Results 91 to 100 of about 826,950 (244)
Epileptic Disorders, EarlyView.Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by refractory seizures and frequently recurring epileptic activity with neurodevelopmental delay or regression that usually begin in early life. We aimed to define the relationship between electroclinical features and etiology, as well as the genotype–phenotype ...
Burcu Yaman +7 more
wiley +1 more source
A clinical and pathological study in patients with sudden unexpected death in Epilepsy
Acta Epileptologica, 2019 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
Increased susceptibility to kainate-induced tonic-clonic seizures in the mutant mice.
, 2013 A, The graph represents the percentage of mice with the generalized tonic-clonic seizures 1 h after drug administration ...
Toshiya Manabe (375132) +10 more
core +1 more source
Localizing value of verbal automatisms, vocal automatisms, singing, and humming: A systematic review
Epileptic Disorders, EarlyView.Abstract Objective We performed a systematic review of the localizing and lateralizing value of verbal automatisms, vocal automatisms, ictal singing, and humming in focal epilepsy with the view to summarize the state‐of‐the‐art clinico‐anatomical correlations in the field and help guide interpretation of ictal semiology within the framework of ...
Vit Vsiansky, Martin Pail, Milan Brazdil
wiley +1 more source
Circadian patterns of generalized tonic-clonic evolutions in pediatric epilepsy patients.
, 2012 ObjectiveTo investigate the sleep/wake, day/night, and 24-h periodicity of pediatric evolution to generalized tonic–clonic seizures (GTC).MethodsCharts of 407 consecutive patients aged 0–21years undergoing continuous video-EEG monitoring for epilepsy ...
Ramgopal, Sriram +9 more
core +1 more source
KBG syndrome: A scoping review of electroclinical features of patients with epilepsy
Epileptic Disorders, EarlyView.Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini +6 more
wiley +1 more source
Epileptic Disorders, EarlyView.Abstract Objective Epilepsy with eyelid myoclonia is a childhood‐onset generalized epilepsy syndrome with variable recognition of eyelid myoclonia, eye‐closure sensitivity, and photosensitivity during follow‐up. We aimed to characterize longitudinal clinical and electroencephalographic features in pediatric epilepsy with eyelid myoclonia, focusing on ...
Hande Aygün +3 more
wiley +1 more source
Magnetic Resonance Imaging and Its Benefit in Epilepsy and Seizure Disorders Diagnosis
The Iraqi Journal of Medical SciencesBackground: Brain magnetic resonance imaging (MRI) is one of the most important investigations in epilepsy, which can detect any structural abnormality such as infarctions, gliosis, tumors and other different abnormalities.
Hasanain H. Obaid +2 more
doaj +6 more sources