. Aug 2005 A1
20050182287 Becker Aug 2005 A1
20050182288 Zabara Aug 2005 A1
20050182389 LaPorte et al. Aug 2005 A1
20050182450 Hunter et al. Aug 2005 A1
20050182453 Whitehurst et al. Aug 2005 A1
20050182456 Ziobro et al. Aug 2005 A1
20050182467 Hunter et al. Aug 2005 A1
20050182468 Hunter et al. Aug 2005 A1
20050182469 Hunter et al. Aug 2005 A1
20050187600 Hunter et al. Aug 2005 A1
20050192514 Kearby et al. Sep 2005 A1
20050192644 Boveja et al. Sep 2005 A1
20050192647 Hunter et al. Sep 2005 A1
20050197590 Osorio et al. Sep 2005 A1
20050197675 David et al. Sep 2005 A1
20050197678 Boveja et al. Sep 2005 A1
20050209512 Heruth et al. Sep 2005 A1
20050209517 Diab et al. Sep 2005 A1
20050209654 Boveja et al. Sep 2005 A1
20050209664 Hunter et al. Sep 2005 A1
20050209665 Hunter et al. Sep 2005 A1
20050209666 Hunter et al. Sep 2005 A1
20050215889 Patterson Sep 2005 A1
20050216070 Boveja et al. Sep 2005 A1
20050216071 Devlin et al. Sep 2005 A1
20050222522 Heruth et al. Oct 2005 A1
20050222639 Seifritz et al. Oct 2005 A1
20050228451 Jaax et al. Oct 2005 A1
20050228785 Wolcott et al. Oct 2005 A1
20050240087 Keenan et al. Oct 2005 A1
20050240229 Whitehurst et al. Oct 2005 A1
20050240253 Tyler et al. Oct 2005 A1
20050244045 Eriksson Nov 2005 A1
20050245796 Woods et al. Nov 2005 A1
20050251055 Zhirnov et al. Nov 2005 A1
20050251220 Barrett et al. Nov 2005 A1
20050256378 Takai et al. Nov 2005 A1
20050256385 Diab et al. Nov 2005 A1
20050256418 Mietus et al. Nov 2005 A1
20050267011 Deisseroth et al. Dec 2005 A1
20050267343 Woods et al. Dec 2005 A1
20050267344 Woods et al. Dec 2005 A1
20050267362 Mietus et al. Dec 2005 A1
20050267542 David et al. Dec 2005 A1
20050273017 Gordon Dec 2005 A1
20050277813 Katz et al. Dec 2005 A1
20050277912 John Dec 2005 A1
20050283053 deCharms Dec 2005 A1
20050283090 Wells Dec 2005 A1
20060004298 Kennedy et al. Jan 2006 A1
20060004422 De Ridder Jan 2006 A1
20060009704 Okada et al. Jan 2006 A1
20060009815 Boveja et al. Jan 2006 A1
20060014753 Shamloo et al. Jan 2006 A1
20060015034 Martinerie et al. Jan 2006 A1
20060015153 Gliner et al. Jan 2006 A1
20060018525 Barbour Jan 2006 A1
20060020184 Woods et al. Jan 2006 A1
20060036152 Kozel Feb 2006 A1
20060036153 Laken Feb 2006 A1
20060041201 Behbehani et al. Feb 2006 A1
20060047187 Goyal et al. Mar 2006 A1
20060047216 Dorr et al. Mar 2006 A1
20060047324 Tass Mar 2006 A1
20060047325 Thimineur et al. Mar 2006 A1
20060051814 Jackowski et al. Mar 2006 A1
20060052386 Wieloch et al. Mar 2006 A1
20060052657 Zabara Mar 2006 A9
20060052706 Hynynen et al. Mar 2006 A1
20060058590 Shaw et al. Mar 2006 A1
20060058683 Chance Mar 2006 A1
20060058856 Morrell Mar 2006 A1
20060061544 Min et al. Mar 2006 A1
20060064138 Velasco et al. Mar 2006 A1
20060064139 Chung et al. Mar 2006 A1
20060064140 Whitehurst et al. Mar 2006 A1
20060069059 Schaller et al. Mar 2006 A1
20060069415 Cameron et al. Mar 2006 A1
20060074290 Chen et al. Apr 2006 A1
20060074298 Borsook et al. Apr 2006 A1
20060074334 Coyle Apr 2006 A1
20060074822 Eda et al. Apr 2006 A1
20060078183 deCharms Apr 2006 A1
20060079936 Boveja et al. Apr 2006 A1
20060082727 Bolger et al. Apr 2006 A1
20060084858 Marks Apr 2006 A1
20060084877 Ujhazy et al. Apr 2006 A1
20060087746 Lipow Apr 2006 A1
20060089541 Braun et al. Apr 2006 A1
20060089549 Diab et al. Apr 2006 A1
20060094968 Drew May 2006 A1
20060094970 Drew May 2006 A1
20060094971 Drew May 2006 A1
20060094972 Drew May 2006 A1
20060095091 Drew May 2006 A1
20060095092 Drew May 2006 A1
20060100526 Yamamoto et al. May 2006 A1
20060100530 Kliot et al. May 2006 A1
20060100671 Ridder May 2006 A1
20060102171 Gavish May 2006 A1
20060106274 Thomas et al. May 2006 A1
20060106326 Krebs et al. May 2006 A1
20060106430 Fowler et al. May 2006 A1
20060106434 Padgitt et al. May 2006 A1
20060111644 Guttag et al. May 2006 A1
20060116556 Duhamel Jun 2006 A1
20060122481 Sievenpiper et al. Jun 2006 A1
20060129022 Venza et al. Jun 2006 A1
20060129202 Armstrong Jun 2006 A1
20060129277 Wu et al. Jun 2006 A1
20060129324 Rabinoff et al. Jun 2006 A1
20060135879 Liley Jun 2006 A1
20060135880 Sarkela Jun 2006 A1
20060136135 Little et al. Jun 2006 A1
20060142802 Armstrong Jun 2006 A1
20060149144 Lynn et al. Jul 2006 A1
20060149160 Kofol et al. Jul 2006 A1
20060149337 John Jul 2006 A1
20060152227 Hammer Jul 2006 A1
20060153396 John Jul 2006 A1
20060155206 Lynn Jul 2006 A1
20060155207 Lynn et al. Jul 2006 A1
20060155348 deCharms Jul 2006 A1
20060155495 Osorio et al. Jul 2006 A1
20060161071 Lynn et al. Jul 2006 A1
20060161075 Kurtz Jul 2006 A1
20060161217 Jaax et al. Jul 2006 A1
20060161218 Danilov Jul 2006 A1
20060161384 Osorio et al. Jul 2006 A1
20060167370 Greenwald et al. Jul 2006 A1
20060167497 Armstrong et al. Jul 2006 A1
20060167564 Flaherty et al. Jul 2006 A1
20060167722 Struys et al. Jul 2006 A1
20060170424 Kasevich Aug 2006 A1
20060173259 Flaherty et al. Aug 2006 A1
20060173364 Clancy et al. Aug 2006 A1
20060173493 Armstrong et al. Aug 2006 A1
20060173494 Armstrong et al. Aug 2006 A1
20060173495 Armstrong et al. Aug 2006 A1
20060173510 Besio et al. Aug 2006 A1
20060176062 Yang et al. Aug 2006 A1
20060178709 Foster et al. Aug 2006 A1
20060184058 Silberstein Aug 2006 A1
20060184059 Jadidi Aug 2006 A1
20060188134 Quist Aug 2006 A1
20060189866 Thomas et al. Aug 2006 A1
20060189880 Lynn et al. Aug 2006 A1
20060189882 Thomas Aug 2006 A1
20060189899 Flaherty et al. Aug 2006 A1
20060191543 Becker et al. Aug 2006 A1
20060195039 Drew et al. Aug 2006 A1
20060195154 Jaax et al. Aug 2006 A1
20060195155 Firlik et al. Aug 2006 A1
20060200013 Smith et al. Sep 2006 A1
20060200016 Diab et al. Sep 2006 A1
20060200034 Ricci et al. Sep 2006 A1
20060200035 Ricci et al. Sep 2006 A1
20060200206 Firlik et al. Sep 2006 A1
20060204532 John Sep 2006 A1
20060206033 Guerrero et al. Sep 2006 A1
20060206108 Hempel Sep 2006 A1
20060206155 Ben-David et al. Sep 2006 A1
20060206165 Jaax et al. Sep 2006 A1
20060206174 Honeycutt et al. Sep 2006 A1
20060212090 Lozano et al. Sep 2006 A1
20060212091 Lozano et al. Sep 2006 A1
20060217609 Diab et al. Sep 2006 A1
20060217781 John Sep 2006 A1
20060217816 Pesaran et al. Sep 2006 A1
20060224216 Pless et al. Oct 2006 A1
20060224421 St. Ores et al. Oct 2006 A1
20060225437 Kazami Oct 2006 A1
20060229164 Einav Oct 2006 A1
20060233390 Causevic et al. Oct 2006 A1
20060235315 Akselrod et al. Oct 2006 A1
20060235324 Lynn Oct 2006 A1
20060235484 Jaax et al. Oct 2006 A1
20060235489 Drew et al. Oct 2006 A1
20060239482 Hatoum Oct 2006 A1
20060241373 Strychacz et al. Oct 2006 A1
20060241382 Li et al. Oct 2006 A1
20060241562 John et al. Oct 2006 A1
20060241718 Tyler et al. Oct 2006 A1
20060247728 Foster et al. Nov 2006 A1
20060251303 He et al. Nov 2006 A1
20060252978 Vesely et al. Nov 2006 A1
20060252979 Vesely et al. Nov 2006 A1
20060258896 Haber et al. Nov 2006 A1
20060258950 Hargrove et al. Nov 2006 A1
20060259077 Pardo et al. Nov 2006 A1
20060265022 John et al. Nov 2006 A1
20060276695 Lynn et al. Dec 2006 A9
20060281543 Sutton et al. Dec 2006 A1
20060281980 Randlov et al. Dec 2006 A1
20060282123 Hunter et al. Dec 2006 A1
20060287691 Drew Dec 2006 A1
20060293578 Rennaker Dec 2006 A1
20060293721 Tarver et al. Dec 2006 A1
20060293723 Whitehurst et al. Dec 2006 A1
20070000372 Rezai et al. Jan 2007 A1
20070005115 Lozano et al. Jan 2007 A1
20070005391 Repucci et al. Jan 2007 A1
20070007454 Stoddart et al. Jan 2007 A1
20070008172 Hewett et al. Jan 2007 A1
20070014454 Sawyer et al. Jan 2007 A1
20070015985 Tolvanen-Laakso et al. Jan 2007 A1
20070016095 Low et al. Jan 2007 A1
20070016264 Falci Jan 2007 A1
20070019846 Bullitt et al. Jan 2007 A1
20070021673 Arbel et al. Jan 2007 A1
20070021675 Childre et al. Jan 2007 A1
20070021800 Whitehurst et al. Jan 2007 A1
20070025608 Armstrong Feb 2007 A1
20070027486 Armstrong Feb 2007 A1
20070027498 Maschino et al. Feb 2007 A1
20070027499 Maschino et al. Feb 2007 A1
20070027500 Maschino et al. Feb 2007 A1
20070027501 Jensen et al. Feb 2007 A1
20070031798 Gottfried Feb 2007 A1
20070032733 Burton Feb 2007 A1
20070032737 Causevic et al. Feb 2007 A1
20070032834 Gliner et al. Feb 2007 A1
20070036355 Terauchi et al. Feb 2007 A1
20070036402 Cahill et al. Feb 2007 A1
20070038067 Kandori et al. Feb 2007 A1
20070038264 Jaax et al. Feb 2007 A1
20070038382 Keenan Feb 2007 A1
20070043392 Gliner et al. Feb 2007 A1
20070043401 John Feb 2007 A1
20070049844 Rosenfeld Mar 2007 A1
20070049988 Carbunaru et al. Mar 2007 A1
20070050715 Behar Mar 2007 A1
20070055145 Zelnik et al. Mar 2007 A1
20070060830 Le et al. Mar 2007 A1
20070060831 Le et al. Mar 2007 A1
20070060954 Cameron et al. Mar 2007 A1
20070060974 Lozano Mar 2007 A1
20070060984 Webb et al. Mar 2007 A1
20070066403 Conkwright Mar 2007 A1
20070066914 Le et al. Mar 2007 A1
20070066915 Frei et al. Mar 2007 A1
20070066997 He et al. Mar 2007 A1
20070067003 Sanchez et al. Mar 2007 A1
20070067004 Boveja et al. Mar 2007 A1
20070072857 Teegarden et al. Mar 2007 A1
20070078134 Teegarden et al. Apr 2007 A1
20070081712 Huang et al. Apr 2007 A1
20070083128 Cote et al. Apr 2007 A1
20070093721 Lynn et al. Apr 2007 A1
20070093870 Maschino Apr 2007 A1
20070100246 Hyde May 2007 A1
20070100251 Prichep May 2007 A1
20070100278 Frei et al. May 2007 A1
20070100377 Armstrong et al. May 2007 A1
20070100378 Maschino May 2007 A1
20070100389 Jaax et al. May 2007 A1
20070100392 Maschino et al. May 2007 A1
20070100398 Sloan May 2007 A1
20070100666 Stivoric et al. May 2007 A1
20070112404 Mann et al. May 2007 A1
20070118197 Loeb May 2007 A1
20070127793 Beckett et al. Jun 2007 A1
20070129647 Lynn Jun 2007 A1
20070129769 Bourget et al. Jun 2007 A1
20070129774 Bourget et al. Jun 2007 A1
20070135724 Ujhazy et al. Jun 2007 A1
20070135728 Snyder et al. Jun 2007 A1
20070138886 Krebs et al. Jun 2007 A1
20070142862 Dilorenzo Jun 2007 A1
20070142873 Esteller et al. Jun 2007 A1
20070142874 John Jun 2007 A1
20070149860 Lynn et al. Jun 2007 A1
20070150024 Leyde et al. Jun 2007 A1
20070150025 Dilorenzo et al. Jun 2007 A1
20070150026 Bourget et al. Jun 2007 A1
20070150029 Bourget et al. Jun 2007 A1
20070156180 Jaax et al. Jul 2007 A1
20070156457 Brown Jul 2007 A1
20070159185 Yang et al. Jul 2007 A1
20070161919 DiLorenzo Jul 2007 A1
20070162085 DiLorenzo Jul 2007 A1
20070162086 DiLorenzo Jul 2007 A1
20070165915 Fuchs Jul 2007 A1
20070167694 Causevic et al. Jul 2007 A1
20070167723 Park et al. Jul 2007 A1
20070167853 Melker et al. Jul 2007 A1
20070167858 Virtanen et al. Jul 2007 A1
20070167991 DiLorenzo Jul 2007 A1
20070173733 Le et al. Jul 2007 A1
20070173902 Maschino et al. Jul 2007 A1
20070179395 Sotos et al. Aug 2007 A1
20070179396 Le et al. Aug 2007 A1
20070179534 Firlik et al. Aug 2007 A1
20070179558 Gliner et al. Aug 2007 A1
20070179734 Chmiel et al. Aug 2007 A1
20070184507 Jackowski et al. Aug 2007 A1
20070191688 Lynn Aug 2007 A1
20070191691 Polanco Aug 2007 A1
20070191697 Lynn et al. Aug 2007 A1
20070191704 DeCharms Aug 2007 A1
20070191727 Fadem Aug 2007 A1
20070197930 Sarkela Aug 2007 A1
20070198063 Hunter et al. Aug 2007 A1
20070203401 Gordon et al. Aug 2007 A1
20070203448 Melker et al. Aug 2007 A1
20070208212 DiLorenzo Sep 2007 A1
20070208269 Mumford et al. Sep 2007 A1
20070209669 Derchak Sep 2007 A1
20070213785 Osorio et al. Sep 2007 A1
20070213786 Sackellares et al. Sep 2007 A1
20070225581 Diab et al. Sep 2007 A1
20070225674 Molnar et al. Sep 2007 A1
20070225774 Eskandar et al. Sep 2007 A1
20070225932 Halford Sep 2007 A1
20070233192 Craig Oct 2007 A1
20070233193 Craig Oct 2007 A1
20070238934 Viswanathan Oct 2007 A1
20070239059 McIver Oct 2007 A1
20070244387 Rodriguez Ponce et al. Oct 2007 A1
20070244407 Osorio Oct 2007 A1
20070249918 Diab et al. Oct 2007 A1
20070249949 Hadley Oct 2007 A1
20070249952 Rubin et al. Oct 2007 A1
20070250119 Tyler et al. Oct 2007 A1
20070250138 Nofzinger Oct 2007 A1
20070255122 Vol et al. Nov 2007 A1
20070255135 Kalafut et al. Nov 2007 A1
20070255155 Drew et al. Nov 2007 A1
20070255320 Inman et al. Nov 2007 A1
20070255379 Williams et al. Nov 2007 A1
20070255531 Drew Nov 2007 A1
20070259323 Brown et al. Nov 2007 A1
20070260151 Clifford Nov 2007 A1
20070265508 Sheikhzadeh-Nadjar et al. Nov 2007 A1
20070265533 Tran Nov 2007 A1
20070273504 Tran Nov 2007 A1
20070273611 Torch Nov 2007 A1
20070276270 Tran Nov 2007 A1
20070276278 Coyle et al. Nov 2007 A1
20070276279 Echauz et al. Nov 2007 A1
20070276441 Goetz Nov 2007 A1
20070276609 Greenwald Nov 2007 A1
20070280508 Ernst et al. Dec 2007 A1
20070282228 Einav et al. Dec 2007 A1
20070287896 Derchak et al. Dec 2007 A1
20070291832 Diab et al. Dec 2007 A1
20070293760 Schaafsma Dec 2007 A1
20070299370 Bystritsky Dec 2007 A1
20070299371 Einav et al. Dec 2007 A1
20080001600 deCharms Jan 2008 A1
20080001735 Tran Jan 2008 A1
20080004514 Diab et al. Jan 2008 A1
20080004550 Einav et al. Jan 2008 A1
20080004904 Tran Jan 2008 A1
20080009685 Kim et al. Jan 2008 A1
20080009772 Tyler et al. Jan 2008 A1
20080013747 Tran Jan 2008 A1
20080015458 Buarque de Macedo et al. Jan 2008 A1
20080015459 Llinas Jan 2008 A1
20080021332 Brainard Jan 2008 A1
20080021336 Dobak Jan 2008 A1
20080021340 Sarkela Jan 2008 A1
20080021341 Harris et al. Jan 2008 A1
20080021342 Echauz et al. Jan 2008 A1
20080021345 Kern et al. Jan 2008 A1
20080027347 Harris et al. Jan 2008 A1
20080027348 Harris et al. Jan 2008 A1
20080027515 Harris et al. Jan 2008 A1
20080033266 Diab et al. Feb 2008 A1
20080033291 Rousso et al. Feb 2008 A1
20080033297 Sliwa Feb 2008 A1
20080033502 Harris et al. Feb 2008 A1
20080033503 Fowler et al. Feb 2008 A1
20080033508 Frei et al. Feb 2008 A1
20080033513 Man et al. Feb 2008 A1
20080036752 Diab et al. Feb 2008 A1
20080039677 Adams Feb 2008 A1
20080039698 Burton Feb 2008 A1
20080039737 Breiter et al. Feb 2008 A1
20080039904 Bulkes et al. Feb 2008 A1
20080042067 Rousso et al. Feb 2008 A1
20080045775 Lozano Feb 2008 A1
20080045823 Diab et al. Feb 2008 A1
20080045844 Arbel et al. Feb 2008 A1
20080046012 Covalin et al. Feb 2008 A1
20080046035 Fowler et al. Feb 2008 A1
20080049376 Stevenson et al. Feb 2008 A1
20080051669 Meyer et al. Feb 2008 A1
20080051858 Haber et al. Feb 2008 A1
20080058664 Mirro Mar 2008 A1
20080058668 Seyed Momen et al. Mar 2008 A1
20080058773 John Mar 2008 A1
20080064934 Frei et al. Mar 2008 A1
20080065183 Whitehurst et al. Mar 2008 A1
20080069446 Ancelin Mar 2008 A1
20080071150 Miesel et al. Mar 2008 A1
20080071326 Heruth et al. Mar 2008 A1
20080074307 Boric-Lubecke et al. Mar 2008 A1
20080077010 Cohen-Solal et al. Mar 2008 A1
20080077015 Boric-Lubecke et al. Mar 2008 A1
20080077191 Morrell Mar 2008 A1
20080081963 Naghavi et al. Apr 2008 A1
20080082018 Sackner et al. Apr 2008 A1
20080086182 Ben-David et al. Apr 2008 A1
20080091118 Georgopoulos Apr 2008 A1
20080091240 Ben-David et al. Apr 2008 A1
20080097197 Kalafut et al. Apr 2008 A1
20080097235 Ofek et al. Apr 2008 A1
20080097553 John Apr 2008 A1
20080097785 Ali Apr 2008 A1
20080103547 Okun et al. May 2008 A1
20080103548 Fowler et al. May 2008 A1
20080109050 John May 2008 A1
20080119716 Boric-Lubecke et al. May 2008 A1
20080119747 Mietus et al. May 2008 A1
20080119763 Wiener May 2008 A1
20080119900 DiLorenzo May 2008 A1
20080123927 Miga et al. May 2008 A1
20080125669 Suffin et al. May 2008 A1
20080125829 Velasco et al. May 2008 A1
20080125830 Morrell May 2008 A1
20080125831 Morrell May 2008 A1
20080128626 Rousso et al. Jun 2008 A1
20080132383 Einav et al. Jun 2008 A1
20080139953 Baker et al. Jun 2008 A1
20080140141 Ben-David et al. Jun 2008 A1
20080140149 John et al. Jun 2008 A1
20080140403 Hughes et al. Jun 2008 A1
20080147137 Cohen et al. Jun 2008 A1
20080154111 Wu et al. Jun 2008 A1
20080154126 Culver et al. Jun 2008 A1
20080154148 Chung et al. Jun 2008 A1
20080154331 John et al. Jun 2008 A1
20080154332 Rezai Jun 2008 A1
20080157980 Sachanandani et al. Jul 2008 A1
20080161700 Sachanandani et al. Jul 2008 A1
20080161879 Firlik et al. Jul 2008 A1
20080161880 Firlik et al. Jul 2008 A1
20080161881 Firlik et al. Jul 2008 A1
20080161886 Stevenson et al. Jul 2008 A1
20080161894 Ben-David et al. Jul 2008 A1
20080162182 Cazares et al. Jul 2008 A1
20080167535 Stivoric et al. Jul 2008 A1
20080167540 Korhonen et al. Jul 2008 A1
20080167569 Ermes et al. Jul 2008 A1
20080167571 Gevins Jul 2008 A1
20080177195 Armitstead Jul 2008 A1
20080177196 Burdick et al. Jul 2008 A1
20080177197 Lee et al. Jul 2008 A1
20080183072 Robertson et al. Jul 2008 A1
20080183097 Leyde et al. Jul 2008 A1
20080188765 Stolarski et al. Aug 2008 A1
20080194981 Sarkela et al. Aug 2008 A1
20080195166 Sun et al. Aug 2008 A1
20080200831 Sturzebecher Aug 2008 A1
20080208072 Fadem et al. Aug 2008 A1
20080208073 Causevic Aug 2008 A1
20080208280 Lindenthaler et al. Aug 2008 A1
20080208285 Fowler et al. Aug 2008 A1
20080214902 Lee et al. Sep 2008 A1
20080215112 Firlik et al. Sep 2008 A1
20080219917 Koruga Sep 2008 A1
20080221400 Lee et al. Sep 2008 A1
20080221401 Derchak et al. Sep 2008 A1
20080221441 Bjornerud et al. Sep 2008 A1
20080221472 Lee et al. Sep 2008 A1
20080221969 Lee et al. Sep 2008 A1
20080228077 Wilk et al. Sep 2008 A1
