Dravet syndrome - considerable delay in making the diagnosis
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.2011.01609.x/fullpdf
Reference19 articles.
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2. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009;Berg;Epilepsia,2010
3. Polymorphic epilepsy in children. Study of 12 patients;Lambarri San Martin;An Esp Pediatr,1997
4. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy in infancy;Claes;Am J Hum Genet,2001
5. Spectrum of SCN1A mutations in severe myoclonic epilepsy in infancy;Nabbout;Neurology,2003
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3. A Retrospective Study of the Profile and Outcome of Children with Dravet Syndrome in a Tertiary Care Hospital of Southern India;Journal of Pediatric Epilepsy;2022-11-21
4. The role of vagus nerve stimulation in genetic etiologies of drug-resistant epilepsy: a meta-analysis;Journal of Neurosurgery: Pediatrics;2022-06-01
5. Genetics and clinical correlation of Dravet syndrome and its mimics – experience of a tertiary center in Taiwan;Pediatrics & Neonatology;2021-09
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