02595nas a2200421 4500008004100000022001400041245009200055210006900147260001200216300001100228490000700239520137400246653001001620653000901630653003401639653002801673653003001701653002801731653002701759653003501786653001101821653001101832653000901843653001601852653001901868653002301887653002801910653001801938100002001956700002101976700002601997700001902023700001902042700001902061700002102080700002402101856004802125 2014 eng d a2167-922300aBrain-computer interface (BCI) evaluation in people with amyotrophic lateral sclerosis.0 aBraincomputer interface BCI evaluation in people with amyotrophi c06/2014 a207-150 v153 aBrain-computer interfaces (BCIs) might restore communication to people severely disabled by amyotrophic lateral sclerosis (ALS) or other disorders. We sought to: 1) define a protocol for determining whether a person with ALS can use a visual P300-based BCI; 2) determine what proportion of this population can use the BCI; and 3) identify factors affecting BCI performance. Twenty-five individuals with ALS completed an evaluation protocol using a standard 6 × 6 matrix and parameters selected by stepwise linear discrimination. With an 8-channel EEG montage, the subjects fell into two groups in BCI accuracy (chance accuracy 3%). Seventeen averaged 92 (± 3)% (range 71-100%), which is adequate for communication (G70 group). Eight averaged 12 (± 6)% (range 0-36%), inadequate for communication (L40 subject group). Performance did not correlate with disability: 11/17 (65%) of G70 subjects were severely disabled (i.e. ALSFRS-R < 5). All L40 subjects had visual impairments (e.g. nystagmus, diplopia, ptosis). P300 was larger and more anterior in G70 subjects. A 16-channel montage did not significantly improve accuracy. In conclusion, most people severely disabled by ALS could use a visual P300-based BCI for communication. In those who could not, visual impairment was the principal obstacle. For these individuals, auditory P300-based BCIs might be effective.10aAdult10aAged10aAmyotrophic Lateral Sclerosis10aBiofeedback, Psychology10abrain-computer interfaces10aCommunication Disorders10aElectroencephalography10aEvent-Related Potentials, P30010aFemale10aHumans10aMale10aMiddle Aged10aOnline Systems10aPhotic Stimulation10aPsychomotor Performance10aReaction Time1 aMcCane, Lynn, M1 aSellers, Eric, W1 aMcFarland, Dennis, J.1 aMak, Joseph, N1 aCarmack, Steve1 aZeitlin, Debra1 aWolpaw, Jonathan1 aVaughan, Theresa, M uhttp://www.ncbi.nlm.nih.gov/pubmed/2455584307041nas a2200313 4500008004100000022001400041245008200055210006900137260001200206300001100218490000600229520615100235653002806386653001006414653001806424653002706442653002106469653003106490653001106521653002406532653001306556653002806569100001906597700001506616700001306631700001606644700001906660856004806679 2011 eng d a1741-255200aCurrent Trends in Hardware and Software for Brain-Computer Interfaces (BCIs).0 aCurrent Trends in Hardware and Software for BrainComputer Interf c04/2011 a0250010 v83 a

brain-computer interface (BCI) provides a non-muscular communication channel to people with and without disabilities. BCI devices consist of hardware and software. BCI hardware records signals from the brain, either invasively or non-invasively, using a series of device components. BCI software then translates these signals into device output commands and provides feedback. One may categorize different types of BCI applications into the following four categories: basic research, clinical/translational research, consumer products, and emerging applications. These four categories use BCI hardware and software, but have different sets of requirements. For example, while basic research needs to explore a wide range of system configurations, and thus requires a wide range of hardware and software capabilities, applications in the other three categories may be designed for relatively narrow purposes and thus may only need a very limited subset of capabilities. This paper summarizes technical aspects for each of these four categories of BCI applications. The results indicate that BCI technology is in transition from isolated demonstrations to systematic research and commercial development. This process requires several multidisciplinary efforts, including the development of better integrated and more robust BCI hardware and software, the definition of standardized interfaces, and the developmentof certification, dissemination and reimbursement procedures.

10aBiofeedback, Psychology10aBrain10aBrain Mapping10aElectroencephalography10aEquipment Design10aEquipment Failure Analysis10aHumans10aMan-Machine Systems10aSoftware10aUser-Computer Interface1 aBrunner, Peter1 aBianchi, L1 aGuger, C1 aCincotti, F1 aSchalk, Gerwin uhttp://www.ncbi.nlm.nih.gov/pubmed/2143653607936nas a2200361 4500008004100000022001400041245009600055210006900151260001200220300001100232490000800243520694900251653001507200653001007215653002807225653002007253653001007273653002507283653002407308653001107332653001107343653000907354653001607363653001907379653001607398100001607414700001907430700002207449700001707471700001707488700002107505856004807526 2010 eng d a1091-649000aCortical activity during motor execution, motor imagery, and imagery-based online feedback.0 aCortical activity during motor execution motor imagery and image c03/2010 a4430-50 v1073 a

Imagery of motor movement plays an important role in learning of complex motor skills, from learning to serve in tennis to perfecting a pirouette in ballet. What and where are the neural substrates that underlie motor imagery-based learning? We measured electrocorticographic cortical surface potentials in eight human subjects during overt action and kinesthetic imagery of the same movement, focusing on power in "high frequency" (76-100 Hz) and "low frequency" (8-32 Hz) ranges. We quantitatively establish that the spatial distribution of local neuronal population activity during motor imagery mimics the spatial distribution of activity during actual motor movement. By comparing responses to electrocortical stimulation with imagery-induced cortical surface activity, we demonstrate the role of primary motor areas in movement imagery. The magnitude of imagery-induced cortical activity change was approximately 25% of that associated with actual movement. However, when subjects learned to use this imagery to control a computer cursor in a simple feedback task, the imagery-induced activity change was significantly augmented, even exceeding that of overt movement.

