[HTML][HTML] Febrile seizures: an overview

AKC Leung, KL Hon, TNH Leung - Drugs in context, 2018 - ncbi.nlm.nih.gov
Febrile seizures: an overview - PMC Back to Top Skip to main content NIH NLM Logo Access
keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation Preview …

Developmental and epileptic encephalopathies

IE Scheffer, S Zuberi, HC Mefford, R Guerrini… - Nature Reviews …, 2024 - nature.com
Developmental and epileptic encephalopathies, the most severe group of epilepsies, are
characterized by seizures and frequent epileptiform activity associated with developmental …

ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions

SM Zuberi, E Wirrell, E Yozawitz, JM Wilmshurst… - …, 2022 - Wiley Online Library
Abstract The International League Against Epilepsy (ILAE) Task Force on Nosology and
Definitions proposes a classification and definition of epilepsy syndromes in the neonate …

ILAE definition of the idiopathic generalized epilepsy syndromes: position statement by the ILAE task force on nosology and definitions

E Hirsch, J French, IE Scheffer, A Bogacz, T Alsaadi… - …, 2022 - Wiley Online Library
Abstract In 2017, the International League Against Epilepsy (ILAE) Classification of
Epilepsies described the “genetic generalized epilepsies”(GGEs), which contained the …

Methodology for classification and definition of epilepsy syndromes with list of syndromes: report of the ILAE Task Force on Nosology and Definitions

EC Wirrell, R Nabbout, IE Scheffer, T Alsaadi… - …, 2022 - Wiley Online Library
Epilepsy syndromes have been recognized for> 50 years, as distinct electroclinical
phenotypes with therapeutic and prognostic implications. Nonetheless, no formally accepted …

The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications

A Brunklaus, T Brünger, T Feng, C Fons, A Lehikoinen… - Brain, 2022 - academic.oup.com
Brain voltage-gated sodium channel NaV1. 1 (SCN1A) loss-of-function variants cause the
severe epilepsy Dravet syndrome, as well as milder phenotypes associated with genetic …

The genetics of epilepsy

P Perucca, M Bahlo, SF Berkovic - Annual review of genomics …, 2020 - annualreviews.org
Epilepsy encompasses a group of heterogeneous brain diseases that affect more than 50
million people worldwide. Epilepsy may have discernible structural, infectious, metabolic …

SCN1A‐related phenotypes: epilepsy and beyond

IE Scheffer, R Nabbout - Epilepsia, 2019 - Wiley Online Library
SCN1A, encoding the alpha 1 subunit of the sodium channel, is associated with several
epilepsy syndromes and a range of other diseases. SCN1A represents the archetypal …

Deciphering the concepts behind “Epileptic encephalopathy” and “Developmental and epileptic encephalopathy”

IE Scheffer, J Liao - European journal of paediatric neurology, 2020 - Elsevier
The recent introduction of the term 'developmental and epileptic encephalopathy'by the
International League Against Epilepsy has added another conceptual layer to …

Management of pediatric febrile seizures

D Laino, E Mencaroni, S Esposito - International journal of environmental …, 2018 - mdpi.com
Febrile seizures (FS), events associated with a fever in the absence of an intracranial
infection, hypoglycaemia, or an acute electrolyte imbalance, occur in children between six …