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Journal of Neuroimmunology|December 10, 1998
T cell receptor beta-chain repertoire in inclusion body myositisI M Fyhr, A R Moslemi, C Lindberg, et al.
Cardiology|December 9, 2000
Fatal dilated cardiomyopathy associated with a mitochondrial DNA deletionA R Moslemi, N Selimovic, C H Bergh, 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|June 24, 2014
Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutationsS Roos, U Lindgren, C Ehrstedt, et al.
Neurology|March 7, 2007
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutationH Tajsharghi, E Kimber, D Holmgren, et al.
Brain : a Journal of Neurology|April 1, 1993
Mitochondrial DNA deletions in inclusion body myositisA Oldfors, N G Larsson, C Lindberg, et al.
Neurology|January 27, 1998
Rhabdomyolysis in autosomal dominant progressive external ophthalmoplegiaA Melberg, E Holme, A Oldfors, et al.
Scandinavian Journal of Immunology|January 1, 1996
Limited T-cell receptor V gene usage in inclusion body myositisI M Fyhr, A R Moslemi, A Tarkowski, 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.
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.
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