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Neuromuscular Disorders : NMD|December 7, 2007
Dropped head syndrome as prominent clinical feature in MuSK-positive Myasthenia Gravis with thymus hyperplasiaKonstantinos Spengos, Sofia Vassilopoulou, Georgios Papadimas, et al.Neuromuscular Disorders : NMD|January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindredDavid O Hutchinson, Amanda Charlton, Nigel G Laing, et al.Neuromuscular Disorders : NMD|January 24, 2006
Health related quality of life in people with hereditary neuromuscular diseases: an investigation of test-retest agreement with comparison between two generic questionnaires, the Nottingham health profile and the short form-36 itemsF Boyer, I Morrone, I Laffont, et al.Neuromuscular Disorders : NMD|March 18, 2006
First evaluation of the potential effectiveness in muscular dystrophy of a novel chimeric compound, BN 82270, acting as calpain-inhibitor and anti-oxidantRosa Burdi, Maria Paola Didonna, Bernadette Pignol, et al.Neuromuscular Disorders : NMD|February 21, 2006
Wheelchair economy class syndrome in amyotrophic lateral sclerosisFumiharu Kimura, Simon Ishida, Daisuke Furutama, et al.Neuromuscular Disorders : NMD|February 21, 2006
Improvement in survival and muscle function in an mdx/utrn(-/-) double mutant mouse using a human retinal dystrophin transgeneRoger Gaedigk, Douglas J Law, Kathleen M Fitzgerald-Gustafson, et al.Neuromuscular Disorders : NMD|January 3, 2026
The complexity of dystrophin transcription and processing: implications of transcript imbalance on dystrophin gene targeting strategiesRachele Rossi, Annemieke Aartsma-Rus, Francesco Muntoni, et al.Neuromuscular Disorders : NMD|November 26, 1998
Impaired aerobic glycolysis in muscle phosphofructokinase deficiency results in biphasic post-exercise phosphocreatine recovery in 31P magnetic resonance spectroscopyT Grehl, K Müller, M Vorgerd, et al.Neuromuscular Disorders : NMD|October 1, 1996
Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutationT Tyni, A Majander, H Kalimo, et al.Neuromuscular Disorders : NMD|October 1, 1996
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophyP Melacini, A Vianello, C Villanova, et al.Pageof 340