Enhanced Endothelium-Dependent Vasodilation in Fabry Disease

BACKGROUND AND PURPOSE: Fabry disease is an X-linked lysosomal storage disease secondary to deficiency of α-galactosidase A with resulting glycolipid accumulation, particularly globotriaosylceramide in arterial smooth muscle and endothelial cells. A systemic vasculopathy, including early-onset strok...

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Publicat a:Stroke
Autors principals: Altarescu, Gheona, Moore, David F., Pursley, Randall, Campia, Umberto, Goldstein, Seth, Bryant, Melissa, Panza, Julio A., Schiffmann, Raphael
Format: Artigo
Idioma:Inglês
Publicat: 2001
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4770460/
https://ncbi.nlm.nih.gov/pubmed/11441201
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