Skeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patients

Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine extensor muscle dystrophy, due to defective lysosomal acid maltase. With the exception of the few patients who present with a dramatically accelerated clinical course, standard diagnostic imaging fail to detect a...

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Detalles Bibliográficos
Autores principales: Carlier, Pierre G., Azzabou, Noura, de Sousa, Paulo Loureiro, Hicks, Arnaud, Boisserie, Jean-Marc, Amadon, Alexis, Carlier, Robert-Yves, Wary, Claire, Orlikowski, David, Laforêt, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2015
Materias:
Glycogenoses
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432102/
https://www.ncbi.nlm.nih.gov/pubmed/25749708
http://dx.doi.org/10.1007/s10545-015-9825-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432102/
https://www.ncbi.nlm.nih.gov/pubmed/25749708
http://dx.doi.org/10.1007/s10545-015-9825-9

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