Cardiac magnetic resonance in Fabry disease

Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by deficient a-galactosidase A activity that leads to an accumulation of glycolipids, mainly globotriaosylceramide (Gb3) and globotriaosylsphingosine, in affected tissues, including the heart. Cardiovascular involvemen...

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Detalles Bibliográficos
Autores principales: Lanzillo, Chiara, Fedele, Elisa, Martino, Annamaria, Ferrazza, Alessandro, Fusco, Armando, Silvetti, Elisa, Canestrelli, Stefano, Romeo, Fabiana, Canali, Emanuele, De Luca, Lucia, Golia, Paolo, Crescenzi, Cinzia, Stefanini, Matteo, Calò, Leonardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
PLACE 2022 Supplement Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132562/
https://www.ncbi.nlm.nih.gov/pubmed/37125302
http://dx.doi.org/10.1093/eurheartjsupp/suad045

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132562/
https://www.ncbi.nlm.nih.gov/pubmed/37125302
http://dx.doi.org/10.1093/eurheartjsupp/suad045

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