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1 all clinical and EEG information (including intracranial EEG).
2 s, such as those that would be recorded with intracranial EEG.
3 6 women) monitored with simultaneous MEG and intracranial EEG.
4 unctional networks derived from coregistered intracranial EEG.
5 are largely based on functional mapping via intracranial EEG.
6 f high-gamma activity recorded using MEG and intracranial EEG.
7 p electroencephalography (EEG), MRI, PET and intracranial EEG.
8 egions with accuracy comparable with that of intracranial EEG.
9 6 and 1994, 28 patients had IBTL seizures on intracranial EEG.
10 epsy often requires recording seizures using intracranial EEG.
11 t outcomes, only 9 of 31 patients undergoing intracranial EEG (29%) and only 9 of 85 patient with non
12 24 of these 31 patients undergoing long-term intracranial EEG (77%), a seizure focus was identified a
13 fically between white matter connections and intracranial EEG, across pre-ictal and ictal periods in
14 anial EEG recordings to a normative atlas of intracranial EEG activity and connectivity can reliably
15 clinical signs of loss of consciousness and intracranial EEG activity during 129 focal impaired awar
18 otably, the sounds also elicited oscillatory intracranial EEG activity, including increases in theta,
19 e 16 features for early seizure detection in intracranial EEG and compared them and their frequency r
20 nd without spikes across different bands for intracranial EEG and electric/magnetic source imaging an
21 amma-range) in rare, simultaneously recorded intracranial EEG and fMRI in humans, and source-localize
22 the presumed epileptogenic zone based on the intracranial EEG and MRI abnormalities while maximally p
23 was compared with the seizure onset zone at intracranial EEG and with surface IED-related potentials
25 asible to detect interictal abnormalities in intracranial EEG, and of potential clinical value to ide
26 l intervention based on synchronizability of intracranial EEG (area under the receiver operating char
33 ed seizure onset zone and the spike onset on intracranial EEG channels by estimating their overlap wi
34 ed MRI and functional imaging and subsequent intracranial EEG confirmation of the seizure-onset zone
36 found to have partially dissociable resting intracranial EEG correlates, reflecting different underl
43 ultaneous EEG/fMRI data in healthy subjects, intracranial EEG data in epilepsy patients, comparison w
45 sed related models, and fitting the model to intracranial EEG data uncovers two regularities across h
48 FC and DLPFC in human epilepsy patients with intracranial EEG electrodes during an auditory Stroop ex
49 of the resection zone and determining which intracranial EEG electrodes lie within it; (ii) validati
51 vious exposure of the images while recording intracranial EEG from the higher-order visual cortex of
53 ly comparing source imaging results with the intracranial EEG (iEEG) findings and surgical resection
54 pert musicians and non-musicians, as well as intracranial EEG (iEEG) from six neurological patients,
57 TMS) with intracranial micro-sEEG (usEEG) or intracranial EEG (iEEG) have significantly advanced our
58 investigated the neural effects of TBS using intracranial EEG (iEEG) in 10 pre-surgical epilepsy part
61 electrodes can replace prolonged interictal intracranial EEG (iEEG) recording, making the process mo
63 tional magnetic resonance imaging (fMRI) and intracranial EEG (iEEG) recordings to delineate place-se
64 g surgical resection can involve presurgical intracranial EEG (iEEG) recordings to detect seizures an
66 sify active electrodes showing event-related intracranial EEG (iEEG) responses from 115 patients perf
68 how high-frequency activity captured through intracranial EEG (iEEG) supports human memory retrieval.
69 rchitecture, which enables interpretation of intracranial EEG (iEEG) transients driving classificatio
70 estigated the feasibility of recording human intracranial EEG (iEEG) using a benchtop version of the
72 stimating a transfer function model from the intracranial EEG 'impulse' or single-pulse electrical st
81 iated with better chance of concordance with intracranial EEG localization, and with excellent postsu
83 ations were found between source imaging and intracranial EEG measures (0.4 <= rho <= 0.9, P < 0.05).
84 naturally occurring epilepsy had continuous intracranial EEG (median 298 days) using novel implantab
85 onsuming process wherein a patient undergoes intracranial EEG monitoring, and a team of clinicians wa
90 produces large amplitude oscillations in the intracranial EEG network that propagate seizure activity
91 onses occur when there is 'resonance' in the intracranial EEG network, and the resonant frequency can
94 , we reveal neocortical gating mechanisms in intracranial EEG patients by identifying rapid, within-t
95 Here, we investigated this question using intracranial EEG recorded from seventeen pediatric, adol
99 ns between hippocampus and lateral PFC using intracranial EEG recordings (26 participants, 16 females
100 sed 38 focal epilepsy patients who underwent intracranial EEG recordings and diffusion-weighted imagi
101 nvestigate these questions here by examining intracranial EEG recordings as 28 participants with elec
103 egular samples of IED rates from multi-month intracranial EEG recordings from ambulatory humans, we u
109 ocampal-cortical coupling were measured with intracranial EEG recordings in patients with epilepsy.
112 Here, we use data from a large cohort of intracranial EEG recordings to investigate the neurophys
114 areal communication in the human brain using intracranial EEG recordings, acquired following 29,055 s
115 ing a multimodal analysis of functional MRI, intracranial EEG recordings, and large-scale neural popu
119 can explain the variability in the timing of intracranial EEG responses to sounds: cortical electrode
121 ological Institute, we aggregated interictal intracranial EEG retrospectively across 166 subjects com
124 n during these periods, measured by spectral intracranial EEG similarity, predicts subsequent recall.
127 mpal longitudinal specialization in 32 human intracranial EEG subjects as they performed an associati
128 interpretation of ictal activity observed by intracranial EEG that challenges the traditional concept
129 e we leverage the high temporal precision of intracranial EEG to examine sub-second changes in functi
131 ized on the high spatiotemporal precision of intracranial EEG to localize such abstract decision sign
133 EEG was localizing in 35 patients (66%) and intracranial EEG was localizing in 22 patients (85%) (of
139 uantitative measures derived from interictal intracranial EEG yield potentially appealing biomarkers