Results 31 to 40 of about 4,983 (178)
Pediatric Neurology Briefs, 1991 A 14 year old girl with epilepsia partialis continua complicated by palatal myoclonus of focal cortical origin is reported from the Comprehensive Epilepsy Center, Graduate Hospital; and University of Pennsylvania School of Medicine, Philadelphia, PA.
J Gordon Millichap
doaj +1 more source
Epilepsia, EarlyView.Abstract Objective This study was undertaken to evaluate whether seizure freedom in pregnancy predicts seizure freedom in the postpartum period in women with epilepsy (WWE). Prior studies have shown that seizure freedom prior to conception strongly predicts seizure freedom during pregnancy.
Emma C. Osterhaus +7 more
wiley +1 more source
Low diagnostic yield of presurgical genetic testing in adult patients with epilepsy
Epilepsia, EarlyView.Abstract Objective To determine the diagnostic yield of genetic testing in patients undergoing presurgical evaluation for epilepsy. Methods We conducted a cohort study including 115 adult patients who underwent presurgical evaluation in the Calgary Epilepsy Program between 2019 and 2023 and who had undergone research exome sequencing.
Clara Jünemann +16 more
wiley +1 more source
Epilepsia, EarlyView.Abstract Children with developmental and epileptic encephalopathies (DEEs) face cognitive and behavioral challenges that may have a greater impact than seizures on their quality of life (QoL). The need to assess these nonseizure outcomes for evaluating treatments is increasingly recognized.
Cinzia Correale +9 more
wiley +1 more source
Acta Neurológica Colombiana, 2015 Objetivo: presentar la evidencia publicada hasta el momento acerca de la utilidad de la lacosamida en población pediátrica con epilepsia refractaria.
Johann Sebastián Ortiz de la Rosa +2 more
doaj +1 more source
Epilepsia, EarlyView.Abstract Objective Infantile epileptic spasms syndrome (IESS) is an epileptic encephalopathy requiring rapid diagnosis and treatment to optimize neurodevelopmental outcomes. Although multiple national and regional guidelines exist, recommendations vary.
Gozde Erdemir +21 more
wiley +1 more source
Archives of Epilepsy, 2019 Seizures may occur in frontotemporal lobar degeneration syndromes as an element of a heterogeneous group of disorders, according to both clinical phenotype and neuropathology.
Yasemin DİNÇ, Gönül ÇELİK AKDAĞ
doaj +1 more source
Arquivos de Neuro-Psiquiatria, 2009 BACKGROUND: Epileptic syndromes with absence seizures (AS) possess unique clinical and electroencephalographic (EEG) characteristics. In typical or atypical AS, ictal phenomenology may include various characteristics.
Soniza Vieira Alves-Leon +3 more
doaj +1 more source
Individualização do tratamento com topiramato em pacientes infantis com epilepsia focal
Revista Brasileira de Ciências Biomédicas, 2023 O topiramato é um medicamento antiepilético utilizado em crises de epilepsia parciais em adultos e crianças, atuando no sistema nervoso central (SNC) e trazendo equilíbrio às células neurológicas. O estudo tem aplicação em pacientes infantis, em que são demonstrados os efeitos benéficos da individualização, principalmente por se tratar de um fraco ...
Isabelle Fernandes Inocencio +5 more
openaire +1 more source
Epilepsia, EarlyView.Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by drug‐resistant seizures and developmental slowing/regression. We examined the efficacy and tolerability of fenfluramine (FFA) in pediatric and adult patients with Lennox–Gastaut syndrome (LGS), Dravet syndrome (DS), and other DEEs.
Vicente Villanueva +29 more
wiley +1 more source