The spectrum of SCN1A-related infantile epileptic encephalopathies-Reference-Cited by-同舟云学术

The spectrum of SCN1A-related infantile epileptic encephalopathies

Published:2007-03-01 Issue:3 Volume:130 Page:843-852
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Harkin Louise A.,McMahon Jacinta M.,Iona Xenia,Dibbens Leanne,Pelekanos James T.,Zuberi Sameer M.,Sadleir Lynette G.,Andermann Eva,Gill Deepak,Farrell Kevin,Connolly Mary,Stanley Thorsten,Harbord Michael,Andermann Frederick,Wang Jing,Batish Sat Dev,Jones Jeffrey G.,Seltzer William K.,Gardner Alison,Sutherland Grant,Berkovic Samuel F.,Mulley John C.,Scheffer Ingrid E.,

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/130/3/843/23665428/awm002.pdf

Reference56 articles.

1. The Lennox-Gastaut syndrome;Beaumanoir,2005

2. De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study;Berkovic;Lancet Neurol,2006

3. Clinical and electroencephalographic correlates of the multiple independent spike foci pattern in children;Blume;Ann Neurol,1978

4. Multifocal independent epileptiform discharges in children: ictal correlates and surgical therapy;Burnstine;Neurology,1991

5. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001

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