20080228100 Navakatikyan Sep 2008 A1
20080228239 Tyler et al. Sep 2008 A1
20080229408 Dinges et al. Sep 2008 A1
20080230702 Rousso et al. Sep 2008 A1
20080230705 Rousso et al. Sep 2008 A1
20080234113 Einav Sep 2008 A1
20080234601 Wexelman Sep 2008 A1
20080235469 Drew Sep 2008 A1
20080241804 Pennebaker Oct 2008 A1
20080242521 Einav Oct 2008 A1
20080242976 Robertson et al. Oct 2008 A1
20080243005 Jung et al. Oct 2008 A1
20080243014 Moussavi et al. Oct 2008 A1
20080243017 Moussavi et al. Oct 2008 A1
20080243021 Causevic et al. Oct 2008 A1
20080244003 Springer Oct 2008 A1
20080247618 Laine et al. Oct 2008 A1
20080249430 John et al. Oct 2008 A1
20080249589 Cornejo Cruz et al. Oct 2008 A1
20080255469 Shieh et al. Oct 2008 A1
20080255816 Neville Oct 2008 A1
20080255949 Genco et al. Oct 2008 A1
20080257349 Hedner et al. Oct 2008 A1
20080260212 Moskal et al. Oct 2008 A1
20080262327 Kato Oct 2008 A1
20080262367 Mugler et al. Oct 2008 A1
20080262371 Causevic Oct 2008 A1
20080269542 Zabara Oct 2008 A1
20080269652 Reiner Oct 2008 A1
20080269812 Gerber et al. Oct 2008 A1
20080269833 Scott et al. Oct 2008 A1
20080269834 Byerman et al. Oct 2008 A1
20080269840 Scott et al. Oct 2008 A1
20080269843 Gerber et al. Oct 2008 A1
20080275327 Faarbaek et al. Nov 2008 A1
20080275340 Beach et al. Nov 2008 A1
20080275526 Lozano Nov 2008 A1
20080279436 Razifar et al. Nov 2008 A1
20080281238 Oohashi et al. Nov 2008 A1
20080281381 Gerber et al. Nov 2008 A1
20080281667 Chen et al. Nov 2008 A1
20080286453 Koruga Nov 2008 A1
20080287774 Katz-Brull Nov 2008 A1
20080287821 Jung et al. Nov 2008 A1
20080288018 Rezai et al. Nov 2008 A1
20080294019 Tran Nov 2008 A1
20080294063 Bibian et al. Nov 2008 A1
20080298653 Amunts et al. Dec 2008 A1
20080298659 Spence et al. Dec 2008 A1
20080304691 Lai Dec 2008 A1
20080304731 Kimura Dec 2008 A1
20080306365 Bunce et al. Dec 2008 A1
20080310697 Razifar et al. Dec 2008 A1
20080311549 Belitsiotis Dec 2008 A1
20080317317 Shekhar et al. Dec 2008 A1
20080319326 Behbehani et al. Dec 2008 A1
20080319505 Boyden et al. Dec 2008 A1
20090005654 Jung et al. Jan 2009 A1
20090005667 Cui et al. Jan 2009 A1
20090005675 Grunwald et al. Jan 2009 A1
20090006001 Niculescu et al. Jan 2009 A1
20090009284 Sako Jan 2009 A1
20090012387 Hanson et al. Jan 2009 A1
20090018407 Jung et al. Jan 2009 A1
20090018419 Torch Jan 2009 A1
20090018429 Saliga et al. Jan 2009 A1
20090018431 Feiweier et al. Jan 2009 A1
20090018432 He et al. Jan 2009 A1
20090018462 Bell Jan 2009 A1
20090022825 Kerkman et al. Jan 2009 A1
20090024007 Lee et al. Jan 2009 A1
20090024050 Jung et al. Jan 2009 A1
20090030476 Hargrove Jan 2009 A1
20090030930 Pradeep et al. Jan 2009 A1
20090033333 Gribova et al. Feb 2009 A1
20090036781 Utsugi et al. Feb 2009 A1
20090036791 Plenz Feb 2009 A1
20090036950 Armstrong et al. Feb 2009 A1
20090039889 Wilt et al. Feb 2009 A1
20090043221 Kaplan et al. Feb 2009 A1
20090048507 Feiweier et al. Feb 2009 A1
20090048530 Sarkela et al. Feb 2009 A1
20090054788 Hauger et al. Feb 2009 A1
20090054800 Martinerie et al. Feb 2009 A1
20090054801 Hinrikus et al. Feb 2009 A1
20090054946 Sommer et al. Feb 2009 A1
20090054958 Nofzinger Feb 2009 A1
20090058660 Torch Mar 2009 A1
20090062660 Chance Mar 2009 A1
20090062670 Sterling et al. Mar 2009 A1
20090062676 Kruglikov et al. Mar 2009 A1
20090062679 Tan et al. Mar 2009 A1
20090062680 Sandford Mar 2009 A1
20090062696 Nathan et al. Mar 2009 A1
20090062698 Einav et al. Mar 2009 A1
20090069707 Sandford Mar 2009 A1
20090074279 Razifar et al. Mar 2009 A1
20090076339 Quintin et al. Mar 2009 A1
20090076399 Arbel et al. Mar 2009 A1
20090076400 Diab et al. Mar 2009 A1
20090076406 Graham et al. Mar 2009 A1
20090076407 John et al. Mar 2009 A1
20090076567 Fowler et al. Mar 2009 A1
20090078875 Rousso et al. Mar 2009 A1
20090082688 Wagner Mar 2009 A1
20090082689 Guttag et al. Mar 2009 A1
20090082690 Phillips et al. Mar 2009 A1
20090082829 Panken et al. Mar 2009 A1
20090083071 Phillips et al. Mar 2009 A1
20090088658 Luo et al. Apr 2009 A1
20090088680 Aravanis et al. Apr 2009 A1
20090093403 Zhang et al. Apr 2009 A1
20090093862 Gliner et al. Apr 2009 A1
20090094305 Johnson Apr 2009 A1
20090099474 Pineda et al. Apr 2009 A1
20090099627 Molnar et al. Apr 2009 A1
20090099783 Reisberg Apr 2009 A1
20090105785 Wei et al. Apr 2009 A1
20090112117 Rewari Apr 2009 A1
20090112273 Wingeier et al. Apr 2009 A1
20090112277 Wingeier et al. Apr 2009 A1
20090112278 Wingeier et al. Apr 2009 A1
20090112279 Wingeier et al. Apr 2009 A1
20090112280 Wingeier et al. Apr 2009 A1
20090112281 Miyazawa et al. Apr 2009 A1
20090112523 Townsend et al. Apr 2009 A1
20090118593 Jung et al. May 2009 A1
20090118610 Karmarkar et al. May 2009 A1
20090118622 Durkin et al. May 2009 A1
20090118636 Collura May 2009 A1
20090118780 DiLorenzo May 2009 A1
20090118786 Meadows et al. May 2009 A1
20090118787 Moffitt et al. May 2009 A1
20090119154 Jung et al. May 2009 A1
20090124869 Hu et al. May 2009 A1
20090124921 Milgramm et al. May 2009 A1
20090124922 Milgramm et al. May 2009 A1
20090124923 Sackellares et al. May 2009 A1
20090131995 Sloan et al. May 2009 A1
20090132275 Jung et al. May 2009 A1
20090137915 Childre et al. May 2009 A1
20090137923 Suffin et al. May 2009 A1
20090143654 Funane et al. Jun 2009 A1
20090148019 Hamada et al. Jun 2009 A1
20090149148 Kurtz et al. Jun 2009 A1
20090149736 Skidmore et al. Jun 2009 A1
20090156907 Jung et al. Jun 2009 A1
20090156954 Cox et al. Jun 2009 A1
20090156955 Jung et al. Jun 2009 A1
20090156956 Milgramm et al. Jun 2009 A1
20090157323 Jung et al. Jun 2009 A1
20090157481 Jung et al. Jun 2009 A1
20090157482 Jung et al. Jun 2009 A1
20090157625 Jung et al. Jun 2009 A1
20090157660 Jung et al. Jun 2009 A1
20090157662 Suffin et al. Jun 2009 A1
20090157751 Jung et al. Jun 2009 A1
20090157813 Jung et al. Jun 2009 A1
20090163777 Jung et al. Jun 2009 A1
20090163980 Stevenson Jun 2009 A1
20090163981 Stevenson et al. Jun 2009 A1
20090163982 deCharms Jun 2009 A1
20090164131 Jung et al. Jun 2009 A1
20090164132 Jung et al. Jun 2009 A1
20090164302 Jung et al. Jun 2009 A1
20090164401 Jung et al. Jun 2009 A1
20090164403 Jung et al. Jun 2009 A1
20090164458 Jung et al. Jun 2009 A1
20090164503 Jung et al. Jun 2009 A1
20090164549 Jung et al. Jun 2009 A1
20090171164 Jung et al. Jul 2009 A1
20090171232 Hu et al. Jul 2009 A1
20090171240 Aguilar et al. Jul 2009 A1
20090171405 Craig Jul 2009 A1
20090172540 Jung et al. Jul 2009 A1
20090177050 Griffiths et al. Jul 2009 A1
20090177090 Grunwald et al. Jul 2009 A1
20090177108 Shieh et al. Jul 2009 A1
20090177144 Masmanidis et al. Jul 2009 A1
20090179642 deCharms Jul 2009 A1
20090182211 Diab et al. Jul 2009 A1
20090187230 Dilorenzo Jul 2009 A1
20090191131 Fossheim et al. Jul 2009 A1
20090192394 Guttag et al. Jul 2009 A1
20090192556 Wu et al. Jul 2009 A1
20090198144 Phillips et al. Aug 2009 A1
20090198145 Chow Aug 2009 A1
20090204015 Phillips et al. Aug 2009 A1
20090209831 Kucharczyk et al. Aug 2009 A1
20090209835 Diab et al. Aug 2009 A1
20090209845 Christen et al. Aug 2009 A1
20090210018 Lozano Aug 2009 A1
20090216091 Arndt Aug 2009 A1
20090216146 Teicher et al. Aug 2009 A1
20090216288 Schiff et al. Aug 2009 A1
20090220425 Moxon et al. Sep 2009 A1
20090220429 Johnsen et al. Sep 2009 A1
20090221904 Shealy et al. Sep 2009 A1
20090221928 Einav Sep 2009 A1
20090221930 Laken Sep 2009 A1
20090227876 Tran Sep 2009 A1
20090227877 Tran Sep 2009 A1
20090227882 Foo Sep 2009 A1
20090227889 John et al. Sep 2009 A2
20090234419 Maschino et al. Sep 2009 A1
20090240119 Schwaibold et al. Sep 2009 A1
20090243756 Stevenson et al. Oct 2009 A1
20090246138 Santosh et al. Oct 2009 A1
20090247893 Lapinlampi et al. Oct 2009 A1
20090247894 Causevic Oct 2009 A1
20090259277 Cornejo Cruz et al. Oct 2009 A1
20090261832 DePavia et al. Oct 2009 A1
20090264785 Causevic et al. Oct 2009 A1
20090264789 Molnar et al. Oct 2009 A1
20090264952 Jassemidis et al. Oct 2009 A1
20090264954 Rise et al. Oct 2009 A1
20090264955 Giftakis et al. Oct 2009 A1
20090264956 Rise et al. Oct 2009 A1
20090264957 Giftakis et al. Oct 2009 A1
20090264958 Hsu et al. Oct 2009 A1
20090264967 Giftakis et al. Oct 2009 A1
20090267758 Hyde et al. Oct 2009 A1
20090270687 Hyde et al. Oct 2009 A1
20090270688 Hyde et al. Oct 2009 A1
20090270692 Hyde et al. Oct 2009 A1
20090270693 Hyde et al. Oct 2009 A1
20090270694 Hyde et al. Oct 2009 A1
20090270754 Moridaira Oct 2009 A1
20090270758 Eagleman et al. Oct 2009 A1
20090270786 Hyde et al. Oct 2009 A1
20090270944 Whitehurst et al. Oct 2009 A1
20090271011 Hyde et al. Oct 2009 A1
20090271120 Hyde et al. Oct 2009 A1
20090271122 Hyde et al. Oct 2009 A1
20090271347 Hyde et al. Oct 2009 A1
20090275853 Sarkela Nov 2009 A1
20090276011 Hyde et al. Nov 2009 A1
20090276012 Hyde et al. Nov 2009 A1
20090280153 Hunter et al. Nov 2009 A1
20090281400 McCraty et al. Nov 2009 A1
20090281448 Wright et al. Nov 2009 A1
20090281594 King et al. Nov 2009 A1
20090287035 Dietrich et al. Nov 2009 A1
20090287107 Beck-Nielsen et al. Nov 2009 A1
20090287108 Levy Nov 2009 A1
20090287271 Blum et al. Nov 2009 A1
20090287272 Kokones et al. Nov 2009 A1
20090287273 Carlton et al. Nov 2009 A1
20090287274 De Ridder Nov 2009 A1
20090287467 Sparks et al. Nov 2009 A1
20090290767 Jung et al. Nov 2009 A1
20090290772 Avinash et al. Nov 2009 A1
20090292180 Mirow Nov 2009 A1
20090292478 Avinash et al. Nov 2009 A1
20090292551 Sirohey et al. Nov 2009 A1
20090292713 Jung et al. Nov 2009 A1
20090292724 Jung et al. Nov 2009 A1
20090297000 Shahaf et al. Dec 2009 A1
20090299126 Fowler et al. Dec 2009 A1
20090299169 deCharms Dec 2009 A1
20090299435 Gliner et al. Dec 2009 A1
20090304582 Rousso et al. Dec 2009 A1
20090306491 Haggers Dec 2009 A1
20090306531 Leuthardt et al. Dec 2009 A1
20090306532 Tucker Dec 2009 A1
20090306534 Pizzagalli Dec 2009 A1
20090306741 Hogle et al. Dec 2009 A1
20090311655 Karkanias et al. Dec 2009 A1
20090312595 Leuthardt et al. Dec 2009 A1
20090312624 Berridge et al. Dec 2009 A1
20090312646 Binder et al. Dec 2009 A1
20090312663 John et al. Dec 2009 A1
20090312664 Rodriguez Villegas et al. Dec 2009 A1
20090312668 Leuthardt et al. Dec 2009 A1
20090312808 Tyler et al. Dec 2009 A1
20090312817 Hogle et al. Dec 2009 A1
20090312998 Berckmans et al. Dec 2009 A1
20090316925 Eisenfeld et al. Dec 2009 A1
20090316968 Fueyo et al. Dec 2009 A1
20090316969 Fueyo et al. Dec 2009 A1
20090318773 Jung et al. Dec 2009 A1
20090318779 Tran Dec 2009 A1
20090318794 DeCharms Dec 2009 A1
20090319000 Firlik et al. Dec 2009 A1
20090319001 Schiff Dec 2009 A1
20090319002 Simon Dec 2009 A1
20090319004 Sabel Dec 2009 A1
20090322331 Buracas Dec 2009 A1
20090323049 Addison et al. Dec 2009 A1
20090326353 Watson et al. Dec 2009 A1
20090326604 Tyler et al. Dec 2009 A1
20090326605 Morrell Dec 2009 A1
20090327068 Pradeep et al. Dec 2009 A1
20100003656 Kilgard et al. Jan 2010 A1
20100004500 Gliner et al. Jan 2010 A1
20100004705 Kilgard et al. Jan 2010 A1
20100004717 Kilgard et al. Jan 2010 A1
20100004762 Leuthardt et al. Jan 2010 A1
20100004977 Marci et al. Jan 2010 A1
20100010289 Clare Jan 2010 A1
20100010316 Fueyo et al. Jan 2010 A1
20100010363 Fueyo et al. Jan 2010 A1
20100010364 Verbitskiy Jan 2010 A1
20100010365 Terao et al. Jan 2010 A1
20100010366 Silberstein Jan 2010 A1
20100010383 Skelton et al. Jan 2010 A1
20100010388 Panken et al. Jan 2010 A1
20100010391 Skelton et al. Jan 2010 A1
20100010392 Skelton et al. Jan 2010 A1
20100010571 Skelton et al. Jan 2010 A1
20100010572 Skelton et al. Jan 2010 A1
20100010573 Skelton et al. Jan 2010 A1
20100010574 Skelton et al. Jan 2010 A1
20100010575 Skelton et al. Jan 2010 A1
20100010576 Skelton et al. Jan 2010 A1
20100010577 Skelton et al. Jan 2010 A1
20100010578 Skelton et al. Jan 2010 A1
20100010579 Skelton et al. Jan 2010 A1
20100010580 Skelton et al. Jan 2010 A1
20100010584 Skelton et al. Jan 2010 A1
20100010585 Davis et al. Jan 2010 A1
20100010587 Skelton et al. Jan 2010 A1
20100010588 Skelton et al. Jan 2010 A1
20100010589 Skelton et al. Jan 2010 A1
20100010590 Skelton et al. Jan 2010 A1
20100010844 Isaksen Jan 2010 A1
20100014730 Hahn et al. Jan 2010 A1
20100014732 Vija et al. Jan 2010 A1
20100015583 Leuthardt et al. Jan 2010 A1
20100016783 Bourke, Jr. et al. Jan 2010 A1
20100017001 Leuthardt et al. Jan 2010 A1
20100021378 Rousso et al. Jan 2010 A1
20100022820 Leuthardt et al. Jan 2010 A1
20100023089 DiLorenzo Jan 2010 A1
20100028841 Eatough Feb 2010 A1
20100030073 Kalafut Feb 2010 A1
20100030089 Hyde et al. Feb 2010 A1
20100030097 Silberstein Feb 2010 A1
20100030287 Jaax et al. Feb 2010 A1
20100036211 La Rue et al. Feb 2010 A1
20100036233 Zhu et al. Feb 2010 A1
20100036276 Ochs Feb 2010 A1
20100036453 Hulvershorn et al. Feb 2010 A1
20100041949 Tolkowsky Feb 2010 A1
20100041958 Leuthardt et al. Feb 2010 A1
20100041962 Causevic et al. Feb 2010 A1
20100041964 Hyde et al. Feb 2010 A1
20100042011 Doidge et al. Feb 2010 A1
20100042578 Leuthardt et al. Feb 2010 A1
20100043795 Ujhazy et al. Feb 2010 A1
20100045467 Sachanandani et al. Feb 2010 A1
20100049069 Tarassenko et al. Feb 2010 A1
20100049075 Bolger et al. Feb 2010 A1
20100049276 Blum et al. Feb 2010 A1
20100049482 He et al. Feb 2010 A1
20100056276 Silberstein Mar 2010 A1
20100056854 Chang Mar 2010 A1
20100056939 Tarassenko et al. Mar 2010 A1
20100057159 Lozano Mar 2010 A1
20100057160 De Ridder Mar 2010 A1
20100057655 Jacobson et al. Mar 2010 A1
20100063368 Leuthardt et al. Mar 2010 A1
20100063563 Craig Mar 2010 A1
20100068751 Eberle Mar 2010 A1
20100069724 Leuthardt et al. Mar 2010 A1
20100069739 deCharms Mar 2010 A1
20100069762 Mietus et al. Mar 2010 A1
20100069775 Milgramm et al. Mar 2010 A1
20100069777 Marks Mar 2010 A1
20100069780 Schuette et al. Mar 2010 A1
20100070001 Goetz Mar 2010 A1
20100076249 Leuthardt et al. Mar 2010 A1
20100076253 Altman et al. Mar 2010 A1
20100076274 Severson Mar 2010 A1
20100076333 Burton et al. Mar 2010 A9
20100076334 Rothblatt Mar 2010 A1
20100076338 Kwak Mar 2010 A1
20100076525 Skelton et al. Mar 2010 A1
20100079292 Lynn et al. Apr 2010 A1
20100080432 Lilja et al. Apr 2010 A1
20100081860 Leuthardt et al. Apr 2010 A1
20100081861 Leuthardt et al. Apr 2010 A1
20100082506 Avinash et al. Apr 2010 A1
20100087719 Benni Apr 2010 A1
20100087900 Flint Apr 2010 A1
20100090835 Liu et al. Apr 2010 A1
20100092934 Silberstein Apr 2010 A1
20100094103 Kaplan et al. Apr 2010 A1
20100094152 Semmlow Apr 2010 A1
20100094154 Schalk et al. Apr 2010 A1
20100094155 Prichep Apr 2010 A1
20100098289 Tognoli et al. Apr 2010 A1
20100099954 Dickinson et al. Apr 2010 A1
20100099975 Faro et al. Apr 2010 A1
20100100036 Leuthardt et al. Apr 2010 A1
20100100164 Johnson et al. Apr 2010 A1
20100106041 Ghovanloo et al. Apr 2010 A1
20100106043 Robinson et al. Apr 2010 A1
20100106044 Linderman Apr 2010 A1
20100106217 Colborn Apr 2010 A1
20100113959 Pascual-Leone et al. May 2010 A1
20100114190 Bendett et al. May 2010 A1
20100114192 Jaax et al. May 2010 A1
20100114193 Lozano et al. May 2010 A1
20100114237 Giftakis et al. May 2010 A1
20100114272 Haidarliu et al. May 2010 A1
20100114813 Zalay et al. May 2010 A1
20100121415 Skelton et al. May 2010 A1
20100125219 Harris et al. May 2010 A1
20100125304 Faltys May 2010 A1
20100125561 Leuthardt et al. May 2010 A1
20100130811 Leuthardt et al. May 2010 A1
20100130812 Martel May 2010 A1
20100130869 Hauger et al. May 2010 A1
20100130878 Lasso et al. May 2010 A1
20100131030 Firlik et al. May 2010 A1
20100131034 Gliner et al. May 2010 A1
20100132448 Donadille et al. Jun 2010 A1
20100134113 DePavia et al. Jun 2010 A1
20100135556 Razifar et al. Jun 2010 A1
20100137728 Govari Jun 2010 A1
20100137937 John et al. Jun 2010 A1
20100142774 Ben-Haim et al. Jun 2010 A1
20100143256 Suffin et al. Jun 2010 A1
20100145215 Pradeep et al. Jun 2010 A1
20100145219 Grey Jun 2010 A1
20100145427 Gliner et al. Jun 2010 A1
20100145428 Cameron et al. Jun 2010 A1
20100152621 Janna et al. Jun 2010 A1
20100160737 Shachar et al. Jun 2010 A1
20100163027 Hyde et al. Jul 2010 A1
20100163028 Hyde et al. Jul 2010 A1
20100163035 Hyde et al. Jul 2010 A1
20100165593 Townsend et al. Jul 2010 A1
20100168053 Kurtz Jul 2010 A1
20100168525 Hyde et al. Jul 2010 A1
20100168529 Hyde et al. Jul 2010 A1
20100168602 Hyde et al. Jul 2010 A1
20100172567 Prokoski Jul 2010 A1
20100174161 Lynn Jul 2010 A1
20100174533 Pakhomov Jul 2010 A1
20100179415 Wenzel et al. Jul 2010 A1
20100179447 Hunt Jul 2010 A1
20100185113 Peot et al. Jul 2010 A1
20100189318 Chang et al. Jul 2010 A1
20100191095 Felblinger et al. Jul 2010 A1
20100191124 Prokoski Jul 2010 A1
20100191139 Jacquin et al. Jul 2010 A1
20100191304 Scott Jul 2010 A1
20100191305 Imran et al. Jul 2010 A1
20100195770 Ricci et al. Aug 2010 A1
20100197610 Lian et al. Aug 2010 A1
20100197993 Vasishta Aug 2010 A1
20100198090 Hudson et al. Aug 2010 A1
20100198098 Osorio et al. Aug 2010 A1
20100198101 Song et al. Aug 2010 A1
20100198282 Rogers Aug 2010 A1
20100198296 Ignagni et al. Aug 2010 A1
20100198519 Wilt et al. Aug 2010 A1
20100204604 Liley et al. Aug 2010 A1
20100204614 Lindquist et al. Aug 2010 A1
20100204748 Lozano et al. Aug 2010 A1
