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An evidence-based review of the potential benefits of taliglucerase alfa in the treatment of patients with Gaucher disease

Gaucher disease is an inherited lysosomal storage disorder, characterized by deficient activity of glucocerebrosidase leading to storage of glucocerebroside in tissue macrophages. Type I disease, the most prevalent form, lacks central nervous system involvement but presents primarily with variable d...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijä: Hollak, Carla EM
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove Medical Press 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3363131/
https://ncbi.nlm.nih.gov/pubmed/22654679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CE.S20201
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