Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry
Author:
Funder
Sanofi Genzyme
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference43 articles.
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2. Alpha-galactosidase A deficiency: Fabry disease;Desnick,2001
3. Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry;Wilcox;Mol. Genet. Metab.,2008
4. Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy;Schiffmann;Nephrol. Dial. Transplant.,2009
5. Cardiovascular events in patients with Fabry disease natural history data from the Fabry registry;Patel;J. Am. Coll. Cardiol.,2011
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