Natural history of the cerebrovascular complications of Fabry disease

Author:

Mehta A,Ginsberg L

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology, and Child Health

Reference22 articles.

1. Desnick, R and Ioannou, Y and Eng, C.(2001) α-Galactosidase A deficiency: Fabry disease. In The metabolic and molecular basis of inherited disease8th ed. ( pp. 3733 - 74 ). New York : McGraw-Hill.

2. Mehta, A. (2002) New developments in the management of Anderson–Fabry disease QJM, 95, pp. 647 - 53.

3. Altarescu, G and Moore, D and Pursley, R and Campia, U and Goldstein, S and Bryant, M and (2001) Enhanced endothelium-dependent vasodilation in Fabry disease Stroke, 32, pp. 1559 - 62.

4. Meikle, P and Hopwood, J and Clague, A and Carey, W. (1999) Prevalence of lysosomal storage disorders JAMA, 281, pp. 249 - 54.

5. Desnick, R and Bishop, D.(1989) Fabry disease: α-galactosidase deficiency and Schindler disease: α-N-acetylgalactosaminidase deficiency. In The metabolic and molecular basis of inherited disease6th ed. ( pp. 1751 - 96 ). New York : McGraw–Hill.

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