10aAdolescent10aAdult10aBiofeedback, Psychology10aCerebral Cortex10aChild10aElectric Stimulation10aElectrocardiography10aFemale10aHumans10aMale10aMiddle Aged10aMotor Activity10aYoung Adult1 aMiller, K J1 aSchalk, Gerwin1 aFetz, Eberhard, E1 aNijs, Marcel1 aOjemann, J G1 aRao, Rajesh, P N uhttp://www.ncbi.nlm.nih.gov/pubmed/2016008405892nas a2200361 4500008004100000022001400041245010100055210006900156260001200225300001000237490000800247520480000255653001505055653002805070653001805098653002005116653002705136653002405163653001105187653000905198653001105207653003105218653003205249653002805281653004105309653002205350653002805372100002305400700002005423700002005443700001905463856004805482 2008 eng d a0165-027000aExtraction and localization of mesoscopic motor control signals for human ECoG neuroprosthetics.0 aExtraction and localization of mesoscopic motor control signals  c01/2008 a63-810 v1673 a

Electrocorticogram (ECoG) recordings for neuroprosthetics provide a mesoscopic level of abstraction of brain function between microwire single neuron recordings and the electroencephalogram (EEG). Single-trial ECoG neural interfaces require appropriate feature extraction and signal processing methods to identify and model in real-time signatures of motor events in spontaneous brain activity. Here, we develop the clinical experimental paradigm and analysis tools to record broadband (1Hz to 6kHz) ECoG from patients participating in a reaching and pointing task. Motivated by the significant role of amplitude modulated rate coding in extracellular spike based brain-machine interfaces (BMIs), we develop methods to quantify spatio-temporal intermittent increased ECoG voltages to determine if they provide viable control inputs for ECoG neural interfaces. This study seeks to explore preprocessing modalities that emphasize amplitude modulation across frequencies and channels in the ECoG above the level of noisy background fluctuations in order to derive the commands for complex, continuous control tasks. Preliminary experiments show that it is possible to derive online predictive models and spatially localize the generation of commands in the cortex for motor tasks using amplitude modulated ECoG.

10aAdolescent10aBiofeedback, Psychology10aBrain Mapping10aCerebral Cortex10aElectroencephalography10aEpilepsies, Partial10aFemale10aHand10aHumans10aMagnetic Resonance Imaging10aPhysical Therapy Modalities10aPsychomotor Performance10aSignal Processing, Computer-Assisted10aSpectrum Analysis10aUser-Computer Interface1 aSanchez, Justin, C1 aGunduz, Aysegul1 aCarney, Paul, R1 aPrincipe, Jose uhttp://www.ncbi.nlm.nih.gov/pubmed/1758250703153nas a2200481 4500008004100000022001400041245008200055210006900137260001200206300001000218490000700228520180600235653001002041653002802051653002002079653003602099653002402135653002702159653002402186653001102210653001102221653001602232653000902248653001602257653001902273653001702292653004102309653001302350653002502363653001702388653002802405653001202433100002002445700001802465700001302483700002502496700002402521700001802545700001802563700002102581700002102602856004802623 2008 eng d a1525-506900aVoluntary brain regulation and communication with electrocorticogram signals.0 aVoluntary brain regulation and communication with electrocortico c08/2008 a300-60 v133 a

Brain-computer interfaces (BCIs) can be used for communication in writing without muscular activity or for learning to control seizures by voluntary regulation of brain signals such as the electroencephalogram (EEG). Three of five patients with epilepsy were able to spell their names with electrocorticogram (ECoG) signals derived from motor-related areas within only one or two training sessions. Imagery of finger or tongue movements was classified with support-vector classification of autoregressive coefficients derived from the ECoG signals. After training of the classifier, binary classification responses were used to select letters from a computer-generated menu. Offline analysis showed increased theta activity in the unsuccessful patients, whereas the successful patients exhibited dominant sensorimotor rhythms that they could control. The high spatial resolution and increased signal-to-noise ratio in ECoG signals, combined with short training periods, may offer an alternative for communication in complete paralysis, locked-in syndrome, and motor restoration.

10aAdult10aBiofeedback, Psychology10aCerebral Cortex10aCommunication Aids for Disabled10aDominance, Cerebral10aElectroencephalography10aEpilepsies, Partial10aFemale10aHumans10aImagination10aMale10aMiddle Aged10aMotor Activity10aMotor Cortex10aSignal Processing, Computer-Assisted10aSoftware10aSomatosensory Cortex10aTheta Rhythm10aUser-Computer Interface10aWriting1 aHinterberger, T1 aWidman, Guido1 aLal, T N1 aHill, Jeremy, Jeremy1 aTangermann, Michael1 aRosenstiel, W1 aSchölkopf, B1 aElger, Christian1 aBirbaumer, Niels uhttp://www.ncbi.nlm.nih.gov/pubmed/18495541