20100204749 Thimineur et al. Aug 2010 A1
20100204750 Hargrove et al. Aug 2010 A1
20100217100 LeBoeuf et al. Aug 2010 A1
20100217146 Osvath Aug 2010 A1
20100217341 John et al. Aug 2010 A1
20100217348 DiLorenzo Aug 2010 A1
20100219820 Skidmore et al. Sep 2010 A1
20100222640 Anderson et al. Sep 2010 A1
20100222694 Causevic Sep 2010 A1
20100222845 Goetz Sep 2010 A1
20100224188 John et al. Sep 2010 A1
20100231221 Rosthal et al. Sep 2010 A1
20100231327 Johnson et al. Sep 2010 A1
20100234705 Lynn Sep 2010 A1
20100234752 Sullivan et al. Sep 2010 A1
20100234753 Ma Sep 2010 A1
20100238763 Gzara et al. Sep 2010 A1
20100241020 Zaidel et al. Sep 2010 A1
20100241195 Meadows et al. Sep 2010 A1
20100241449 Firminger et al. Sep 2010 A1
20100245093 Kobetski et al. Sep 2010 A1
20100248275 Jackowski et al. Sep 2010 A1
20100249573 Marks Sep 2010 A1
20100249627 Zhang et al. Sep 2010 A1
20100249635 Van Der Reijden Sep 2010 A1
20100249638 Liley Sep 2010 A1
20100256592 Gerber et al. Oct 2010 A1
20100258126 Ujhazy et al. Oct 2010 A1
20100260402 Axelsson et al. Oct 2010 A1
20100261977 Seely Oct 2010 A1
20100261993 van der Kouwe et al. Oct 2010 A1
20100262377 Jensen Oct 2010 A1
20100268055 Jung et al. Oct 2010 A1
20100268057 Firminger et al. Oct 2010 A1
20100268108 Firminger et al. Oct 2010 A1
20100268288 Hunter et al. Oct 2010 A1
20100274106 Heruth et al. Oct 2010 A1
20100274141 Patangay et al. Oct 2010 A1
20100274147 Patangay et al. Oct 2010 A1
20100274303 Bukhman Oct 2010 A1
20100274305 Gliner et al. Oct 2010 A1
20100274308 Scott Oct 2010 A1
20100274577 Firminger et al. Oct 2010 A1
20100274578 Firminger et al. Oct 2010 A1
20100280332 Hyde et al. Nov 2010 A1
20100280334 Carlson et al. Nov 2010 A1
20100280335 Carlson et al. Nov 2010 A1
20100280372 Poolman et al. Nov 2010 A1
20100280403 Erdogmus et al. Nov 2010 A1
20100280500 Skelton et al. Nov 2010 A1
20100280571 Sloan Nov 2010 A1
20100280574 Carlson et al. Nov 2010 A1
20100280579 Denison et al. Nov 2010 A1
20100286549 John et al. Nov 2010 A1
20100286747 Sabesan Nov 2010 A1
20100292602 Worrell et al. Nov 2010 A1
20100292752 Bardakjian et al. Nov 2010 A1
20100293002 Firminger et al. Nov 2010 A1
20100293115 Seyed Momen Nov 2010 A1
20100298624 Becker Nov 2010 A1
20100298735 Suffin Nov 2010 A1
20100303101 Lazar et al. Dec 2010 A1
20100305962 Firminger et al. Dec 2010 A1
20100305963 Firminger et al. Dec 2010 A1
20100312188 Robertson et al. Dec 2010 A1
20100312579 Firminger et al. Dec 2010 A1
20100318025 John Dec 2010 A1
20100318160 Stevenson et al. Dec 2010 A1
20100322488 Virtue et al. Dec 2010 A1
20100322497 Dempsey et al. Dec 2010 A1
20100324441 Hargrove et al. Dec 2010 A1
20100331649 Chou Dec 2010 A1
20100331715 Addison et al. Dec 2010 A1
20100331976 Pesaran et al. Dec 2010 A1
20110004115 Shahaf et al. Jan 2011 A1
20110004270 Sheffield et al. Jan 2011 A1
20110004283 Stevenson et al. Jan 2011 A1
20110004412 Shahaf et al. Jan 2011 A1
20110007129 Martin et al. Jan 2011 A1
20110009715 O' Reilly et al. Jan 2011 A1
20110009729 Shin et al. Jan 2011 A1
20110009752 Chen et al. Jan 2011 A1
20110009777 Reichow et al. Jan 2011 A1
20110009920 Whitehurst et al. Jan 2011 A1
20110009928 Gerber et al. Jan 2011 A1
20110015209 Shamloo et al. Jan 2011 A1
20110015469 Walter et al. Jan 2011 A1
20110015501 Lynn et al. Jan 2011 A1
20110015515 deCharms Jan 2011 A1
20110015536 Milgramm et al. Jan 2011 A1
20110015539 deCharms Jan 2011 A1
20110021899 Arps et al. Jan 2011 A1
20110021970 Vo-Dinh et al. Jan 2011 A1
20110022981 Mahajan et al. Jan 2011 A1
20110028798 Hyde et al. Feb 2011 A1
20110028799 Hyde et al. Feb 2011 A1
20110028802 Addison et al. Feb 2011 A1
20110028825 Douglas et al. Feb 2011 A1
20110028827 Sitaram et al. Feb 2011 A1
20110028859 Chian Feb 2011 A1
20110029038 Hyde et al. Feb 2011 A1
20110029044 Hyde et al. Feb 2011 A1
20110034812 Patangay et al. Feb 2011 A1
20110034821 Ekpar Feb 2011 A1
20110034822 Phillips et al. Feb 2011 A1
20110034912 de Graff et al. Feb 2011 A1
20110035231 Firminger et al. Feb 2011 A1
20110038515 Jacquin et al. Feb 2011 A1
20110038850 Bagnol et al. Feb 2011 A1
20110040202 Luo et al. Feb 2011 A1
20110040356 Schiffer Feb 2011 A1
20110040546 Gerber et al. Feb 2011 A1
20110040547 Gerber et al. Feb 2011 A1
20110040713 Colman et al. Feb 2011 A1
20110043759 Bushinsky Feb 2011 A1
20110046451 Horn et al. Feb 2011 A1
20110046473 Pradeep et al. Feb 2011 A1
20110046491 Diamond Feb 2011 A1
20110050232 Wilt et al. Mar 2011 A1
20110054272 Derchak Mar 2011 A1
20110054279 Reisfeld et al. Mar 2011 A1
20110054345 Nagatani Mar 2011 A1
20110054562 Gliner Mar 2011 A1
20110054569 Zitnik et al. Mar 2011 A1
20110060382 Jaax et al. Mar 2011 A1
20110066005 Rotenberg Mar 2011 A1
20110066041 Pandia et al. Mar 2011 A1
20110066042 Pandia et al. Mar 2011 A1
20110066053 Yazicioglu Mar 2011 A1
20110074396 Liao et al. Mar 2011 A1
20110077503 Bonilha et al. Mar 2011 A1
20110077538 Liu et al. Mar 2011 A1
20110077548 Torch Mar 2011 A1
20110077721 Whitehurst et al. Mar 2011 A1
20110082154 Oksenberg et al. Apr 2011 A1
20110082360 Fuchs et al. Apr 2011 A1
20110082381 Uthman et al. Apr 2011 A1
20110082522 Bourget et al. Apr 2011 A1
20110087125 Causevic Apr 2011 A1
20110087127 Sarkela et al. Apr 2011 A1
20110092800 Yoo et al. Apr 2011 A1
20110092834 Yazicioglu et al. Apr 2011 A1
20110092839 Alshaer et al. Apr 2011 A1
20110092882 Firlik et al. Apr 2011 A1
20110093033 Nekhendzy Apr 2011 A1
20110098583 Pandia et al. Apr 2011 A1
20110098778 Thimineur et al. Apr 2011 A1
20110105859 Popovic et al. May 2011 A1
20110105915 Bauer et al. May 2011 A1
20110105938 Hardt May 2011 A1
20110105998 Zhang et al. May 2011 A1
20110106206 Schiff May 2011 A1
20110106750 Pradeep et al. May 2011 A1
20110110868 Akhtari et al. May 2011 A1
20110112379 Li et al. May 2011 A1
20110112381 Sun et al. May 2011 A1
20110112394 Mishelevich May 2011 A1
20110112426 Causevic May 2011 A1
20110112427 Phillips et al. May 2011 A1
20110112590 Wu et al. May 2011 A1
20110115624 Tran May 2011 A1
20110118536 Phillips et al. May 2011 A1
20110118618 John et al. May 2011 A1
20110118619 Burton et al. May 2011 A1
20110119212 De Bruin et al. May 2011 A1
20110125046 Burton et al. May 2011 A1
20110125048 Causevic et al. May 2011 A1
20110125077 Denison et al. May 2011 A1
20110125078 Denison et al. May 2011 A1
20110125203 Simon et al. May 2011 A1
20110125238 Nofzinger May 2011 A1
20110129129 Avinash et al. Jun 2011 A1
20110130615 Mishelevich Jun 2011 A1
20110130643 Derchak et al. Jun 2011 A1
20110130675 Bibian et al. Jun 2011 A1
20110137371 Giftakis et al. Jun 2011 A1
20110137381 Lee et al. Jun 2011 A1
20110144520 Causevic et al. Jun 2011 A1
20110144521 Molnar et al. Jun 2011 A1
20110150253 Corona-Strauss et al. Jun 2011 A1
20110152284 Wieloch et al. Jun 2011 A1
20110152710 Kim et al. Jun 2011 A1
20110152729 Oohashi et al. Jun 2011 A1
20110152967 Simon et al. Jun 2011 A1
20110152988 Whitehurst et al. Jun 2011 A1
20110160543 Parsey et al. Jun 2011 A1
20110160607 John et al. Jun 2011 A1
20110160608 Hargrove Jun 2011 A1
20110160795 Osorio Jun 2011 A1
20110160796 Lane et al. Jun 2011 A1
20110161011 Hasson et al. Jun 2011 A1
20110162645 John et al. Jul 2011 A1
20110166430 Harris et al. Jul 2011 A1
20110166471 Drew et al. Jul 2011 A1
20110166546 Jaax et al. Jul 2011 A1
20110172500 Van Dooren et al. Jul 2011 A1
20110172509 Chance Jul 2011 A1
20110172553 John et al. Jul 2011 A1
20110172554 Leyde et al. Jul 2011 A1
20110172562 Sahasrabudhe et al. Jul 2011 A1
20110172564 Drew Jul 2011 A1
20110172567 Panken et al. Jul 2011 A1
20110172725 Wells et al. Jul 2011 A1
20110172732 Maschino Jul 2011 A1
20110172738 Davis et al. Jul 2011 A1
20110172739 Mann et al. Jul 2011 A1
20110172743 Davis et al. Jul 2011 A1
20110172927 Sahasrabudhe et al. Jul 2011 A1
20110178359 Hirschman et al. Jul 2011 A1
20110178441 Tyler Jul 2011 A1
20110178442 Mishelevich Jul 2011 A1
20110178581 Haber et al. Jul 2011 A1
20110181422 Tran Jul 2011 A1
20110182501 Mercier et al. Jul 2011 A1
20110184305 Liley Jul 2011 A1
20110184487 Alberts et al. Jul 2011 A1
20110184650 Hymel Jul 2011 A1
20110190569 Simon et al. Aug 2011 A1
20110190600 McKenna et al. Aug 2011 A1
20110190846 Ruffini et al. Aug 2011 A1
20110191275 Lujan et al. Aug 2011 A1
20110191350 Zhang et al. Aug 2011 A1
20110196693 Hargrove et al. Aug 2011 A1
20110201944 Higgins et al. Aug 2011 A1
20110207988 Ruohonen et al. Aug 2011 A1
20110208012 Gerber et al. Aug 2011 A1
20110208094 Mishelevich Aug 2011 A1
20110208264 Gliner et al. Aug 2011 A1
20110208539 Lynn Aug 2011 A1
20110213200 Mishelevich Sep 2011 A1
20110213222 Leyde et al. Sep 2011 A1
20110217240 Ferris Sep 2011 A1
20110218405 Avinash et al. Sep 2011 A1
20110218453 Hirata et al. Sep 2011 A1
20110218456 Graham et al. Sep 2011 A1
20110218950 Mirowski et al. Sep 2011 A1
20110224569 Isenhart et al. Sep 2011 A1
20110224570 Causevic Sep 2011 A1
20110224571 Pascual-Leone et al. Sep 2011 A1
20110224602 Struijk et al. Sep 2011 A1
20110224749 Ben-David et al. Sep 2011 A1
20110229005 Den Harder et al. Sep 2011 A1
20110230701 Simon et al. Sep 2011 A1
20110230738 Chance Sep 2011 A1
20110230755 MacFarlane et al. Sep 2011 A1
20110230938 Simon et al. Sep 2011 A1
20110238130 Bourget et al. Sep 2011 A1
20110238136 Bourget et al. Sep 2011 A1
20110245709 Greenwald Oct 2011 A1
20110245734 Wagner et al. Oct 2011 A1
20110251583 Miyazawa et al. Oct 2011 A1
20110251985 Waxman et al. Oct 2011 A1
20110256520 Siefert Oct 2011 A1
20110257501 Huys et al. Oct 2011 A1
20110257517 Guttag et al. Oct 2011 A1
20110257519 Bj?rnerud et al. Oct 2011 A1
20110263962 Marks Oct 2011 A1
20110263968 Quattrocki-Knight et al. Oct 2011 A1
20110263995 Chen Oct 2011 A1
20110264182 Cowley Oct 2011 A1
20110270074 deCharms Nov 2011 A1
20110270095 Bukhman Nov 2011 A1
20110270096 Osorio et al. Nov 2011 A1
20110270117 Warwick et al. Nov 2011 A1
20110270346 Frei et al. Nov 2011 A1
20110270347 Frei et al. Nov 2011 A1
20110270348 Goetz Nov 2011 A1
20110270579 Watson et al. Nov 2011 A1
20110270914 Jung et al. Nov 2011 A1
20110275927 Wagner et al. Nov 2011 A1
20110276107 Simon et al. Nov 2011 A1
20110276112 Simon et al. Nov 2011 A1
20110282225 Anderson et al. Nov 2011 A1
20110282230 Liley Nov 2011 A9
20110282234 Ochs Nov 2011 A1
20110288119 Chesworth et al. Nov 2011 A1
20110288400 Russell et al. Nov 2011 A1
20110288424 Kanai et al. Nov 2011 A1
20110288431 Alshaer et al. Nov 2011 A1
20110293193 Garg et al. Dec 2011 A1
20110295142 Chakravarthy et al. Dec 2011 A1
20110295143 Leuthardt et al. Dec 2011 A1
20110295166 Dalton Dec 2011 A1
20110295338 Rickert et al. Dec 2011 A1
20110295344 Wells et al. Dec 2011 A1
20110295345 Wells et al. Dec 2011 A1
20110295346 Wells et al. Dec 2011 A1
20110295347 Wells et al. Dec 2011 A1
20110298706 Mann Dec 2011 A1
20110301436 Teixeira Dec 2011 A1
20110301439 Albert et al. Dec 2011 A1
20110301441 Bandic et al. Dec 2011 A1
20110301448 deCharms Dec 2011 A1
20110301486 Van Hek et al. Dec 2011 A1
20110301487 Abeyratne et al. Dec 2011 A1
20110301488 Schuette et al. Dec 2011 A1
20110301529 Zhang et al. Dec 2011 A1
20110306845 Osorio Dec 2011 A1
20110306846 Osorio Dec 2011 A1
20110307029 Hargrove Dec 2011 A1
20110307030 John Dec 2011 A1
20110307079 Oweiss et al. Dec 2011 A1
20110308789 Zhang et al. Dec 2011 A1
20110311021 Tsukagoshi Dec 2011 A1
20110311489 Deisseroth et al. Dec 2011 A1
20110313268 Kokones et al. Dec 2011 A1
20110313274 Subbarao Dec 2011 A1
20110313308 Zavoronkovs et al. Dec 2011 A1
20110313487 Kokones et al. Dec 2011 A1
20110313760 Ricci et al. Dec 2011 A1
20110319482 Blower et al. Dec 2011 A1
20110319724 Cox Dec 2011 A1
20110319726 Sachanandani et al. Dec 2011 A1
20110319975 Ho et al. Dec 2011 A1
20120003615 Ochs Jan 2012 A1
20120004518 D'Souza et al. Jan 2012 A1
20120004561 John Jan 2012 A1
20120004564 Dobak Jan 2012 A1
20120004579 Luo et al. Jan 2012 A1
20120004749 Abeyratne et al. Jan 2012 A1
20120010493 Semenov Jan 2012 A1
20120010536 Bolger et al. Jan 2012 A1
20120011927 Badri et al. Jan 2012 A1
20120016218 Lau et al. Jan 2012 A1
20120016252 Melker et al. Jan 2012 A1
20120016336 Whitehurst et al. Jan 2012 A1
20120016430 Lozano Jan 2012 A1
20120016432 Westendorp et al. Jan 2012 A1
20120016435 Rom Jan 2012 A1
20120021394 deCharms Jan 2012 A1
20120022336 Teixeira Jan 2012 A1
20120022340 Heruth et al. Jan 2012 A1
20120022343 Shastri et al. Jan 2012 A1
20120022350 Teixeira Jan 2012 A1
20120022351 Starr Jan 2012 A1
20120022365 Mansfield Jan 2012 A1
20120022384 Teixeira Jan 2012 A1
20120022392 Leuthardt et al. Jan 2012 A1
20120022611 Firlik et al. Jan 2012 A1
20120022844 Teixeira Jan 2012 A1
20120022884 Chillemi Jan 2012 A1
20120029320 Watson et al. Feb 2012 A1
20120029378 Low Feb 2012 A1
20120029379 Sivadas Feb 2012 A1
20120029591 Simon et al. Feb 2012 A1
20120029601 Simon et al. Feb 2012 A1
20120035428 Roberts et al. Feb 2012 A1
20120035431 Sun et al. Feb 2012 A1
20120035433 Chance Feb 2012 A1
20120035698 Johnson et al. Feb 2012 A1
20120035765 Sato et al. Feb 2012 A1
20120036004 Pradeep et al. Feb 2012 A1
20120041279 Freeman et al. Feb 2012 A1
20120041318 Taylor Feb 2012 A1
20120041319 Taylor et al. Feb 2012 A1
20120041320 Taylor Feb 2012 A1
20120041321 Taylor et al. Feb 2012 A1
20120041322 Taylor et al. Feb 2012 A1
20120041323 Taylor et al. Feb 2012 A1
20120041324 Taylor et al. Feb 2012 A1
20120041330 Prichep et al. Feb 2012 A1
20120041498 Gliner et al. Feb 2012 A1
20120041735 Taylor Feb 2012 A1
20120041739 Taylor Feb 2012 A1
20120046531 Hua Feb 2012 A1
20120046535 Lin et al. Feb 2012 A1
20120046711 Osorio Feb 2012 A1
20120046715 Moffitt et al. Feb 2012 A1
20120046971 Walker et al. Feb 2012 A1
20120052469 Sobel et al. Mar 2012 A1
20120052905 Lim et al. Mar 2012 A1
20120053394 Honeycutt Mar 2012 A1
20120053433 Chamoun et al. Mar 2012 A1
20120053449 Moses et al. Mar 2012 A1
20120053473 Johnson et al. Mar 2012 A1
20120053476 Hopenfeld Mar 2012 A1
20120053478 Johnson et al. Mar 2012 A1
20120053479 Hopenfeld Mar 2012 A1
20120053483 Doidge et al. Mar 2012 A1
20120053491 Nathan et al. Mar 2012 A1
20120053508 Wu et al. Mar 2012 A1
20120053919 Taylor Mar 2012 A1
20120053921 Taylor Mar 2012 A1
20120059246 Taylor Mar 2012 A1
20120059273 Meggiolaro et al. Mar 2012 A1
20120059431 Williams et al. Mar 2012 A1
20120060851 Amberg Mar 2012 A1
20120065536 Causevic et al. Mar 2012 A1
20120070044 Avinash et al. Mar 2012 A1
20120071771 Behar Mar 2012 A1
20120078115 Lonky Mar 2012 A1
20120078323 Osorio Mar 2012 A1
20120078327 Sloan et al. Mar 2012 A1
20120080305 Koruga Apr 2012 A1
20120083668 Pradeep et al. Apr 2012 A1
20120083690 Semenov Apr 2012 A1
20120083700 Osorio Apr 2012 A1
20120083701 Osorio Apr 2012 A1
20120083708 Rajdev et al. Apr 2012 A1
20120088987 Braun et al. Apr 2012 A1
20120088992 Armitstead Apr 2012 A1
20120089004 Hsu et al. Apr 2012 A1
20120089205 Boyden et al. Apr 2012 A1
20120092156 Tran Apr 2012 A1
20120092157 Tran Apr 2012 A1
20120095352 Tran Apr 2012 A1
20120095357 Tran Apr 2012 A1
20120100514 Desain et al. Apr 2012 A1
20120101326 Simon et al. Apr 2012 A1
20120101387 Ji et al. Apr 2012 A1
20120101401 Faul et al. Apr 2012 A1
20120101402 Nguyen Apr 2012 A1
20120101430 Robertson et al. Apr 2012 A1
20120101544 Hoberman et al. Apr 2012 A1
20120108909 Slobounov et al. May 2012 A1
20120108918 Jarvik et al. May 2012 A1
20120108995 Pradeep et al. May 2012 A1
20120108997 Guan et al. May 2012 A1
20120108998 Molnar et al. May 2012 A1
20120108999 Leininger et al. May 2012 A1
20120109020 Wagner et al. May 2012 A1
20120116149 Pilla et al. May 2012 A1
20120116179 Drew et al. May 2012 A1
20120116235 Trumble et al. May 2012 A1
20120116244 McIntyre et al. May 2012 A1
20120116475 Nelson et al. May 2012 A1
20120116741 Choi et al. May 2012 A1
20120123232 Najarian et al. May 2012 A1
20120123290 Kidmose et al. May 2012 A1
20120125337 Asanoi May 2012 A1
20120128683 Shantha May 2012 A1
20120130204 Basta et al. May 2012 A1
20120130228 Zellers et al. May 2012 A1
20120130229 Zellers et al. May 2012 A1
20120130300 Stavchansky et al. May 2012 A1
20120130641 Morrison et al. May 2012 A1
20120136242 Qi et al. May 2012 A1
20120136274 Burdea et al. May 2012 A1
20120136605 Addison et al. May 2012 A1
20120143038 Georgopoulos Jun 2012 A1
20120143074 Shin et al. Jun 2012 A1
20120143075 Tansey Jun 2012 A1
20120143104 Tee et al. Jun 2012 A1
20120143285 Wang et al. Jun 2012 A1
20120145152 Lain et al. Jun 2012 A1
20120149042 Jackowski et al. Jun 2012 A1
20120149997 Diab et al. Jun 2012 A1
20120150255 Lindenthaler et al. Jun 2012 A1
20120150257 Aur et al. Jun 2012 A1
20120150262 Gliner et al. Jun 2012 A1
20120150516 Taylor et al. Jun 2012 A1
20120150545 Simon Jun 2012 A1
20120157804 Rogers et al. Jun 2012 A1
20120157963 Imran Jun 2012 A1
20120158092 Thimineur et al. Jun 2012 A1
20120159656 Gerber et al. Jun 2012 A1
20120162002 Semenov Jun 2012 A1
20120163689 Bottger et al. Jun 2012 A1
20120164613 Jung et al. Jun 2012 A1
20120165624 Diab et al. Jun 2012 A1
20120165631 Diab et al. Jun 2012 A1
20120165696 Arns Jun 2012 A1
20120165898 Moffitt Jun 2012 A1
20120165899 Gliner Jun 2012 A1
20120165904 Lee et al. Jun 2012 A1
