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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.Gut|December 15, 2000
Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tractP F Chinnery, S Jones, L Sviland, et al.Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.Journal of Neuropathology and Experimental Neurology|July 20, 2000
Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorderD A Cottrell, P G Ince, E L Blakely, et al.Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.Heart (British Cardiac Society)|March 27, 1999
Diagnostic utility of metabolic exercise testing in a patient with cardiovascular diseaseP M Elliott, M G Hanna, S A Ward, et al.American Journal of Medical Genetics|July 16, 1999
Nonrandom tissue distribution of mutant mtDNAP F Chinnery, P J Zwijnenburg, M Walker, et al.Biochemical and Biophysical Research Communications|February 25, 1998
A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosisR W Taylor, P F Chinnery, M J Bates, et al.Diabetic Medicine : a Journal of the British Diabetic Association|June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic populationJ E Newkirk, R W Taylor, N Howell, et al.Journal of Internal Medicine|March 19, 2020
Inheritance of mitochondrial DNA in humans: implications for rare and common diseasesW Wei, P F ChinneryPageof 27