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Spotlight on taliglucerase alfa in the treatment of pediatric patients with type 1 Gaucher disease

Gaucher disease (GD) is a heritable storage disorder caused by functional defects of the lysosomal acid β-glucosidase and the accumulation of glucosylceramide within macrophages, resulting in multiple organ dysfunction. There are three commercially available enzyme replacement therapy (ERT) products...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Pediatric Health Med Ther
Egile Nagusiak: Gupta, Punita, Pastores, Gregory M
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Dove Medical Press 2017
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5774592/
https://ncbi.nlm.nih.gov/pubmed/29388611
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PHMT.S93634
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