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

Year Number of Results
1987 1
1988 1
1989 3
1992 6
1993 5
1994 5
1995 4
1996 8
1997 10
1998 21
1999 15
2000 13
2001 16
2002 10
2003 19
2004 19
2005 13
2006 25
2007 28
2008 21
2009 20
2010 21
2011 24
2012 27
2013 18
2014 12
2015 26
2016 12
2017 13
2018 16
2019 13
2020 9
2021 16
2022 5
Text availability
Article attribute
Article type
Publication date

Search Results

421 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.
Mitochondrial medicine.
Koene S, Smeitink J. Koene S, et al. Among authors: smeitink j. J Inherit Metab Dis. 2011 Apr;34(2):247-8. doi: 10.1007/s10545-011-9292-x. J Inherit Metab Dis. 2011. PMID: 21365464 Free PMC article. No abstract available.
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.
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.
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.
Exome sequencing in paediatric patients with movement disorders.
Kwong AK, Tsang MH, Fung JL, Mak CC, Chan KL, Rodenburg RJT, Lek M, Huang S, Pajusalu S, Yau MM, Tsoi C, Fung S, Liu KT, Ma CK, Wong S, Yau EK, Tai SM, Fung EL, Wu NS, Tsung LY, Smeitink J, Chung BH, Fung CW. Kwong AK, et al. Among authors: smeitink j. Orphanet J Rare Dis. 2021 Jan 15;16(1):32. doi: 10.1186/s13023-021-01688-6. Orphanet J Rare Dis. 2021. PMID: 33446253 Free PMC article.
421 results