Bone density in patients with late onset Pompe disease

BACKGROUND: Pompe disease is an inherited metabolic disorder characterized by α-glycosidase deficiency, which leads to lysosomal glycogen accumulation in many different tissues. The infantile form is the most severe with a rapidly fatal outcome, while the late onset form has a greater phenotypic var...

Descripción completa

Detalles Bibliográficos
Autores principales: Papadimas, George, Terzis, Gerassimos, Papadopoulos, Constantinos, Areovimata, Anna, Spengos, Konstantinos, Kavouras, Stavros, Manta, Panagiota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693639/
https://www.ncbi.nlm.nih.gov/pubmed/23843830
http://dx.doi.org/10.5812/ijem.4967

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693639/
https://www.ncbi.nlm.nih.gov/pubmed/23843830
http://dx.doi.org/10.5812/ijem.4967

Ejemplares similares