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

Year Number of Results
2014 7
2015 46
2016 28
2017 24
2018 21
2019 12
2020 3
2022 9
2023 4
2024 0

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136 results

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Page 1
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.
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJ, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZ, Rahman S, Chinnery PF. Parikh S, et al. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.107. doi: 10.1038/gim.2017.107. Epub 2017 Jul 27. Genet Med. 2017. PMID: 28749475 Free PMC article. Review.
Mitochondrial Matchmaking.
Chinnery PF, Zeviani M. Chinnery PF, et al. N Engl J Med. 2016 Nov 10;375(19):1894-1896. doi: 10.1056/NEJMcibr1608715. N Engl J Med. 2016. PMID: 27959648 No abstract available.
Mitochondrial heteroplasmy beyond the oocyte bottleneck.
van den Ameele J, Li AYZ, Ma H, Chinnery PF. van den Ameele J, et al. Semin Cell Dev Biol. 2020 Jan;97:156-166. doi: 10.1016/j.semcdb.2019.10.001. Epub 2019 Oct 11. Semin Cell Dev Biol. 2020. PMID: 31611080 Review.
The Human Phenotype Ontology in 2017.
Köhler S, Vasilevsky NA, Engelstad M, Foster E, McMurry J, Aymé S, Baynam G, Bello SM, Boerkoel CF, Boycott KM, Brudno M, Buske OJ, Chinnery PF, Cipriani V, Connell LE, Dawkins HJ, DeMare LE, Devereau AD, de Vries BB, Firth HV, Freson K, Greene D, Hamosh A, Helbig I, Hum C, Jähn JA, James R, Krause R, F Laulederkind SJ, Lochmüller H, Lyon GJ, Ogishima S, Olry A, Ouwehand WH, Pontikos N, Rath A, Schaefer F, Scott RH, Segal M, Sergouniotis PI, Sever R, Smith CL, Straub V, Thompson R, Turner C, Turro E, Veltman MW, Vulliamy T, Yu J, von Ziegenweidt J, Zankl A, Züchner S, Zemojtel T, Jacobsen JO, Groza T, Smedley D, Mungall CJ, Haendel M, Robinson PN. Köhler S, et al. Nucleic Acids Res. 2017 Jan 4;45(D1):D865-D876. doi: 10.1093/nar/gkw1039. Epub 2016 Nov 28. Nucleic Acids Res. 2017. PMID: 27899602 Free PMC article. Review.
Mitochondrial disease: mimics and chameleons.
Martikainen MH, Chinnery PF. Martikainen MH, et al. Pract Neurol. 2015 Dec;15(6):424-35. doi: 10.1136/practneurol-2015-001191. Epub 2015 Jul 22. Pract Neurol. 2015. PMID: 26201977 Review.
Mitochondrial DNA mutations in neurodegeneration.
Keogh MJ, Chinnery PF. Keogh MJ, et al. Biochim Biophys Acta. 2015 Nov;1847(11):1401-11. doi: 10.1016/j.bbabio.2015.05.015. Epub 2015 May 23. Biochim Biophys Acta. 2015. PMID: 26014345 Free article. Review.
Emerging therapies for mitochondrial disorders.
Nightingale H, Pfeffer G, Bargiela D, Horvath R, Chinnery PF. Nightingale H, et al. Brain. 2016 Jun;139(Pt 6):1633-48. doi: 10.1093/brain/aww081. Epub 2016 May 3. Brain. 2016. PMID: 27190030 Free PMC article. Review.
136 results