Showing results (1861-1870 of 3,403) with videos related to
Sort By:
Pageof 341
Neuromuscular Disorders : NMD|July 1, 1995
Cytochrome c oxidase deficiency presenting as recurrent neonatal myoglobinuriaP Saunier, D Chretien, C Wood, et al.Neuromuscular Disorders : NMD|July 1, 1995
Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transferL Morandi, P Bernasconi, M Gebbia, et al.Neuromuscular Disorders : NMD|July 1, 1995
Focal myositis: a clinicopathological studyC J Caldwell, M Swash, J D Van der Walt, et al.Neuromuscular Disorders : NMD|March 1, 1993
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriersM Vainzof, L V Nicholson, D E Bulman, et al.Neuromuscular Disorders : NMD|March 1, 1996
Controlled trial of nimodipine in amyotrophic lateral sclerosisR G Miller, R Shepherd, H Dao, et al.Neuromuscular Disorders : NMD|January 1, 1993
Dystrophin and dystrophin-related proteins: a review of protein and RNA studiesD R Love, B C Byth, J M Tinsley, et al.Neuromuscular Disorders : NMD|January 1, 1993
Very small dystrophin molecule in a family with a mild form of Becker dystrophyL Morandi, M Mora, P Bernasconi, et al.Neuromuscular Disorders : NMD|January 1, 1996
Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's diseaseS Tsujino, S Shanske, S J Valberg, et al.Neuromuscular Disorders : NMD|January 1, 1996
Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effectC L Grosson, J Esteban, D McKenna-Yasek, et al.Neuromuscular Disorders : NMD|January 1, 1996
The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidismA Papadimitriou, G M Hadjigeorgiou, R Divari, et al.Pageof 341