Infantile epileptic encephalopathy with a hyperkinetic movement disorder and hand stereotypies associated with a novel SCN1A mutation-Reference-Cited by-同舟云学术

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Infantile epileptic encephalopathy with a hyperkinetic movement disorder and hand stereotypies associated with a novel SCN1A mutation

Published:2014-06 Issue:2 Volume:16 Page:208-212
ISSN:1294-9361
Container-title:Epileptic Disorders
language:
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Author:

Ohashi Tsukasa,Akasaka Noriyuki,Kobayashi Yu,Magara Shinichi,Kawashima Hideshi,Matsumoto Naomichi,Saitsu Hirotomo,Tohyama Jun

Publisher

John Libbey Eurotext

Subject

Clinical Neurology,Neurology,General Medicine

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Novel Case of SCN1A Mutation Presenting as Hyperkinetic Movement Disorder;Annals of Indian Academy of Neurology;2024-04-12

2. Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis: A case report with a novel missense variant of SCN1A;Brain and Development;2023-10

3. Epileptic Channelopathies and Neuromuscular Disorders in Newborns: A Narrative Review;Cureus;2023-08-18

4. Genetic and clinical variations of developmental epileptic encephalopathies;Neurological Research;2023-02-02

5. Gain of function SCN1A disease‐causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication;Epilepsia;2023-01-26

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