Showing results (2001-2010 of 3,405) with videos related to
Sort By:
Pageof 341
Neuromuscular Disorders : NMD|October 4, 2016
Clinical manifestation of late onset Pompe disease patients in Hong KongYim Pui Chu, Bun Sheng, Kwok Kwong Lau, et al.Neuromuscular Disorders : NMD|January 24, 2017
Gene co-expression network analysis of dysferlinopathy: Altered cellular processes and functional prediction of TOR1AIP1, a novel muscular dystrophy geneAyse Ece Cali-Daylan, Pervin DincerNeuromuscular Disorders : NMD|February 14, 2017
Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathyKira Philipsen Prahm, Ulla Feldt-Rasmussen, John VissingNeuromuscular Disorders : NMD|August 19, 2003
Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiencyClaire Wary, Pascal Laforêt, Bruno Eymard, et al.Neuromuscular Disorders : NMD|August 19, 2003
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Reinhard Kiefer, Emma L Blakely, et al.Neuromuscular Disorders : NMD|October 17, 2003
Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicineJ Andoni Urtizberea, Qi Shi Fan, Elizabeth Vroom, et al.Neuromuscular Disorders : NMD|March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.Neuromuscular Disorders : NMD|March 24, 2004
Subclinical cardiac involvement in myotonic dystrophy manifesting as decreased myocardial Doppler velocitiesDragos Vinereanu, Balwinder P S Bajaj, Jane Fenton-May, et al.Neuromuscular Disorders : NMD|March 24, 2004
Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in bloodMassoud Houshmand, Ann Gardner, Tore Hällström, et al.Neuromuscular Disorders : NMD|March 24, 2004
Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during agingF Chevessier, I Marty, M Paturneau-Jouas, et al.Pageof 341