Results 21 to 30 of about 1,727,832 (292)

Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy [PDF]

open access: yesSeizure, 2018
Children with Childhood Absence Epilepsy (CAE) may develop generalized tonic-clonic seizure or juvenile myoclonic epilepsy. A possible evolution to Eyelid Myoclonia with Absence Epilepsy (EMA) hasn't been documented yet. We report the electroclinical features of a case series of children with CAE that evolved to EMA after therapy withdrawal.Of 108 ...
Galli, Jessica   +4 more
openaire   +3 more sources

Prognosis of Early Onset Absence Epilepsy

open access: yesPediatric Neurology Briefs, 2013
Investigators from University of Chieti and several other centers in Italy conducted a multicenter retrospective 36-month follow-up study of the electroclinical course of epilepsy in all children with typical absence seizures (TAS) starting in the first ...
J Gordon Millichap
doaj   +1 more source

Hormones and Absence Epilepsy☆ [PDF]

open access: yes, 2017
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Luijtelaar, E.L.J.M. van   +2 more
openaire   +3 more sources

Role of neurotrophins and neuropeptides in Genetic Absence Epilepsy Rats from Strasbourg (GAERS) : a model for human generalized absence seizures [PDF]

open access: yes, 2010
Several studies have shown that neurotrophins and neuropeptides contribute to epileptogenesis but their impact on idiopathic generalized epilepsies is not yet elucidated.
Landweer, Svenja
core   +1 more source

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14 [PDF]

open access: yes, 2009
Childhood absence epilepsy (CAE) is an idiopathic generalised epilepsy (IGE) characterised by typical absence seizures manifested by transitory loss of awareness with 2.5–4 Hz spike-wave complexes on ictal EEG.
Sander, Thomas   +51 more
core   +1 more source

The S100B Protein in Epilepsy

open access: yes, 2023
Epilepsy is a chronic disease caused by an increased excitability of nerve cells in the brain, characterized by two or more unprovoked seizures, which can be attributed to genetic or acquired causes.
Ahmet Eren Seçen   +5 more
core   +1 more source

Epilepsy Spectrum Associated with PRRT2 Variants: Case Presentations [PDF]

open access: yes, 2023
Variations in the PRRT2 gene have been shown to cause a variety of diseases, including benign familial infantile epilepsy (BFIE) and paroxysmal kinesigenic dyskinesia (PKD).
Gözde Yeşı̇l Sayın   +4 more
core   +1 more source

Treatment priorities for idiopathic generalized epilepsy

open access: yesЭпилепсия и пароксизмальные состояния, 2021
The report presents the current principles of treatment of various types of epileptic seizures and forms of epilepsy. High efficacy and good tolerability in mono- and combination therapy with lamotrigine are shown, including its beneficial effects on ...
K. Yu. Mukhin
doaj   +1 more source

Electroencephalographic differences between WAG/Rij and GAERS rat models of absence epilepsy

open access: yes, 2010
The inbred Wistar Albino Glaxo Rats from Rijswijk (WAG/Rij) and the Genetic Absence Epilepsy Rats from Strasbourg (GAERS) are well-validated genetic models of absence epilepsy.
ONAT, FİLİZ
core   +3 more sources

Absence Epilepsy Psychosocial Outcome

open access: yesPediatric Neurology Briefs, 1997
The long-term psychosocial outcome in 56 patients aged 18 years or older with typical absence epilepsy and 61 controls with juvenile rheumatoid arthritis (JRA) was studied at the Royal University Hospital, Saskatoon, Saskatchewan, and the Izaak Walton ...
J Gordon Millichap
doaj   +1 more source

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