Survival and associated factors in 268 adults with Pompe disease prior to treatment with enzyme replacement therapy

BACKGROUND: Pompe disease is a rare lysosomal storage disorder characterized by muscle weakness and wasting. The majority of adult patients have slowly progressive disease, which gradually impairs mobility and respiratory function and may lead to wheelchair and ventilator dependency. It is as yet un...

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Detalles Bibliográficos
Autores principales: Güngör, Deniz, de Vries, Juna M, Hop, Wim CJ, Reuser, Arnold JJ, van Doorn, Pieter A, van der Ploeg, Ans T, Hagemans, Marloes LC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135500/
https://www.ncbi.nlm.nih.gov/pubmed/21631931
http://dx.doi.org/10.1186/1750-1172-6-34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135500/
https://www.ncbi.nlm.nih.gov/pubmed/21631931
http://dx.doi.org/10.1186/1750-1172-6-34

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