Myoclonic Absence Seizures in Dravet Syndrome
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health
Reference15 articles.
1. The core Dravet syndrome phenotype;Dravet;Epilepsia,2011
2. An unexpected EEG course in Dravet syndrome;Nabbout;Epilepsy Res,2008
3. Molecular genetics of Dravet syndrome;De Jonghe;Dev Med Child Neurol,2011
4. Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms;Wallace;Neurology,2003
5. Epilepsy with myoclonic absences;Genton;CNS Drugs,2006
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1. Atypical absence seizures and gene variants: A gene-based review of etiology, electro-clinical features, and associated epilepsy syndrome;Epilepsy & Behavior;2024-02
2. Genetics of Dravet Syndrome and its Targeted Therapy by Nanomedicine: A Roadmap for Future Treatment of Drug Resistant Seizures;Current Molecular Pharmacology;2023-06
3. Dravet syndrome: Advances in etiology, clinical presentation, and treatment;Epilepsy Research;2022-12
4. A case of Dravet syndrome with focal cortical myoclonus;Acta Epileptologica;2022-09-06
5. International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions;Epilepsia;2022-05-03
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