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	21.	Prevalence and progression of diabetes in mitochondrial disease. [electronic resource] by Whittaker, R G Schaefer, A M McFarland, R Taylor, R W Walker, M Turnbull, D M Producer: 20080215 In: Diabetologia vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutation. [electronic resource] by Betts, J Barron, M J Needham, S J Schaefer, A M Taylor, R W Turnbull, D M Producer: 20080515 In: Neurology vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy. [electronic resource] by Barron, M J Chinnery, P F Howel, D Blakely, E L Schaefer, A M Taylor, R W Turnbull, D M Producer: 20060207 In: Neuromuscular disorders : NMD vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Mitochondrial DNA deletion in "identical" twin brothers. [electronic resource] by Blakely, E L He, L Taylor, R W Chinnery, P F Lightowlers, R N Schaefer, A M Turnbull, D M Producer: 20040223 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement. [electronic resource] by Betts, J Jaros, E Perry, R H Schaefer, A M Taylor, R W Abdel-All, Z Lightowlers, R N Turnbull, D M Producer: 20060919 In: Neuropathology and applied neurobiology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	A scale to monitor progression and treatment of mitochondrial disease in children. [electronic resource] by Phoenix, C Schaefer, A M Elson, J L Morava, E Bugiani, M Uziel, G Smeitink, J A Turnbull, D M McFarland, R Producer: 20070223 In: Neuromuscular disorders : NMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions. [electronic resource] by Betts-Henderson, J Jaros, E Krishnan, K J Perry, R H Reeve, A K Schaefer, A M Taylor, R W Turnbull, D M Producer: 20090309 In: Neuropathology and applied neurobiology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO). [electronic resource] by Agostino, A Valletta, L Chinnery, P F Ferrari, G Carrara, F Taylor, R W Schaefer, A M Turnbull, D M Tiranti, V Zeviani, M Producer: 20040114 In: Neurology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions. [electronic resource] by Hudson, G Deschauer, M Taylor, R W Hanna, M G Fialho, D Schaefer, A M He, L-P Blakely, E Turnbull, D M Chinnery, P F Producer: 20060612 In: Neurology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) gene. [electronic resource] by Taylor, R W Schaefer, A M McDonnell, M T Petty, R K H Thomas, A M Blakely, E L Hayes, C M McFarland, R Turnbull, D M Producer: 20040810 In: Neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation. [electronic resource] by Deschauer, M Chinnery, P F Schaefer, A M Turnbull, D M Taylor, R W Zierz, S Shanske, S DiMauro, S Majamaa, K Wilichowski, E Thorburn, D R Producer: 20040818 In: Journal of neurology, neurosurgery, and psychiatry vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Homoplasmy, heteroplasmy, and mitochondrial dystonia. [electronic resource] by McFarland, R Chinnery, P F Blakely, E L Schaefer, A M Morris, A A M Foster, S M Tuppen, H A L Ramesh, V Dorman, P J Turnbull, D M Taylor, R W Producer: 20070928 In: Neurology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions. [electronic resource] by Fratter, C Raman, P Alston, C L Blakely, E L Craig, K Smith, C Evans, J Seller, A Czermin, B Hanna, M G Poulton, J Brierley, C Staunton, T G Turnpenny, P D Schaefer, A M Chinnery, P F Horvath, R Turnbull, D M Gorman, G S Taylor, R W Producer: 20110818 In: Neurology vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)