Showing results (441-450 of 3,396) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|July 16, 2002
Dose-dependent effect of individualized respiratory muscle training in children with Duchenne muscular dystrophyNathalie Topin, Stefan Matecki, Stephanie Le Bris, et al.
Neuromuscular Disorders : NMD|March 23, 2013
Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 geneNomazulu Dlamini, Dragana J Josifova, Simon M L Paine, et al.
Neuromuscular Disorders : NMD|January 3, 2012
Assessment of cardiac function in three mouse dystrophinopathies by magnetic resonance imagingIngrid E C Verhaart, Rianne J M van Duijn, Brigit den Adel, et al.
Neuromuscular Disorders : NMD|June 12, 2012
Evaluation of muscle oxygenation by near-infrared spectroscopy in patients with Becker muscular dystrophyE Allart, N Olivier, H Hovart, et al.
Neuromuscular Disorders : NMD|June 12, 2012
Winged scapula in patients with myotonic dystrophy type 1Tadanori Hamano, Tatsuro Mutoh, Mikio Hirayama, et al.
Neuromuscular Disorders : NMD|May 15, 2012
Single deletions in mitochondrial DNA--molecular mechanisms and disease phenotypes in clinical practiceR D S Pitceathly, S Rahman, M G Hanna
Neuromuscular Disorders : NMD|April 26, 2011
Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutationsYoshiaki Saito, Hirofumi Komaki, Ayako Hattori, et al.
Neuromuscular Disorders : NMD|April 26, 2011
King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) geneJames J Dowling, Suzanne Lillis, Kimberley Amburgey, et al.
Neuromuscular Disorders : NMD|May 17, 2011
Electrocardiographic abnormalities in very young Duchenne muscular dystrophy patients precede the onset of cardiac dysfunctionJeanne James, Kathleen Kinnett, Yu Wang, et al.
Pageof 340