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Neuromuscular Disorders : NMD|January 1, 1991
Role of persisting basement membrane in the reorganization of myofibres originating from myogenic cell grafts in the ratH S Alameddine, D Hantaï, M Dehaupas, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Type III glycogen storage disease: an adult case with mild disease but complete absence of debrancher proteinB Z Yang, C Stewart, J H Ding, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Imaging methods reveal unexpected patchy lesions in late onset distal myopathyB Udd, A Lamminen, H Somer
Neuromuscular Disorders : NMD|March 14, 2008
Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutationNicola Carboni, Marco Mura, Giovanni Marrosu, et al.
Neuromuscular Disorders : NMD|March 14, 2008
Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-CanadiansNicolas Dupré, Nicolas Chrestian, Jean-Pierre Bouchard, et al.
Neuromuscular Disorders : NMD|March 14, 2008
A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3)Maria Jedrzejowska, Barbara Ryniewicz, Dagmara Kabzińska, et al.
Neuromuscular Disorders : NMD|May 27, 2008
Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonismFederica Invernizzi, Sara Varanese, Astrid Thomas, et al.
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