Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials-Reference-Cited by-同舟云学术

Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials

Published:2021-08-02 Issue:9 Volume:62 Page:2205-2217
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Li Wenhui¹²,Schneider Amy L.²^ORCID,Scheffer Ingrid E.²³⁴^ORCID

Affiliation:

1. Children's Hospital of Fudan University Shanghai China

2. Department of Medicine Austin Health Epilepsy Research Centre University of Melbourne Heidelberg Vic. Australia

3. Florey Institute of Neuroscience and Mental Health Heidelberg Vic. Australia

4. Murdoch Children's Research Institute and Department of Paediatrics Royal Children's Hospital University of Melbourne Parkville Vic. Australia

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.17015

Reference38 articles.

1. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

2. De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

3. The genetic landscape of the epileptic encephalopathies of infancy and childhood

4. Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome;Han Z;Sci Transl Med,2020

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