A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients-Reference-Cited by-同舟云学术

A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients

Published:2011-02 Issue:2 Volume:33 Page:131-139
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Kraoua Ichraf,Sedel Frédéric,Caillaud Catherine,Froissart Roseline,Stirnemann Jérôme,Chaurand Guy,Flodrops Hugues,Tari Saliha,Gourfinkel-An Isabelle,Mathieu Sophie,Belmatoug Nadia,Billette de Villemeur Thierry,Mignot Cyril

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference31 articles.

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3. Hydrops fetalis: lysosomal storage disorders in extremis;Stone;Adv Pediatr,1999

4. Type 2 Gaucher disease: 15 new cases and review of the literature;Mignot;Brain Dev,2006

5. New perspectives in type 2 Gaucher disease;Sidransky;Adv Pediatr,1997

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