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

Year Number of Results
1996 1
2007 1
2008 3
2010 3
2011 5
2012 8
2013 7
2014 2
2015 8
2016 4
2017 6
2018 4
2019 4
2020 3
2021 3
2023 2

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56 results

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Page 1
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.
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.
Exome sequencing: how to understand it.
Keogh MJ, Daud D, Chinnery PF. Keogh MJ, et al. Pract Neurol. 2013 Dec;13(6):399-407. doi: 10.1136/practneurol-2012-000498. Epub 2013 Jun 1. Pract Neurol. 2013. PMID: 23727621 Review. No abstract available.
Response to Simon et al.
Wei W, Keogh MJ, Ironside JW, Chinnery PF. Wei W, et al. Among authors: keogh mj. Acta Neuropathol Commun. 2017 Apr 29;5(1):34. doi: 10.1186/s40478-017-0434-8. Acta Neuropathol Commun. 2017. PMID: 28454558 Free PMC article. No abstract available.
How to spot mitochondrial disease in adults.
Keogh MJ, Chinnery PF. Keogh MJ, et al. Clin Med (Lond). 2013 Feb;13(1):87-92. doi: 10.7861/clinmedicine.13-1-87. Clin Med (Lond). 2013. PMID: 23472503 Free PMC article. Review. No abstract available.
Awareness of venous thromboembolism prophylaxis must be increased.
Findlay JM, Keogh MJ, Tatman E, Leach S. Findlay JM, et al. Among authors: keogh mj. Br J Hosp Med (Lond). 2008 May;69(5):244-5. doi: 10.12968/hmed.2008.69.5.29351. Br J Hosp Med (Lond). 2008. PMID: 18557542 No abstract available.
Germline selection shapes human mitochondrial DNA diversity.
Wei W, Tuna S, Keogh MJ, Smith KR, Aitman TJ, Beales PL, Bennett DL, Gale DP, Bitner-Glindzicz MAK, Black GC, Brennan P, Elliott P, Flinter FA, Floto RA, Houlden H, Irving M, Koziell A, Maher ER, Markus HS, Morrell NW, Newman WG, Roberts I, Sayer JA, Smith KGC, Taylor JC, Watkins H, Webster AR, Wilkie AOM, Williamson C; NIHR BioResource–Rare Diseases; 100,000 Genomes Project–Rare Diseases Pilot; Ashford S, Penkett CJ, Stirrups KE, Rendon A, Ouwehand WH, Bradley JR, Raymond FL, Caulfield M, Turro E, Chinnery PF. Wei W, et al. Among authors: keogh mj. Science. 2019 May 24;364(6442):eaau6520. doi: 10.1126/science.aau6520. Epub 2019 May 23. Science. 2019. PMID: 31123110 Free article.
Early neuropsychiatry features in neuroferritinopathy.
Keogh MJ, Singh B, Chinnery PF. Keogh MJ, et al. Mov Disord. 2013 Aug;28(9):1310-3. doi: 10.1002/mds.25371. Epub 2013 Feb 23. Mov Disord. 2013. PMID: 23436236 No abstract available.
56 results