Functional Electrical Stimulation: A Possible Strategy to Improve Muscle Function in Central Core Disease?

Central Core Disease (CCD) is a congenital myopathy characterized by presence of amorphous central areas (or cores) lacking glycolytic/oxidative enzymes and mitochondria in skeletal muscle fibers. Most CCD families are linked to mutations in ryanodine receptor type-1 (RYR1), the gene encoding for th...

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Detalles Bibliográficos
Autores principales: Iodice, Pierpaolo, Boncompagni, Simona, Pietrangelo, Laura, Galli, Lucia, Pierantozzi, Enrico, Rossi, Daniela, Fusella, Aurora, Caulo, Massimo, Kern, Helmut, Sorrentino, Vincenzo, Protasi, Feliciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548841/
https://www.ncbi.nlm.nih.gov/pubmed/31191425
http://dx.doi.org/10.3389/fneur.2019.00479

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548841/
https://www.ncbi.nlm.nih.gov/pubmed/31191425
http://dx.doi.org/10.3389/fneur.2019.00479

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