Enzyme replacement therapy for Anderson-Fabry disease: A complementary overview of a Cochrane publication through a linear regression and a pooled analysis of proportions from cohort studies

BACKGROUND: Anderson-Fabry disease (AFD) is an X-linked recessive inborn error of glycosphingolipid metabolism caused by a deficiency of alpha-galactosidase A. Renal failure, heart and cerebrovascular involvement reduce survival. A Cochrane review provided little evidence on the use of enzyme replac...

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Detalles Bibliográficos
Autores principales: El Dib, Regina, Gomaa, Huda, Ortiz, Alberto, Politei, Juan, Kapoor, Anil, Barreto, Fellype
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351840/
https://www.ncbi.nlm.nih.gov/pubmed/28296917
http://dx.doi.org/10.1371/journal.pone.0173358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351840/
https://www.ncbi.nlm.nih.gov/pubmed/28296917
http://dx.doi.org/10.1371/journal.pone.0173358

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