20120172682 Linderman et al. Jul 2012 A1
20120172689 Albert et al. Jul 2012 A1
20120172743 Aguilar et al. Jul 2012 A1
20120177716 Ho et al. Jul 2012 A1
20120179071 Skelton Jul 2012 A1
20120179228 DeCharms Jul 2012 A1
20120184801 Simon et al. Jul 2012 A1
20120184826 Keenan et al. Jul 2012 A1
20120185020 Simon et al. Jul 2012 A1
20120191000 Adachi et al. Jul 2012 A1
20120191158 Craig Jul 2012 A1
20120191542 Nurmi Jul 2012 A1
20120195860 Walker et al. Aug 2012 A1
20120197092 Luo et al. Aug 2012 A1
20120197153 Kraus et al. Aug 2012 A1
20120197163 Mishelevich Aug 2012 A1
20120197322 Skelton et al. Aug 2012 A1
20120203079 McLaughlin Aug 2012 A1
20120203087 McKenna et al. Aug 2012 A1
20120203130 Bernhard Aug 2012 A1
20120203131 DiLorenzo Aug 2012 A1
20120203133 Jadidi Aug 2012 A1
20120203725 Stoica Aug 2012 A1
20120207362 Fueyo et al. Aug 2012 A1
20120209126 Amos et al. Aug 2012 A1
20120209136 Ma Aug 2012 A1
20120209139 John Aug 2012 A1
20120209346 Bikson et al. Aug 2012 A1
20120212353 Fung et al. Aug 2012 A1
20120215114 Gratton et al. Aug 2012 A1
20120215448 Hu et al. Aug 2012 A1
20120219195 Wu et al. Aug 2012 A1
20120219507 Santosh et al. Aug 2012 A1
20120220843 Diab et al. Aug 2012 A1
20120220889 Sullivan et al. Aug 2012 A1
20120221310 Sarrafzadeh et al. Aug 2012 A1
20120226091 Mishelevich Sep 2012 A1
20120226130 De Graff et al. Sep 2012 A1
20120226185 Chung et al. Sep 2012 A1
20120226334 Gardiner et al. Sep 2012 A1
20120232327 Lozano et al. Sep 2012 A1
20120232376 Crevecoeur et al. Sep 2012 A1
20120232433 Mishelevich Sep 2012 A1
20120238890 Baker et al. Sep 2012 A1
20120242501 Tran et al. Sep 2012 A1
20120245464 Tran Sep 2012 A1
20120245474 Ofek et al. Sep 2012 A1
20120245481 Blanco et al. Sep 2012 A1
20120245493 Mishelevich Sep 2012 A1
20120245655 Spitzer et al. Sep 2012 A1
20120249274 Toda et al. Oct 2012 A1
20120253101 Wang et al. Oct 2012 A1
20120253141 Addison et al. Oct 2012 A1
20120253168 Hu et al. Oct 2012 A1
20120253219 Suffin et al. Oct 2012 A1
20120253249 Wilson Oct 2012 A1
20120253261 Poletto et al. Oct 2012 A1
20120253421 Gliner et al. Oct 2012 A1
20120253429 Schiffer Oct 2012 A1
20120253434 Nissila et al. Oct 2012 A1
20120253442 Gliner et al. Oct 2012 A1
20120259249 Khuri-Yakub et al. Oct 2012 A1
20120262250 Stevenson et al. Oct 2012 A1
20120262558 Boger et al. Oct 2012 A1
20120263393 Yahil Oct 2012 A1
20120265080 Yu et al. Oct 2012 A1
20120265262 Osorio Oct 2012 A1
20120265267 Blum et al. Oct 2012 A1
20120265270 Cornejo Cruz et al. Oct 2012 A1
20120265271 Goetz Oct 2012 A1
20120268272 Lee et al. Oct 2012 A1
20120269385 Lee et al. Oct 2012 A1
20120271148 Nelson Oct 2012 A1
20120271151 LaVoilette et al. Oct 2012 A1
20120271183 Sachanandani et al. Oct 2012 A1
20120271189 Nelson et al. Oct 2012 A1
20120271190 Mortensen et al. Oct 2012 A1
20120271374 Nelson et al. Oct 2012 A1
20120271375 Wu et al. Oct 2012 A1
20120271376 Kokones et al. Oct 2012 A1
20120271377 Hagedorn et al. Oct 2012 A1
20120271380 Roberts et al. Oct 2012 A1
20120277545 Teixeira Nov 2012 A1
20120277548 Burton Nov 2012 A1
20120277816 Zhang et al. Nov 2012 A1
20120277833 Gerber et al. Nov 2012 A1
20120283502 Mishelevich et al. Nov 2012 A1
20120283604 Mishelevich Nov 2012 A1
20120288143 Ernst et al. Nov 2012 A1
20120289854 Yamada et al. Nov 2012 A1
20120289869 Tyler Nov 2012 A1
20120290058 Langevin et al. Nov 2012 A1
20120296182 Hornero S Nchez et al. Nov 2012 A1
20120296241 Mishelevich Nov 2012 A1
20120296253 Mathews et al. Nov 2012 A1
20120296569 Shahaf et al. Nov 2012 A1
20120302842 Kurtz et al. Nov 2012 A1
20120302845 Lynn et al. Nov 2012 A1
20120302856 Chang et al. Nov 2012 A1
20120302867 Ichimura Nov 2012 A1
20120302894 Diab et al. Nov 2012 A1
20120302912 Moffitt et al. Nov 2012 A1
20120303080 Ben-David et al. Nov 2012 A1
20120303087 Moffitt et al. Nov 2012 A1
20120310050 Osorio Dec 2012 A1
20120310100 Galen et al. Dec 2012 A1
20120310105 Feingold et al. Dec 2012 A1
20120310106 Cavuoto Dec 2012 A1
20120310107 Doidge et al. Dec 2012 A1
20120310298 Besio et al. Dec 2012 A1
20120316622 Whitehurst et al. Dec 2012 A1
20120316630 Firlik et al. Dec 2012 A1
20120316793 Jung et al. Dec 2012 A1
20120321152 Carroll Dec 2012 A1
20120321160 Carroll Dec 2012 A1
20120321759 Marinkovich et al. Dec 2012 A1
20120323108 Carroll Dec 2012 A1
20120323132 Warner et al. Dec 2012 A1
20120330109 Tran Dec 2012 A1
20120330369 Osorio et al. Dec 2012 A1
20130006124 Eyal et al. Jan 2013 A1
20130006332 Sommer et al. Jan 2013 A1
20130009783 Tran Jan 2013 A1
20130011819 Horseman Jan 2013 A1
20130012786 Horseman Jan 2013 A1
20130012787 Horseman Jan 2013 A1
20130012788 Horseman Jan 2013 A1
20130012789 Horseman Jan 2013 A1
20130012790 Horseman Jan 2013 A1
20130012802 Horseman Jan 2013 A1
20130012804 deCharms Jan 2013 A1
20130012830 Leininger et al. Jan 2013 A1
20130013327 Horseman Jan 2013 A1
20130013339 Goldman et al. Jan 2013 A1
20130013667 Serena Jan 2013 A1
20130018435 De Ridder Jan 2013 A1
20130018438 Chow Jan 2013 A1
20130018439 Chow et al. Jan 2013 A1
20130018440 Chow et al. Jan 2013 A1
20130018592 Mollicone et al. Jan 2013 A1
20130018596 Bottger et al. Jan 2013 A1
20130019325 Deisseroth et al. Jan 2013 A1
20130023783 Snyder et al. Jan 2013 A1
20130028496 Panin et al. Jan 2013 A1
20130030241 Smith Jan 2013 A1
20130030257 Nakata et al. Jan 2013 A1
20130031038 Horne Jan 2013 A1
20130034837 Clapp et al. Feb 2013 A1
20130035579 Le et al. Feb 2013 A1
20130039498 Adachi et al. Feb 2013 A1
20130041235 Rogers et al. Feb 2013 A1
20130041281 Park et al. Feb 2013 A1
20130046151 Bsoul et al. Feb 2013 A1
20130046193 Guttag et al. Feb 2013 A1
20130046358 Leyde Feb 2013 A1
20130046715 Castermans et al. Feb 2013 A1
20130053656 Mollicone et al. Feb 2013 A1
20130054214 Taylor Feb 2013 A1
20130054215 Stubna et al. Feb 2013 A1
20130058548 Garg et al. Mar 2013 A1
20130060110 Lynn et al. Mar 2013 A1
20130060125 Zeman et al. Mar 2013 A1
20130060158 Perez-Velazquez et al. Mar 2013 A1
20130063434 Miga et al. Mar 2013 A1
20130063550 Ritchey et al. Mar 2013 A1
20130064438 Taylor et al. Mar 2013 A1
20130066350 Mishelevich Mar 2013 A1
20130066391 Hulvershorn et al. Mar 2013 A1
20130066392 Simon et al. Mar 2013 A1
20130066394 Saab Mar 2013 A1
20130066395 Simon et al. Mar 2013 A1
20130066618 Taylor et al. Mar 2013 A1
20130069780 Tran et al. Mar 2013 A1
20130070929 Adachi et al. Mar 2013 A1
20130072292 Sutton et al. Mar 2013 A1
20130072775 Rogers et al. Mar 2013 A1
20130072780 Espy et al. Mar 2013 A1
20130072807 Tran Mar 2013 A1
20130072996 Kilgard et al. Mar 2013 A1
20130073022 Ollivier Mar 2013 A1
20130076885 Kobetski et al. Mar 2013 A1
20130079606 McGonigle et al. Mar 2013 A1
20130079621 Shoham et al. Mar 2013 A1
20130079647 McGonigle et al. Mar 2013 A1
20130079656 Dripps et al. Mar 2013 A1
20130079657 Ochs et al. Mar 2013 A1
20130080127 Shahaf et al. Mar 2013 A1
20130080489 Ochs et al. Mar 2013 A1
20130085678 Jung et al. Apr 2013 A1
20130089503 Deisseroth et al. Apr 2013 A1
20130090454 Deisseroth et al. Apr 2013 A1
20130090706 Nudo et al. Apr 2013 A1
20130091941 Huh et al. Apr 2013 A1
20130095459 Tran Apr 2013 A1
20130096391 Osorio et al. Apr 2013 A1
20130096393 Osorio et al. Apr 2013 A1
20130096394 Gupta et al. Apr 2013 A1
20130096408 He et al. Apr 2013 A1
20130096441 Osorio Apr 2013 A1
20130096453 Chung et al. Apr 2013 A1
20130096454 Jang et al. Apr 2013 A1
20130096839 Osorio et al. Apr 2013 A1
20130096840 Osorio et al. Apr 2013 A1
20130102833 John et al. Apr 2013 A1
20130102877 Mori et al. Apr 2013 A1
20130102897 Kalafut et al. Apr 2013 A1
20130102907 Funane et al. Apr 2013 A1
20130102919 Schiff Apr 2013 A1
20130104066 Soederstroem Apr 2013 A1
20130109995 Rothman et al. May 2013 A1
20130109996 Turnbull et al. May 2013 A1
20130110616 Bakalash et al. May 2013 A1
20130113816 Sudarsky et al. May 2013 A1
20130116520 Roham et al. May 2013 A1
20130116540 Li et al. May 2013 A1
20130116561 Rothberg et al. May 2013 A1
20130116578 An et al. May 2013 A1
20130116588 Yazicioglu et al. May 2013 A1
20130116748 Bokil et al. May 2013 A1
20130118494 Ujhazy et al. May 2013 A1
20130120246 Schuette et al. May 2013 A1
20130121984 Haslett et al. May 2013 A1
20130123568 Hamilton et al. May 2013 A1
20130123584 Sun et al. May 2013 A1
20130123607 Leuthardt et al. May 2013 A1
20130123684 Giuffrida et al. May 2013 A1
20130127708 Jung et al. May 2013 A1
20130127980 Haddick et al. May 2013 A1
20130130799 Van Hulle et al. May 2013 A1
20130131438 Brewer et al. May 2013 A1
20130131461 Jorge et al. May 2013 A1
20130131537 Tam May 2013 A1
20130131746 Simon et al. May 2013 A1
20130131753 Simon et al. May 2013 A1
20130131755 Panken et al. May 2013 A1
20130132029 Mollicone et al. May 2013 A1
20130137717 Chesworth et al. May 2013 A1
20130137936 Baker, Jr. et al. May 2013 A1
20130137938 Peters May 2013 A1
20130138002 Weng et al. May 2013 A1
20130138176 Goetz May 2013 A1
20130138177 DeRidder May 2013 A1
20130141103 Roshtal et al. Jun 2013 A1
20130144106 Phillips et al. Jun 2013 A1
20130144107 Phillips et al. Jun 2013 A1
20130144108 Phillips et al. Jun 2013 A1
20130144183 John et al. Jun 2013 A1
20130144192 Mischelevich et al. Jun 2013 A1
20130144353 Lozano Jun 2013 A1
20130144537 Schalk et al. Jun 2013 A1
20130150650 Phillips et al. Jun 2013 A1
20130150651 Phillips et al. Jun 2013 A1
20130150659 Shaw et al. Jun 2013 A1
20130150702 Hokari Jun 2013 A1
20130150921 Singhal et al. Jun 2013 A1
20130151163 Taylor et al. Jun 2013 A1
20130158883 Hasegawa et al. Jun 2013 A1
20130159041 Jayaraman et al. Jun 2013 A1
20130165766 Nishikawa et al. Jun 2013 A1
20130165804 Johnson et al. Jun 2013 A1
20130165812 Aksenova et al. Jun 2013 A1
20130165846 Peyman Jun 2013 A1
20130165996 Meadows et al. Jun 2013 A1
20130167360 Masmanidis et al. Jul 2013 A1
20130172663 Leonard Jul 2013 A1
20130172686 Addison et al. Jul 2013 A1
20130172691 Tran Jul 2013 A1
20130172716 Lozano et al. Jul 2013 A1
20130172763 Wheeler Jul 2013 A1
20130172767 Dripps et al. Jul 2013 A1
20130172772 Alshaer et al. Jul 2013 A1
20130172774 Crowder et al. Jul 2013 A1
20130178693 Neuvonen et al. Jul 2013 A1
20130178718 Tran et al. Jul 2013 A1
20130178733 Langleben Jul 2013 A1
20130178913 Lozano Jul 2013 A1
20130182860 Adachi et al. Jul 2013 A1
20130184218 Paul et al. Jul 2013 A1
20130184516 Genereux et al. Jul 2013 A1
20130184552 Westermann et al. Jul 2013 A1
20130184558 Gallant et al. Jul 2013 A1
20130184597 Hopenfeld Jul 2013 A1
20130184603 Rothman Jul 2013 A1
20130184639 Whitehurst et al. Jul 2013 A1
20130184728 Mishelevich Jul 2013 A1
20130184781 Eskandar et al. Jul 2013 A1
20130184786 Goetz Jul 2013 A1
20130184792 Simon et al. Jul 2013 A1
20130184997 Mott Jul 2013 A1
20130185144 Pradeep et al. Jul 2013 A1
20130185145 Pradeep et al. Jul 2013 A1
20130188830 Ernst et al. Jul 2013 A1
20130188854 Bilgic et al. Jul 2013 A1
20130189663 Tuchschmid et al. Jul 2013 A1
20130190577 Brunner et al. Jul 2013 A1
20130190642 Muesch et al. Jul 2013 A1
20130197321 Wilson Aug 2013 A1
20130197322 Tran Aug 2013 A1
20130197328 Diab et al. Aug 2013 A1
20130197339 Bardakjian et al. Aug 2013 A1
20130197401 Sato et al. Aug 2013 A1
20130197944 Drew et al. Aug 2013 A1
20130203019 Nolen Aug 2013 A1
20130204085 Alexander et al. Aug 2013 A1
20130204122 Hendler et al. Aug 2013 A1
20130204144 Colborn et al. Aug 2013 A1
20130204150 Similowski et al. Aug 2013 A1
20130211183 Schiffer Aug 2013 A1
20130211224 Isenhart et al. Aug 2013 A1
20130211238 DeCharms Aug 2013 A1
20130211276 Luo et al. Aug 2013 A1
20130211291 Tran Aug 2013 A1
20130211728 Taylor et al. Aug 2013 A1
20130217982 Behzadi Aug 2013 A1
20130218043 Yoshida Aug 2013 A1
20130218053 Kaiser et al. Aug 2013 A1
20130218232 Giftakis et al. Aug 2013 A1
20130218233 Warschewske et al. Aug 2013 A1
20130218819 Lujan et al. Aug 2013 A1
20130221961 Liu Aug 2013 A1
20130223709 Wagner Aug 2013 A1
20130225940 Fujita et al. Aug 2013 A1
20130225953 Oliviero et al. Aug 2013 A1
20130225992 Osorio Aug 2013 A1
20130226261 Sparks et al. Aug 2013 A1
20130226408 Fung et al. Aug 2013 A1
20130226464 Marci et al. Aug 2013 A1
20130231574 Tran Sep 2013 A1
20130231580 Chen et al. Sep 2013 A1
20130231709 Lozano Sep 2013 A1
20130231716 Skelton et al. Sep 2013 A1
20130231721 DeCharms Sep 2013 A1
20130231947 Shusterman Sep 2013 A1
20130234823 Kahn et al. Sep 2013 A1
20130235550 Stevenson et al. Sep 2013 A1
20130237541 Teegarden et al. Sep 2013 A1
20130237874 Zoicas Sep 2013 A1
20130238049 Simon et al. Sep 2013 A1
20130238050 Simon et al. Sep 2013 A1
20130238053 Ignagni et al. Sep 2013 A1
20130238063 Nofzinger Sep 2013 A1
20130242262 Lewis Sep 2013 A1
20130243287 Thomson et al. Sep 2013 A1
20130244323 Deisseroth et al. Sep 2013 A1
20130245416 Yarmush et al. Sep 2013 A1
20130245422 D'arcy et al. Sep 2013 A1
20130245424 deCharms Sep 2013 A1
20130245464 Colborn et al. Sep 2013 A1
20130245466 Sachanandani et al. Sep 2013 A1
20130245485 Mashour et al. Sep 2013 A1
20130245486 Simon et al. Sep 2013 A1
20130245711 Simon et al. Sep 2013 A1
20130245712 Simon et al. Sep 2013 A1
20130245886 Fung et al. Sep 2013 A1
20130251641 Akhtari et al. Sep 2013 A1
20130253363 Juffali et al. Sep 2013 A1
20130253612 Chow Sep 2013 A1
20130255586 Gerashchenko Oct 2013 A1
20130261490 Truccolo et al. Oct 2013 A1
20130261506 Mishelevich Oct 2013 A1
20130261703 Chow et al. Oct 2013 A1
20130266163 Morikawa et al. Oct 2013 A1
20130267760 Jin Oct 2013 A1
20130267866 Nakashima et al. Oct 2013 A1
20130267928 Imran et al. Oct 2013 A1
20130274562 Ghaffari et al. Oct 2013 A1
20130274580 Madsen et al. Oct 2013 A1
20130274586 Miyazaki et al. Oct 2013 A1
20130274625 Sarma et al. Oct 2013 A1
20130275159 Seely Oct 2013 A1
20130281758 Solvason et al. Oct 2013 A1
20130281759 Hagedorn et al. Oct 2013 A1
20130281811 Imran Oct 2013 A1
20130281879 Raniere Oct 2013 A1
20130281890 Mishelevich Oct 2013 A1
20130282075 De Ridder Oct 2013 A1
20130282339 Ricci et al. Oct 2013 A1
20130289360 Hyde et al. Oct 2013 A1
20130289364 Colman et al. Oct 2013 A1
20130289385 Lozano et al. Oct 2013 A1
20130289386 Deisseroth et al. Oct 2013 A1
20130289401 Colbaugh et al. Oct 2013 A1
20130289413 Ochs et al. Oct 2013 A1
20130289417 Grunwald et al. Oct 2013 A1
20130289424 Brockway et al. Oct 2013 A1
20130289433 Jin et al. Oct 2013 A1
20130289653 Kilgard et al. Oct 2013 A1
20130289669 Deisseroth et al. Oct 2013 A1
20130293844 Gross et al. Nov 2013 A1
20130295016 Gerber et al. Nov 2013 A1
20130296406 Deisseroth et al. Nov 2013 A1
20130296637 Kilgard et al. Nov 2013 A1
20130300573 Brown et al. Nov 2013 A1
20130303828 Hargrove Nov 2013 A1
20130303934 Collura Nov 2013 A1
20130304153 Hargrove et al. Nov 2013 A1
20130304159 Simon et al. Nov 2013 A1
20130304472 Pakhomov Nov 2013 A1
20130308099 Stack Nov 2013 A1
20130309278 Peyman Nov 2013 A1
20130310422 Brown et al. Nov 2013 A1
20130310660 Zuckerman-Stark et al. Nov 2013 A1
20130310909 Simon et al. Nov 2013 A1
20130314243 Le Nov 2013 A1
20130317380 Liley et al. Nov 2013 A1
20130317382 Le Nov 2013 A1
20130317384 Le Nov 2013 A1
20130317474 Rezai et al. Nov 2013 A1
20130317568 Skelton Nov 2013 A1
20130317580 Simon et al. Nov 2013 A1
20130318546 Kothuri et al. Nov 2013 A1
20130324880 Adachi et al. Dec 2013 A1
20130330428 Geng Dec 2013 A1
20130338449 Warwick et al. Dec 2013 A1
20130338450 Osorio et al. Dec 2013 A1
20130338459 Lynn et al. Dec 2013 A1
20130338518 Zoica Dec 2013 A1
20130338526 Howard Dec 2013 A1
20130338738 Garcia Molina et al. Dec 2013 A1
20130338803 Maoz et al. Dec 2013 A1
20130339043 Bakar et al. Dec 2013 A1
20130344465 Dickinson et al. Dec 2013 A1
20130345522 Sun et al. Dec 2013 A1
20130345523 Diab et al. Dec 2013 A1
20140000630 Ford Jan 2014 A1
20140003696 Taghva Jan 2014 A1
20140005518 Ko et al. Jan 2014 A1
20140005743 Giuffrida et al. Jan 2014 A1
20140005744 Hershey et al. Jan 2014 A1
20140005988 Brockway Jan 2014 A1
20140012061 Song et al. Jan 2014 A1
20140012110 Watson et al. Jan 2014 A1
20140012133 Sverdlik et al. Jan 2014 A1
20140012153 Greenwald Jan 2014 A1
20140015852 Kantartzis et al. Jan 2014 A1
20140018649 Jespersen et al. Jan 2014 A1
20140018792 Gang et al. Jan 2014 A1
20140019165 Horseman Jan 2014 A1
20140023999 Greder Jan 2014 A1
20140025133 Lozano Jan 2014 A1
20140025396 Horseman Jan 2014 A1
20140025397 Horseman Jan 2014 A1
20140029830 Vija et al. Jan 2014 A1
20140031703 Rayner et al. Jan 2014 A1
20140031889 Mashiach Jan 2014 A1
20140031903 Mashiach Jan 2014 A1
20140032512 Drew et al. Jan 2014 A1
20140038147 Morrow Feb 2014 A1
20140039279 Jarvik et al. Feb 2014 A1
20140039290 De Graff et al. Feb 2014 A1
20140039336 Osorio et al. Feb 2014 A1
20140039571 Wolpaw et al. Feb 2014 A1
20140039577 Kothandaraman et al. Feb 2014 A1
20140039578 Whitehurst et al. Feb 2014 A1
20140039975 Hill Feb 2014 A1
20140046203 Osorio et al. Feb 2014 A1
20140046208 Sejdic et al. Feb 2014 A1
20140046407 Ben-Ezra et al. Feb 2014 A1
20140051044 Badower et al. Feb 2014 A1
20140051960 Badower et al. Feb 2014 A1
20140051961 Badower et al. Feb 2014 A1
20140052213 Osorio Feb 2014 A1
20140055284 Tran et al. Feb 2014 A1
20140056815 Peyman Feb 2014 A1
20140057232 Wetmore et al. Feb 2014 A1
