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Neuromuscular Disorders : NMD|August 25, 2011
Double trouble: spinal muscular atrophy type II and seropositive myasthenia gravis in the same patientManu Jokela, Bjarne Udd, Markku Päivärinta
Neuromuscular Disorders : NMD|June 14, 2011
Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutationVéronique Bissay, Kathelijn Keymolen, Willy Lissens, et al.
Neuromuscular Disorders : NMD|December 15, 2010
Duchenne muscular dystrophy: survival by cardio-respiratory interventionsYuka Ishikawa, Toshihiko Miura, Yukitoshi Ishikawa, et al.
Neuromuscular Disorders : NMD|December 7, 2010
Infantile onset myofibrillar myopathy due to recessive CRYAB mutationsKatharine M L Forrest, Safa Al-Sarraj, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|May 17, 2011
Age-matched comparison reveals early electrocardiography and echocardiography changes in dystrophin-deficient dogsDeborah M Fine, Jin-Hong Shin, Yongping Yue, et al.
Neuromuscular Disorders : NMD|June 3, 2011
Inflammatory changes in infantile-onset LMNA-associated myopathyHirofumi Komaki, Yukiko K Hayashi, Rie Tsuburaya, et al.
Neuromuscular Disorders : NMD|March 8, 2011
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locusPeter Hackman, Satu Sandell, Jaakko Sarparanta, et al.
Neuromuscular Disorders : NMD|March 9, 2011
Cognitive impairment and McArdle disease: Is there a link?M Mancuso, D Orsucci, D Volterrani, et al.
Neuromuscular Disorders : NMD|March 12, 2011
Pre-clinical study of 21 approved drugs in the mdx mouseMaïté Carre-Pierrat, Aude Lafoux, Guillaume Tanniou, et al.
Neuromuscular Disorders : NMD|July 12, 2011
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypesSonia Nouioua, Tarik Hamadouche, Benoit Funalot, et al.
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