Turnbull D - Search Results

1

Chinnery P, Majamaa K, Turnbull D, Thorburn D. Chinnery P, et al. Among authors: turnbull 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.

2

Treatment for mitochondrial disorders.

Pfeffer G, Majamaa K, Turnbull DM, Thorburn D, Chinnery PF. Pfeffer G, et al. Among authors: turnbull dm. 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.

3

Mitochondrial diseases.

Gorman GS, Chinnery PF, DiMauro S, Hirano M, Koga Y, McFarland R, Suomalainen A, Thorburn DR, Zeviani M, Turnbull DM. Gorman GS, et al. Nat Rev Dis Primers. 2016 Oct 20;2:16080. doi: 10.1038/nrdp.2016.80. Nat Rev Dis Primers. 2016. PMID: 27775730 Review.

4

Can mitochondrial DNA mutations cause sperm dysfunction?

Spiropoulos J, Turnbull DM, Chinnery PF. Spiropoulos J, et al. Mol Hum Reprod. 2002 Aug;8(8):719-21. doi: 10.1093/molehr/8.8.719. Mol Hum Reprod. 2002. PMID: 12149402

5

Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?

Chinnery PF, Samuels DC, Elson J, Turnbull DM. Chinnery PF, et al. Lancet. 2002 Oct 26;360(9342):1323-5. doi: 10.1016/S0140-6736(02)11310-9. Lancet. 2002. PMID: 12414225

6

Changes in the human mitochondrial genome after treatment of malignant disease.

Wardell TM, Ferguson E, Chinnery PF, Borthwick GM, Taylor RW, Jackson G, Craft A, Lightowlers RN, Howell N, Turnbull DM. Wardell TM, et al. Mutat Res. 2003 Apr 9;525(1-2):19-27. doi: 10.1016/s0027-5107(02)00313-5. Mutat Res. 2003. PMID: 12650902

7

Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial cells.

McDonnell MT, Schaefer AM, Blakely EL, McFarland R, Chinnery PF, Turnbull DM, Taylor RW. McDonnell MT, et al. Eur J Hum Genet. 2004 Sep;12(9):778-81. doi: 10.1038/sj.ejhg.5201216. Eur J Hum Genet. 2004. PMID: 15199381

8

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

9

The epidemiology of mitochondrial disorders--past, present and future.

Schaefer AM, Taylor RW, Turnbull DM, Chinnery PF. Schaefer AM, et al. Biochim Biophys Acta. 2004 Dec 6;1659(2-3):115-20. doi: 10.1016/j.bbabio.2004.09.005. Biochim Biophys Acta. 2004. PMID: 15576042 Free article. Review.

10

Progressive depletion of mtDNA in mitochondrial myopathy.

Durham SE, Brown DT, Turnbull DM, Chinnery PF. Durham SE, et al. Neurology. 2006 Aug 8;67(3):502-4. doi: 10.1212/01.wnl.0000227961.55640.2f. Neurology. 2006. PMID: 16894115

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