20140058189 Stubbeman Feb 2014 A1
20140058218 Randlov et al. Feb 2014 A1
20140058219 Kiraly Feb 2014 A1
20140058241 Apparies et al. Feb 2014 A1
20140058289 Panken et al. Feb 2014 A1
20140058292 Alford et al. Feb 2014 A1
20140058528 Contreras-Vidal et al. Feb 2014 A1
20140062472 Nishikawa Mar 2014 A1
20140063054 Osterhout et al. Mar 2014 A1
20140063055 Osterhout et al. Mar 2014 A1
20140066739 He et al. Mar 2014 A1
20140066763 Rothberg et al. Mar 2014 A2
20140066796 Davis et al. Mar 2014 A1
20140067740 Solari Mar 2014 A1
20140070958 Foo Mar 2014 A1
20140072127 Adachi et al. Mar 2014 A1
20140072130 Adachi et al. Mar 2014 A1
20140073863 Engelbrecht et al. Mar 2014 A1
20140073864 Engelbrecht et al. Mar 2014 A1
20140073866 Engelbrecht et al. Mar 2014 A1
20140073870 Engelbrecht et al. Mar 2014 A1
20140073875 Engelbrecht et al. Mar 2014 A1
20140073876 Rodriguez-Llorente et al. Mar 2014 A1
20140073877 Wooder Mar 2014 A1
20140073878 Engelbrecht et al. Mar 2014 A1
20140073898 Engelbrecht et al. Mar 2014 A1
20140073948 Engelbrecht et al. Mar 2014 A1
20140073949 Engelbrecht et al. Mar 2014 A1
20140073951 Engelbrecht et al. Mar 2014 A1
20140073953 Engelbrecht et al. Mar 2014 A1
20140073954 Engelbrecht et al. Mar 2014 A1
20140073955 Engelbrecht et al. Mar 2014 A1
20140073956 Engelbrecht et al. Mar 2014 A1
20140073960 Rodriguez-Llorente et al. Mar 2014 A1
20140073961 Rodriguez-Llorente et al. Mar 2014 A1
20140073963 Engelbrecht et al. Mar 2014 A1
20140073965 Engelbrecht et al. Mar 2014 A1
20140073966 Engelbrecht et al. Mar 2014 A1
20140073967 Engelbrecht et al. Mar 2014 A1
20140073968 Engelbrecht et al. Mar 2014 A1
20140073974 Engelbrecht Mar 2014 A1
20140073975 Engelbrecht et al. Mar 2014 A1
20140074060 Imran Mar 2014 A1
20140074179 Heldman et al. Mar 2014 A1
20140074180 Heldman et al. Mar 2014 A1
20140074188 Armstrong et al. Mar 2014 A1
20140077612 Onuma et al. Mar 2014 A1
20140077946 Tran Mar 2014 A1
20140081071 Simon et al. Mar 2014 A1
20140081114 Shachar et al. Mar 2014 A1
20140081115 Gu Mar 2014 A1
20140081347 Nelson et al. Mar 2014 A1
20140081353 Cook et al. Mar 2014 A1
20140088341 Altman et al. Mar 2014 A1
20140088377 Manzke et al. Mar 2014 A1
20140094710 Sarma et al. Apr 2014 A1
20140094719 Mishelevich Apr 2014 A1
20140094720 Tyler Apr 2014 A1
20140098981 Lunner et al. Apr 2014 A1
20140100467 Baker et al. Apr 2014 A1
20140100633 Mann et al. Apr 2014 A1
20140101084 Li et al. Apr 2014 A1
20140104059 Tran Apr 2014 A1
20140105436 Adachi et al. Apr 2014 A1
20140107397 Simon et al. Apr 2014 A1
20140107398 Simon et al. Apr 2014 A1
20140107401 Anderson et al. Apr 2014 A1
20140107464 Aksenova et al. Apr 2014 A1
20140107519 Musha et al. Apr 2014 A1
20140107521 Galan Apr 2014 A1
20140107525 Tass Apr 2014 A1
20140107728 Fried et al. Apr 2014 A1
20140107935 Taylor Apr 2014 A1
20140111335 Kleiss et al. Apr 2014 A1
20140113367 Deisseroth et al. Apr 2014 A1
20140114165 Walker et al. Apr 2014 A1
20140114205 Braun et al. Apr 2014 A1
20140114207 Patterson Apr 2014 A1
20140114242 Eckle Apr 2014 A1
20140114889 Dagum Apr 2014 A1
20140119621 Uber May 2014 A1
20140121446 Phillips et al. May 2014 A1
20140121476 Tran et al. May 2014 A1
20140121554 Sarma et al. May 2014 A1
20140121565 Kim May 2014 A1
20140122379 Moffiit et al. May 2014 A1
20140128762 Han et al. May 2014 A1
20140128763 Fadem May 2014 A1
20140128764 Gandhi May 2014 A1
20140128938 Craig May 2014 A1
20140133720 Lee et al. May 2014 A1
20140133722 Lee et al. May 2014 A1
20140135642 Ekpar May 2014 A1
20140135680 Peyman May 2014 A1
20140135873 An et al. May 2014 A1
20140135879 Flint May 2014 A1
20140135886 Cook et al. May 2014 A1
20140136585 Brockway May 2014 A1
20140140567 LeBoeuf et al. May 2014 A1
20140142448 Bae et al. May 2014 A1
20140142653 Osorio May 2014 A1
20140142654 Simon et al. May 2014 A1
20140142669 Cook et al. May 2014 A1
20140143064 Tran May 2014 A1
20140148479 Chesworth et al. May 2014 A1
20140148657 Hendler et al. May 2014 A1
20140148693 Taylor May 2014 A1
20140148716 Hopenfeld et al. May 2014 A1
20140148723 Nierenberg et al. May 2014 A1
20140148726 Wagner May 2014 A1
20140148872 Goldwasser et al. May 2014 A1
20140151563 Rousso et al. Jun 2014 A1
20140152673 Lynn et al. Jun 2014 A1
20140154647 Nolen Jun 2014 A1
20140154650 Stack Jun 2014 A1
20140155430 Chesworth et al. Jun 2014 A1
20140155706 Kochs et al. Jun 2014 A1
20140155714 Gavish Jun 2014 A1
20140155730 Bansal et al. Jun 2014 A1
20140155740 Semenov Jun 2014 A1
20140155770 Taylor Jun 2014 A1
20140155772 Frei et al. Jun 2014 A1
20140155952 Lozano et al. Jun 2014 A1
20140156000 Campin et al. Jun 2014 A1
20140159862 Yang et al. Jun 2014 A1
20140161352 Buyens et al. Jun 2014 A1
20140163328 Geva et al. Jun 2014 A1
20140163330 Horseman Jun 2014 A1
20140163331 Horseman Jun 2014 A1
20140163332 Horseman Jun 2014 A1
20140163333 Horseman Jun 2014 A1
20140163335 Horseman Jun 2014 A1
20140163336 Horseman Jun 2014 A1
20140163337 Horseman Jun 2014 A1
20140163368 Rousso et al. Jun 2014 A1
20140163385 Kelleher et al. Jun 2014 A1
20140163409 Arndt Jun 2014 A1
20140163425 Tran Jun 2014 A1
20140163627 Starr et al. Jun 2014 A1
20140163643 Craig Jun 2014 A1
20140163893 Harumatsu et al. Jun 2014 A1
20140163897 Lynn et al. Jun 2014 A1
20140171749 Chin et al. Jun 2014 A1
20140171757 Kawato et al. Jun 2014 A1
20140171819 Patterson Jun 2014 A1
20140171820 Causevic Jun 2014 A1
20140174277 Mann Jun 2014 A1
20140175261 Addison et al. Jun 2014 A1
20140176944 Addison et al. Jun 2014 A1
20140179980 Phillips et al. Jun 2014 A1
20140180088 Rothberg et al. Jun 2014 A1
20140180092 Rothberg et al. Jun 2014 A1
20140180093 Rothberg et al. Jun 2014 A1
20140180094 Rothberg et al. Jun 2014 A1
20140180095 Rothberg et al. Jun 2014 A1
20140180096 Rothberg et al. Jun 2014 A1
20140180097 Rothberg et al. Jun 2014 A1
20140180099 Rothberg et al. Jun 2014 A1
20140180100 Rothberg et al. Jun 2014 A1
20140180112 Rothberg et al. Jun 2014 A1
20140180113 Rothberg et al. Jun 2014 A1
20140180145 Kanai et al. Jun 2014 A1
20140180153 Zia et al. Jun 2014 A1
20140180160 Brown et al. Jun 2014 A1
20140180161 Bolger et al. Jun 2014 A1
20140180176 Rothberg et al. Jun 2014 A1
20140180177 Rothberg et al. Jun 2014 A1
20140180194 Lozano Jun 2014 A1
20140180358 Giftakis et al. Jun 2014 A1
20140180597 Brown et al. Jun 2014 A1
20140184550 Hennessey et al. Jul 2014 A1
20140187901 Cui et al. Jul 2014 A1
20140187994 Thornton Jul 2014 A1
20140188006 Alshaer et al. Jul 2014 A1
20140188770 Agrafioti et al. Jul 2014 A1
20140193336 Rousso et al. Jul 2014 A1
20140194702 Tran Jul 2014 A1
20140194720 Hua Jul 2014 A1
20140194726 Mishelevich et al. Jul 2014 A1
20140194758 Korenberg Jul 2014 A1
20140194759 Weiland et al. Jul 2014 A1
20140194768 Nierenberg et al. Jul 2014 A1
20140194769 Nierenberg et al. Jul 2014 A1
20140194780 Alshaer et al. Jul 2014 A1
20140194793 Nakata et al. Jul 2014 A1
20140200414 Osorio Jul 2014 A1
20140200432 Banerji et al. Jul 2014 A1
20140200623 Lindenthaler et al. Jul 2014 A1
20140203797 Stivoric et al. Jul 2014 A1
20140206981 Nagasaka Jul 2014 A1
20140207224 Simon Jul 2014 A1
20140207432 Taylor Jul 2014 A1
20140211593 Tyler et al. Jul 2014 A1
20140213842 Simon et al. Jul 2014 A1
20140213843 Pilla et al. Jul 2014 A1
20140213844 Pilla et al. Jul 2014 A1
20140213937 Bianchi et al. Jul 2014 A1
20140213961 Whitehurst et al. Jul 2014 A1
20140214135 Ben-David et al. Jul 2014 A1
20140214330 Iyer et al. Jul 2014 A1
20140214335 Siefert Jul 2014 A1
20140221726 Pilla et al. Aug 2014 A1
20140221866 Quy Aug 2014 A1
20140222113 Gliner et al. Aug 2014 A1
20140222406 Taylor Aug 2014 A1
20140226131 Lopez et al. Aug 2014 A1
20140226888 Skidmore Aug 2014 A1
20140228620 Vasishta Aug 2014 A1
20140228649 Rayner et al. Aug 2014 A1
20140228651 Causevic et al. Aug 2014 A1
20140228653 Kiraly Aug 2014 A1
20140228702 Shahaf et al. Aug 2014 A1
20140232516 Stivoric et al. Aug 2014 A1
20140235826 Deisseroth et al. Aug 2014 A1
20140235965 Tran Aug 2014 A1
20140236039 Strokova Aksenova et al. Aug 2014 A1
20140236077 Robertson et al. Aug 2014 A1
20140236272 Simon et al. Aug 2014 A1
20140236492 Taylor Aug 2014 A1
20140237073 Schiff Aug 2014 A1
20140243608 Hunt Aug 2014 A1
20140243613 Osorio Aug 2014 A1
20140243614 Rothberg et al. Aug 2014 A1
20140243621 Weng et al. Aug 2014 A1
20140243628 Ochs et al. Aug 2014 A1
20140243647 Clark et al. Aug 2014 A1
20140243652 Pashko Aug 2014 A1
20140243663 Taylor Aug 2014 A1
20140243694 Baker et al. Aug 2014 A1
20140243714 Ward et al. Aug 2014 A1
20140243926 Carcieri Aug 2014 A1
20140243934 Vo-Dinh et al. Aug 2014 A1
20140245191 Serena Aug 2014 A1
20140247970 Taylor Sep 2014 A1
20140249360 Jaeger et al. Sep 2014 A1
20140249396 Shacham-Diamand et al. Sep 2014 A1
20140249429 Tran Sep 2014 A1
20140249445 Deadwyler et al. Sep 2014 A1
20140249447 Sereno et al. Sep 2014 A1
20140249454 Carpentier Sep 2014 A1
20140249608 Rogers Sep 2014 A1
20140249791 Taylor Sep 2014 A1
20140249792 Taylor Sep 2014 A1
20140257047 Sillay et al. Sep 2014 A1
20140257073 Machon et al. Sep 2014 A1
20140257118 DiLorenzo et al. Sep 2014 A1
20140257128 Moxon et al. Sep 2014 A1
20140257132 Kilgard et al. Sep 2014 A1
20140257147 John et al. Sep 2014 A1
20140257430 Kilgard et al. Sep 2014 A1
20140257437 Simon et al. Sep 2014 A1
20140257438 Simon et al. Sep 2014 A1
20140266696 Addison et al. Sep 2014 A1
20140266787 Tran Sep 2014 A1
20140270438 Declerck et al. Sep 2014 A1
20140271483 Satchi-Fainaro et al. Sep 2014 A1
20140275716 Connor Sep 2014 A1
20140275741 Vandenbelt et al. Sep 2014 A1
20140275807 Redei Sep 2014 A1
20140275847 Perryman et al. Sep 2014 A1
20140275851 Amble et al. Sep 2014 A1
20140275886 Teixeira Sep 2014 A1
20140275889 Addison et al. Sep 2014 A1
20140275891 Muehlemann et al. Sep 2014 A1
20140275944 Semenov Sep 2014 A1
20140276012 Semenov Sep 2014 A1
20140276013 Muehlemann et al. Sep 2014 A1
20140276014 Khanicheh et al. Sep 2014 A1
20140276090 Breed Sep 2014 A1
20140276123 Yang Sep 2014 A1
20140276130 Mirelman et al. Sep 2014 A1
20140276181 Sun et al. Sep 2014 A1
20140276183 Badower Sep 2014 A1
20140276185 Carlson et al. Sep 2014 A1
20140276187 Iasemidis et al. Sep 2014 A1
20140276194 Osorio Sep 2014 A1
20140276549 Osorio Sep 2014 A1
20140276702 McKay et al. Sep 2014 A1
20140276944 Farritor et al. Sep 2014 A1
20140277255 Sabesan Sep 2014 A1
20140277256 Osorio Sep 2014 A1
20140277282 Jaax Sep 2014 A1
20140277286 Cinbis Sep 2014 A1
20140277582 Leuthardt et al. Sep 2014 A1
20140279341 Bhardwaj et al. Sep 2014 A1
20140279746 De Bruin et al. Sep 2014 A1
20140280189 Tang Sep 2014 A1
20140288381 Faarbaek et al. Sep 2014 A1
20140288614 Hagedorn et al. Sep 2014 A1
20140288620 DiLorenzo Sep 2014 A1
20140288953 Lynn et al. Sep 2014 A1
20140289172 Rothman et al. Sep 2014 A1
20140296646 Wingeier et al. Oct 2014 A1
20140296655 Akhbardeh et al. Oct 2014 A1
20140296724 Guttag et al. Oct 2014 A1
20140296733 Omurtag et al. Oct 2014 A1
20140296750 Einav et al. Oct 2014 A1
20140297397 Bakalash et al. Oct 2014 A1
20140300532 Karkkainen et al. Oct 2014 A1
20140303424 Glass Oct 2014 A1
20140303425 Pilla et al. Oct 2014 A1
20140303452 Ghaffari Oct 2014 A1
20140303453 Seely et al. Oct 2014 A1
20140303454 Clifton et al. Oct 2014 A1
20140303486 Baumgartner et al. Oct 2014 A1
20140303508 Plotnik-Peleg et al. Oct 2014 A1
20140303511 Sajda et al. Oct 2014 A1
20140304773 Woods et al. Oct 2014 A1
20140309484 Chang Oct 2014 A1
20140309614 Frei et al. Oct 2014 A1
20140309881 Fung et al. Oct 2014 A1
20140309943 Grundlehner et al. Oct 2014 A1
20140313303 Davis et al. Oct 2014 A1
20140315169 Bohbot Oct 2014 A1
20140316191 de Zambotti et al. Oct 2014 A1
20140316192 de Zambotti et al. Oct 2014 A1
20140316217 Purdon et al. Oct 2014 A1
20140316221 Rothman Oct 2014 A1
20140316230 Denison et al. Oct 2014 A1
20140316235 Davis et al. Oct 2014 A1
20140316243 Niedermeyer Oct 2014 A1
20140316248 deCharms Oct 2014 A1
20140316278 Addison et al. Oct 2014 A1
20140323849 Deisseroth et al. Oct 2014 A1
20140323899 Silberstein Oct 2014 A1
20140323900 Bibian et al. Oct 2014 A1
20140323924 Mishelevich Oct 2014 A1
20140323946 Bourke, Jr. et al. Oct 2014 A1
20140324118 Simon et al. Oct 2014 A1
20140324138 Wentz et al. Oct 2014 A1
20140328487 Hiroe Nov 2014 A1
20140330093 Pedro Nov 2014 A1
20140330102 Zbrzeski et al. Nov 2014 A1
20140330157 Snook Nov 2014 A1
20140330159 Costa et al. Nov 2014 A1
20140330268 Palti et al. Nov 2014 A1
20140330334 Errico et al. Nov 2014 A1
20140330335 Errico et al. Nov 2014 A1
20140330336 Errico et al. Nov 2014 A1
20140330337 Linke et al. Nov 2014 A1
20140330345 John Nov 2014 A1
20140330357 Stevenson et al. Nov 2014 A1
20140330394 Leuthardt et al. Nov 2014 A1
20140330404 Abdelghani et al. Nov 2014 A1
20140330580 Grima et al. Nov 2014 A1
20140335489 DeCharms Nov 2014 A1
20140336473 Greco Nov 2014 A1
20140336489 Angotzi et al. Nov 2014 A1
20140336514 Peyman Nov 2014 A1
20140336547 Tass et al. Nov 2014 A1
20140336730 Simon et al. Nov 2014 A1
20140340084 Alon Nov 2014 A1
20140343397 Kim et al. Nov 2014 A1
20140343399 Posse Nov 2014 A1
20140343408 Tolkowsky Nov 2014 A1
20140343463 Mishelevich Nov 2014 A1
20140343882 Taulu et al. Nov 2014 A1
20140347265 Aimone et al. Nov 2014 A1
20140347491 Connor Nov 2014 A1
20140348183 Kim et al. Nov 2014 A1
20140348412 Taylor Nov 2014 A1
20140350353 Connor Nov 2014 A1
20140350369 Budiman et al. Nov 2014 A1
20140350380 Eidelberg Nov 2014 A1
20140350431 Hagedorn Nov 2014 A1
20140350436 Nathan et al. Nov 2014 A1
20140350634 Grill et al. Nov 2014 A1
20140350636 King et al. Nov 2014 A1
20140350864 Fang et al. Nov 2014 A1
20140354278 Subbarao Dec 2014 A1
20140355859 Taylor et al. Dec 2014 A1
20140357507 Umansky et al. Dec 2014 A1
20140357932 Lozano Dec 2014 A1
20140357935 Ilmoniemi et al. Dec 2014 A1
20140357936 Simon et al. Dec 2014 A1
20140357962 Harrington et al. Dec 2014 A1
20140358024 Nelson et al. Dec 2014 A1
20140358025 Parhi et al. Dec 2014 A1
20140358067 Deisseroth et al. Dec 2014 A1
20140358193 Lyons et al. Dec 2014 A1
20140358199 Lim Dec 2014 A1
20140364721 Lee et al. Dec 2014 A1
20140364746 Addison et al. Dec 2014 A1
20140369537 Pontoppidan et al. Dec 2014 A1
20140370479 Gazzaley Dec 2014 A1
20140371515 John Dec 2014 A1
20140371516 Tsai et al. Dec 2014 A1
20140371544 Wu et al. Dec 2014 A1
20140371573 Komoto et al. Dec 2014 A1
20140371599 Wu et al. Dec 2014 A1
20140371611 Kim Dec 2014 A1
20140371984 Fung et al. Dec 2014 A1
20140378809 Weitnauer et al. Dec 2014 A1
20140378810 Davis et al. Dec 2014 A1
20140378815 Huang et al. Dec 2014 A1
20140378830 Li Dec 2014 A1
20140378851 Frei et al. Dec 2014 A1
20140378941 Su et al. Dec 2014 A1
20140379620 Sarrafzadeh et al. Dec 2014 A1
20150002815 Gross et al. Jan 2015 A1
20150003698 Davis et al. Jan 2015 A1
20150003699 Davis et al. Jan 2015 A1
20150005592 Osorio Jan 2015 A1
20150005594 Chamoun et al. Jan 2015 A1
20150005640 Davis et al. Jan 2015 A1
20150005644 Rhoads Jan 2015 A1
20150005646 Balakrishnan et al. Jan 2015 A1
20150005660 Kraus et al. Jan 2015 A1
20150005680 Lipani Jan 2015 A1
20150005839 Sabesan et al. Jan 2015 A1
20150005840 Pal et al. Jan 2015 A1
20150005841 Pal et al. Jan 2015 A1
20150006186 Davis et al. Jan 2015 A1
20150008916 Le Prado et al. Jan 2015 A1
20150010223 Sapiro et al. Jan 2015 A1
20150011866 Baumgartner Jan 2015 A1
20150011877 Baumgartner Jan 2015 A1
20150011907 Purdon et al. Jan 2015 A1
20150012054 Kilgard et al. Jan 2015 A1
20150012057 Carlson et al. Jan 2015 A1
20150012111 Contreras-Vidal et al. Jan 2015 A1
20150012466 Sapiro et al. Jan 2015 A1
20150016618 Adachi et al. Jan 2015 A1
20150017115 Satchi-Fainaro et al. Jan 2015 A1
20150018665 Jasanoff et al. Jan 2015 A1
20150018699 Zeng et al. Jan 2015 A1
20150018702 Galloway et al. Jan 2015 A1
20150018705 Barlow et al. Jan 2015 A1
20150018706 Segal Jan 2015 A1
20150018758 John Jan 2015 A1
20150018893 Kilgard et al. Jan 2015 A1
20150018905 Nofzinger et al. Jan 2015 A1
20150019241 Bennett et al. Jan 2015 A1
20150019266 Stempora Jan 2015 A1
20150024356 Hillyer et al. Jan 2015 A1
20150025351 Govari Jan 2015 A1
20150025408 Wingeier et al. Jan 2015 A1
20150025410 Wolpaw et al. Jan 2015 A1
20150025421 Wagner et al. Jan 2015 A1
20150025422 Tyler Jan 2015 A1
20150025610 Wingeier et al. Jan 2015 A1
20150025917 Stempora Jan 2015 A1
20150026446 Kim et al. Jan 2015 A1
20150029087 Klappert et al. Jan 2015 A1
20150030220 Cho et al. Jan 2015 A1
20150032017 Babaeizadeh et al. Jan 2015 A1
20150032044 Peyman Jan 2015 A9
20150032178 Simon et al. Jan 2015 A1
20150033245 Klappert et al. Jan 2015 A1
20150033258 Klappert et al. Jan 2015 A1
20150033259 Klappert et al. Jan 2015 A1
20150033262 Klappert et al. Jan 2015 A1
20150033266 Klappert et al. Jan 2015 A1
20150033363 Pinsky et al. Jan 2015 A1
20150035959 Amble et al. Feb 2015 A1
20150038804 Younes Feb 2015 A1
20150038812 Ayaz et al. Feb 2015 A1
20150038822 Wingeier et al. Feb 2015 A1
20150038869 Simon et al. Feb 2015 A1
20150039066 Wingeier et al. Feb 2015 A1
20150039110 Abeyratne et al. Feb 2015 A1
20150042477 Kobetski et al. Feb 2015 A1
20150044138 Lansbergen et al. Feb 2015 A1
