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American Journal of Human Genetics|February 1, 1992
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her childN G Larsson, H G Eiken, H Boman, 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.Free Radical Research|November 8, 2001
Human cultured skin fibroblasts survive profound inherited ubiquinone depletionV Geromel, N Kadhom, I Ceballos-Picot, 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.Heart (British Cardiac Society)|March 22, 2002
Idebenone and reduced cardiac hypertrophy in Friedreich's ataxiaA O Hausse, Y Aggoun, D Bonnet, et al.The Journal of Clinical Investigation|March 1, 1993
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300)A Rötig, V Cormier, P Chatelain, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Biochemical and molecular investigations in respiratory chain deficienciesP Rustin, D Chretien, T Bourgeron, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|December 22, 1999
[Metabolic and genetic investigations in childhood cardiomyopathies]D Bonnet, P Rustin, A Rötig, et al.Biochemical and Biophysical Research Communications|December 13, 1996
Absence of relationship between the level of electron transport chain activities and aging in human skeletal muscleA Barrientos, J Casademont, A Rötig, et al.Human Molecular Genetics|October 9, 2001
Disabled early recruitment of antioxidant defenses in Friedreich's ataxiaK Chantrel-Groussard, V Geromel, H Puccio, et al.Pageof 18