Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patients
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2003.630107.x/fullpdf
Reference23 articles.
1. Fabry disease (α-galactosidase A deficiency): pathophysiology, clinical signs and genetics aspects;Germain;J Soc Biol,2002
2. Prevalence of lysosomal storage disorders;Meikle;J Am Med Assoc,1999
3. Safety and efficacy of recombinant human α-galactosidase replacement therapy in Fabry's disease;Eng;New Engl J Med,2001
4. Enzyme replacement therapy in Fabry disease: a randomized controlled trial;Schiffmann;J Am Med Assoc,2001
5. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings;Devereux;Am J Cardiol,1986
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