Anderson-Fabry Disease: From Endothelial Dysfunction to Emerging Therapies

• Váldodahkkit: Cosimo A. Stamerra (Dahkki), Rita Del Pinto (Dahkki), Paolo di Giosia (Dahkki), Claudio Ferri (Dahkki), Amirhossein Sahebkar (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Hindawi Limited, 2021-01-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

The Anderson-Fabry disease is a rare, X-linked, multisystemic, progressive lysosomal storage disease caused by α-galactosidase A total or partial deficiency. The resulting syndrome is mainly characterized by early-onset autonomic neuropathy and life-threatening multiorgan involvement, including rena...