Operculoinsular cortex encodes pain intensity at the earliest stages of cortical processing as indicated by amplitude of laser-evoked potentials in humans.
about
Somatosensory spatial attention modulates amplitudes, latencies, and latency jitter of laser-evoked brain potentialsChanges in cortical activity associated with adaptive behavior during repeated balance perturbation of unpredictable timing.Multiple linear regression to estimate time-frequency electrophysiological responses in single trialsCortical responses to salient nociceptive and not nociceptive stimuli in vegetative and minimal conscious state.Topographically organized projection to posterior insular cortex from the posterior portion of the ventral medial nucleus in the long-tailed macaque monkey.Taking into account latency, amplitude, and morphology: improved estimation of single-trial ERPs by wavelet filtering and multiple linear regressionDeterminants of laser-evoked EEG responses: pain perception or stimulus saliency?Cortical activity evoked by inoculation needle prick in infants up to one-year old.Laser-evoked potentials are graded and somatotopically organized anteroposteriorly in the operculoinsular cortex of anesthetized monkeys.Automated classification of pain perception using high-density electroencephalography data.Similar nociceptive afferents mediate psychophysical and electrophysiological responses to heat stimulation of glabrous and hairy skin in humans.Laser-evoked cortical potentials in cluster headache.Gamma oscillations in human primary somatosensory cortex reflect pain perception.Analgesic and antinociceptive effects of peripheral nerve neurostimulation in an advanced human experimental model.Central pain processing in chronic chemotherapy-induced peripheral neuropathy: a functional magnetic resonance imaging studyMultiple somatotopic representations of heat and mechanical pain in the operculo-insular cortex: a high-resolution fMRI study.Dishabituation of laser-evoked EEG responses: dissecting the effect of certain and uncertain changes in stimulus modality.Negative expectations interfere with the analgesic effect of safety cues on pain perception by priming the cortical representation of pain in the midcingulate cortex.Cortical activation changes during repeated laser stimulation: a magnetoencephalographic studyPharmacological modulation of pain-related brain activity during normal and central sensitization states in humans.Neurofeedback of the difference in activation of the anterior cingulate cortex and posterior insular cortex: two functionally connected areas in the processing of pain.Unique, common, and interacting cortical correlates of thirst and pain.Transcranial magnetic stimulation over human secondary somatosensory cortex disrupts perception of pain intensity.Virtual visual effect of hospital waiting room on pain modulation in healthy subjects and patients with chronic migraine.Baroreceptor activation attenuates attentional effects on pain-evoked potentials.Introducing the event related fixed interval area (ERFIA) multilevel technique: a method to analyze the complete epoch of event-related potentials at single trial level.Innocuous peripheral nerve stimulation shifts stimulus-response function of painful laser stimulation in manHeightened eating drive and visual food stimuli attenuate central nociceptive processing.Perceiving monetary loss as due to inequity reduces behavioral and cortical responses to pain.On the Agreement between Manual and Automated Methods for Single-Trial Detection and Estimation of Features from Event-Related Potentials.The Analgesic Effect of Oxytocin in Humans: A Double-Blind, Placebo-Controlled Cross-Over Study Using Laser-Evoked Potentials.Nociceptive Local Field Potentials Recorded from the Human Insula Are Not Specific for NociceptionThe relationship between nociceptive brain activity, spinal reflex withdrawal and behaviour in newborn infantsBOLD responses in somatosensory cortices better reflect heat sensation than pain.Normalization of Pain-Evoked Neural Responses Using Spontaneous EEG Improves the Performance of EEG-Based Cross-Individual Pain Prediction.Neural correlates of heat-evoked pain memory in humans.Viewing the body modulates both pain sensations and pain responsesThe perception of pain and its management in disorders of consciousness.Assessing pain objectively: the use of physiological markers.Differential fMRI activation to noxious heat and tactile stimuli in parasylvian areas of new world monkeys.
