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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.Diabetologia|March 11, 2003
Heteroplasmic ratio of the A3243G mitochondrial DNA mutation in single pancreatic beta cellsS Lynn, G M Borthwick, R M Charnley, et al.Diabetes|July 26, 2000
Decreased insulin responsiveness of glucose uptake in cultured human skeletal muscle cells from insulin-resistant nondiabetic relatives of type 2 diabetic familiesS Jackson, S M Bagstaff, S Lynn, et al.Diabetologia|July 27, 2007
Prevalence and progression of diabetes in mitochondrial diseaseR G Whittaker, A M Schaefer, R McFarland, et al.Diabetic Medicine : a Journal of the British Diabetic Association|April 1, 1996
Relationship between insulin sensitivity and insulin receptor substrate-1 mutations in non-diabetic relatives of NIDDM familiesM Armstrong, F Haldane, P J Avery, et al.Diabetologia|June 6, 2008
Age-related decline in mitochondrial DNA copy number in isolated human pancreatic isletsL M Cree, S K Patel, A Pyle, et al.Journal of Internal Medicine|February 5, 2009
Batteries not included: diagnosis and management of mitochondrial diseaseR McFarland, D M TurnbullJournal of Neurology, Neurosurgery, and Psychiatry|November 1, 1985
The comparative efficacy of antiepileptic drugs for partial and tonic-clonic seizuresD Chadwick, D M TurnbullDiabetologia|March 1, 1996
Variant sequences of the Hexokinase II gene in familial NIDDMR W Taylor, R L Printz, M Armstrong, et al.Quarterly Journal of Experimental Physiology (Cambridge, England)|April 1, 1984
Mitochondrial oxidative enzyme activity in individual fibre types in hypo- and hyperthyroid rat skeletal musclesM A Johnson, D M TurnbullPageof 509