Mutations in the mitochondrial glutamate carrierSLC25A22in neonatal epileptic encephalopathy with suppression bursts-Reference-Cited by-同舟云学术

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Mutations in the mitochondrial glutamate carrierSLC25A22in neonatal epileptic encephalopathy with suppression bursts

Published:2009-08 Issue:2 Volume:76 Page:188-194
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Molinari F,Kaminska A,Fiermonte G,Boddaert N,Raas-Rothschild A,Plouin P,Palmieri L,Brunelle F,Palmieri F,Dulac O,Munnich A,Colleaux L

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01236.x/fullpdf

Reference24 articles.

1. Aicardi syndrome: a longitudinal clinical and electroencephalographic study;Ohtsuka;Epilepsia,1993

2. Infantile epileptic syndromes and metabolic etiologies;Vigevano;J Child Neurol,2002

3. Epileptic syndromes in infancy and childhood;Nabbout;Curr Opin Neurol,2008

4. Ohtahara syndrome: with special reference to its developmental aspects for differentiating from early myoclonic encephalopathy;Ohtahara;Epilepsy Res,2006

5. Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other?;Djukic;Epilepsy Res,2006

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