Showing results (11-20 of 28) with videos related to
Sort By:
Pageof 3
Human Genetics|March 1, 1996
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gneM Houshmand, N G Larsson, A Oldfors, et al.Neuropediatrics|October 12, 2005
Two new mutations in the MTATP6 gene associated with Leigh syndromeA-R Moslemi, N Darin, M Tulinius, et al.Acta Neuropathologica|January 1, 1990
Neuropathology in Kearns-Sayre syndromeA Oldfors, I M Fyhr, E Holme, et al.Acta Neuropathologica|January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosisA Oldfors, M Tulinius, E Holme, et al.Neurology|October 15, 2003
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiencyA-R Moslemi, M Tulinius, N Darin, et al.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.Neuropediatrics|May 28, 2008
Progressive encephalopathy and complex I deficiency associated with mutations in MTND1A-R Moslemi, N Darin, M Tulinius, et al.Neuropediatrics|December 19, 2003
Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiencyN Darin, A-R Moslemi, S Lebon, et al.Pageof 3