P2860
Q30387220-580517EF-1E83-4AC2-A614-522422BDC1B3Q30399590-F063169C-C8DC-4833-9B80-AD9F7E5A92C3Q30413215-8DFCA3FD-66ED-4791-A817-D0C6C774EDFFQ30418682-C4135BD2-71DF-4CE5-8B62-F39D701391A8Q30421875-428EB37B-D87D-4CEB-9897-DAF3170F7978Q30460345-CDF422FE-7384-423C-BF6D-4C5FBB61E332Q30487797-BC4FBF0A-D11B-455C-8D05-9CE42A0BE56AQ30618772-70546E2E-A015-40BA-822F-E31DA636D85EQ30821780-E60DD0CA-3059-48B6-9825-73479986A691Q31146220-FD77A508-0F62-44A9-94C0-4E90C3BC16CFQ33257625-31F06929-CB7D-4AD6-8764-6ECFA93A2127Q33281817-8F8016B8-4206-4971-8E29-02A5185CCE2CQ33282654-78B84F29-7203-4026-81C3-6DE30B231B83Q33299643-7880DC9A-20F9-483B-9B0D-F986880BF6FCQ33599361-99362429-3ED6-4779-85C8-57140B003C1EQ33672728-179A784D-8DC2-444D-A251-9BBF244718ABQ33803261-C6690CAA-17A9-4F45-88F1-246619D5787CQ33860048-92DEDD36-9E3D-4DDE-91C0-AF93CEA86C1AQ33900214-553AE1EA-B621-4402-887C-F74660EFF71EQ34193899-03929C56-97D2-4D15-B142-E2CE6C20F8A1Q34341612-B8F25088-0F86-44C9-B8AA-7C1B38B682E6Q34479279-E8CF14BD-2C3A-4AF9-B079-3E9AFAF51D15Q34537109-B70D8AF1-A199-47BD-91BB-B0674243CA74Q34568440-57DF7BDF-6D79-4AF3-8F7E-2F645AAA6580Q34571062-DC1B6A7D-0F1B-4A2C-A334-9BCAC18EDC75Q35041530-443940D4-A167-4BA9-8A02-DEF4C3AD06E6Q35044363-D1BFBF21-4481-48E7-8E4B-6B49EAE4791DQ35138388-815C2CF4-1166-43D8-AA4A-78757FD3A015Q35143476-C784ECD8-B663-4829-8C5B-BBA0EC7184BAQ35741341-5A8521DF-2CDA-4725-8AF1-5B3D8897C611Q35867587-CA9EFBF8-BAE5-44FF-8751-D01C54450510Q35886477-86639BC0-F3D3-42A1-91BE-E53A46DBDF4FQ35905701-D844F2F5-3B36-4C12-B451-7F5D3B3A6A7AQ35944148-0E01EAF0-0613-4ADC-8819-45B779A97E4DQ36009094-FFDA07F0-1F98-43A1-98E0-9011C2F0B9F2Q36729849-A68340EE-6F68-4327-BD14-8A4F350C2884Q36968663-3020973C-1F7F-46DF-A5D1-E90AE28755F3Q38146883-7343354D-A47B-48D5-B281-75175AA7D14CQ38378808-1475C677-2BE3-452F-99F0-19CD3D216533Q39987216-571DAA34-6FDC-4456-8A8F-6859917A7930
P2860
Operculoinsular cortex encodes pain intensity at the earliest stages of cortical processing as indicated by amplitude of laser-evoked potentials in humans.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Operculoinsular cortex encodes ...... r-evoked potentials in humans.
@ast
Operculoinsular cortex encodes ...... r-evoked potentials in humans.
@en
type
label
Operculoinsular cortex encodes ...... r-evoked potentials in humans.
@ast
Operculoinsular cortex encodes ...... r-evoked potentials in humans.
@en
prefLabel
Operculoinsular cortex encodes ...... r-evoked potentials in humans.
@ast
Operculoinsular cortex encodes ...... r-evoked potentials in humans.
@en
P2093
P1433
P1476
Operculoinsular cortex encodes ...... er-evoked potentials in humans
@en
P2093
P304
P356
10.1016/J.NEUROSCIENCE.2004.10.035
P407
P577
2005-01-01T00:00:00Z