Histoire naturelle des leucodystrophies avec mutation EIF2B : étude rétrospective multicentrique de 24 cas adultes-Reference-Cited by-同舟云学术

Histoire naturelle des leucodystrophies avec mutation EIF2B : étude rétrospective multicentrique de 24 cas adultes

Published:2011-11 Issue:11 Volume:167 Page:802-811
ISSN:0035-3787
Container-title:Revue Neurologique
language:fr
Short-container-title:Revue Neurologique

Author:

Carra-Dalliere C.,Horzinski L.,Ayrignac X.,Vukusic S.,Rodriguez D.,Mauguiere F.,Peter L.,Goizet C.,Bouhour F.,Denier C.,Confavreux C.,Obadia M.,Blanc F.,de Seze J.,Sedel F.,Guennoc A.-M.,Sartori E.,Laplaud D.,Antoine J.-C.,Fogli A.,Boespflug-Tanguy O.,Labauge P.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference24 articles.

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2. Ovarian failure related to eukaryotic initiation factor 2B mutations;Fogli;Am J Hum Genet,2003

3. The effect of genotype on the natural history of eIF2B-related leukodystrophies;Fogli;Neurology,2004

4. Fatal infantile leukodystrophy. A severe variant of CACH/VWM syndrome, allelic to chromosome 3q27;Francalanci;Neurology,2001

5. Steroids and glial cell function;Garcia-Segura;Glia,2006

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