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European Journal of Neurology|April 22, 2008
Beta-tropomyosin mutations alter tropomyosin isoform compositionJ Nilsson, H TajsharghiNeuromuscular Disorders : NMD|July 4, 2012
Myopathies associated with β-tropomyosin mutationsH Tajsharghi, M Ohlsson, L Palm, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 21, 2004
Myopathies associated with myosin heavy chain mutationsA Oldfors, H Tajsharghi, N Darin, et al.Neuromuscular Disorders : NMD|September 1, 2004
Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1)M Ohlsson, H Tajsharghi, N Darin, et al.Neurology|March 7, 2007
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutationH Tajsharghi, E Kimber, D Holmgren, et al.Neurology|August 23, 2006
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposisE Kimber, H Tajsharghi, A-K Kroksmark, et al.Acta Neurologica Scandinavica|July 10, 2004
The effects of endurance training in persons with a hereditary myosin myopathyK S Sunnerhagen, N Darin, H Tajsharghi, et al.Neuromuscular Disorders : NMD|September 29, 2006
Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys)M Li, A Lionikas, F Yu, et al.Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa geneT Martinsson, A Oldfors, N Darin, et al.Neurology|March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with ageH Tajsharghi, L-E Thornell, N Darin, et al.Pageof 2