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Neuromuscular Disorders : NMD|July 1, 2008
Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophyLawrence Korngut, Victoria M Siu, Shannon L Venance, et al.Neuromuscular Disorders : NMD|June 27, 2008
Autosomal dominant congenital spinal muscular atrophy--a possible developmental deficiency of motor neurones?S Reddel, R A Ouvrier, G Nicholson, et al.Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.Neuromuscular Disorders : NMD|January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patientsM Fanin, G A Danieli, L Vitiello, et al.Neuromuscular Disorders : NMD|January 1, 1992
Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostainingM P Chevron, S Tuffery, B Echenne, et al.Neuromuscular Disorders : NMD|June 24, 2004
Myofibrillar myopathy with desmin accumulation in a young Australian Shepherd dogG Diane Shelton, Veronique Sammut, Saschiko Homma, et al.Neuromuscular Disorders : NMD|June 24, 2004
New potent mexiletine and tocainide analogues evaluated in vivo and in vitro as antimyotonic agents on the myotonic ADR mouseAnnamaria De Luca, Sabata Pierno, Antonella Liantonio, et al.Neuromuscular Disorders : NMD|June 24, 2004
Functional characterization of malignant hyperthermia-associated RyR1 mutations in exon 44, using the human myotube modelMarkus Wehner, Henrik Rueffert, Fritjoff Koenig, et al.Neuromuscular Disorders : NMD|July 13, 2005
Impaired primary hemostasis with normal platelet function in Duchenne muscular dystrophy during highly-invasive spinal surgeryFrancesco Turturro, Bianca Rocca, Stefano Gumina, et al.Neuromuscular Disorders : NMD|October 17, 2003
Involvement of 3Na+/2K+ ATP-ase and Pi-3 kinase in the response of skeletal muscle ATP-sensitive K+ channels to insulinDomenico Tricarico, Loredana Montanari, Diana Conte CamerinoPageof 341