Inherited restrictive cardiomyopathy in a 74-year-old woman: A case of Fabry's disease
- 1 January 1995
- journal article
- case report
- Published by Elsevier in American Heart Journal
- Vol. 129 (1), 199-202
- https://doi.org/10.1016/0002-8703(95)90062-4
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Fabry disease: Detection of 13-bp deletion in ?-galactosidase a gene and its application to gene diagnosis of heterozygotesAnnals of Neurology, 1991
- An Atypical Variant of Fabry's Disease with Manifestations Confined to the MyocardiumNew England Journal of Medicine, 1991
- Endomyocardial Biopsy in Patients with Unexplained Congestive Heart FailureAnnals of Internal Medicine, 1988
- Cardiac valvular anomalies in Fabry disease. Clinical, morphologic, and biochemical studies.Circulation, 1976
- Replacement Therapy for Inherited Enzyme DeficiencyNew England Journal of Medicine, 1973
- Angiokeratoma corporis diffusum universale (Fabry's disease) in female subjectsAmerican Journal Of Medicine, 1967