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Annals of Neurology|August 26, 1998
Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuolesN Darin, M Kyllerman, J Wahlström, et al.Biochimica Et Biophysica Acta|May 24, 1995
Inheritance and expression of mitochondrial DNA point mutationsE Holme, M H Tulinius, N G Larsson, et al.Neurology|January 25, 2006
Mitochondrial abnormalities in inclusion-body myositisA Oldfors, A R Moslemi, L Jonasson, et al.Muscle & Nerve. Supplement|January 1, 1995
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomasN G Larsson, M H Tulinius, E Holme, et al.Biochemical and Biophysical Research Communications|May 16, 1994
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletionN G Larsson, A Oldfors, E Holme, 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.Annals of Neurology|November 1, 1991
Leber's hereditary optic neuropathy and complex I deficiency in muscleN G Larsson, O Andersen, E Holme, et al.American Journal of Human Genetics|April 17, 1999
Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1T Martinsson, N Darin, M Kyllerman, et al.Acta Neuropathologica|July 27, 2000
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathyM Jansson, N Darin, M Kyllerman, et al.Journal of Neuroimmunology|December 12, 1997
Oligoclonal expansion of muscle infiltrating T cells in inclusion body myositisI M Fyhr, A R Moslemi, A A Mosavi, et al.Pageof 22