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Results by year

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

Year Number of Results
1989 2
1992 2
1993 5
1994 3
1995 4
1996 8
1997 8
1998 13
1999 11
2000 11
2001 8
2002 5
2003 14
2004 14
2005 9
2006 19
2007 21
2008 17
2009 14
2010 14
2011 19
2012 22
2013 16
2014 12
2015 22
2016 8
2017 7
2018 11
2019 7
2020 8
2021 10
2022 4
2023 1
Text availability
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Search Results

305 results
Results by year
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Page 1
A guide to diagnosis and treatment of Leigh syndrome.
Baertling F, Rodenburg RJ, Schaper J, Smeitink JA, Koopman WJ, Mayatepek E, Morava E, Distelmaier F. Baertling F, et al. Among authors: smeitink ja. J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):257-65. doi: 10.1136/jnnp-2012-304426. Epub 2013 Jun 14. J Neurol Neurosurg Psychiatry. 2014. PMID: 23772060 Review.
Monogenic mitochondrial disorders.
Koopman WJ, Willems PH, Smeitink JA. Koopman WJ, et al. Among authors: smeitink ja. N Engl J Med. 2012 Mar 22;366(12):1132-41. doi: 10.1056/NEJMra1012478. N Engl J Med. 2012. PMID: 22435372 Free article. Review. No abstract available.
OXPHOS mutations and neurodegeneration.
Koopman WJ, Distelmaier F, Smeitink JA, Willems PH. Koopman WJ, et al. Among authors: smeitink ja. EMBO J. 2013 Jan 9;32(1):9-29. doi: 10.1038/emboj.2012.300. Epub 2012 Nov 13. EMBO J. 2013. PMID: 23149385 Free PMC article. Review.
Mitochondrial ATP synthase: architecture, function and pathology.
Jonckheere AI, Smeitink JA, Rodenburg RJ. Jonckheere AI, et al. Among authors: smeitink ja. J Inherit Metab Dis. 2012 Mar;35(2):211-25. doi: 10.1007/s10545-011-9382-9. Epub 2011 Aug 27. J Inherit Metab Dis. 2012. PMID: 21874297 Free PMC article. Review.
Peroxisomal disorders: a review.
Fournier B, Smeitink JA, Dorland L, Berger R, Saudubray JM, Poll-The BT. Fournier B, et al. Among authors: smeitink ja. J Inherit Metab Dis. 1994;17(4):470-86. doi: 10.1007/BF00711362. J Inherit Metab Dis. 1994. PMID: 7967497 Review.
Respiratory chain complex I deficiency.
Triepels RH, Van Den Heuvel LP, Trijbels JM, Smeitink JA. Triepels RH, et al. Among authors: smeitink ja. Am J Med Genet. 2001 Spring;106(1):37-45. doi: 10.1002/ajmg.1397. Am J Med Genet. 2001. PMID: 11579423 Review.
van Proosdij JM, Smeitink JA. van Proosdij JM, et al. Among authors: smeitink ja. Tijdschr Kindergeneeskd. 1989 Apr;57(2):49-53. Tijdschr Kindergeneeskd. 1989. PMID: 2741158 Dutch.
Smith-Lemli-Opitz syndrome and the DHCR7 gene.
Jira PE, Waterham HR, Wanders RJ, Smeitink JA, Sengers RC, Wevers RA. Jira PE, et al. Among authors: smeitink ja. Ann Hum Genet. 2003 May;67(Pt 3):269-80. doi: 10.1046/j.1469-1809.2003.00034.x. Ann Hum Genet. 2003. PMID: 12914579 Review.
305 results