Onset and progression of the Anderson–Fabry disease related cardiomyopathy-Reference-Cited by-同舟云学术

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Onset and progression of the Anderson–Fabry disease related cardiomyopathy

Published:2008-11 Issue:3 Volume:130 Page:367-373
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Kampmann Christoph,Linhart Ales,Baehner Frank,Palecek Tomas,Wiethoff Christiane M.,Miebach Elke,Whybra Catharina,Gal Andreas,Bultas Jan,Beck Michael

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference54 articles.

1. Fabry's disease: alpha-galactosidase deficiency;Kint;Science,1970

2. Enzymatic defect in Fabry's disease: ceramidetrihexosidase deficiency;Brady;N Engl J Med,1967

3. The early clinical phenotype of Fabry disease: a study on 35 European children and adolescents;Ries;Eur J Pediatr,2003

4. Natural history of Fabry renal disease: influence of a-galactosidase A activity and genetic mutations on clinical course;Branton;Medicine,2002

5. The heart in Fabry's disease. A histochemical and electron microscopic study;Ferrans;Am J Cardiol,1969

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