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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 11
2022 13
2023 10
2024 6

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295 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
Commentary from the Editor.
Oldfors A. Oldfors A. Neuromuscul Disord. 2023 Jan;33(1):1-4. doi: 10.1016/j.nmd.2022.12.010. Epub 2022 Dec 16. Neuromuscul Disord. 2023. PMID: 36609118 No abstract available.
Commentary from the Editor.
Oldfors A. Oldfors A. Neuromuscul Disord. 2024 Jan;34:123-125. doi: 10.1016/j.nmd.2023.12.013. Epub 2023 Dec 22. Neuromuscul Disord. 2024. PMID: 38199149 No abstract available.
Polyglucosan storage myopathies.
Hedberg-Oldfors C, Oldfors A. Hedberg-Oldfors C, et al. Among authors: oldfors a. Mol Aspects Med. 2015 Dec;46:85-100. doi: 10.1016/j.mam.2015.08.006. Epub 2015 Aug 13. Mol Aspects Med. 2015. PMID: 26278982 Review.
Inclusion body myositis.
Oldfors A, Lindberg C. Oldfors A, et al. Curr Opin Neurol. 1999 Oct;12(5):527-33. doi: 10.1097/00019052-199910000-00006. Curr Opin Neurol. 1999. PMID: 10590889 Review.
[No title available]
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.
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study.
Schiava M, Ikenaga C, Villar-Quiles RN, Caballero-Ávila M, Topf A, Nishino I, Kimonis V, Udd B, Schoser B, Zanoteli E, Souza PVS, Tasca G, Lloyd T, Lopez-de Munain A, Paradas C, Pegoraro E, Nadaj-Pakleza A, De Bleecker J, Badrising U, Alonso-Jiménez A, Kostera-Pruszczyk A, Miralles F, Shin JH, Bevilacqua JA, Olivé M, Vorgerd M, Kley R, Brady S, Williams T, Domínguez-González C, Papadimas GK, Warman-Chardon J, Claeys KG, de Visser M, Muelas N, LaForet P, Malfatti E, Alfano LN, Nair SS, Manousakis G, Kushlaf HA, Harms MB, Nance C, Ramos-Fransi A, Rodolico C, Hewamadduma C, Cetin H, García-García J, Pál E, Farrugia ME, Lamont PJ, Quinn C, Nedkova-Hristova V, Peric S, Luo S, Oldfors A, Taylor K, Ralston S, Stojkovic T, Weihl C, Diaz-Manera J; VCP International Study Group; VCP International Study Group. Schiava M, et al. Among authors: oldfors a. J Neurol Neurosurg Psychiatry. 2022 Jul 27:jnnp-2022-328921. doi: 10.1136/jnnp-2022-328921. Online ahead of print. J Neurol Neurosurg Psychiatry. 2022. PMID: 35896379 Free PMC article.
Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem Proteinopathy.
Schiava M, Ikenaga C, Topf A, Caballero-Ávila M, Chou TF, Li S, Wang F, Daw J, Stojkovic T, Villar-Quiles R, Nishino I, Inoue M, Nishimori Y, Saito Y, Katsuno M, Noda S, Ito C, Otsuka M, Nahir S, Manousakis G, Walk D, Quinn C, Alfano L, Sahenk Z, Tasca G, Monforte M, Sabatelli M, Bisogni G, Oldfors A, Rydeliu A, Pal E, Paradas C, Velez B, De Bleecker JL, Farugia ME, Longman C, Harms MB, Ralston S, Zanoteli E, Macedo Serafim da Silva A, Sotoca J, Juntas-Morales R, Bevilacqua J, Balart M, Talbot S, Straub V, Guglieri M, Marini-Bettolo C, Diaz-Manera J, Weihl CC. Schiava M, et al. Among authors: oldfors a. Neurol Genet. 2023 Aug 15;9(5):e200093. doi: 10.1212/NXG.0000000000200093. eCollection 2023 Oct. Neurol Genet. 2023. PMID: 37588275 Free PMC article.
Thick filament diseases.
Oldfors A, Lamont PJ. Oldfors A, et al. Adv Exp Med Biol. 2008;642:78-91. doi: 10.1007/978-0-387-84847-1_7. Adv Exp Med Biol. 2008. PMID: 19181095 Review.
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.
295 results