Use of imaging biomarkers to assess perfusion and glucose metabolism in the skeletal muscle of dystrophic mice

BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disease that affects 1 in 3500 boys. The disease is characterized by progressive muscle degeneration that results from mutations in or loss of the cytoskeletal protein, dystrophin, from the glycoprotein membrane complex, thus in...

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Detalles Bibliográficos
Autores principales: Ahmad, Nabeel, Welch, Ian, Grange, Robert, Hadway, Jennifer, Dhanvantari, Savita, Hill, David, Lee, Ting-Yim, Hoffman, Lisa M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141608/
https://www.ncbi.nlm.nih.gov/pubmed/21639930
http://dx.doi.org/10.1186/1471-2474-12-127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141608/
https://www.ncbi.nlm.nih.gov/pubmed/21639930
http://dx.doi.org/10.1186/1471-2474-12-127

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