Anderson-Fabry disease (AFD) is a rare genetic lysosomal storage disorder caused by deficient activity of the enzyme α-galactosidase A, leading to progressive intracellular accumulation of neutral glycosphingolipids in different organs, including the heart.
Graziani, F., Lillo, R., Panaioli, E., Spagnoletti, G., Bruno, I., Leccisotti, L., Marano, R., Manna, R., Crea, F., Massive Coronary Microvascular Dysfunction in Severe Anderson-Fabry Disease Cardiomyopathy, <<CIRCULATION. CARDIOVASCULAR IMAGING>>, 2019; 12 (6): N/A-e009104. [doi:10.1161/CIRCIMAGING.119.009104] [http://hdl.handle.net/10807/148144]
Massive Coronary Microvascular Dysfunction in Severe Anderson-Fabry Disease Cardiomyopathy
Graziani, Francesca;Lillo, Rosa;Panaioli, Elena;Spagnoletti, Gionata;Bruno, Isabella;Leccisotti, Lucia;Marano, Riccardo;Manna, Raffaele;Crea, Filippo
2019
Abstract
Anderson-Fabry disease (AFD) is a rare genetic lysosomal storage disorder caused by deficient activity of the enzyme α-galactosidase A, leading to progressive intracellular accumulation of neutral glycosphingolipids in different organs, including the heart.
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