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5PSQ-010 Efficacy and safety of agalsidase alfa in fabry disease

BACKGROUND: Fabry disease is included within the lipid deposition diseases that occur due to mutations in the gene that encodes the α-galactosidase enzyme. As a consequence, a fatty substance, globotriosilceramide (GL-3), is responsible for the illness of different organs such as the heart, eyes or...

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Dettagli Bibliografici
Pubblicato in:Eur J Hosp Pharm
Autori principali: Rosa, V González, Gil, E Atienza, Torres, MI Sierra, Rascón, M Zaragoza, Alonso, M Pajares
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Group 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7535223/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ejhpharm-2018-eahpconf.364
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