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

Year Number of Results
1977 2
1978 1
1979 2
1980 2
1981 3
1982 1
1983 2
1985 1
1986 6
1987 2
1988 3
1989 10
1990 6
1991 6
1992 5
1993 2
1994 7
1995 9
1996 6
1997 3
1998 6
1999 7
2000 5
2001 4
2002 7
2003 8
2004 8
2005 11
2006 9
2007 13
2008 8
2009 7
2010 6
2011 10
2012 14
2013 14
2014 13
2015 11
2016 9
2017 10
2018 13
2019 14
2020 9
2021 6
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267 results
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Page 1
Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Trifunovic A, Wredenberg A, Falkenberg M, Spelbrink JN, Rovio AT, Bruder CE, Bohlooly-Y M, Gidlöf S, Oldfors A, Wibom R, Törnell J, Jacobs HT, Larsson NG. Trifunovic A, et al. Among authors: oldfors a. Nature. 2004 May 27;429(6990):417-23. doi: 10.1038/nature02517. Nature. 2004. PMID: 15164064
Oldfors A. Oldfors A. Neuromuscul Disord. 2020 Oct;30(10):795. doi: 10.1016/j.nmd.2020.09.030. Epub 2020 Sep 23. Neuromuscul Disord. 2020. PMID: 33011058 No abstract available.
Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric Cores.
Donkervoort S, Kutzner CE, Hu Y, Lornage X, Rendu J, Stojkovic T, Baets J, Neuhaus SB, Tanboon J, Maroofian R, Bolduc V, Mroczek M, Conijn S, Kuntz NL, Töpf A, Monges S, Lubieniecki F, McCarty RM, Chao KR, Governali S, Böhm J, Boonyapisit K, Malfatti E, Sangruchi T, Horkayne-Szakaly I, Hedberg-Oldfors C, Efthymiou S, Noguchi S, Djeddi S, Iida A, di Rosa G, Fiorillo C, Salpietro V, Darin N, Fauré J, Houlden H, Oldfors A, Nishino I, de Ridder W, Straub V, Pokrzywa W, Laporte J, Foley AR, Romero NB, Ottenheijm C, Hoppe T, Bönnemann CG. Donkervoort S, et al. Among authors: oldfors a. Am J Hum Genet. 2020 Dec 3;107(6):1078-1095. doi: 10.1016/j.ajhg.2020.11.002. Epub 2020 Nov 19. Am J Hum Genet. 2020. PMID: 33217308 Free PMC article.
Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles.
Hedberg-Oldfors C, Meyer R, Nolte K, Abdul Rahim Y, Lindberg C, Karason K, Thuestad IJ, Visuttijai K, Geijer M, Begemann M, Kraft F, Lausberg E, Hitpass L, Götzl R, Luna EJ, Lochmüller H, Koschmieder S, Gramlich M, Gess B, Elbracht M, Weis J, Kurth I, Oldfors A, Knopp C. Hedberg-Oldfors C, et al. Among authors: oldfors a. Brain. 2020 Aug 1;143(8):2406-2420. doi: 10.1093/brain/awaa206. Brain. 2020. PMID: 32779703 Free PMC article.
Myosinopathies: pathology and mechanisms.
Tajsharghi H, Oldfors A. Tajsharghi H, et al. Among authors: oldfors a. Acta Neuropathol. 2013 Jan;125(1):3-18. doi: 10.1007/s00401-012-1024-2. Epub 2012 Aug 5. Acta Neuropathol. 2013. PMID: 22918376 Free PMC article. Review.
Progressive external ophthalmoplegia associated with novel MT-TN mutations.
Visuttijai K, Hedberg-Oldfors C, Lindgren U, Nordström S, Elíasdóttir Ó, Lindberg C, Oldfors A. Visuttijai K, et al. Among authors: oldfors a. Acta Neurol Scand. 2021 Jan;143(1):103-108. doi: 10.1111/ane.13339. Epub 2020 Sep 19. Acta Neurol Scand. 2021. PMID: 32869280 Free PMC article.
Myopathology in the times of modern genetics.
Schuelke M, Øien NC, Oldfors A. Schuelke M, et al. Among authors: oldfors a. Neuropathol Appl Neurobiol. 2017 Feb;43(1):44-61. doi: 10.1111/nan.12374. Neuropathol Appl Neurobiol. 2017. PMID: 28009443 Review.
267 results
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