Results 51 to 60 of about 6,465 (257)
The hidden burden of sleep in adolescents with idiopathic generalized epilepsy
Abstract Background Idiopathic Generalized Epilepsies (IGEs) are electroclinical syndromes characterized by distinct seizure types, EEG patterns, and presumed polygenic inheritance. While seizure prognosis is often favorable, sleep disturbances, behavioral and emotional difficulties, and executive function impairment are common, especially during ...
Carlo Alberto Quaranta +8 more
wiley +1 more source
Status epilepticus in patients with genetic (idiopathic) generalized epilepsy
Magdalena Bosak,1 Dominika Pawełczak,2 Agnieszka Słowik11Department of Neurology, Jagiellonian University Medical College, Krakow, Poland; 2Department of Neurology, Jagiellonian University Medical College, Krakow, PolandAim of the study: Genetic ...
Bosak M, Pawełczak D, Słowik A
doaj
Background We performed this meta-analysis to investigate the association between GABRG2 rs211037polymorphism and the risk for idiopathic generalized epilepsies (IGEs).
Xiaohui Yang +7 more
doaj +1 more source
Headache in juvenile myoclonic epilepsy [PDF]
The objective of this study was to assess the prevalence of and risk factors for primary headaches in juvenile myoclonic epilepsy (JME). Headache was classified in 75 patients with JME using a questionnaire, and its prevalence was correlated with the literature on the general population and clinical data. Headache was present in 47 patients. Thirty-one
Schankin, Christoph J. +6 more
openaire +2 more sources
De novo TANC2 stop‐loss variant associated with developmental impairment and drug‐resistant epilepsy
Epileptic Disorders, EarlyView.
Matthew A. Hintermayer, Kenneth A. Myers
wiley +1 more source
Exploring the efficacy and safety of perampanel in epilepsia partialis continua: A case series
Abstract Background Epilepsia partialis continua (EPC) is a form of focal motor status epilepticus (SE), which is commonly drug‐resistant requiring treatment with multiple antiseizure medications (ASM). There are no established guidelines for pharmacological management.
Setareh Lahsaee +3 more
wiley +1 more source
Absence seizures are idiopathic epilepsies characterized by impairment of consciousness and generalized 2.5-4 Hz spike and slow wave discharges.
Ozge Uysal-Soyer +2 more
doaj
Abstract Objective To develop and evaluate a simple‐to‐use checklist to support physicians with the timely diagnosis of Lennox–Gastaut syndrome (LGS). Methods A panel of 10 pediatric and adult epileptologists used the International League Against Epilepsy (ILAE) criteria for LGS classification and definition to develop seven questions for the checklist,
Nicola Specchio +9 more
wiley +1 more source

