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American Journal of Medical Genetics|October 2, 2001
Epidemiology and treatment of mitochondrial disordersP F Chinnery, D M TurnbullCurrent Opinion in Neurology|December 16, 1998
Fatty acid oxidation defects in muscleA A Morris, D M TurnbullMolecular Medicine Today|November 14, 2000
Mitochondrial DNA mutations in the pathogenesis of human diseaseP F Chinnery, D M TurnbullBiochemical Medicine and Metabolic Biology|June 1, 1993
Assay of acyl-CoA dehydrogenase activity in frozen muscle biopsies: application to medium-chain acyl-CoA dehydrogenase deficiencyM A Verity, D M TurnbullCurrent Opinion in Clinical Nutrition and Metabolic Care|November 21, 2000
Mitochondria and ageingD A Cottrell, D M TurnbullActa Neurologica Scandinavica. Supplementum|July 2, 2009
Mitochondrial DNA depletion in progressive external ophthalmoplegia caused by POLG1 mutationsC Tzoulis, M Papingji, T Fiskestrand, et al.European Journal of Biochemistry|March 15, 1994
Redox control of beta-oxidation in rat liver mitochondriaS Eaton, D M Turnbull, K BartlettAnalytical Biochemistry|February 15, 1993
A rapid fluorometric method for the determination of carnitine palmitoyltransferaseJ Schäfer, D M Turnbull, H ReichmannAnnals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.Current Topics in Developmental Biology|January 16, 2007
Mitochondrial disease--its impact, etiology, and pathologyR McFarland, R W Taylor, D M TurnbullPageof 22