Vasculopathy in patients with Fabry disease: Current controversies and research directions

Author:

Rombach S.M.,Twickler Th.B.,Aerts J.M.F.G.,Linthorst G.E.,Wijburg F.A.,Hollak C.E.M.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference113 articles.

1. Enzymatic defect in Fabry’s disease. Ceramidetrihexosidase deficiency;Brady;N. Engl. J. Med.,1967

2. Fabry’s disease: alpha-galactosidase deficiency;Kint;Science,1970

3. R.J. Desnick, Y.A. Ioannou, M.E. Eng, α-Galactosidase A deficiency: Fabry disease. In: C.R. Scriver, A.L.S.W. Beaudet, D. Valle (Eds.), The metabolic and molecular bases of inherited disease, eighth ed., McGraw-Hill, New York, 2001, pp. 3733–3774.

4. The cerebral vasculopathy of Fabry disease;Moore;J. Neurol. Sci.,2007

5. Fabry disease;Schiffmann;Pharmacol. Ther.,2009

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