Results 31 to 40 of about 41,822 (309)

Electroencephalogram of Healthy Horses During Inhaled Anesthesia. [PDF]

open access: yes, 2015
BackgroundPrevious study of the diagnostic validity of electroencephalography (EEG) to detect abnormalities in equine cerebral cortical function relied on the administration of various drugs for sedation, induction, and maintenance of general anesthesia ...
Aleman, MR   +8 more
core   +1 more source

Different patterns of epileptiform-like activity are generated in the sclerotic hippocampus from patients with drug-resistant temporal lobe epilepsy

open access: yesScientific Reports, 2018
Human hippocampal slice preparations from patients with temporal lobe epilepsy (TLE) associated with hippocampal sclerosis (HS) are excellent material for the characterization of epileptiform-like activity.
Selvin Z. Reyes-Garcia   +8 more
doaj   +1 more source

EEG changes in children born to epileptic parents

open access: yesНеврология, нейропсихиатрия, психосоматика, 2015
Epileptiform EEG changes are much more common in children whose parents are epileptic than in the population. There is evidence that subclinical epileptiform activity affects children’s intellect and behavior.
D. V. Morozov
doaj   +1 more source

Electroencephalography in young onset dementia

open access: yesBMC Neurology, 2023
Background Young onset dementia (YOD) is a major diagnostic and management problem. Methods We set out to explore if electroencephalography (EEG) might be useful in the diagnosis of young onset Alzheimer’s disease (YOAD) and young onset frontotemporal ...
Casey W Brown   +2 more
doaj   +1 more source

Influence of metallic artifact filtering on MEG signals for source localization during interictal epileptiform activity [PDF]

open access: yes, 2016
Objective. Medical intractable epilepsy is a common condition that affects 40% of epileptic patients that generally have to undergo resective surgery.
Alonso López, Joan Francesc   +5 more
core   +2 more sources

AUTISTIC EPILEPTIFORM REGRESSION (A REVIEW)

open access: yesРусский журнал детской неврологии, 2015
The author represents the review of current scientific literature devoted to autistic epileptiform regression — the special form of autistic disorder, characterized by development of severe communicative disorders in children as a result of continuous ...
L. Yu. Glukhova
doaj   +1 more source

Epilepsy and autism: The authors’ study data

open access: yesНеврология, нейропсихиатрия, психосоматика, 2013
A study was conducted to investigate electroclinical features in patients with epilepsy and autism and to determine the efficiency of antiepileptic therapy. A group of 113 patients aged 8 months to 10 years with autistic disorders was followed up.
K. V. Voronkova   +5 more
doaj   +1 more source

Anti-epileptic effect of Ganoderma lucidum polysaccharides by inhibition of intracellular calcium accumulation and stimulation of expression of CaMKII a in epileptic hippocampal neurons [PDF]

open access: yes, 2014
Purpose: To investigate the mechanism of the anti-epileptic effect of Ganoderma lucidum polysaccharides (GLP), the changes of intracellular calcium and CaMK II a expression in a model of epileptic neurons were investigated.
A Hudmon   +57 more
core   +3 more sources

Microphysiology of Epileptiform Activity in Human Neocortex [PDF]

open access: yesJournal of Clinical Neurophysiology, 2008
The authors report the use of dense two-dimensional microelectrode array recordings to characterize fine resolution electrocortical activity ("microEEG") in epileptogenic human cortex. A 16-mm(2) 96 microelectrode array with 400-mum interelectrode spacing was implanted in five patients undergoing invasive EEG monitoring for medically refractory ...
Catherine A, Schevon   +9 more
openaire   +2 more sources

EPILEPSY IN 11 PATIENTS WITH TYPICAL RETT SYNDROME CAUSED BY MECP2 MUTATION: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS, COURSE, THERAPY (RESULTS OF THE AUTHORS’ OBSERVATIONS)

open access: yesРусский журнал детской неврологии, 2016
Examinations were made in 11 female patients aged 3 to 23 years with Rett syndrome and typical mutation in the MECP2 gene, who had been followed up from 2006 to 2015.
M. Yu. Bobylova   +6 more
doaj   +1 more source

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