20150045606 Hagedorn et al. Feb 2015 A1
20150045607 Hakansson Feb 2015 A1
20150045686 Lynn Feb 2015 A1
20150051655 Kilgard et al. Feb 2015 A1
20150051656 Kilgard et al. Feb 2015 A1
20150051657 Kilgard et al. Feb 2015 A1
20150051658 Kilgard et al. Feb 2015 A1
20150051659 Kilgard et al. Feb 2015 A1
20150051663 Hagedorn Feb 2015 A1
20150051668 Bahmer Feb 2015 A1
20150057512 Kapoor Feb 2015 A1
20150057715 Kilgard et al. Feb 2015 A1
20150065803 Douglas et al. Mar 2015 A1
20150065831 Popovic et al. Mar 2015 A1
20150065838 Wingeier et al. Mar 2015 A1
20150065839 Farah et al. Mar 2015 A1
20150065845 Takiguchi Mar 2015 A1
20150066124 Stevenson et al. Mar 2015 A1
20150068069 Tran et al. Mar 2015 A1
20150069846 Hokari Mar 2015 A1
20150071907 Crombez et al. Mar 2015 A1
20150072394 Deisseroth et al. Mar 2015 A1
20150073141 Teegarden et al. Mar 2015 A1
20150073237 Osorio Mar 2015 A1
20150073249 Musha Mar 2015 A1
20150073294 Zhang et al. Mar 2015 A1
20150073306 Abeyratne et al. Mar 2015 A1
20150073505 Errico et al. Mar 2015 A1
20150073722 Taylor et al. Mar 2015 A1
20150080327 Paul et al. Mar 2015 A1
20150080671 Christensen et al. Mar 2015 A1
20150080674 Drew et al. Mar 2015 A1
20150080695 Rogers et al. Mar 2015 A1
20150080703 Reiman Mar 2015 A1
20150080746 Bleich et al. Mar 2015 A1
20150080753 Miyazaki et al. Mar 2015 A1
20150080985 Yun et al. Mar 2015 A1
20150081226 Baki Mar 2015 A1
20150081299 Jasinschi et al. Mar 2015 A1
20150087931 Banerjee et al. Mar 2015 A1
20150088015 Taylor Mar 2015 A1
20150088024 Sackellares Mar 2015 A1
20150088093 Goetz Mar 2015 A1
20150088120 Garcia et al. Mar 2015 A1
20150088224 Goldwasser et al. Mar 2015 A1
20150088228 Moffitt Mar 2015 A1
20150088478 Taylor Mar 2015 A1
20150091730 Kangas et al. Apr 2015 A1
20150091791 Segal Apr 2015 A1
20150092949 Adachi et al. Apr 2015 A1
20150093729 Plans et al. Apr 2015 A1
20150094962 Hoegh et al. Apr 2015 A1
20150096564 Cosnek Apr 2015 A1
20150099941 Tran Apr 2015 A1
20150099946 Sahin Apr 2015 A1
20150099959 Bonmassar et al. Apr 2015 A1
20150099962 Weiss et al. Apr 2015 A1
20150103360 Addison et al. Apr 2015 A1
20150105631 Tran et al. Apr 2015 A1
20150105641 Austin et al. Apr 2015 A1
20150105701 Mayer et al. Apr 2015 A1
20150105837 Aguilar Domingo Apr 2015 A1
20150105844 Tass et al. Apr 2015 A1
20150112222 Sun et al. Apr 2015 A1
20150112403 Ruffini et al. Apr 2015 A1
20150112409 Hagedorn Apr 2015 A1
20150112899 Dagum Apr 2015 A1
20150119652 Hyde et al. Apr 2015 A1
20150119658 Osorio Apr 2015 A1
20150119689 Pascual-Leone et al. Apr 2015 A1
20150119698 Eyal et al. Apr 2015 A1
20150119743 Maksym et al. Apr 2015 A1
20150119745 Similowski et al. Apr 2015 A1
20150119746 Conradsen Apr 2015 A1
20150119794 Peyman Apr 2015 A1
20150119898 Desalles et al. Apr 2015 A1
20150119956 Libbus et al. Apr 2015 A1
20150120007 Guez et al. Apr 2015 A1
20150123653 Nagasaka May 2015 A1
20150124220 Gross et al. May 2015 A1
20150126821 Kempfner et al. May 2015 A1
20150126845 Jin et al. May 2015 A1
20150126848 Baker et al. May 2015 A1
20150126873 Connor May 2015 A1
20150133716 Suhami et al. May 2015 A1
20150133811 Suzuki et al. May 2015 A1
20150133812 deCharms May 2015 A1
20150133830 Dirks et al. May 2015 A1
20150134031 Moffitt et al. May 2015 A1
20150134264 Tansey May 2015 A1
20150137817 Wilson et al. May 2015 A1
20150137988 Gravenstein et al. May 2015 A1
20150140528 Sikstrom et al. May 2015 A1
20150141529 Hargrove May 2015 A1
20150141773 Einav et al. May 2015 A1
20150141789 Knight et al. May 2015 A1
20150141794 Foo May 2015 A1
20150142082 Simon et al. May 2015 A1
20150145519 Lee et al. May 2015 A1
20150145676 Adhikari et al. May 2015 A1
20150148617 Friedman May 2015 A1
20150148619 Berg et al. May 2015 A1
20150148700 Mhuircheartaigh et al. May 2015 A1
20150148878 Yoo et al. May 2015 A1
20150150122 Son et al. May 2015 A1
20150150473 Knight et al. Jun 2015 A1
20150150475 Varcoe Jun 2015 A1
20150150530 Taylor et al. Jun 2015 A1
20150150753 Racette Jun 2015 A1
20150151142 Tyler et al. Jun 2015 A1
20150153477 Wikelski et al. Jun 2015 A1
20150154721 Thompson Jun 2015 A1
20150154764 Xie et al. Jun 2015 A1
20150154889 Tuchschmid et al. Jun 2015 A1
20150157235 Jelen et al. Jun 2015 A1
20150157266 Machon et al. Jun 2015 A1
20150157271 Zhang Jun 2015 A1
20150157859 Besio Jun 2015 A1
20150161326 Taylor et al. Jun 2015 A1
20150161348 Taylor et al. Jun 2015 A1
20150161738 Stempora Jun 2015 A1
20150164349 Gopalakrishnan et al. Jun 2015 A1
20150164362 Morrow Jun 2015 A1
20150164375 Schindhelm et al. Jun 2015 A1
20150164404 Euliano et al. Jun 2015 A1
20150164431 Terry et al. Jun 2015 A1
20150165226 Simon et al. Jun 2015 A1
20150165239 Mishelevich Jun 2015 A1
20150167459 Sen et al. Jun 2015 A1
20150174362 Panova et al. Jun 2015 A1
20150174398 Chow et al. Jun 2015 A1
20150174403 Pal et al. Jun 2015 A1
20150174405 Kilgard et al. Jun 2015 A1
20150174406 Lamensdorf et al. Jun 2015 A1
20150174407 Osorio Jun 2015 A1
20150174418 Tyler et al. Jun 2015 A1
20150177413 Wilt et al. Jun 2015 A1
20150178631 Thomas et al. Jun 2015 A1
20150178978 Durand et al. Jun 2015 A1
20150181840 Tupin, Jr. et al. Jul 2015 A1
20150182417 Nagatani Jul 2015 A1
20150182753 Harris et al. Jul 2015 A1
20150182756 Peyman Jul 2015 A1
20150186923 Gurumoorthy et al. Jul 2015 A1
20150190062 Han et al. Jul 2015 A1
20150190070 Bonmassar et al. Jul 2015 A1
20150190077 Kim et al. Jul 2015 A1
20150190085 Nathan et al. Jul 2015 A1
20150190094 Lee et al. Jul 2015 A1
20150190636 Simon et al. Jul 2015 A1
20150190637 Simon et al. Jul 2015 A1
20150192532 Clevenson et al. Jul 2015 A1
20150192776 Lee et al. Jul 2015 A1
20150196213 Pandia et al. Jul 2015 A1
20150196246 Osorio Jul 2015 A1
20150196249 Brown et al. Jul 2015 A1
20150196800 Macri et al. Jul 2015 A1
20150199010 Coleman et al. Jul 2015 A1
20150199121 Gulaka et al. Jul 2015 A1
20150200046 Park et al. Jul 2015 A1
20150201849 Taylor Jul 2015 A1
20150201879 Hargrove Jul 2015 A1
20150202330 Yang et al. Jul 2015 A1
20150202428 Miller Jul 2015 A1
20150202447 Afshar et al. Jul 2015 A1
20150203822 Tremolada et al. Jul 2015 A1
20150206051 McIntosh et al. Jul 2015 A1
20150206174 Barnett et al. Jul 2015 A1
20150208940 Addison et al. Jul 2015 A1
20150208975 Ghajar Jul 2015 A1
20150208978 Osorio et al. Jul 2015 A1
20150208982 Ho et al. Jul 2015 A1
20150208994 Rapoport Jul 2015 A1
20150212168 Shah et al. Jul 2015 A1
20150213012 Marvit et al. Jul 2015 A1
20150213019 Marvit et al. Jul 2015 A1
20150213020 Marvit et al. Jul 2015 A1
20150213191 Abdelghani et al. Jul 2015 A1
20150215412 Marvit et al. Jul 2015 A1
20150216436 Bosl et al. Aug 2015 A1
20150216439 Muraskin et al. Aug 2015 A1
20150216468 Vidal-Naquet et al. Aug 2015 A1
20150216469 DiLorenzo et al. Aug 2015 A1
20150216762 Oohashi et al. Aug 2015 A1
20150217082 Kang et al. Aug 2015 A1
20150219729 Takahashi Aug 2015 A1
20150219732 Diamond et al. Aug 2015 A1
20150220486 Karakonstantis et al. Aug 2015 A1
20150220830 Li et al. Aug 2015 A1
20150223721 De Ridder Aug 2015 A1
20150223731 Sahin Aug 2015 A1
20150223743 Pathangay et al. Aug 2015 A1
20150223905 Karmarkar et al. Aug 2015 A1
20150226813 Yu et al. Aug 2015 A1
20150227702 Krishna et al. Aug 2015 A1
20150227793 Ernst et al. Aug 2015 A1
20150230719 Berg et al. Aug 2015 A1
20150230744 Faubert et al. Aug 2015 A1
20150230750 McDarby et al. Aug 2015 A1
20150231330 Lozano et al. Aug 2015 A1
20150231395 Saab Aug 2015 A1
20150231397 Nudo, Jr. et al. Aug 2015 A1
20150231405 Okada Aug 2015 A1
20150231408 Williams et al. Aug 2015 A1
20150234477 Abovitz et al. Aug 2015 A1
20150235088 Abovitz et al. Aug 2015 A1
20150235370 Abovitz et al. Aug 2015 A1
20150235441 Abovitz et al. Aug 2015 A1
20150235447 Abovitz et al. Aug 2015 A1
20150238104 Tass Aug 2015 A1
20150238106 Lappalainen et al. Aug 2015 A1
20150238112 Park et al. Aug 2015 A1
20150238137 Eyal et al. Aug 2015 A1
20150238693 Skelton et al. Aug 2015 A1
20150238761 Sabesan Aug 2015 A1
20150238765 Zhu Aug 2015 A1
20150241705 Abovitz et al. Aug 2015 A1
20150241916 Choi et al. Aug 2015 A1
20150241959 Abovitz et al. Aug 2015 A1
20150242575 Abovitz et al. Aug 2015 A1
20150242608 Kim et al. Aug 2015 A1
20150242943 Abovitz et al. Aug 2015 A1
20150243100 Abovitz et al. Aug 2015 A1
20150243105 Abovitz et al. Aug 2015 A1
20150243106 Abovitz et al. Aug 2015 A1
20150245781 Hua Sep 2015 A1
20150245800 Sorensen et al. Sep 2015 A1
20150246238 Moses et al. Sep 2015 A1
20150247723 Abovitz et al. Sep 2015 A1
20150247921 Rothberg et al. Sep 2015 A1
20150247975 Abovitz et al. Sep 2015 A1
20150247976 Abovitz et al. Sep 2015 A1
20150248167 Turbell et al. Sep 2015 A1
20150248169 Abovitz et al. Sep 2015 A1
20150248170 Abovitz et al. Sep 2015 A1
20150248470 Coleman et al. Sep 2015 A1
20150248615 Parra et al. Sep 2015 A1
20150248764 Keskin et al. Sep 2015 A1
20150248765 Criminisi et al. Sep 2015 A1
20150248787 Abovitz et al. Sep 2015 A1
20150248788 Abovitz et al. Sep 2015 A1
20150248789 Abovitz et al. Sep 2015 A1
20150248791 Abovitz et al. Sep 2015 A1
20150248792 Abovitz et al. Sep 2015 A1
20150248793 Abovitz et al. Sep 2015 A1
20150250393 Tran Sep 2015 A1
20150250401 Tveit Sep 2015 A1
20150250415 Leininger et al. Sep 2015 A1
20150251016 Vo-Dinh et al. Sep 2015 A1
20150253391 Toda et al. Sep 2015 A1
20150253410 Warfield et al. Sep 2015 A1
20150254413 Soederstroem Sep 2015 A1
20150257645 Bae et al. Sep 2015 A1
20150257648 Semenov Sep 2015 A1
20150257649 Semenov Sep 2015 A1
20150257673 Lawrence et al. Sep 2015 A1
20150257674 Jordan et al. Sep 2015 A1
20150257700 Fu Sep 2015 A1
20150257712 Sarrafzadeh et al. Sep 2015 A1
20150262016 Rothblatt Sep 2015 A1
20150264492 Laudanski et al. Sep 2015 A1
20150265164 Gopalakrishnan et al. Sep 2015 A1
20150265207 Wu et al. Sep 2015 A1
20150265583 Chesworth et al. Sep 2015 A1
20150265830 Simon et al. Sep 2015 A1
20150265836 Simon et al. Sep 2015 A1
20150269825 Tran Sep 2015 A1
20150272448 Fonte et al. Oct 2015 A1
20150272461 Morimoto et al. Oct 2015 A1
20150272465 Ishii Oct 2015 A1
20150272496 Klappert et al. Oct 2015 A1
20150272510 Chin Oct 2015 A1
20150272652 Ghaffari et al. Oct 2015 A1
20150273211 Ollivier Oct 2015 A1
20150273223 John Oct 2015 A1
20150282705 Avital Oct 2015 A1
20150282730 Knight et al. Oct 2015 A1
20150282749 Zand et al. Oct 2015 A1
20150282755 Deriche et al. Oct 2015 A1
20150282760 Badower et al. Oct 2015 A1
20150283019 Feingold Oct 2015 A1
20150283265 Peyman Oct 2015 A1
20150283379 Venkatesan Oct 2015 A1
20150283393 Schmidt Oct 2015 A1
20150287223 Bresler et al. Oct 2015 A1
20150289217 Ban et al. Oct 2015 A1
20150289779 Fischl et al. Oct 2015 A1
20150289813 Lipov Oct 2015 A1
20150289929 Toth et al. Oct 2015 A1
20150290419 Kare et al. Oct 2015 A1
20150290420 Nofzinger Oct 2015 A1
20150290453 Tyler et al. Oct 2015 A1
20150290454 Tyler et al. Oct 2015 A1
20150293004 Adolphi et al. Oct 2015 A1
20150294067 Kare et al. Oct 2015 A1
20150294074 Kawato et al. Oct 2015 A1
20150294085 Kare et al. Oct 2015 A1
20150294086 Kare et al. Oct 2015 A1
20150294445 Sakaue Oct 2015 A1
20150296288 Anastas Oct 2015 A1
20150297106 Pasley et al. Oct 2015 A1
20150297108 Chase et al. Oct 2015 A1
20150297109 Garten et al. Oct 2015 A1
20150297139 Toth Oct 2015 A1
20150297141 Siegel et al. Oct 2015 A1
20150297444 Tass Oct 2015 A1
20150297719 Deisseroth et al. Oct 2015 A1
20150297889 Simon et al. Oct 2015 A1
20150297893 Kokones et al. Oct 2015 A1
20150301218 Donderici Oct 2015 A1
20150304048 Kim et al. Oct 2015 A1
20150304101 Gupta et al. Oct 2015 A1
20150305685 Shahaf et al. Oct 2015 A1
20150305686 Coleman et al. Oct 2015 A1
20150305689 Gourmelon et al. Oct 2015 A1
20150305799 Trieu Oct 2015 A1
20150305800 Trieu Oct 2015 A1
20150305801 Trieu Oct 2015 A1
20150306057 Goodenowe Oct 2015 A1
20150306340 Giap et al. Oct 2015 A1
20150306390 Zalay et al. Oct 2015 A1
20150306391 Wu et al. Oct 2015 A1
20150306392 Sabesan Oct 2015 A1
20150309563 Connor Oct 2015 A1
20150309582 Gupta Oct 2015 A1
20150310862 Dauphin et al. Oct 2015 A1
20150313496 Connor Nov 2015 A1
20150313498 Coleman et al. Nov 2015 A1
20150313535 Alshaer et al. Nov 2015 A1
20150313539 Connor Nov 2015 A1
20150313540 Deuchar et al. Nov 2015 A1
20150313949 Cutillo Nov 2015 A1
20150313971 Haslett et al. Nov 2015 A1
20150315554 Shekdar et al. Nov 2015 A1
20150317447 Helleputte et al. Nov 2015 A1
20150317796 Schett et al. Nov 2015 A1
20150320591 Smith et al. Nov 2015 A1
20150321000 Rosenbluth et al. Nov 2015 A1
20150324544 Maslowski et al. Nov 2015 A1
20150324545 Fonte Nov 2015 A1
20150324692 Ritchey et al. Nov 2015 A1
20150325151 Tuchschmid et al. Nov 2015 A1
20150327813 Fu Nov 2015 A1
20150327837 Qi et al. Nov 2015 A1
20150328330 Satchi-Fainaro et al. Nov 2015 A1
20150328455 Meadows et al. Nov 2015 A1
20150331929 El-Saban et al. Nov 2015 A1
20150332015 Taylor Nov 2015 A1
20150335281 Scroggins Nov 2015 A1
20150335288 Toth et al. Nov 2015 A1
20150335292 Mittal Nov 2015 A1
20150335294 Witcher et al. Nov 2015 A1
20150335295 Park et al. Nov 2015 A1
20150335303 Chandelier et al. Nov 2015 A1
20150335876 Jeffery et al. Nov 2015 A1
20150335877 Jeffery et al. Nov 2015 A1
20150338915 Publicover et al. Nov 2015 A1
20150339363 Moldoveanu et al. Nov 2015 A1
20150339459 Taylor Nov 2015 A1
20150342472 Semenov Dec 2015 A1
20150342478 Galen et al. Dec 2015 A1
20150342493 Hardt Dec 2015 A1
20150343215 De Ridder Dec 2015 A1
20150343222 Kilgard et al. Dec 2015 A1
20150343242 Tyler et al. Dec 2015 A1
20150351655 Coleman Dec 2015 A1
20150351690 Toth et al. Dec 2015 A1
20150351701 Moxon et al. Dec 2015 A1
20150352362 Craig Dec 2015 A1
20150352363 McIntyre et al. Dec 2015 A1
20150359431 Bakalash et al. Dec 2015 A1
20150359441 Giovangrandi et al. Dec 2015 A1
20150359450 Lee et al. Dec 2015 A1
20150359452 Giovangrandi et al. Dec 2015 A1
20150359467 Tran Dec 2015 A1
20150359486 Kovacs et al. Dec 2015 A1
20150359492 Giovangrandi et al. Dec 2015 A1
20150360026 Wagner Dec 2015 A1
20150360030 Cartledge et al. Dec 2015 A1
20150360039 Lempka et al. Dec 2015 A1
20150363941 Taylor Dec 2015 A1
20150366482 Lee Dec 2015 A1
20150366497 Cavuoto et al. Dec 2015 A1
20150366503 Sjaaheim et al. Dec 2015 A1
20150366504 Connor Dec 2015 A1
20150366516 Dripps et al. Dec 2015 A1
20150366518 Sampson Dec 2015 A1
20150366656 Wortz et al. Dec 2015 A1
20150366659 Wortz et al. Dec 2015 A1
20150369864 Marlow et al. Dec 2015 A1
20150370320 Connor Dec 2015 A1
20150370325 Jarosiewicz et al. Dec 2015 A1
20150374250 Hatano et al. Dec 2015 A1
20150374285 Chang et al. Dec 2015 A1
20150374292 Wyeth et al. Dec 2015 A1
20150374300 Najarian et al. Dec 2015 A1
20150374973 Morrell Dec 2015 A1
20150374983 Simon et al. Dec 2015 A1
20150374986 Bahmer Dec 2015 A1
20150374987 Bahmer Dec 2015 A1
20150374993 Morrell Dec 2015 A1
20150375006 Denison et al. Dec 2015 A1
20150379230 Taylor Dec 2015 A1
20150379370 Clifton et al. Dec 2015 A1
20150379878 Walter et al. Dec 2015 A1
20150380009 Chang et al. Dec 2015 A1
20160000348 Kitajo et al. Jan 2016 A1
20160000354 Hagedorn et al. Jan 2016 A1
20160000383 Lee et al. Jan 2016 A1
20160001065 Wingeier et al. Jan 2016 A1
20160001096 Mishelevich Jan 2016 A1
20160001098 Wingeier et al. Jan 2016 A1
20160002523 Huh et al. Jan 2016 A1
20160004298 Mazed et al. Jan 2016 A1
20160004396 Gulaka et al. Jan 2016 A1
20160004821 Fueyo et al. Jan 2016 A1
20160004957 Solari Jan 2016 A1
20160005235 Fateh Jan 2016 A1
20160005320 deCharms et al. Jan 2016 A1
20160007899 Durkee et al. Jan 2016 A1
20160007904 Vardy Jan 2016 A1
20160007915 Berka et al. Jan 2016 A1
20160007918 Badower et al. Jan 2016 A1
20160007945 Taylor Jan 2016 A1
20160008489 Korzus Jan 2016 A1
20160008568 Attia et al. Jan 2016 A1
20160008598 McLaughlin et al. Jan 2016 A1
20160008600 Hershey et al. Jan 2016 A1
20160008620 Stubbeman Jan 2016 A1
20160008632 Wetmore et al. Jan 2016 A1
20160012011 Llinas et al. Jan 2016 A1
20160012583 Cales et al. Jan 2016 A1
20160012749 Connor Jan 2016 A1
20160015281 McKenna et al. Jan 2016 A1
20160015289 Simon et al. Jan 2016 A1
20160015307 Kothuri Jan 2016 A1
20160015673 Goodenowe Jan 2016 A1
20160016014 Wagner et al. Jan 2016 A1
20160019434 Caldwell Jan 2016 A1
20160019693 Silbersweig et al. Jan 2016 A1
20160022141 Mittal et al. Jan 2016 A1
20160022156 Kovacs et al. Jan 2016 A1
20160022164 Brockway et al. Jan 2016 A1
20160022165 Sackellares et al. Jan 2016 A1
20160022167 Simon Jan 2016 A1
20160022168 Luczak et al. Jan 2016 A1
20160022206 Simon et al. Jan 2016 A1
20160022207 Roberts et al. Jan 2016 A1
20160022981 Wingeier et al. Jan 2016 A1
20160023016 Bonmassar et al. Jan 2016 A1
20160026913 Moon et al. Jan 2016 A1
20160027178 Yu et al. Jan 2016 A1
20160027293 Esteller et al. Jan 2016 A1
20160027342 Ben-Haim Jan 2016 A1
20160027423 Deuel et al. Jan 2016 A1
20160029896 Lee et al. Feb 2016 A1
20160029917 Baker et al. Feb 2016 A1
20160029918 Baker et al. Feb 2016 A1
20160029946 Simon et al. Feb 2016 A1
20160029950 Chang et al. Feb 2016 A1
20160029958 Le et al. Feb 2016 A1
20160029959 Le et al. Feb 2016 A1
20160029965 Simon Feb 2016 A1
20160029998 Brister et al. Feb 2016 A1
20160030666 Lozano et al. Feb 2016 A1
