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Neurology|July 17, 1999
Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletionsA R Moslemi, A Melberg, 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.Acta Neuropathologica|January 1, 1995
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibresA Oldfors, E Holme, M Tulinius, et al.Acta Neuropathologica|January 1, 1989
Cytochrome c oxidase deficiency in infancyA Oldfors, H Sommerland, E Holme, 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.Pediatric Research|August 1, 1990
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndromeN G Larsson, E Holme, B Kristiansson, et al.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.Acta Neuropathologica|January 1, 1990
Neuropathology in Kearns-Sayre syndromeA Oldfors, I M Fyhr, E Holme, et al.Neuromuscular Disorders : NMD|December 9, 2003
A novel mutation in the mitochondrial tRNA(Phe) gene associated with mitochondrial myopathyA-R Moslemi, C Lindberg, J Toft, et al.Acta Neuropathologica|January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosisA Oldfors, M Tulinius, E Holme, et al.Pageof 22