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1 ECoG based decoding performance negatively correlated wi
2 ECoG ClusterFlow supports the comparison of spatio-tempo
3 ECoG from 63 subdural electrodes (500 Hz/channel) chroni
4 ECoG HV-LV cyclicity was reduced 4-5 h prior to spontane
5 ECoG patterns changed 7 to 4 h prior to spontaneous onse
6 ECoG responses in visual cortex can be separated into tw
7 ECoG revealed a striking anatomical and functional corre
8 ECoG signal changes on the hemisphere ipsilateral to HIF
9 ECoG signals were purified by a denoising procedure of w
10 ECoG signals were recorded with a high-density 32-electr
11 ECoG spectral analysis utilized a mixed-effects analysis
12 ECoG spectral analysis utilized a mixed-effects analysis
13 ECoG was also recorded when subjects passively listened
14 imately 3 Torr, LD-CBF increased 48 +/- 10%, ECoG shifted to chiefly the HVLF state, SEF(90) decrease
16 show that network metrics computed from all ECoG channels capture the dynamics of the seizure onset
20 ways: across stimuli, the BOLD amplitude and ECoG broadband power were positively correlated, the BOL
21 counts for the relationship between BOLD and ECoG data from human visual cortex in V1, V2, and V3, wi
24 oscillations were similarly tuned in LFP and ECoG to stimulus orientation, contrast and spatial frequ
26 ectrodes to simultaneously map MUA, LFP, and ECoG RFs from the primary visual cortex of awake monkeys
27 highest temporal resolution for EEG/MEG and ECoG were shown as ~200 ms and ~10 ms and are now correc
28 ing a hybrid array containing both micro and ECoG electrodes implanted in the primary visual cortex o
29 ed array containing both microelectrodes and ECoG electrodes to simultaneously map MUA, LFP, and ECoG
30 oppler flowmeter, fluorescent O(2) probe and ECoG electrodes, we measured laser Doppler CBF (LD-CBF),
31 fferences between electrical stimulation and ECoG that were partially related to the reciprocity of c
35 G and complete resection of IEDs on baseline ECoG are associated with better outcomes following stand
37 ECoG contacts, followed by coherence between ECoG and deep cortical local field potential (LFP), and
39 was coherence at approximately 1 Hz between ECoG and basal ganglia LFPs, with much of the coherent a
40 where the highest coherence occurred between ECoG contacts, followed by coherence between ECoG and de
41 4 h ECoG patterns, (2) relationships between ECoG and myometrial contractility, and (3) 24 h ECoG pat
43 we show that the architecture of whole-brain ECoG networks and the factors that shape it can be studi
45 nship: When the raw fluctuation in broadband ECoG activity is closer to the across-trial mean, hit ra
47 uency (beta, gamma) oscillations recorded by ECoG were altered at acute and chronic time points follo
48 luate interregional functional connectivity, ECoG data from electrodes situated over specific cortica
49 projection approach to decode the continuous ECoG data stream spontaneously, predicting the occurrenc
50 be an attractive alternative to conventional ECoG grids with regard to mechanical properties, 3-T MR
52 that functional responsiveness of different ECoG high-gamma sub-bands can discriminate cognitive tas
55 LC neuronal activity increases cortical EEG (ECoG) and hippocampal EEG (HEEG) indices of arousal bila
61 simultaneously acquired electrocorticogram (ECoG) in discrete brain states representative of global
62 r framework by analysing electrocorticogram (ECoG) recordings from patients who have undergone epilep
64 both microelectrodes and electrocorticogram (ECoG) electrodes in the primary visual cortex of 2 femal
66 tecture as determined by electrocorticogram (ECoG) and electromyogram (EMG) activity over a 7-day sub
68 of STN units and frontal electrocorticogram (ECoG) to cortical stimulation in anaesthetized rats.
69 , local field potential, electrocorticogram (ECoG), and EEG, and compared their information and decod
70 ave been recorded in the electrocorticogram (ECoG) of rats weeks and months after fluid percussion in
71 eorganization affect the electrocorticogram (ECoG) responses to various neurotransmitter agonists.
72 e obtained by averaging electrocorticograms (ECoGs) recorded from the perisylvian and extrasylvian ba
73 ent with these changes, electrocorticograms (ECoGs) reveal suppressed ketamine-evoked y oscillations.
