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Neuromuscular Disorders : NMD|April 25, 2020
"Status myotonicus" in Nav1.4-M1592V channelopathyTorge Rempe, S H Subramony
Neuromuscular Disorders : NMD|March 1, 2003
Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant miceL T Guo, X U Zhang, W Kuang, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiencyKeiko Ishigaki, Delphine Nicolle, Eric Krejci, et al.
Neuromuscular Disorders : NMD|June 12, 2003
Inhibition of dystroglycan cleavage causes muscular dystrophy in transgenic miceVianney Jayasinha, Holly H Nguyen, Bing Xia, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophyC Billard, P Gillet, J L Signoret, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A randomized controlled trial of early surgery in Duchenne muscular dystrophyA Y Manzur, S A Hyde, E Rodillo, et al.
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