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Human Mutation|January 1, 1997
Analysis of multiple mitochondrial DNA deletions in inclusion body myositisA R Moslemi, C Lindberg, A OldforsActa Neurologica Scandinavica|September 27, 2007
MELAS syndrome in a patient with a point mutation in MTTS1C Lindberg, A-R Moslemi, A OldforsNeurology|July 17, 1999
Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletionsA R Moslemi, A Melberg, E Holme, et al.Scandinavian Journal of Immunology|July 19, 2003
Inclusion body myositis: clonal expansions of muscle-infiltrating T cells persist over timeK Müntzing, C Lindberg, A-R Moslemi, et al.Neuromuscular Disorders : NMD|July 23, 1998
Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibresA R Moslemi, M Tulinius, E Holme, et al.Annals of Neurology|November 1, 1996
Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegiaA R Moslemi, A Melberg, E Holme, et al.Clinical and Experimental Rheumatology|July 25, 2006
A Western blot and molecular genetic investigation of the estrogen receptor beta in giant cell arteritisK Larsson, C Nordborg, A-R Moslemi, et al.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.Human Mutation|March 25, 1999
A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspringM Houshmand, C Lindberg, A R Moslemi, et al.Pageof 3