SCN1A Mutation Analysis in Myoclonic Astatic Epilepsy and Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures-Reference-Cited by-同舟云学术

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SCN1A Mutation Analysis in Myoclonic Astatic Epilepsy and Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures

Published:2005-06 Issue:3 Volume:36 Page:210-213
ISSN:0174-304X
Container-title:Neuropediatrics
language:de
Short-container-title:Neuropediatrics

Author:

Ebach K.,Joos H.,Doose H.,Stephani U.,Kurlemann G.,Fiedler B.,Hahn A.,Hauser E.,Hundt K.,Holthausen H.,Müller U.,Neubauer B. A.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2005-865607.pdf

Cited by 49 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. Genetic mechanisms in generalized epilepsies;Acta Epileptologica;2023-03-10

2. SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis;Frontiers in Neurology;2021-12-24

3. The relation of etiology based on the 2017 ILAE classification to the effectiveness of the ketogenic diet in drug‐resistant epilepsy in childhood;Epilepsia;2021-08-28

4. New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies;Epilepsy & Behavior;2021-08

5. Genetics and gene therapy in Dravet syndrome;Epilepsy & Behavior;2021-05

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