Endothelial markers and homocysteine in patients with classic Fabry disease
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2002.tb03112.x/fullpdf
Reference23 articles.
1. Enzymatic defect in Fabry's disease: ceramidetrihexosidase deficiency;Brady;N Engl J Med,1967
2. Clinical features of and recent advances in therapy for Fabry disease;Brady;J Am Med Assoc,2000
3. Fabry disease (α-galactosidase A deficiency): pathophysiology, clinical signs and genetic aspects;Germain;J Soc Biol,2002
4. Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease;Schiffmann;Proc Natl Acad Sci U S A,2000
5. A phase 1/2 clinical trial of enzyme replacement in Fabry disease: pharmacokinetic, substrate clearance, and safety studies;Eng;Am J Hum Genet,2001
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