@article{1a8d8dcc47b245cbbf3e6fa1ac95b1c5,
title = "Muscle histology vs MRI in Duchenne muscular dystrophy",
abstract = "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 well-preserved muscle of recruited patients. The choice of the muscles to be studied and the role of noninvasive methods to assess muscle preservation therefore require further evaluation.",
keywords = "Adolescent, Child, Foot, Humans, Leg, Magnetic Resonance Imaging, Male, Muscle, Skeletal, Muscular Dystrophy, Duchenne, Adolescent, Child, Foot, Humans, Leg, Magnetic Resonance Imaging, Male, Muscle, Skeletal, Muscular Dystrophy, Duchenne",
author = "M. Kinali and V. Arechavala-Gomeza and S. Cirak and A. Glover and M. Guglieri and L. Feng and Hollingsworth, {K. G.} and D. Hunt and H. Jungbluth and Roper, {H. P.} and Quinlivan, {R. M.} and Gosalakkal, {J. A.} and S. Jayawant and A. Nadeau and L. Hughes-Carre and Manzur, {A. Y.} and Mercuri, {Eugenio Maria} and Morgan, {J. E.} and V. Straub and K. Bushby and C. Sewry and M. Rutherford and F. Muntoni",
year = "2011",
doi = "10.1212/WNL.0b013e318208811f",
language = "English",
volume = "76",
pages = "346--353",
journal = "Neurology",
issn = "0028-3878",
publisher = "Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL:
[email protected], INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320",
}