Muscle histology vs MRI in Duchenne muscular dystrophy

OBJECTIVE: There are currently no effective treatments to halt the muscle breakdown in Duchenne muscular dystrophy (DMD), although genetic-based clinical trials are being piloted. Most of these trials have as an endpoint the restoration of dystrophin in muscle fibers, hence requiring sufficiently we...

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Bibliografiset tiedot
Päätekijät: Kinali, M., Arechavala-Gomeza, V., Cirak, S., Glover, A., Guglieri, M., Feng, L., Hollingsworth, K.G., Hunt, D., Jungbluth, H., Roper, H.P., Quinlivan, R.M., Gosalakkal, J.A., Jayawant, S., Nadeau, A., Hughes-Carre, L., Manzur, A.Y., Mercuri, E., Morgan, J.E., Straub, V., Bushby, K., Sewry, C., Rutherford, M., Muntoni, F.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Lippincott Williams & Wilkins 2011
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Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3034418/
https://ncbi.nlm.nih.gov/pubmed/21263136
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e318208811f
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