20160030702 Yang Feb 2016 A1
20160030749 Carcieri et al. Feb 2016 A1
20160030750 Bokil et al. Feb 2016 A1
20160030834 Brown et al. Feb 2016 A1
20160031479 Fung et al. Feb 2016 A1
20160035093 Kateb et al. Feb 2016 A1
20160038037 Kovacs Feb 2016 A1
20160038038 Kovacs Feb 2016 A1
20160038042 Mulligan et al. Feb 2016 A1
20160038043 Mulligan et al. Feb 2016 A1
20160038049 Geva et al. Feb 2016 A1
20160038069 Stack Feb 2016 A1
20160038091 Krishnaswamy et al. Feb 2016 A1
20160038559 Palmer et al. Feb 2016 A1
20160038770 Tyler et al. Feb 2016 A1
20160040514 Rahmani et al. Feb 2016 A1
20160044841 Chamberlain Feb 2016 A1
20160045128 Sitt et al. Feb 2016 A1
20160045150 Leininger et al. Feb 2016 A1
20160045162 De Graff et al. Feb 2016 A1
20160045731 Simon et al. Feb 2016 A1
20160045756 Phillips et al. Feb 2016 A1
20160048659 Pereira et al. Feb 2016 A1
20160048948 Bajic Feb 2016 A1
20160048965 Stehle et al. Feb 2016 A1
20160051161 Labyt et al. Feb 2016 A1
20160051162 Durand et al. Feb 2016 A1
20160051187 Damadian Feb 2016 A1
20160051195 Pang et al. Feb 2016 A1
20160051793 Gibson-Horn Feb 2016 A1
20160051812 Montgomery, Jr. et al. Feb 2016 A1
20160051818 Simon et al. Feb 2016 A1
20160055236 Frank et al. Feb 2016 A1
20160055304 Russell et al. Feb 2016 A1
20160055415 Baxi Feb 2016 A1
20160055842 DeFranks et al. Feb 2016 A1
20160058301 Shusterman Mar 2016 A1
20160058304 Emblem et al. Mar 2016 A1
20160058322 Brister et al. Mar 2016 A1
20160058354 Phan et al. Mar 2016 A1
20160058359 Osorio Mar 2016 A1
20160058366 Choi et al. Mar 2016 A1
20160058376 Baek et al. Mar 2016 A1
20160058392 Hasson et al. Mar 2016 A1
20160058673 Francis Mar 2016 A1
20160060926 Kim et al. Mar 2016 A1
20160062459 Publicover et al. Mar 2016 A1
20160063207 Schmidt Mar 2016 A1
20160063883 Jeyanandarajan Mar 2016 A1
20160065724 Lee et al. Mar 2016 A1
20160065840 Kim et al. Mar 2016 A1
20160066788 Tran et al. Mar 2016 A1
20160066789 Rogers et al. Mar 2016 A1
20160066828 Phan et al. Mar 2016 A1
20160066838 DeCharms Mar 2016 A1
20160067485 Lindenthaler et al. Mar 2016 A1
20160067492 Wolpaw et al. Mar 2016 A1
20160067494 Lipani Mar 2016 A1
20160067496 Gliner et al. Mar 2016 A1
20160067526 Yang Mar 2016 A1
20160070436 Thomas et al. Mar 2016 A1
20160073886 Connor Mar 2016 A1
20160073916 Aksenova et al. Mar 2016 A1
20160073947 Anderson Mar 2016 A1
20160073991 Taylor Mar 2016 A1
20160074657 Kwan et al. Mar 2016 A1
20160074660 Osorio et al. Mar 2016 A1
20160074661 Lipani Mar 2016 A1
20160077547 Aimone et al. Mar 2016 A1
20160078780 Alexander et al. Mar 2016 A1
20160081577 Sridhar et al. Mar 2016 A1
20160081610 Osorio et al. Mar 2016 A1
20160081613 Braun et al. Mar 2016 A1
20160081616 Li Mar 2016 A1
20160081625 Kim et al. Mar 2016 A1
20160081793 Galstian et al. Mar 2016 A1
20160082180 Toth et al. Mar 2016 A1
20160082319 Macri et al. Mar 2016 A1
20160084925 Le Prado et al. Mar 2016 A1
20160085302 Publicover et al. Mar 2016 A1
20160086622 Yamamoto Mar 2016 A1
20160087603 Ricci et al. Mar 2016 A1
20160089031 Hu Mar 2016 A1
20160091448 Soleimani Mar 2016 A1
20160095546 Sahasrabudhe et al. Apr 2016 A1
20160095838 Satchi-Fainaro et al. Apr 2016 A1
20160096025 Moffitt et al. Apr 2016 A1
20160097824 Fujii et al. Apr 2016 A1
20160100769 Kim et al. Apr 2016 A1
20160101260 Austin et al. Apr 2016 A1
20160102500 Donderici et al. Apr 2016 A1
20160103487 Crawford et al. Apr 2016 A1
20160103963 Mishra Apr 2016 A1
20160104006 Son et al. Apr 2016 A1
20160106331 Zorick et al. Apr 2016 A1
20160106344 Nazari Apr 2016 A1
20160106513 De Stavola et al. Apr 2016 A1
20160106950 Vasapollo Apr 2016 A1
20160106997 Arendash et al. Apr 2016 A1
20160107309 Walsh et al. Apr 2016 A1
20160107653 Fung et al. Apr 2016 A1
20160109851 Tsang Apr 2016 A1
20160109959 Heo Apr 2016 A1
20160110517 Taylor Apr 2016 A1
20160110866 Taylor Apr 2016 A1
20160110867 Taylor Apr 2016 A1
20160112022 Butts Apr 2016 A1
20160112684 Connor Apr 2016 A1
20160113517 Lee et al. Apr 2016 A1
20160113528 Taylor Apr 2016 A1
20160113539 Sinharay et al. Apr 2016 A1
20160113545 Kim et al. Apr 2016 A1
20160113567 Osvath et al. Apr 2016 A1
20160113569 Zhao et al. Apr 2016 A1
20160113587 Kothe et al. Apr 2016 A1
20160113726 Taylor Apr 2016 A1
20160114165 Levine et al. Apr 2016 A1
20160116472 Ay Apr 2016 A1
20160116553 Kim et al. Apr 2016 A1
20160117815 Taylor Apr 2016 A1
20160117816 Taylor Apr 2016 A1
20160117819 Taylor Apr 2016 A1
20160119726 Pontoppidan et al. Apr 2016 A1
20160120048 Seo et al. Apr 2016 A1
20160120428 Yoshida et al. May 2016 A1
20160120432 Sridhar et al. May 2016 A1
20160120433 Hughes et al. May 2016 A1
20160120434 Park et al. May 2016 A1
20160120436 Silberstein May 2016 A1
20160120437 Graham et al. May 2016 A1
20160120457 Wu et al. May 2016 A1
20160120464 Lau et al. May 2016 A1
20160120480 Turnbull et al. May 2016 A1
20160121074 Ashby May 2016 A1
20160121114 Simon et al. May 2016 A1
20160121116 Simon et al. May 2016 A1
20160125228 Son et al. May 2016 A1
20160125572 Yoo et al. May 2016 A1
20160128589 Tabib-Azar May 2016 A1
20160128596 Morshed et al. May 2016 A1
20160128597 Lin et al. May 2016 A1
20160128632 Wiebe et al. May 2016 A1
20160128661 Taylor May 2016 A1
20160128864 Nofzinger et al. May 2016 A1
20160129249 Yun et al. May 2016 A1
20160131723 Nagasaka May 2016 A1
20160132654 Rothman et al. May 2016 A1
20160133015 Taylor May 2016 A1
20160135691 Dripps et al. May 2016 A1
20160135727 Osorio May 2016 A1
20160135748 Lin et al. May 2016 A1
20160135754 Marshall et al. May 2016 A1
20160136423 Simon et al. May 2016 A1
20160136427 De Ridder May 2016 A1
20160136429 Massoumi et al. May 2016 A1
20160136430 Moffitt et al. May 2016 A1
20160136443 Grandhe et al. May 2016 A1
20160139215 Fujii May 2016 A1
20160140306 Hua et al. May 2016 A1
20160140313 Taylor May 2016 A1
20160140707 Abe et al. May 2016 A1
20160140834 Tran May 2016 A1
20160140975 Kamamoto et al. May 2016 A1
20160143540 Gencer et al. May 2016 A1
20160143541 He et al. May 2016 A1
20160143554 Lim et al. May 2016 A1
20160143560 Grunwald et al. May 2016 A1
20160143574 Jones et al. May 2016 A1
20160143582 Connor May 2016 A1
20160143594 Moorman et al. May 2016 A1
20160144175 Simon et al. May 2016 A1
20160144186 Kaemmerer et al. May 2016 A1
20160147964 Corey et al. May 2016 A1
20160148077 Cox et al. May 2016 A1
20160148371 Itu et al. May 2016 A1
20160148372 Itu et al. May 2016 A1
20160148400 Bajic May 2016 A1
20160148531 Bleich et al. May 2016 A1
20160150988 Prerau et al. Jun 2016 A1
20160151014 Ujhazy et al. Jun 2016 A1
20160151018 Machon et al. Jun 2016 A1
20160151628 Simon et al. Jun 2016 A1
20160152233 Fung et al. Jun 2016 A1
20160155005 Varkuti et al. Jun 2016 A1
20160157742 Huang et al. Jun 2016 A1
20160157773 Baek et al. Jun 2016 A1
20160157777 Attal et al. Jun 2016 A1
20160157828 Sumi et al. Jun 2016 A1
20160158553 Panken et al. Jun 2016 A1
20160158554 Graig Jun 2016 A1
20160162652 Siekmeier Jun 2016 A1
20160164813 Anderson et al. Jun 2016 A1
20160165852 Goldfain Jun 2016 A1
20160165853 Goldfain Jun 2016 A1
20160166169 Badower et al. Jun 2016 A1
20160166197 Venkatraman et al. Jun 2016 A1
20160166199 Sun et al. Jun 2016 A1
20160166205 Ernst et al. Jun 2016 A1
20160166207 Falconer Jun 2016 A1
20160166208 Girouard et al. Jun 2016 A1
20160166219 Majewski et al. Jun 2016 A1
20160167672 Krueger Jun 2016 A1
20160168137 Van Leyen et al. Jun 2016 A1
20160170996 Frank et al. Jun 2016 A1
20160170998 Frank et al. Jun 2016 A1
20160171514 Frank et al. Jun 2016 A1
20160174099 Goldfain Jun 2016 A1
20160174862 Yu et al. Jun 2016 A1
20160174863 Foerster et al. Jun 2016 A1
20160174867 Hatano et al. Jun 2016 A1
20160174907 Colman et al. Jun 2016 A1
20160175557 Tass Jun 2016 A1
20160175607 Deisseroth et al. Jun 2016 A1
20160176053 Rognini et al. Jun 2016 A1
20160178392 Goldfain Jun 2016 A1
20160180042 Menon et al. Jun 2016 A1
20160180054 Luo et al. Jun 2016 A1
20160180055 Fonte Jun 2016 A1
20160183812 Zhang et al. Jun 2016 A1
20160183828 Ouyang et al. Jun 2016 A1
20160183861 Hayes et al. Jun 2016 A1
20160183881 Keenan et al. Jun 2016 A1
20160184029 Peng et al. Jun 2016 A1
20160184596 Fried et al. Jun 2016 A1
20160184599 Segal Jun 2016 A1
20160187524 Suhami Jun 2016 A1
20160191517 Bae et al. Jun 2016 A1
20160192841 Inagaki et al. Jul 2016 A1
20160192842 Inagaki Jul 2016 A1
20160192847 Inagaki Jul 2016 A1
20160192879 Yamashita Jul 2016 A1
20160193499 Kim et al. Jul 2016 A1
20160196185 Gu et al. Jul 2016 A1
20160196393 Avinash et al. Jul 2016 A1
20160196635 Cho et al. Jul 2016 A1
20160196758 Causevic et al. Jul 2016 A1
20160198950 Gross et al. Jul 2016 A1
20160198963 Addison et al. Jul 2016 A1
20160198966 Uematsu et al. Jul 2016 A1
20160198968 Plenz et al. Jul 2016 A1
20160198973 Fukuda et al. Jul 2016 A1
20160199241 Rapoport Jul 2016 A1
20160199577 Hyde et al. Jul 2016 A1
20160199656 Phillips Jul 2016 A1
20160199662 Wundrich et al. Jul 2016 A1
20160202755 Connor Jul 2016 A1
20160203597 Chang et al. Jul 2016 A1
20160203726 Hibbs et al. Jul 2016 A1
20160204937 Edwards et al. Jul 2016 A1
20160205450 Gartseev et al. Jul 2016 A1
20160205489 Jabri Jul 2016 A1
20160206236 Dilorenzo et al. Jul 2016 A1
20160206241 Cho et al. Jul 2016 A1
20160206380 Sparks et al. Jul 2016 A1
20160206581 Wittkowski Jul 2016 A1
20160206671 Geng Jul 2016 A1
20160206871 Weisend Jul 2016 A1
20160206877 Hargrove Jul 2016 A1
20160206880 Koubeissi Jul 2016 A1
20160210872 Roberts et al. Jul 2016 A1
20160213261 Fleischer et al. Jul 2016 A1
20160213276 Gadot et al. Jul 2016 A1
20160213314 Zuckerman-Stark et al. Jul 2016 A1
20160213317 Richardson et al. Jul 2016 A1
20160213947 Han et al. Jul 2016 A1
20160216760 Trutna et al. Jul 2016 A1
20160217586 Dickrell et al. Jul 2016 A1
20160217595 Han et al. Jul 2016 A1
20160219345 Knight et al. Jul 2016 A1
20160220133 Inagaki Aug 2016 A1
20160220134 Inagaki Aug 2016 A1
20160220136 Schultz Aug 2016 A1
20160220163 Yamada et al. Aug 2016 A1
20160220166 Thornton Aug 2016 A1
20160220439 Wojciechowski et al. Aug 2016 A1
20160220821 O'Connell et al. Aug 2016 A1
20160220836 Parks Aug 2016 A1
20160220837 Jin Aug 2016 A1
20160220850 Tyler Aug 2016 A1
20160222073 Deisseroth et al. Aug 2016 A1
20160223622 Yu et al. Aug 2016 A1
20160223627 Shah et al. Aug 2016 A1
20160223703 Wu et al. Aug 2016 A1
20160224757 Melkonyan Aug 2016 A1
20160224803 Frank et al. Aug 2016 A1
20160228019 Grunwald et al. Aug 2016 A1
20160228028 Van Der Kooi et al. Aug 2016 A1
20160228029 Ware Aug 2016 A1
20160228059 Badower Aug 2016 A1
20160228064 Jung et al. Aug 2016 A1
20160228204 Quaid et al. Aug 2016 A1
20160228640 Pindado et al. Aug 2016 A1
20160228702 Kempe et al. Aug 2016 A1
20160228705 Crowder et al. Aug 2016 A1
20160231401 Wang et al. Aug 2016 A1
20160232330 Dowson Aug 2016 A1
20160232625 Akutagawa et al. Aug 2016 A1
20160232667 Taylor Aug 2016 A1
20160232811 Connor Aug 2016 A9
20160235323 Tadi et al. Aug 2016 A1
20160235324 Mershin et al. Aug 2016 A1
20160235341 Choi et al. Aug 2016 A1
20160235351 Intrator Aug 2016 A1
20160235352 DiLorenzo Aug 2016 A1
20160235359 Cho et al. Aug 2016 A1
20160235980 Berman et al. Aug 2016 A1
20160235983 Berman et al. Aug 2016 A1
20160238673 Honkura Aug 2016 A1
20160239084 Connor Aug 2016 A1
20160239966 Parsey et al. Aug 2016 A1
20160239968 Parsey et al. Aug 2016 A1
20160240212 Wilson et al. Aug 2016 A1
20160240765 Washington et al. Aug 2016 A1
20160242645 Muller Aug 2016 A1
20160242659 Yamashita et al. Aug 2016 A1
20160242665 Galloway et al. Aug 2016 A1
20160242669 Muraskin et al. Aug 2016 A1
20160242670 Suzuki et al. Aug 2016 A1
20160242690 Principe et al. Aug 2016 A1
20160242699 Das et al. Aug 2016 A1
20160243362 Hehrmann et al. Aug 2016 A1
20160243381 Alford et al. Aug 2016 A1
20160245670 Nelson et al. Aug 2016 A1
20160245766 Nelson et al. Aug 2016 A1
20160245952 Dupuis et al. Aug 2016 A1
20160246939 Taylor Aug 2016 A1
20160247064 Yoo et al. Aug 2016 A1
20160248434 Govari Aug 2016 A1
20160248994 Liu Aug 2016 A1
20160249826 Derchak Sep 2016 A1
20160249841 Gerber et al. Sep 2016 A1
20160249846 Yoo et al. Sep 2016 A1
20160249857 Choi et al. Sep 2016 A1
20160249864 Kang et al. Sep 2016 A1
20160250355 Macknik Sep 2016 A1
20160250465 Simon et al. Sep 2016 A1
20160250473 Alberts et al. Sep 2016 A1
20160256063 Friedman et al. Sep 2016 A1
20160256086 Byrd et al. Sep 2016 A1
20160256105 Boyle et al. Sep 2016 A1
20160256108 Yun et al. Sep 2016 A1
20160256109 Semenov Sep 2016 A1
20160256112 Brockway et al. Sep 2016 A1
20160256118 Iyer et al. Sep 2016 A1
20160256130 Hamilton et al. Sep 2016 A1
20160256690 Cecchi et al. Sep 2016 A1
20160256691 Cecchi et al. Sep 2016 A1
20160256693 Parramon Sep 2016 A1
20160257957 Greenberg et al. Sep 2016 A1
20160259085 Wilson et al. Sep 2016 A1
20160259905 Park et al. Sep 2016 A1
20160260216 Wu et al. Sep 2016 A1
20160261962 Petersen et al. Sep 2016 A1
20160262623 Semenov Sep 2016 A1
20160262664 Linderman Sep 2016 A1
20160262680 Martucci et al. Sep 2016 A1
20160262685 Wagner et al. Sep 2016 A1
20160262695 Zhang et al. Sep 2016 A1
20160262703 MacCallum Sep 2016 A1
20160263318 Osorio Sep 2016 A1
20160263376 Yoo et al. Sep 2016 A1
20160263380 Starr et al. Sep 2016 A1
20160263393 Vo-Dinh et al. Sep 2016 A1
20160267809 deCharms et al. Sep 2016 A1
20160270656 Samec et al. Sep 2016 A1
20160270723 Deisseroth et al. Sep 2016 A1
20160274660 Publicover et al. Sep 2016 A1
20160275536 Anderson Sep 2016 A1
20160278651 Lu et al. Sep 2016 A1
20160278653 Clark et al. Sep 2016 A1
20160278662 Brister et al. Sep 2016 A1
20160278672 Cho et al. Sep 2016 A1
20160278687 Xia Sep 2016 A1
20160278697 John et al. Sep 2016 A1
20160278713 Shoaran et al. Sep 2016 A1
20160278736 Hamilton et al. Sep 2016 A1
20160278870 Quaid et al. Sep 2016 A1
20160279021 Hyde et al. Sep 2016 A1
20160279022 Hyde et al. Sep 2016 A1
20160279023 Hyde et al. Sep 2016 A1
20160279024 Hyde et al. Sep 2016 A1
20160279025 Hyde et al. Sep 2016 A1
20160279267 Deisseroth et al. Sep 2016 A1
20160279410 Simon et al. Sep 2016 A1
20160279417 Kilgard et al. Sep 2016 A1
20160279435 Hyde et al. Sep 2016 A1
20160282113 Lee Sep 2016 A1
20160282941 Aksenova et al. Sep 2016 A1
20160284082 Varkuti Sep 2016 A1
20160287117 Breakspear et al. Oct 2016 A1
20160287118 Sarma et al. Oct 2016 A1
20160287120 Sun et al. Oct 2016 A1
20160287142 Han et al. Oct 2016 A1
20160287157 Simpson Oct 2016 A1
20160287162 Bardakjian et al. Oct 2016 A1
20160287166 Tran Oct 2016 A1
20160287169 Kortelainen et al. Oct 2016 A1
20160287308 Grant et al. Oct 2016 A1
20160287334 Grant et al. Oct 2016 A1
20160287436 Wingeier et al. Oct 2016 A1
20160287869 Errico et al. Oct 2016 A1
20160287871 Bardakjian et al. Oct 2016 A1
20160287889 Bokil et al. Oct 2016 A1
20160287895 Deisseroth et al. Oct 2016 A1
20160296157 Girouard Oct 2016 A1
20160296287 Taylor Oct 2016 A1
20160296746 Wingeier et al. Oct 2016 A1
20160298449 Orban Oct 2016 A1
20160299568 Segal Oct 2016 A1
20160300252 Frank et al. Oct 2016 A1
20160300352 Raj Oct 2016 A1
20160302683 Lawrence et al. Oct 2016 A1
20160302704 Lynn et al. Oct 2016 A9
20160302709 Mossbridge Oct 2016 A1
20160302711 Frank et al. Oct 2016 A1
20160302720 John et al. Oct 2016 A1
20160302737 Watson et al. Oct 2016 A1
20160303322 John Oct 2016 A1
20160303396 Deisseroth et al. Oct 2016 A9
20160303397 Hirschman et al. Oct 2016 A1
20160303402 Tyler Oct 2016 A1
20160306844 Frank et al. Oct 2016 A1
20160306942 Rapaka et al. Oct 2016 A1
20160310031 Sarkar Oct 2016 A1
20160310070 Sabesan Oct 2016 A1
20160310071 Kim Oct 2016 A1
20160313408 Hatano et al. Oct 2016 A1
20160313417 Kawabata et al. Oct 2016 A1
20160313418 Fujii et al. Oct 2016 A1
20160313798 Connor Oct 2016 A1
20160317056 Moon et al. Nov 2016 A1
20160317060 Connor Nov 2016 A1
20160317077 Sillay Nov 2016 A1
20160317383 Stanfield et al. Nov 2016 A1
20160317824 Moffitt et al. Nov 2016 A1
20160320210 Nelson et al. Nov 2016 A1
20160321742 Phillips et al. Nov 2016 A1
20160324445 Kim et al. Nov 2016 A1
20160324457 Dagum Nov 2016 A1
20160324465 Osvath et al. Nov 2016 A1
20160324478 Goldstein Nov 2016 A1
20160324580 Esterberg Nov 2016 A1
20160324677 Hyde et al. Nov 2016 A1
20160324942 Lester et al. Nov 2016 A1
20160325111 Bourke, Jr. et al. Nov 2016 A1
20160331264 Helms-Tillery et al. Nov 2016 A1
20160331307 Purdon et al. Nov 2016 A1
20160331952 Faltys et al. Nov 2016 A1
20160331970 Lozano Nov 2016 A1
20160331974 Lyons et al. Nov 2016 A1
20160331982 Chow et al. Nov 2016 A1
20160334475 Ueno Nov 2016 A1
20160334534 Mandviwala et al. Nov 2016 A1
20160334866 Mazed et al. Nov 2016 A9
20160338608 Nagasaka et al. Nov 2016 A1
20160338634 Neu et al. Nov 2016 A1
20160338644 Connor Nov 2016 A1
20160338798 Vora et al. Nov 2016 A1
20160338825 Wortz et al. Nov 2016 A1
20160339237 Ahmed et al. Nov 2016 A1
20160339238 Ahmed et al. Nov 2016 A1
20160339239 Yoo et al. Nov 2016 A1
20160339242 Cook et al. Nov 2016 A1
20160339243 Wingeier et al. Nov 2016 A1
20160339300 Todasco Nov 2016 A1
20160341684 Choi Nov 2016 A1
20160342241 Chung et al. Nov 2016 A1
20160342762 Goetz Nov 2016 A1
20160345856 Semenov Dec 2016 A1
20160345895 Loetsch et al. Dec 2016 A1
