Results 11 to 20 of about 2,272,583 (371)

Perisylvian Polymicrogyria Epileptic Syndrome

open access: yesPediatric Neurology Briefs, 1994
The epileptic spectrum and EEG findings in 31 patients with a congenital bilateral perisylvian syndrome are reported from the University of Alabama at Birmingham and the CBPS Multicenter Collaborative Study Group.
J Gordon Millichap
doaj   +4 more sources

Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox–Gastaut Syndrome

open access: yesCNS Drugs, 2021
Cannabidiol (CBD), which is one major constituent of the Cannabis sativa plant, has anti-seizure properties and does not produce euphoric or intrusive side effects.
S. Lattanzi   +6 more
semanticscholar   +1 more source

The syndrome of transient epileptic amnesia: a combined series of 115 cases and literature review

open access: yesBrain Communications, 2021
The term transient epileptic amnesia was coined in 1990 to describe a form of epilepsy causing predominantly amnestic seizures which could be confused with episodes of Transient Global Amnesia.
J. Baker   +6 more
semanticscholar   +1 more source

Insights in classification of seizures and epilepsies – review of key concepts throughout history [PDF]

open access: yesRomanian Journal of Neurology, 2011
Since the Babylonian era up to nowadays, the large complexity of epileptic disorders made the attempt of classifying and organizing concepts one of the most challenging.
Ioana Mindruta   +2 more
doaj   +1 more source

SCN 1A /Na V 1.1 channelopathies: Mechanisms in expression systems, animal models, and human iPSC models [PDF]

open access: yesEpilepsia, Wiley, 2019, 60 (S3), 2022
Pathogenic SCN1A/NaV1.1 mutations cause well defined epilepsies, including Genetic Epilepsy with Febrile Seizures Plus (GEFS+) and the severe epileptic encephalopathy Dravet syndrome. In addition, they cause a severe form of migraine with aura, Familial Hemiplegic Migraine.
arxiv   +1 more source

Diagnostics and age-related evolution of Lennox–Gastaut syndrome. Management in diverse patient age periods

open access: yesЭпилепсия и пароксизмальные состояния, 2022
Lennox–Gastaut syndrome is an epileptic encephalopathy with onset in childhood. The classical triad of diagnostic criteria is well known: 1) presence of various types of refractory epileptic seizures (tonic, atypical absences, myoclonic, tonic/atonic ...
E. D. Belousova   +3 more
doaj   +1 more source

Transient epileptic opercular syndrome [PDF]

open access: yesSeizure, 2007
Ictal transient opercular syndrome is rarely observed in benign epilepsy with centro-temporal spikes in children, and even more rarely in epilepsia partialis continua and symptomatic focal status epilepticus in adults. Here we report the ictal and interictal neuroimaging and electrophysiological findings in an adult female suffering from discontinuous ...
Susanne G. Mueller   +5 more
openaire   +3 more sources

Cortex leads the thalamic centromedian nucleus in generalized epileptic discharges in Lennox‐Gastaut syndrome

open access: yesEpilepsia, 2020
We aimed to assess the roles of the cortex and thalamus (centromedian nucleus [CM]) during epileptic activity in Lennox‐Gastaut syndrome (LGS) patients undergoing deep brain stimulation (DBS) surgery as part of the ESTEL (Electrical Stimulation of the ...
Linda J. Dalic   +6 more
semanticscholar   +1 more source

Epileptogenesis in tuberous sclerosis complex-related developmental and epileptic encephalopathy

open access: yesBrain : a journal of neurology, 2023
Epileptogenesis in infants with tuberous sclerosis complex (TSC) is a gradual and dynamic process, leading to early onset and difficult-to-treat seizures.
E. Aronica   +3 more
semanticscholar   +1 more source

Case Report: Cognitive Assessment Before an Amnesic Seizure in Transient Epileptic Amnesia Syndrome

open access: yesFrontiers in Neurology, 2022
A patient with transient epileptic amnesia syndrome presented a clinically observable amnesic seizure immediately after a neuropsychological assessment.
Coline Bouyer   +2 more
doaj   +1 more source

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