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Current Opinion in Pharmacology|November 20, 2001
The mitochondrial genome and mitochondrial muscle disordersA M Schaefer, R W Taylor, D M TurnbullBiochemical Medicine and Metabolic Biology|April 1, 1992
The measurement of mitochondrial beta-oxidation by release of 3H2O from [9,10-3H]hexadecanoate: application to skeletal muscle and the use of inhibitors as models of metabolic diseaseR S Kler, H S Sherratt, D M TurnbullBiochemical Medicine and Metabolic Biology|December 1, 1991
Immunoreactive enzyme protein in medium-chain acyl-CoA dehydrogenase deficiencyI Ogilvie, S Jackson, K Bartlett, et al.Biochemical Society Transactions|October 25, 2007
Do mitochondrial DNA mutations have a role in neurodegenerative disease?K J Krishnan, A K Reeve, D M TurnbullNeuropathology and Applied Neurobiology|June 12, 2016
Review: Central nervous system involvement in mitochondrial diseaseN Z Lax, G S Gorman, D M TurnbullAnnals of Neurology|October 1, 1996
Trifunctional enzyme deficiency: adult presentation of a usually fatal beta-oxidation defectJ Schaefer, S Jackson, D J Dick, et al.Gene Therapy|July 1, 1995
Gene therapy for mitochondrial DNA defects: is it possible?Z M Chrzanowska-Lightowlers, R N Lightowlers, D M TurnbullActa Neurochirurgica. Supplement|January 1, 1997
Selective impairments of mitochondrial respiratory chain activity during aging and ischemic brain damageM Davis, T Whitely, D M Turnbull, et al.Molecular Biology and Evolution|June 11, 2004
African Haplogroup L mtDNA sequences show violations of clock-like evolutionNeil Howell, Joanna L Elson, D M Turnbull, et al.Diabetic Medicine : a Journal of the British Diabetic Association|February 26, 2008
Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutationR Murphy, D M Turnbull, M Walker, et al.Pageof 22