Fabry Disease (α-Galactosidase A Deficiency)

Author:

Desnick R.J.

Publisher

Elsevier

Reference146 articles.

1. Effect of genetic modifiers on cerebral lesions in Fabry disease;Altarescu;Neurology,2005

2. Gastrointestinal symptoms and delayed gastric emptying in Fabry’s disease: response to metoclopramide;Argoff;Nucl. Med. Commun.,1998

3. 22 novel mutations in the α-galactosidase A gene and genotype/phenotype correlations including mild hemizygotes and severely affected heterozygotes;Ashton-Prolla;J. Invest. Med.,2000

4. Gastrointestinal manifestations of Fabry disease: Clinical response to enzyme replacement therapy;Banikazemi;Mol. Genet. Metab.,2005

5. Fabry’s disease. Light and electron microscopic cardiac findings 12 years after successful kidney transplantation;Bannwart;Schweiz. Med. Wochenschr.,1982

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