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

Year Number of Results
1981 1
1985 1
1993 3
1999 1
2000 2
2001 1
2002 2
2003 4
2004 4
2005 5
2006 1
2007 8
2008 10
2009 3
2010 4
2011 2
2012 5
2013 2
2014 3
2015 2
2016 4
2017 6
2018 3
2019 4
2020 2
2021 8
2022 3
2023 2
2024 0

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PubMed for id: 4540

83 results

Results by year

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Page 1
Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance.
Zhou N, Tang L, Jiang Y, Qin S, Cui J, Wang Y, Zhu W, Zhao W, Pan C, Shu X. Zhou N, et al. Anatol J Cardiol. 2019 Jan;21(1):18-24. doi: 10.14744/AnatolJCardiol.2018.53258. Anatol J Cardiol. 2019. PMID: 30587702 Free PMC article.
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.
Ng YS, Lax NZ, Maddison P, Alston CL, Blakely EL, Hepplewhite PD, Riordan G, Meldau S, Chinnery PF, Pierre G, Chronopoulou E, Du A, Hughes I, Morris AA, Kamakari S, Chrousos G, Rodenburg RJ, Saris CGJ, Feeney C, Hardy SA, Sakakibara T, Sudo A, Okazaki Y, Murayama K, Mundy H, Hanna MG, Ohtake A, Schaefer AM, Champion MP, Turnbull DM, Taylor RW, Pitceathly RDS, McFarland R, Gorman GS. Ng YS, et al. EBioMedicine. 2018 Apr;30:86-93. doi: 10.1016/j.ebiom.2018.02.010. Epub 2018 Feb 24. EBioMedicine. 2018. PMID: 29506874 Free PMC article.
[Mitochondrial ND5 as the causative gene of Leight syndrome].
Wang K, Yan CZ, Wang GX, Jiao JS, Jin M. Wang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Dec;27(6):616-9. doi: 10.3760/cma.j.issn.1003-9406.2010.06.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 21154318 Chinese.
83 results