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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2011 17
2012 86
2013 91
2014 65
2015 66
2016 16
2017 1
2020 0
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280 results
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Page 1
Mutations causing mitochondrial disease: What is new and what challenges remain?
Lightowlers RN, Taylor RW, Turnbull DM. Lightowlers RN, et al. Science. 2015 Sep 25;349(6255):1494-9. doi: 10.1126/science.aac7516. Epub 2015 Sep 24. Science. 2015. PMID: 26404827 Review.
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gorman GS, Schaefer AM, Ng Y, Gomez N, Blakely EL, Alston CL, Feeney C, Horvath R, Yu-Wai-Man P, Chinnery PF, Taylor RW, Turnbull DM, McFarland R. Gorman GS, et al. Ann Neurol. 2015 May;77(5):753-9. doi: 10.1002/ana.24362. Epub 2015 Mar 28. Ann Neurol. 2015. PMID: 25652200 Free PMC article.
Mitochondrial disease: genetics and management.
Ng YS, Turnbull DM. Ng YS, et al. J Neurol. 2016 Jan;263(1):179-91. doi: 10.1007/s00415-015-7884-3. Epub 2015 Aug 28. J Neurol. 2016. PMID: 26315846 Free PMC article. Review.
Meiosis and maternal aging: insights from aneuploid oocytes and trisomy births.
Herbert M, Kalleas D, Cooney D, Lamb M, Lister L. Herbert M, et al. Cold Spring Harb Perspect Biol. 2015 Apr 1;7(4):a017970. doi: 10.1101/cshperspect.a017970. Cold Spring Harb Perspect Biol. 2015. PMID: 25833844 Free PMC article. Review.
Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.
Taylor RW, Pyle A, Griffin H, Blakely EL, Duff J, He L, Smertenko T, Alston CL, Neeve VC, Best A, Yarham JW, Kirschner J, Schara U, Talim B, Topaloglu H, Baric I, Holinski-Feder E, Abicht A, Czermin B, Kleinle S, Morris AA, Vassallo G, Gorman GS, Ramesh V, Turnbull DM, Santibanez-Koref M, McFarland R, Horvath R, Chinnery PF. Taylor RW, et al. JAMA. 2014 Jul 2;312(1):68-77. doi: 10.1001/jama.2014.7184. JAMA. 2014. PMID: 25058219 Free PMC article.
Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease.
Hyslop LA, Blakeley P, Craven L, Richardson J, Fogarty NM, Fragouli E, Lamb M, Wamaitha SE, Prathalingam N, Zhang Q, O'Keefe H, Takeda Y, Arizzi L, Alfarawati S, Tuppen HA, Irving L, Kalleas D, Choudhary M, Wells D, Murdoch AP, Turnbull DM, Niakan KK, Herbert M. Hyslop LA, et al. Nature. 2016 Jun 16;534(7607):383-6. doi: 10.1038/nature18303. Epub 2016 Jun 8. Nature. 2016. PMID: 27281217 Free PMC article.
Neuroferritinopathy.
Keogh MJ, Morris CM, Chinnery PF. Keogh MJ, et al. Int Rev Neurobiol. 2013;110:91-123. doi: 10.1016/B978-0-12-410502-7.00006-5. Int Rev Neurobiol. 2013. PMID: 24209436 Review.
Ageing and Parkinson's disease: why is advancing age the biggest risk factor?
Reeve A, Simcox E, Turnbull D. Reeve A, et al. Ageing Res Rev. 2014 Mar;14(100):19-30. doi: 10.1016/j.arr.2014.01.004. Epub 2014 Feb 3. Ageing Res Rev. 2014. PMID: 24503004 Free PMC article. Review.
Reversible infantile mitochondrial diseases.
Boczonadi V, Bansagi B, Horvath R. Boczonadi V, et al. J Inherit Metab Dis. 2015 May;38(3):427-35. doi: 10.1007/s10545-014-9784-6. Epub 2014 Nov 19. J Inherit Metab Dis. 2015. PMID: 25407320 Review.
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