77 ical tissue (t ), and electrocorticographic (ECoG) activity (high voltage low frequency, HVLF, versus
79 hniques on continuous electrocorticographic (ECoG) recordings (5.4 +/- 1.7 d per patient, mean +/- SD
80 ynthesize speech from electrocorticographic (ECoG) signals acquired across motor, premotor and somato
81 amma-band (25-128 Hz) electrocorticographic (ECoG) activity -- a phenomenon involving large groups of
82 eural oscillations in electrocorticographic (ECoG), electroencephalographic (EEG), and stereoelectroe
83 samples of interictal electrocorticographic (ECoG) signals recorded from patients who became seizure-
84 frequency analyses of electrocorticographic (ECoG) signals, we hypothesized that induced high-gamma-b
86 theories, we recorded electrocorticographic (ECoG) data from 15 human patients with intractable epile
89 ng arrays of subdural electrocorticographic (ECoG) electrodes in human patients performing simple mov
91 we recorded subdural electrocorticographic (ECoG) signals in five clinical subjects while they perfo
92 ationship between the electrocorticographic (ECoG) signal and the observed fMRI response (p < 10(-16)
93 Recent studies using electrocorticographic (ECoG) recordings in humans have shown that functional ac
99 Purpose To develop an electrocorticography (ECoG) grid by using deposition of conductive nanoparticl
100 the feasibility of an electrocorticography (ECoG)-based BCI system in an individual with tetraplegia
101 easured using fMRI and electrocorticography (ECoG) in human visual cortex with a similar set of stimu
104 ive techniques such as electrocorticography (ECoG) offer high decoding accuracy, their surgical requi
106 a 128-channel chronic electrocorticography (ECoG) implant in a paralyzed individual, which allowed s
109 study of high-density electrocorticography (ECoG) recordings from the cortical surface of profoundly
110 e we used high-density electrocorticography (ECoG) recordings to detect when they heard or said an ut
112 aneous recordings from electrocorticography (ECoG) grids and high-density microelectrode arrays to es
113 d auditory and frontal electrocorticography (ECoG) signals in five common awake marmosets performing
115 de evidence from human electrocorticography (ECoG) for an inverted-U brain-behavior relationship: Whe
116 echnologies, including electrocorticography (ECoG) systems, multielectrode arrays (MEAs), Stentrode,
118 EG) and intraoperative electrocorticography (ECoG) are routinely used in the evaluation of magnetic r
120 patients with invasive electrocorticography (ECoG) recordings and compared multilayer directional net
121 monitored by invasive electrocorticography (ECoG; subdural electrodes) and noninvasive scalp EEG dur
122 used a combination of electrocorticography (ECoG) and electrical brain stimulation (EBS) in 10 human
123 through an analysis of electrocorticography (ECoG) data, we identified a timescale hierarchy in the n
124 multimodal approach of electrocorticography (ECoG), high-resolution functional magnetic resonance ima
126 ogy, fiber photometry, electrocorticography (ECoG), optogenetics, and behavior in the Scn8a(+/-)mouse
127 s in non-human primate electrocorticography (ECoG), human electroencephalogram (EEG), and clinical in
128 ral scale by recording electrocorticography (ECoG) signals measured directly from subdural electrode
130 ation and from resting electrocorticography (ECoG) correlations showed similar spatial distributions
131 operative sensorimotor electrocorticography (ECoG) and subthalamic LFP to predict grip-force, a repre
132 analysed simultaneous electrocorticography (ECoG) and neuronal recordings of 34 seizures in a cohort
133 xtraoperative subdural electrocorticography (ECoG) recording could predict long-term seizure outcome.
134 the cortical surface, electrocorticography (ECoG) provides a powerful method to integrate spatial, t
135 fied 0-1 chaos test to electrocorticography (ECoG) and magnetoencephalography (MEG) recordings from t
139 rom two patients using electrocorticography (ECoG) and stereo-electroencephalography (sEEG) recording
144 tentials measured with electrocorticography (ECoG) and the blood oxygen level-dependent (BOLD) respon
145 ubjects implanted with electrocorticography (ECoG) arrays for long-term epilepsy monitoring were trai
146 ts were implanted with electrocorticography (ECoG) electrodes and had multiple opportunities to pract
149 ng on ECoG, we developed a model to estimate ECoG power generated by different firing patterns of the
153 .4-23.0 years), who underwent extraoperative ECoG recording prior to cortical resection for alleviati
154 slow ECoG activity (HV) and low-voltage fast ECoG activity (LV) were determined mathematically, and H
155 enty-four hour rhythms were present in fetal ECoG HV-LV cycles in the 3-5 days prior to spontaneous o
158 t uses a high resolution 32-channel flexible ECoG electrodes array to collect electrical signals of b
159 experiments on a rat show that the flexible ECoG system can accurately record electrical signals of
160 dings reveal a striking convergence of fMRI, ECoG, and EBS, which together offer a rare causal link b
163 The results indicate that high-frequency ECoG reliably differentiates cortical areas associated w
164 with five quantitative metrics computed from ECoG and multiunit data was used to distinguish three ty
168 n sheep fetuses (n = 9) to analyse: (1) 24 h ECoG patterns, (2) relationships between ECoG and myomet
170 derlying cortical population and studied how ECoG power varies with changes in firing rate versus the
172 activity during movement, we analysed human ECoG and subthalamic nucleus (STN) unit activity during
173 d the detection of time of grasps from human ECoG recordings during a sequence of natural and continu
