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Alglucosidase alfa: Long term use in the treatment of patients with Pompe disease

Pompe disease is a lysosomal storage disorder characterized by muscle weakness and cardiomyopathy. It shows a broad variability regarding the clinical severity as well as the age of onset. In the past, two different recombinant enzyme preparations have been developed for the treatment of Pompe patie...

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Bibliografiska uppgifter
Huvudupphovsman: Beck, Michael
Materialtyp: Artigo
Språk:Inglês
Publicerad: Dove Medical Press 2009
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2754091/
https://ncbi.nlm.nih.gov/pubmed/19816575
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