The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients-Reference-Cited by-同舟云学术

The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients

Published:2012 Issue:1 Volume:7 Page:77
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Stirnemann Jérôme,Vigan Marie,Hamroun Dalil,Heraoui Djazia,Rossi-Semerano Linda,Berger Marc G,Rose Christian,Camou Fabrice,de Roux-Serratrice Christine,Grosbois Bernard,Kaminsky Pierre,Robert Alain,Caillaud Catherine,Froissart Roselyne,Levade Thierry,Masseau Agathe,Mignot Cyril,Sedel Frédéric,Dobbelaere Dries,Vanier Marie T,Valayanopoulos Vassili,Fain Olivier,Fantin Bruno,de Villemeur Thierry,Mentré France,Belmatoug Nadia

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference40 articles.

1. Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's disease

2. Lysosomal Storage Disorders in the Newborn

3. Immunochemical Characterization of Two Activator Proteins Stimulating Enzymic Sphingomyelin Degradation in vitro Absence of One of them in a Human Gaucher Disease Variant

4. Recent clinical progress in Gaucher disease

5. Gaucher Disease

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