Results 51 to 60 of about 22,438 (261)
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
Long-term outcomes of generalized tonic-clonic seizures in a childhood absence epilepsy trial [PDF]
To determine incidence and early predictors of generalized tonic-clonic seizures (GTCs) in children with childhood absence epilepsy (CAE).Occurrence of GTCs was determined in 446 children with CAE who participated in a randomized clinical trial comparing ethosuximide, lamotrigine, and valproate as initial therapy for CAE.As of June 2014, the cohort had
Shlomo Shinnar +188 more
openaire +2 more sources
Introduction: Epilepsy remains a challenge, with one-third of patients experiencing refractory seizures despite current anti-seizure medications. The nitrergic system, which involves nitric oxide (NO) and NO synthase (NOS) enzymes, plays a complex role ...
Mohammad Keshavarzi +4 more
doaj +1 more source
Sudden unexpected death in epilepsy in a 14-year-old girl: case report and literature review
Background Sudden unexpected death in epilepsy (SUDEP) is the most common cause of death in people with epilepsy. The pathogenesis of SUDEP is still unclear.
Xinyue Zhang +3 more
doaj +1 more source
Prevalence of childhood and adolescence epilepsy in Upper Egypt (desert areas)
Background A high prevalence of epilepsy in children is frequently found in developing countries. Objective This study aimed to determine the prevalence and clinical pattern of childhood and adolescence epilepsy in Upper Egypt.
Wafaa M. Farghaly +5 more
doaj +1 more source
Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic–clonic seizures
Mutations in SCN1A, the gene encoding the brain voltage‐gated sodium channel α1 subunit (NaV1.1), are associated with genetic forms of epilepsy, including generalized epilepsy with febrile seizures plus (GEFS+ type 2), severe myoclonic epilepsy of infancy (SMEI) and related conditions.
Thomas H, Rhodes +5 more
openaire +3 more sources
This systematic literature review (SLR) assessed the humanistic and economic burden of focal epilepsy and primary generalized tonic–clonic seizures (PGTCS) in adults to evaluate these domains in both populations and identify evidence gaps to inform ...
Simona Boccaletti +4 more
doaj +1 more source
A clinical and pathological study in patients with sudden unexpected death in Epilepsy
Background Sudden unexpected death of epilepsy (SUDEP) is a severe outcome of epilepsy. This study aimed to report the clinical and pathological findings in patients with SUDEP. Methods The record of patients with sudden death was screened.
Weihua Yu +5 more
doaj +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
CLINICAL CASE OF PREGNANT PATIENT WITH TEMPORAL EPILEPSY AND MYOCLONIC EPILEPTIC SEIZURES
Rationale: It is thought that temporal lobe epilepsy tends to show three types of seizures: simple partial seizures, complex partial seizures and secondary generalized motor (tonic ore tonic-clonic) seizures.
V. O. Generalov +6 more
doaj