174 percentage of time spent and duration of HV ECoG increased, and percentage of time spent in LV decre
177 ctral power of low-frequency oscillations in ECoG recordings of R6/2 mice is diminished while the spe
178 down to the sub-millimeter spatial scale in ECoG despite the effects of volume conduction, justifyin
180 rip-force decoding performance of individual ECoG channels across patients by using their connectomic
181 sites at which LC efferents could influence ECoG and HEEG are the medial septum/vertical limb of the
183 s generating IEDs on baseline intraoperative ECoG (P = .02) were associated with excellent outcomes i
185 xploring critical brain dynamics in invasive ECoG recordings from multiple sessions with a single mac
186 whole-brain, interregional and band-limited ECoG networks from a large cohort-in this case, of indiv
189 al distinction using intracranially measured ECoG signals from the human visual cortex in 14 patients
192 We applied the proposed algorithm to 5-min ECoG recordings from human primary auditory cortex obtai
193 tra-flexible, micro-electrocorticography (mu-ECoG) arrays with platinum (Pt) or glassy carbon (GC) el
194 ed a novel technique of analyzing multihuman ECoG recordings to identify cortical regions most releva
195 measured laser Doppler CBF (LD-CBF), tP(O2), ECoG and spectral edge frequency-90 (SEF(90)) in respons
196 yses showed that higher decoding accuracy of ECoG compared with local field potential was not because
199 ctrical stimulation and separate analysis of ECoG gamma changes during spontaneous inter-personal con
205 between correlative versus causal nature of ECoG and EBS, respectively, and provides important insig
206 , we characterized the basic organization of ECoG networks, including frequency-specific architecture
207 e, in shaping the brain-wide organization of ECoG networks, of communication along white matter pathw
209 combined, the specificity and sensitivity of ECoG HGA with respect to ECS were 84% and 43%, respectiv
210 culation, the sensitivity and specificity of ECoG HGA were estimated relative to both ECS-induced imp
211 er with significant HGA), the specificity of ECoG HGA with respect to ECS was 78% for naming and 81%
212 Here, we estimated the spatial spread of ECoG in five behaving monkeys using two different approa
215 portant to determine the "spatial spread" of ECoG (i.e., the extent of cortical tissue that contribut
219 Our results further validate the use of ECoG in clinical and basic cognitive research.SIGNIFICAN
221 nique can be used to evaluate the utility of ECoG biomarkers in epilepsy presurgical evaluation.
222 the potential effects of neuronal firing on ECoG, we developed a model to estimate ECoG power genera
223 Using scRNA-seq and intraoperative patient ECoG recordings, we show that tumors from seizure patien
226 nd spikes in combined pre- and postresection ECoG predict surgical outcome in different tailoring app
227 50 Hz), and spikes in pre- and postresection ECoG sampled at 2,048 Hz in people with refractory focal
228 rrence of FRs in post-ECoG, given FRs in pre-ECoG (+/-, +/+), predicted outcome (hazard ratio, 3.13;
231 In addition to rhythmic brain processes, ECoG potentials also reveal a spectrally broadband motif
233 ing mechanism using intracranial recordings (ECoG), in 12 patients undergoing epilepsy monitoring eng
235 This study indicates that event-related ECoG HGA during confrontation naming predicts ECS interf
237 ine with existing literature, face-selective ECoG responses were present in both left and right FG si
238 We identified FG sites with face-selective ECoG responses, and recorded perceptual reports during E
239 ques (for some stimulus conditions, separate ECoG and microelectrode arrays in two additional male ma
245 tic resonance imaging-negative TLE, standard ECoG performed at the time of surgery, and a minimum fol
246 ingle cortical column.SIGNIFICANCE STATEMENT ECoG methodologically bridges basic neuroscience and und
249 erictal spike frequency measures on subdural ECoG recording may both be useful in predicting the long
251 a novel multi-scale visual analysis system, ECoG ClusterFlow, for the detailed exploration of ECoG d
255 In the fetus, we tested the hypothesis that ECoG pattern is associated closely with cerebral oxygena
258 and conceptual information, suggesting that ECoG recordings can reveal neural correlates of specific
259 Its favourable specificity suggests that ECoG HGA can be used to construct a preliminary function
268 nticorrelations that are not apparent in the ECoG data, it enhances the neuronal-hemodynamic correspo
269 ithin the first 5 weeks of KA injection, the ECoG power shifted towards the lower-frequency range.
270 cile these observations by interrogating the ECoG recordings of 18 presurgical human patients (8 fema
271 teral ventricle were used to investigate the ECoG frequency responses of intracerebroventricularly ap
273 accurately captures the main features of the ECoG time series; in the simulation, the stimulus-locked
276 ECoG reference electrode is identical to the ECoG recording electrodes to significantly improve DC st
277 and clonidine were potentiated, whereas the ECoG effects mediated by GABAA and GABAB receptors remai
279 e normoxic fetus, CBF was closely related to ECoG state, but this association was less evident during
281 of theta and alpha band frequencies to total ECoG activity was significantly lower in the pre-existin
283 These observations suggest that the two ECoG components arise from different neural sources with
285 nces of gamma/high-gamma power in LFP versus ECoG in up to four monkeys, and found them to be surpris
286 roelectrodes are further verified by in-vivo ECoG recordings combined with optogenetics in mice.
287 d increased high voltage and sub-low voltage ECoG and EOG activities, as well as decreased nuchal EMG