Prognostic Indicators of Renal Disease Progression in Adults with Fabry Disease: Natural History Data from the Fabry Registry-Reference-Cited by-同舟云学术

Prognostic Indicators of Renal Disease Progression in Adults with Fabry Disease: Natural History Data from the Fabry Registry

Published:2010-09-02 Issue:12 Volume:5 Page:2220-2228
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Wanner Christoph,Oliveira João P.,Ortiz Alberto,Mauer Michael,Germain Dominique P.,Linthorst Gabor E.,Serra Andreas L.,Maródi László,Mignani Renzo,Cianciaruso Bruno,Vujkovac Bojan,Lemay Roberta,Beitner-Johnson Dana,Waldek Stephen,Warnock David G.

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference31 articles.

1. Desnick RJ Ioannou YA Eng CM : Alpha-galactosidase A deficiency: Fabry disease. In: The Metabolic Bases of Inherited Disease, 8th ed., edited by Scriver C Beaudet A Sly W Valle D New York, McGraw-Hill, 2001, pp 3733–3774

2. Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN)

3. Sustained, Long-Term Renal Stabilization After 54 Months of Agalsidase β Therapy in Patients with Fabry Disease

4. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy

5. Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy

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