Twelve years of experience with miglustat in the treatment of type 1 Gaucher disease: The Spanish ZAGAL project
Author:
Funder
FEETEG
Actelion Pharmaceuticals Ltd
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference36 articles.
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3. Replacement therapy for inherited enzyme deficiency–macrophage-targeted glucocerebrosidase for Gaucher's disease;Barton;N. Engl. J. Med.,1991
4. Low-dose enzyme replacement therapy for Gaucher's disease: effects of age, sex, genotype, and clinical features on response to treatment;Zimran;Am. J. Med.,1994
5. The long-term international safety experience of imiglucerase therapy for Gaucher disease;Starzyk;Mol. Genet. Metab.,2007
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