[HTML][HTML] Febrile seizures: an overview
AKC Leung, KL Hon, TNH Leung - Drugs in context, 2018 - ncbi.nlm.nih.gov
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Developmental and epileptic encephalopathies
Developmental and epileptic encephalopathies, the most severe group of epilepsies, are
characterized by seizures and frequent epileptiform activity associated with developmental …
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 …
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
Abstract In 2017, the International League Against Epilepsy (ILAE) Classification of
Epilepsies described the “genetic generalized epilepsies”(GGEs), which contained the …
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
Epilepsy syndromes have been recognized for> 50 years, as distinct electroclinical
phenotypes with therapeutic and prognostic implications. Nonetheless, no formally accepted …
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 …
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 …
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 …
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 …
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 …
infection, hypoglycaemia, or an acute electrolyte imbalance, occur in children between six …