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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|February 14, 2017
Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathyKira Philipsen Prahm, Ulla Feldt-Rasmussen, John Vissing
Neuromuscular 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.
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