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Neuromuscular Disorders : NMD|April 12, 2001
Activation of calcineurin and stress activated protein kinase/p38-mitogen activated protein kinase in hearts of utrophin-dystrophin knockout miceA Nakamura, G V Harrod, K E DaviesNeuromuscular Disorders : NMD|April 12, 2001
Identification of altered gene expression in skeletal muscles from Duchenne muscular dystrophy patientsA V Tkatchenko, G Piétu, N Cros, et al.Neuromuscular Disorders : NMD|April 12, 2001
Vitamin E and exertional rhabdomyolysis during endurance sled dog racingR J Piercy, K W Hinchcliff, P S Morley, et al.Neuromuscular Disorders : NMD|April 12, 2001
A case of MERRF associated with chronic pancreatitisM Toyono, K Nakano, M Kiuchi, et al.Neuromuscular Disorders : NMD|January 1, 1992
Analysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndromeA Lombès, C Diaz, N B Romero, et al.Neuromuscular Disorders : NMD|January 1, 1992
Unusual course of nemaline myopathyI Hausmanowa-Petrusewicz, A Fidziańska, B BadurskaNeuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.Neuromuscular Disorders : NMD|June 12, 2003
Consequence of parvalbumin deficiency in the mdx mouse: histological, biochemical and mechanical phenotype of a new double mutantJ M Raymackers, H Debaix, M Colson-Van Schoor, et al.Neuromuscular Disorders : NMD|March 20, 2021
Late onset Pompe Disease in India - Beyond the Caucasian phenotypeRatna Dua Puri, Nitika Setia, Vinu N, et al.Neuromuscular Disorders : NMD|March 20, 2021
Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotypeChristian Peña-Padilla, Ivón Romero-Valenzuela, Alejandra Baldomero-López, et al.Pageof 341