20160345901 Connor Dec 2016 A1
20160345911 Leuthardt et al. Dec 2016 A1
20160346530 Jeffery et al. Dec 2016 A1
20160346542 Simon et al. Dec 2016 A1
20160351069 Faubert et al. Dec 2016 A1
20160354003 Baker et al. Dec 2016 A1
20160354027 Benson et al. Dec 2016 A1
20160356911 Wilson et al. Dec 2016 A1
20160357003 Hauger et al. Dec 2016 A1
20160357256 Siefert Dec 2016 A1
20160360100 Kim et al. Dec 2016 A1
20160360965 Tran Dec 2016 A1
20160360970 Tzvieli et al. Dec 2016 A1
20160361021 Salehizadeh et al. Dec 2016 A1
20160361027 Jang et al. Dec 2016 A1
20160361041 Barsimantov et al. Dec 2016 A1
20160361532 Wingeier et al. Dec 2016 A1
20160361534 Weisend Dec 2016 A9
20160361540 Simon et al. Dec 2016 A9
20160361546 Salam et al. Dec 2016 A1
20160363483 Tzvieli et al. Dec 2016 A1
20160364859 Taylor Dec 2016 A1
20160364860 Taylor Dec 2016 A1
20160364861 Taylor Dec 2016 A1
20160366462 Klappert et al. Dec 2016 A1
20160367138 Kim et al. Dec 2016 A1
20160367186 Freeman et al. Dec 2016 A1
20160367195 Park et al. Dec 2016 A1
20160367198 Chon et al. Dec 2016 A1
20160367204 Won et al. Dec 2016 A1
20160367209 Odry et al. Dec 2016 A1
20160367808 Simon et al. Dec 2016 A9
20160367812 De Ridder Dec 2016 A1
20160371387 Serena Dec 2016 A1
20160371455 Taylor Dec 2016 A1
20160371721 Bogdon et al. Dec 2016 A1
20160374581 Jensen Dec 2016 A1
20160374616 Mullins et al. Dec 2016 A1
20160374618 Giovangrandi Dec 2016 A1
20160374990 Teegarden et al. Dec 2016 A1
20160375245 Frei et al. Dec 2016 A1
20160375259 Davis et al. Dec 2016 A1
20160378608 Kong et al. Dec 2016 A1
20160378965 Choe et al. Dec 2016 A1
20170000324 Samec et al. Jan 2017 A1
20170000325 Samec et al. Jan 2017 A1
20170000326 Samec et al. Jan 2017 A1
20170000329 Samec et al. Jan 2017 A1
20170000330 Samec et al. Jan 2017 A1
20170000331 Samec et al. Jan 2017 A1
20170000332 Samec et al. Jan 2017 A1
20170000333 Samec et al. Jan 2017 A1
20170000334 Samec et al. Jan 2017 A1
20170000335 Samec et al. Jan 2017 A1
20170000337 Samec et al. Jan 2017 A1
20170000340 Samec et al. Jan 2017 A1
20170000341 Samec et al. Jan 2017 A1
20170000342 Samec et al. Jan 2017 A1
20170000343 Samec et al. Jan 2017 A1
20170000345 Samec et al. Jan 2017 A1
20170000404 Leininger et al. Jan 2017 A1
20170000422 Moturu et al. Jan 2017 A1
20170000454 Samec et al. Jan 2017 A1
20170000683 Samec et al. Jan 2017 A1
20170001016 De Ridder Jan 2017 A1
20170001032 Samec et al. Jan 2017 A1
20170006931 Guez et al. Jan 2017 A1
20170007111 Samec et al. Jan 2017 A1
20170007115 Samec et al. Jan 2017 A1
20170007116 Samec et al. Jan 2017 A1
20170007122 Samec et al. Jan 2017 A1
20170007123 Samec et al. Jan 2017 A1
20170007165 Jain et al. Jan 2017 A1
20170007173 Adamczyk et al. Jan 2017 A1
20170007182 Samec et al. Jan 2017 A1
20170007450 Samec et al. Jan 2017 A1
20170007799 Samec et al. Jan 2017 A1
20170007820 Simon et al. Jan 2017 A9
20170007828 Monteiro Jan 2017 A1
20170007843 Samec et al. Jan 2017 A1
20170010469 Samec et al. Jan 2017 A1
20170010470 Samec et al. Jan 2017 A1
20170013562 Lim et al. Jan 2017 A1
20170014037 Coppola et al. Jan 2017 A1
20170014080 Macia Barber et al. Jan 2017 A1
20170014083 Diab et al. Jan 2017 A1
20170014625 Rosenbluth et al. Jan 2017 A1
20170014630 Fried et al. Jan 2017 A1
20170017083 Samec et al. Jan 2017 A1
20170020434 Walker et al. Jan 2017 A1
20170020447 Grossman et al. Jan 2017 A1
20170020454 Keteyian et al. Jan 2017 A1
20170020627 Tesar et al. Jan 2017 A1
20170021158 Wingeier et al. Jan 2017 A1
20170021161 De Ridder Jan 2017 A1
20170024886 Dickrell et al. Jan 2017 A1
20170027467 Hagedorn Feb 2017 A1
20170027517 Le et al. Feb 2017 A9
20170027521 Geva et al. Feb 2017 A1
20170027539 Uber Feb 2017 A1
20170027651 Esterberg Feb 2017 A1
20170027812 Hyde et al. Feb 2017 A1
20170028563 Hemken Feb 2017 A1
20170031440 Randolph Feb 2017 A1
20170031441 Muller et al. Feb 2017 A1
20170032098 Ghorbanian et al. Feb 2017 A1
20170032221 Wu et al. Feb 2017 A1
20170032524 Dickrell et al. Feb 2017 A1
20170032527 Murthy et al. Feb 2017 A1
20170032544 Dempsey et al. Feb 2017 A1
20170034638 Anastas Feb 2017 A1
20170035309 Kang et al. Feb 2017 A1
20170035317 Jung et al. Feb 2017 A1
20170035344 Tzvieli et al. Feb 2017 A1
20170035392 Grunwald et al. Feb 2017 A1
20170036024 Hershey et al. Feb 2017 A1
20170039591 Knight et al. Feb 2017 A1
20170039706 Mikhno et al. Feb 2017 A1
20170041699 Mackellar et al. Feb 2017 A1
20170042430 Kovacs Feb 2017 A1
20170042444 Bardy et al. Feb 2017 A1
20170042469 Prerau et al. Feb 2017 A1
20170042474 Widge et al. Feb 2017 A1
20170042475 Verghese et al. Feb 2017 A1
20170042476 Reiman Feb 2017 A1
20170042485 Chung et al. Feb 2017 A1
20170042713 Nurmikko et al. Feb 2017 A1
20170042827 Margel et al. Feb 2017 A1
20170043160 Goodall et al. Feb 2017 A1
20170043166 Choi et al. Feb 2017 A1
20170043167 Widge et al. Feb 2017 A1
20170043178 Vo-Dinh et al. Feb 2017 A1
20170045601 Akhtari Feb 2017 A1
20170046052 Lee et al. Feb 2017 A1
20170046971 Moreno Feb 2017 A1
20170050046 Walder et al. Feb 2017 A1
20170052170 Shekdar et al. Feb 2017 A1
20170053082 Pereira et al. Feb 2017 A1
20170053088 Walker et al. Feb 2017 A1
20170053092 Taylor Feb 2017 A1
20170053461 Pal et al. Feb 2017 A1
20170053513 Savolainen et al. Feb 2017 A1
20170053665 Quatieri, Jr. et al. Feb 2017 A1
20170055839 Levinson et al. Mar 2017 A1
20170055898 Bandyopadhyay et al. Mar 2017 A1
20170055900 Jain et al. Mar 2017 A1
20170055913 Bandyopadhyay et al. Mar 2017 A1
20170056363 Goodenowe Mar 2017 A1
20170056467 Deisseroth et al. Mar 2017 A1
20170056642 Moffitt et al. Mar 2017 A1
20170056655 Lineaweaver Mar 2017 A1
20170056663 Kaemmerer et al. Mar 2017 A1
20170060298 Hwang et al. Mar 2017 A1
20170061034 Ritchey et al. Mar 2017 A1
20170061589 Kuo et al. Mar 2017 A1
20170061760 Lee et al. Mar 2017 A1
20170065199 Meisel Mar 2017 A1
20170065218 Leininger et al. Mar 2017 A1
20170065229 Howard Mar 2017 A1
20170065349 Ourselin et al. Mar 2017 A1
20170065379 Cowburn et al. Mar 2017 A1
20170065638 Fraser Mar 2017 A1
20170065816 Wingeier et al. Mar 2017 A1
20170066806 Deisseroth et al. Mar 2017 A1
20170067323 Katterbauer et al. Mar 2017 A1
20170069306 Asaei et al. Mar 2017 A1
20170071495 Denison et al. Mar 2017 A1
20170071521 Mestha et al. Mar 2017 A1
20170071523 Jain et al. Mar 2017 A1
20170071529 Haugland et al. Mar 2017 A1
20170071532 Greco Mar 2017 A1
20170071537 Jain et al. Mar 2017 A1
20170071546 Jain et al. Mar 2017 A1
20170071551 Jain et al. Mar 2017 A1
20170071552 Harpe et al. Mar 2017 A1
20170076452 Yui et al. Mar 2017 A1
20170079538 Liang et al. Mar 2017 A1
20170079543 Sadeghian-Motahar Mar 2017 A1
20170079573 Osorio Mar 2017 A1
20170079588 Ghaffari et al. Mar 2017 A1
20170079589 Ghaffari et al. Mar 2017 A1
20170079596 Teixeira Mar 2017 A1
20170080050 Deisseroth et al. Mar 2017 A1
20170080234 Gillespie et al. Mar 2017 A1
20170080256 Kim et al. Mar 2017 A1
20170080320 Smith Mar 2017 A1
20170084175 Sedlik et al. Mar 2017 A1
20170084187 Mollicone et al. Mar 2017 A1
20170085547 De Aguiar et al. Mar 2017 A1
20170085855 Roberts et al. Mar 2017 A1
20170086672 Tran Mar 2017 A1
20170086695 Mullins et al. Mar 2017 A1
20170086727 Dagum Mar 2017 A1
20170086729 Bruno Mar 2017 A1
20170086763 Verma et al. Mar 2017 A1
20170087302 Osorio Mar 2017 A1
20170087330 Kahn et al. Mar 2017 A1
20170087354 Stevenson et al. Mar 2017 A1
20170087355 Stevenson et al. Mar 2017 A1
20170087356 Stevenson et al. Mar 2017 A1
20170087364 Cartledge et al. Mar 2017 A1
20170087367 Weisend Mar 2017 A1
20170090475 Choi et al. Mar 2017 A1
20170091418 Chen et al. Mar 2017 A1
20170091567 Wang et al. Mar 2017 A1
20170094385 Lee et al. Mar 2017 A1
20170095157 Tzvieli et al. Apr 2017 A1
20170095174 Fokas et al. Apr 2017 A1
20170095199 Kranck Apr 2017 A1
20170095670 Ghaffari et al. Apr 2017 A1
20170095676 Caparso et al. Apr 2017 A1
20170095721 Bleich et al. Apr 2017 A1
20170099479 Browd et al. Apr 2017 A1
20170099713 Perez et al. Apr 2017 A1
20170100051 Honkura Apr 2017 A1
20170100540 Hyde et al. Apr 2017 A1
20170100591 Nudo et al. Apr 2017 A1
20170103440 Xing et al. Apr 2017 A1
20170105647 Duffy Apr 2017 A1
20170106193 Carcieri Apr 2017 A1
20170107575 Umansky et al. Apr 2017 A1
20170108926 Moon et al. Apr 2017 A1
20170112379 Swiston et al. Apr 2017 A1
20170112403 Doidge et al. Apr 2017 A1
20170112427 Simon et al. Apr 2017 A1
20170112446 Dagum Apr 2017 A1
20170112577 Bonutti et al. Apr 2017 A1
20170112671 Goldstein Apr 2017 A1
20170112947 Abebe Apr 2017 A1
20170113042 Goodall et al. Apr 2017 A1
20170113046 Fried et al. Apr 2017 A1
20170113056 Stocco et al. Apr 2017 A1
20170113057 Goodall et al. Apr 2017 A1
20170117866 Stevenson et al. Apr 2017 A1
20170119270 Juan et al. May 2017 A1
20170119271 Leuthardt et al. May 2017 A1
20170119994 Argaman May 2017 A1
20170120041 Wenger et al. May 2017 A1
20170120043 John May 2017 A1
20170120052 Simon et al. May 2017 A9
20170120054 Moffitt et al. May 2017 A1
20170120066 Phillips et al. May 2017 A1
20170127727 Davidson et al. May 2017 A1
20170127946 Levinson et al. May 2017 A1
20170128006 Seo et al. May 2017 A1
20170128015 Rogers et al. May 2017 A1
20170128032 Buchert et al. May 2017 A1
20170131293 Haslett et al. May 2017 A1
20170132816 Aston et al. May 2017 A1
20170133576 Marcus et al. May 2017 A1
20170133577 Cybart et al. May 2017 A1
20170135594 Hartings et al. May 2017 A1
20170135597 Mann May 2017 A1
20170135604 Kent et al. May 2017 A1
20170135626 Singer May 2017 A1
20170135629 Kent et al. May 2017 A1
20170135631 Zuckerman-Stark et al. May 2017 A1
20170135633 Connor May 2017 A1
20170135640 Gunasekar et al. May 2017 A1
20170136238 Hartig et al. May 2017 A1
20170136240 Mogul May 2017 A1
20170136264 Hyde et al. May 2017 A1
20170136265 Hyde et al. May 2017 A1
20170138132 Wilson et al. May 2017 A1
20170140124 Sehgal et al. May 2017 A1
20170143231 Ostberg et al. May 2017 A1
20170143249 Davis et al. May 2017 A1
20170143255 Babaeizadeh et al. May 2017 A1
20170143257 Kent et al. May 2017 A1
20170143259 Kent et al. May 2017 A1
20170143266 Kovacs et al. May 2017 A1
20170143267 Kovacs et al. May 2017 A1
20170143268 Kovacs et al. May 2017 A1
20170143273 Osorio et al. May 2017 A1
20170143280 Kent et al. May 2017 A1
20170143282 Kovacs et al. May 2017 A1
20170143442 Tesar et al. May 2017 A1
20170143550 Kilgard et al. May 2017 A1
20170143960 Kent et al. May 2017 A1
20170143963 Osorio May 2017 A1
20170143966 Reymers et al. May 2017 A1
20170143986 Deisseroth et al. May 2017 A1
20170146386 Wiard et al. May 2017 A1
20170146387 Wiard et al. May 2017 A1
20170146390 Kovacs May 2017 A1
20170146391 Kovacs et al. May 2017 A1
20170146615 Wolf et al. May 2017 A1
20170146801 Stempora May 2017 A1
20170147578 Hecht et al. May 2017 A1
20170147754 Kovacs May 2017 A1
20170148213 Thomas et al. May 2017 A1
20170148240 Kovacs et al. May 2017 A1
20170148340 Popa-Simil et al. May 2017 A1
20170148592 Tabib-Azir May 2017 A1
20170149945 Lee et al. May 2017 A1
20170150896 Lu et al. Jun 2017 A9
20170150916 Osorio Jun 2017 A1
20170150921 Yun et al. Jun 2017 A1
20170150925 Jung Jun 2017 A1
20170151433 Simon et al. Jun 2017 A1
20170151435 Deadwyler et al. Jun 2017 A1
20170151436 Flaherty et al. Jun 2017 A1
20170154167 Ovtchinnikov Jun 2017 A1
20170156593 Ferber et al. Jun 2017 A1
20170156606 Ferber et al. Jun 2017 A1
20170156622 Mahoor et al. Jun 2017 A1
20170156655 Austin et al. Jun 2017 A1
20170156662 Goodall et al. Jun 2017 A1
20170156674 Hochman Jun 2017 A1
20170157343 Davidson et al. Jun 2017 A1
20170157402 Osorio Jun 2017 A1
20170157410 Moffitt et al. Jun 2017 A1
20170160360 Deisseroth et al. Jun 2017 A1
20170162072 Horseman et al. Jun 2017 A1
20170164861 Cahan et al. Jun 2017 A1
20170164862 Dolev et al. Jun 2017 A1
20170164876 Hyde et al. Jun 2017 A1
20170164878 Connor Jun 2017 A1
20170164893 Narayan et al. Jun 2017 A1
20170164894 Yoo et al. Jun 2017 A1
20170164895 Howard Jun 2017 A1
20170164901 Shusterman Jun 2017 A1
20170165020 Martel Jun 2017 A1
20170165481 Menon Jun 2017 A1
20170165496 Pilla et al. Jun 2017 A1
20170168121 Yu et al. Jun 2017 A1
20170168566 Osterhout et al. Jun 2017 A1
20170168568 Petrov Jun 2017 A1
20170169714 Lin et al. Jun 2017 A1
20170171441 Kearns et al. Jun 2017 A1
20170172414 Nierenberg et al. Jun 2017 A1
20170172446 Kuzum et al. Jun 2017 A1
20170172499 Yoo Jun 2017 A1
20170172501 Badower et al. Jun 2017 A1
20170172520 Kannan et al. Jun 2017 A1
20170172527 Uber Jun 2017 A1
20170173262 Veltz Jun 2017 A1
20170173326 Bloch et al. Jun 2017 A1
20170173391 Wiebe et al. Jun 2017 A1
20170177023 Simon et al. Jun 2017 A1
20170178001 Anderson et al. Jun 2017 A1
20170178340 Schadewaldt et al. Jun 2017 A1
20170180558 Li et al. Jun 2017 A1
20170181252 Wouhaybi et al. Jun 2017 A1
20170181693 Kim et al. Jun 2017 A1
20170182176 Satchi-Fainaro et al. Jun 2017 A1
20170182285 Tyler et al. Jun 2017 A1
20170182312 Durand et al. Jun 2017 A1
20170185149 Oluwafemi et al. Jun 2017 A1
20170185714 Halter et al. Jun 2017 A1
20170185741 Moffitt et al. Jun 2017 A1
20170188862 Kale et al. Jul 2017 A1
20170188865 Nierenberg et al. Jul 2017 A1
20170188866 Kale et al. Jul 2017 A1
20170188868 Kale et al. Jul 2017 A1
20170188869 Kale et al. Jul 2017 A1
20170188870 Hilty Jul 2017 A1
20170188872 Hughes et al. Jul 2017 A1
20170188876 Marci et al. Jul 2017 A1
20170188905 Lee et al. Jul 2017 A1
20170188916 Wang et al. Jul 2017 A1
20170188922 Lee et al. Jul 2017 A1
20170188932 Singer et al. Jul 2017 A1
20170188933 Huggins et al. Jul 2017 A1
20170188947 Connor Jul 2017 A1
20170188992 O'Brien et al. Jul 2017 A1
20170189685 Steinke et al. Jul 2017 A1
20170189686 Steinke et al. Jul 2017 A1
20170189687 Steinke et al. Jul 2017 A1
20170189688 Steinke et al. Jul 2017 A1
20170189689 Steinke et al. Jul 2017 A1
20170189691 De Ridder Jul 2017 A1
20170189700 Moffitt et al. Jul 2017 A1
20170189707 Zabara Jul 2017 A1
20170190765 El-Agnaf Jul 2017 A1
20170193161 Sapiro et al. Jul 2017 A1
20170193831 Walter et al. Jul 2017 A1
20170196497 Ray et al. Jul 2017 A1
20170196501 Watson et al. Jul 2017 A1
20170196503 Narayan et al. Jul 2017 A1
20170196519 Miller et al. Jul 2017 A1
20170197080 Wagner et al. Jul 2017 A1
20170197081 Charlesworth et al. Jul 2017 A1
20170197086 Howard et al. Jul 2017 A1
20170198017 Deisseroth et al. Jul 2017 A1
20170198349 Rice Jul 2017 A1
20170199251 Fujii et al. Jul 2017 A1
20170202474 Banerjee et al. Jul 2017 A1
20170202475 Leuthardt Jul 2017 A1
20170202476 Desain et al. Jul 2017 A1
20170202518 Furman et al. Jul 2017 A1
20170202621 Taylor Jul 2017 A1
20170202633 Liu Jul 2017 A1
20170203154 Solinsky Jul 2017 A1
20170205259 Jang et al. Jul 2017 A1
20170206654 Shiroishi et al. Jul 2017 A1
20170206691 Harrises et al. Jul 2017 A1
20170206913 Nahman et al. Jul 2017 A1
20170209043 Gross et al. Jul 2017 A1
20170209044 Ito et al. Jul 2017 A1
20170209053 Pantelopoulos et al. Jul 2017 A1
20170209062 Iwasaki et al. Jul 2017 A1
20170209083 Zarandi et al. Jul 2017 A1
20170209094 Derchak et al. Jul 2017 A1
20170209225 Wu Jul 2017 A1
20170209389 Toth et al. Jul 2017 A1
20170209737 Tadi et al. Jul 2017 A1
20170212188 Kikitsu et al. Jul 2017 A1
20170213339 Hibbard et al. Jul 2017 A1
20170214786 Lee et al. Jul 2017 A1
20170216595 Geva et al. Aug 2017 A1
20170221206 Han et al. Aug 2017 A1
20170224990 Goldwasser et al. Aug 2017 A1
20170224994 Kilgard et al. Aug 2017 A1
20170231560 Hyde et al. Aug 2017 A1
20170239486 Suryavanshi Aug 2017 A1
20170239489 Bourke, Jr. et al. Aug 2017 A1
20190070386 Raut Mar 2019 A1
Foreign Referenced Citations (4)
Number Date Country
1304073 Apr 2003 EP
1304073 Sep 2003 EP
WO2000025668 Sep 2003 WO
WO2001087153 Sep 2003 WO
Non-Patent Literature Citations (8)
Entry
https://en.wikipedia.org/wiki/Contingent_negative_variation.
https://en.wikipedia.org/wiki/Bereitschaftspotential.
Travers, Eoin, Nima Khalighinejad, Aaron Schurger, and Patrick Haggard. “Do readiness potentials happen all the time?.” NeuroImage 206 (2020): 116286.
Park, Hyeong-Dong, Coline Barnoud, Henri Trang, Oliver A. Kannape, Karl Schaller, and Olaf Blanke. “Breathing is coupled with voluntary action and the cortical readiness potential.” Nature communications 11, No. 1 (2020): 1-8.
Gomes, Gilberto. “Volition and the readiness potential.” Journal of Consciousness Studies 6, No. 8-9 (1999): 59-76.
Cui, R. Q., D. Huter, A. Egkher, W. Lang, G. Lindinger, and L. Deecke. “High resolution DC-EEG mapping of the Bereitschaftspotential preceding simple or complex bimanual sequential finger movement.” Experimental Brain Research 134, No. 1 (2000): 49-57.
Jo, Han-Gue, Marc Wittmann, Thilo Hinterberger, and Stefan Schmidt. “The readiness potential reflects intentional binding.” Frontiers in human neuroscience 8 (2014): 421.
Fuchs, Sven, Angela Carpenter, Meredith Carroll, and Kelly Hale. “A hierarchical adaptation framework for adaptive training systems.” In International Conference on Foundations of Augmented Cognition, pp. 413-421. Springer, Berlin, Heidelberg, 2011.
Related Publications (1)
Number Date Country
20190247662 A1 Aug 2019 US
Provisional Applications (1)
Number Date Country
62594452 Dec 2017 US