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Clinical course of patients with Fabry disease who were switched from agalsidase-β to agalsidase-α

BACKGROUND: Between 2009 and 2012, there was a worldwide shortage of agalsidase-β for the treatment of Fabry disease. Therefore, alternative treatments were needed, including switching to a different enzyme-replacement therapy. PURPOSE: This is an ongoing observational study assessing the effects of...

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Detalhes bibliográficos
Main Authors: Tsuboi, Kazuya, Yamamoto, Hiroshi
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4189383/
https://ncbi.nlm.nih.gov/pubmed/24651606
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2014.28
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