Modeling the effect of enzyme replacement therapy on life-threatening complications in patients with Fabry disease

• Autori principali: V. I. Ignatyeva (Autore), S. V. Moiseev (Autore), N. M. Bulanov (Autore), E. A. Karovajkina (Autore), A S. Moiseev (Autore)
• Natura: Libro
• Pubblicazione: IRBIS LLC, 2019-01-01T00:00:00Z.
• Soggetti: article
• Accesso online: Connect to this object online.

Fabry disease (FD) is a severe lysosome storage disease caused by congenital deficiency of the enzyme α-galactosidase A and characterized by the risk of renal failure combined with cardiovascular and CNS complications. According to the currently available information, the early start of enzyme repla...