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Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study
BACKGROUND: Two recombinant enzymes (agalsidase alfa 0.2 mg/kg/every other week and agalsidase beta 1.0 mg/kg/every other week) have been registered for the treatment of Fabry disease (FD), at equal high costs. An independent international initiative compared clinical and biochemical outcomes of the...
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| Vydáno v: | J Med Genet |
|---|---|
| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5931248/ https://ncbi.nlm.nih.gov/pubmed/29437868 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2017-104863 |
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