Results 71 to 80 of about 24,565 (251)

Refining the electroclinical phenotype of 15q11.2 microdeletion: EEG biomarker overlap with Angelman syndrome

Epileptic Disorders, EarlyView.
Abstract The 15q11.2 microdeletion is a chromosomal condition associated with a broad epileptic phenotype. It is differentiated from Angelman syndrome, which is typically a larger maternal deletion in an overlapping area. We describe a patient with a 15q11.2 microdeletion that has clinical and EEG biomarker features similar to those seen in Angelman ...
Hok Leong Chin, Joshua Chang, Douglas Nordli III   +2 more
wiley   +1 more source

[First generalized tonic-clonic seizure].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 2016
First onset of a generalized tonic-clonic seizure is a frequent reason for hospital admissions. This article aims to provide a brief overview of the epidemiology, etiology, investigation and treatment of a first generalized tonic-clonic seizure.The review is based on a discretionary sample of English-language articles found through a search in PubMed ...
Martha Seim, Realfsen, Siri M Hylleraas, Bø, Morten I, Lossius, Karl O, Nakken   +3 more
openaire   +1 more source

Prolonged visual aura, late-onset migraine-like headaches, and seizures suggest an occipital arteriovenous malformation

Journal of Family Medicine and Primary Care
To report a patient with occipital arteriovenous malformation (AVM), manifested by prolonged visual aura and migraine-like headache as well as rare tonic–clonic seizures. The patient is a 55-year-old woman with a left occipital, unruptured AVM that first
Josef Finsterer, Sounira Mehri
doaj   +1 more source

Peri-Ictal Headaches in Children with Epilepsy

Pediatric Neurology Briefs, 2008
The frequency and character of preictal and postictal headaches in 101 children (aged 5-18 years) with generalized tonic-clonic or partial seizures were determined by interviews and clinic chart reviews, in a study at Alberta Children’s Hospital, Calgary,
J Gordon Millichap
doaj   +1 more source

Adult‐onset CD8‐predominant hemispheric inflammatory epilepsy: Expanding the spectrum of post‐infectious and Rasmussen‐like encephalitis

Epileptic Disorders, EarlyView.
Ramya Raghupathi
wiley   +1 more source

Efficacy of fenfluramine in a pediatric epilepsy patient with a pathogenic SV2A variant: A case report

Epileptic Disorders, EarlyView.
Abstract Pathogenic SV2A gene variants have been reported as causes of epilepsy and are often associated with drug resistance and susceptibility to fever‐related seizures. No highly effective treatments have been established for this condition. We report a female patient with a family history of epilepsy who developed generalized seizures associated ...
Takayuki Mori, Hiroshi Terashima, Yu kakimoto, Mitsuhiro Kato, Shumpei Uchino   +4 more
wiley   +1 more source

Recurrence Risk after a Single Seizure

Pediatric Neurology Briefs, 1990
The risk of recurrence after a single, unprovoked, generalized tonic-clonic seizure was assessed in 119 children aged 2 to 16 years, resident in Normandy and examined at the Hopital General, Le Havre and the Hopital Charles Nicolle, Rouen, France.
J Gordon Millichap
doaj   +1 more source

Metabolic mimicry of perioral myoclonia with absences: A signature of thalamocortical instability in childhood‐onset ornithine transcarbamylase deficiency

Epileptic Disorders, EarlyView.
José Augusto Bragatti, Letícia Grigoletto   +1 more
wiley   +1 more source

The burden of the postictal state in epilepsy: A prospective, single‐center observational cohort study

Epileptic Disorders, EarlyView.
Abstract Objective The postictal state is a major yet underrecognized component of the epilepsy burden. We aimed to develop a structured patient‐reported instrument to quantify postictal recovery, characterize its multidimensional burden, and identify demographic, clinical, psychiatric, and treatment‐related factors associated with postictal severity ...
Ionuț‐Flavius Bratu, Agnès Trébuchon, Fabrice Bartolomei   +2 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, Ying Zhu, Qingshu Li, Xin Tian, Peng Zhang, Yang Lü   +5 more
doaj   +1 more source