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Taliglucerase alfa: safety and efficacy across 6 clinical studies in adults and children with Gaucher disease
Taliglucerase alfa is an enzyme replacement therapy (ERT) approved for treatment of adult and paediatric patients with Type 1 Gaucher disease (GD) in several countries and the first plant cell–expressed recombinant therapeutic protein approved by the US Food and Drug Administration for humans. Here,...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Orphanet J Rare Dis |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2018
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5824466/ https://ncbi.nlm.nih.gov/pubmed/29471850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-018-0776-8 |
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