Showing results (1841-1850 of 3,403) with videos related to

Sort By:
Pageof 341
Neuromuscular Disorders : NMD|June 26, 1999
Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotypeJ R Yates, J Bagshaw, V M Aksmanovic, et al.
Neuromuscular Disorders : NMD|June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3A Driss, R Amouri, C Ben Hamida, et al.
Neuromuscular Disorders : NMD|June 6, 2000
A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophyS A Hyde, I FlŁytrup, S Glent, et al.
Neuromuscular Disorders : NMD|June 6, 2000
Minicore myopathy in children: a clinical and histopathological study of 19 casesH Jungbluth, C Sewry, S C Brown, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin statusE Mercuri, J Gruter-Andrew, J Philpot, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Prominent inflammatory changes on muscle biopsy in patients with Miyoshi myopathyJ Rowin, M N Meriggioli, E J Cochran, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Distribution of ten laminin chains in dystrophic and regenerating musclesB L Patton, A M Connoll, P T Martin, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
Pageof 341