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Page 1
Treatment for mitochondrial disorders.
Pfeffer G, Majamaa K, Turnbull DM, Thorburn D, Chinnery PF. Pfeffer G, et al. Among authors: thorburn d. Cochrane Database Syst Rev. 2012 Apr 18;2012(4):CD004426. doi: 10.1002/14651858.CD004426.pub3. Cochrane Database Syst Rev. 2012. PMID: 22513923 Free PMC article. Review.
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation.
Deschauer M, Chinnery PF, Schaefer AM, Turnbull DM, Taylor RW, Zierz S, Shanske S, DiMauro S, Majamaa K, Wilichowski E, Thorburn DR. Deschauer M, et al. Among authors: thorburn dr. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1204-5. doi: 10.1136/jnnp.2003.026278. J Neurol Neurosurg Psychiatry. 2004. PMID: 15258237 Free PMC article. No abstract available.
Risk of developing a mitochondrial DNA deletion disorder.
Chinnery PF, DiMauro S, Shanske S, Schon EA, Zeviani M, Mariotti C, Carrara F, Lombes A, Laforet P, Ogier H, Jaksch M, Lochmüller H, Horvath R, Deschauer M, Thorburn DR, Bindoff LA, Poulton J, Taylor RW, Matthews JN, Turnbull DM. Chinnery PF, et al. Lancet. 2004 Aug 14-20;364(9434):592-6. doi: 10.1016/S0140-6736(04)16851-7. Lancet. 2004. PMID: 15313359
Mutations of the mitochondrial ND1 gene as a cause of MELAS.
Kirby DM, McFarland R, Ohtake A, Dunning C, Ryan MT, Wilson C, Ketteridge D, Turnbull DM, Thorburn DR, Taylor RW. Kirby DM, et al. Among authors: thorburn dr. J Med Genet. 2004 Oct;41(10):784-9. doi: 10.1136/jmg.2004.020537. J Med Genet. 2004. PMID: 15466014 Free PMC article. No abstract available.
Treatment for mitochondrial disorders.
Chinnery P, Majamaa K, Turnbull D, Thorburn D. Chinnery P, et al. Among authors: thorburn d. Cochrane Database Syst Rev. 2006 Jan 25;(1):CD004426. doi: 10.1002/14651858.CD004426.pub2. Cochrane Database Syst Rev. 2006. PMID: 16437486 Updated. Review.
Biochemical assays of respiratory chain complex activity.
Kirby DM, Thorburn DR, Turnbull DM, Taylor RW. Kirby DM, et al. Methods Cell Biol. 2007;80:93-119. doi: 10.1016/S0091-679X(06)80004-X. Methods Cell Biol. 2007. PMID: 17445690 Review. No abstract available.
Respiratory chain complex I deficiency caused by mitochondrial DNA mutations.
Swalwell H, Kirby DM, Blakely EL, Mitchell A, Salemi R, Sugiana C, Compton AG, Tucker EJ, Ke BX, Lamont PJ, Turnbull DM, McFarland R, Taylor RW, Thorburn DR. Swalwell H, et al. Eur J Hum Genet. 2011 Jul;19(7):769-75. doi: 10.1038/ejhg.2011.18. Epub 2011 Mar 2. Eur J Hum Genet. 2011. PMID: 21364701 Free PMC article.
473 results