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Neuromuscular Disorders : NMD|September 1, 1995
Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patientsP Laforêt, A Lombès, B Eymard, et al.Neuromuscular Disorders : NMD|September 1, 1995
Generalized lysosomal storage in Yunis Varón syndromeF Dworzak, M Mora, C Borroni, et al.Neuromuscular Disorders : NMD|July 1, 1995
New point mutations and deletions of the connexin 32 gene in X-linked Charcot-Marie-Tooth neuropathyV Ionasescu, C Searby, R Ionasescu, et al.Neuromuscular Disorders : NMD|March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patientsM Fanin, E P Hoffman, F A Saad, et al.Neuromuscular Disorders : NMD|March 1, 1993
The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosisJ Goto, D A Figlewicz, J L Haines, et al.Neuromuscular Disorders : NMD|December 1, 1996
Merosin/laminin-2 and muscular dystrophyU M Wewer, E EngvallNeuromuscular Disorders : NMD|December 1, 1996
Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complexD J Duggan, E P HoffmanNeuromuscular Disorders : NMD|March 1, 1997
Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiencyM el-Schahawi, C Bruno, S Tsujino, et al.Neuromuscular Disorders : NMD|March 1, 1997
Abnormal oxidative metabolism in exercise intolerance of undetermined originZ Argov, N De Stefano, T Taivassalo, et al.Neuromuscular Disorders : NMD|March 1, 1997
Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel alpha subunit--a large kindred with a novel phenotypeP Kelly, W S Yang, D Costigan, et al.Pageof 340