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Switching from imiglucerase to miglustat for the treatment of French patients with Gaucher disease type 1: a case series

INTRODUCTION: Gaucher disease is caused by a deficiency of the enzyme β-glucocerebrosidase. Treatment with enzyme replacement therapy has been available for the past two decades but, although effective, enzyme replacement therapy can be delivered only by intravenous infusion every other week. The or...

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Detalhes bibliográficos
Publicado no:J Med Case Rep
Main Authors: Serratrice, Christine, Swiader, Laure, Serratrice, Jacques
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4488047/
https://ncbi.nlm.nih.gov/pubmed/26100396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-015-0617-5
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