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Music effects on event-related potentials of humans on the basis of cultural environment.Bayesian EEG dipole source localization using SA-RJMCMC on realistic head model.Electroencephalographic differences between WAG/Rij and GAERS rat models of absence epilepsy.Topological distribution of oddball 'P300' responses.Wavelet analysis of oddball P300.A wavelet transform based method to determine depth of anesthesia to prevent awareness during general anesthesiaComparative analysis of event-related potentials during Go/NoGo and CPT: decomposition of electrophysiological markers of response inhibition and sustained attention.Human EEG gamma oscillations in neuropsychiatric disorders.Time-frequency analysis of the event-related potentials associated with the Stroop test.P3 and delta band responses in visual oddball paradigm in schizophrenia.Intra-amygdaloid injection of kainic acid in rats with genetic absence epilepsy: the relationship of typical absence epilepsy and temporal lobe epilepsy.Changes in BOLD transients with visual stimuli across 1-44 Hz.A model for P300 generation based on responses to near-threshold visual stimuli.Time-frequency analysis of single-sweep event-related potentials by means of fast wavelet transform.The effects of interstimulus interval on sensory gating and on preattentive auditory memory in the oddball paradigm. Can magnitude of the sensory gating affect preattentive auditory comparison process?Slow cortical potential shifts modulate P300 amplitude and topography in humans.Gamma amplitudes are coupled to theta phase in human EEG during visual perception.N2 and P3 components of event-related potential in first-episode schizophrenic patients: scalp topography, medication, and latency effects.DRD4 and DAT1 polymorphisms modulate human gamma band responses.Achromatic temporal-frequency responses of human lateral geniculate nucleus and primary visual cortex.Cognitive impairment in amyotrophic lateral sclerosis: evidence from neuropsychological investigation and event-related potentials.P3 response during short-term memory retrieval revisited by a spatio-temporal analysis.Wavelet analysis of P3a and P3b.Movement-related cortical potentials: their relationship to the laterality, complexity and learning of a movement.Simultaneous EEG/fMRI analysis of the resonance phenomena in steady-state visual evoked responses.Implementation of low resolution electro-magnetic tomography with FMRI statistical maps on realistic head models.Neuroimaging of event related brain potentials (ERP) using fMRI and dipole source reconstruction.Source localization of subtopographic brain maps for event related potentials (ERP).Interactions of Gamma and Theta Oscillations in the Electroencephalogram (EEG) during Memory ProcessesDesign of an MR-compatible fNIRS instrumentFast rhythms in the hippocampus are a part of the diffuse gamma-response systemEvent-related theta rhythms in cat hippocampus and prefrontal cortex during an omitted stimulus paradigmElectroencephalogram alpha (8-15 Hz) responses to visual stimuli in cat cortex, thalamus, and hippocampus: a distributed alpha network?Decomposition of event-related brain potentials into multiple functional components using wavelet transformEvaluation of the functions of the parvocellular and magnocellular pathways in strabismic amblyopiaAlpha rhythm of the EEG modulates visual detection performance in humansWhat if you are not sure? Electroencephalographic correlates of subjective confidence level about a decisionMeasurement of cognitive dynamics during video watching through event-related potentials (ERPs) and oscillations (EROs)Intrinsic functional connectivity in social anxiety disorder with and without comorbid attention deficit hyperactivity disorder
P50
Q30322784-BE7DF7C0-FD43-4093-96F2-48244F59B8B2Q30365820-E1F35048-C8E5-439F-B35A-94CE412FA01EQ34094098-998556B5-EEB3-426B-AE43-9955EA157770Q34133312-19C330FC-F974-4DD5-B60D-8B304705F7E0Q34133319-7CD466CE-A29B-480D-8683-1F7F80A74761Q34243097-3BAD41A9-47B8-4F7E-BF70-9D9AA78F7E45Q34545248-8718648B-80EB-41E3-8CE8-EFD699753220Q36298870-517D897A-9823-42A8-A788-EF3B8004F67BQ45157853-35303F73-FF3E-435B-915D-4CA4DA35F2CCQ45845438-A3798075-5CDD-43F7-829A-C836C13EDCDAQ46454692-995BF859-5D9A-4942-8977-B71028586B62Q47783402-7C814536-987F-4490-A7FF-79E0C42AB23CQ48227796-1D599472-46C5-450E-90B0-FF88A4264503Q48261513-2A4FC962-FB2E-466F-9C5B-2635200E5B8FQ48322840-E6B6ED8E-6102-4CAE-8FBF-959004C440FCQ48406860-64F626FC-4CE2-49E5-8FD8-07214C9D2719Q48427890-996E767D-B125-4E1F-9510-42C6004F70FAQ48470985-D461A0CA-BBF0-4F23-9861-071C305DD596Q48511322-05304FC0-292B-4A81-9E07-5DFD0FF36708Q48520562-8BA3383E-A117-4ECF-88D4-32B74D4AFB3FQ48577518-3E0DFA55-8AAA-44F2-8CDC-0ED0EA1AAC85Q48629805-26C90B6A-546C-4B58-9BAA-D8BFAF941604Q48801949-A70CE1E2-B857-4C4C-B508-DDB5DC30A3A4Q49079353-22B3C7A6-AFB7-4194-94CB-9D4330EC6EA4Q49162662-165BDD82-A52A-4A67-B040-B64ADD247D57Q50863514-DA7954D8-4260-4337-AFBE-D0ECDF92B131Q50864397-5AE07F19-E070-4DEA-8AB5-3D2D6D02D2FAQ50883595-A0599E6E-9701-4F69-99A9-E8170FA3F4D9Q56966073-D5834067-48AB-447E-9BDA-C0C888641BD3Q60040953-BD628231-DB94-4D93-BBFC-42EB50FFEA84Q71721874-923E9BF6-B3B0-4817-B311-A1ECFE90CD15Q72591500-05305006-276B-4B23-ACA5-157DD1538181Q73039138-849603FD-2FC5-4162-8F3F-0A6509598633Q74397341-A0A03F64-3645-47EC-8350-8508B13A2873Q74538915-8F6FD8D3-DDC0-44C8-A74E-EEFA20BAFA3AQ80370214-0630D783-72A6-4540-BDA1-B3BE1CE313A8Q82691658-5E99651D-4EB8-4311-ABAA-E9F49BDA0331Q91333259-DFB1D1B6-542D-48BF-974D-FFEF4D779718Q92539386-6F0EE19C-4202-4839-9485-B652324E1293
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Tamer Demiralp
@ast
Tamer Demiralp
@en
Tamer Demiralp
@es
Tamer Demiralp
@nl
Tamer Demiralp
@sl
type
label
Tamer Demiralp
@ast
Tamer Demiralp
@en
Tamer Demiralp
@es
Tamer Demiralp
@nl
Tamer Demiralp
@sl
prefLabel
Tamer Demiralp
@ast
Tamer Demiralp
@en
Tamer Demiralp
@es
Tamer Demiralp
@nl
Tamer Demiralp
@sl
P1053
B-2194-2018
P106
P1153
7004701236
P21
P31
P3829
P496
0000-0002-6803-734X
P569
2000-01-01T00:00:00Z