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European Heart Journal|February 20, 2003
Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findingsD Holmgren, H Wåhlander, B O Eriksson, et al.Journal of the Neurological Sciences|July 1, 1992
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibresA Oldfors, N G Larsson, E Holme, et al.American Journal of Human Genetics|March 1, 1993
Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndromeE Holme, N G Larsson, A Oldfors, et al.European Journal of Neurology|February 10, 2017
Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1N Darin, C Hedberg-Oldfors, A-K Kroksmark, et al.Journal of Neuropathology and Experimental Neurology|July 1, 1995
Mitochondrial DNA deletions in muscle fibers in inclusion body myositisA Oldfors, A R Moslemi, I M Fyhr, et al.Neuromuscular Disorders : NMD|March 11, 2000
Neuromuscular disorders in childhood: a descriptive epidemiological study from western SwedenN Darin, M TuliniusHuman 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 OldforsScandinavian 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.Pediatric Research|December 1, 1992
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduriaE Holme, J Greter, C E Jacobson, et al.Pageof 22