Author:
Germain Dominique P.,Waldek Stephen,Banikazemi Maryam,Bushinsky David A.,Charrow Joel,Desnick Robert J.,Lee Philip,Loew Thomas,Vedder Anouk C.,Abichandani Rekha,Wilcox William R.,Guffon Nathalie
Publisher
American Society of Nephrology (ASN)
Subject
Nephrology,General Medicine
Reference18 articles.
1. Barth P: Disorders of sphingolipid metabolism. In: Inborn Metabolic Diseases, edited by Fernandes J, Saudubray J-M, Van den Berghe G, New York, Springer, 2000 , pp 401 –412
2. Desnick R, Ioannou Y, Eng C: Alpha-galactosidase A deficiency: Fabry disease. In: The Metabolic and Molecular Basis of Inherited Disease, edited by Scriver C, Sly W, Childs B, Beaudet A, Valle D, Kinzler A, Vogelstein B, New York, McGraw Hill, 2001 , pp 3733 –3774
3. Enzyme replacement therapy for Fabry disease: lessons from two α-galactosidase A orphan products and one FDA approval
4. Natural history of Fabry disease in females in the Fabry Outcome Survey
5. Cardiac manifestations of Anderson–Fabry disease in heterozygous females
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