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

Year Number of Results
1989 1
1991 2
1992 7
1993 1
1994 3
1995 4
1996 3
1997 2
1998 1
2001 1
2008 1
2012 2
2014 1
2015 2
2016 2
2017 3
2018 2
2019 1
2020 1
2021 1
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39 results
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Page 1
Childhood-onset Leber hereditary optic neuropathy.
Majander A, Bowman R, Poulton J, Antcliff RJ, Reddy MA, Michaelides M, Webster AR, Chinnery PF, Votruba M, Moore AT, Yu-Wai-Man P. Majander A, et al. Br J Ophthalmol. 2017 Nov;101(11):1505-1509. doi: 10.1136/bjophthalmol-2016-310072. Epub 2017 Mar 17. Br J Ophthalmol. 2017. PMID: 28314831 Free article.
[Mitochondrial diseases].
Pihko H, Suomalainen A, Somer H, Haltia M, Majander A. Pihko H, et al. Among authors: majander a. Duodecim. 1992;108(6):578-90. Duodecim. 1992. PMID: 1366118 Review. Finnish. No abstract available.
Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene.
Turunen JA, Wedenoja J, Repo P, Järvinen RS, Jäntti JE, Mörtenhumer S, Riikonen AS, Lehesjoki AE, Majander A, Kivelä TT. Turunen JA, et al. Among authors: majander a. Am J Ophthalmol. 2018 Apr;188:41-50. doi: 10.1016/j.ajo.2018.01.017. Epub 2018 Jan 31. Am J Ophthalmol. 2018. PMID: 29366613 Free article.
Gene defects in Leber hereditary optic neuroretinopathy.
Savontaus ML, Huoponen K, Majander A, Aula P, Nikoskelainen EK. Savontaus ML, et al. Among authors: majander a. Biochim Biophys Acta. 1992 Jul 17;1101(2):204-5. Biochim Biophys Acta. 1992. PMID: 1633186 Review. No abstract available.
39 results
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