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

Year Number of Results
2002 4
2003 2
2004 4
2005 9
2006 4
2007 8
2008 5
2009 7
2010 5
2011 8
2012 11
2013 14
2014 12
2015 10
2016 8
2017 7
2018 11
2019 14
2020 9
2021 11
2022 13
2023 10
2024 1

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152 results

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Page 1
Commentary from the Editor.
Oldfors A. Oldfors A. Neuromuscul Disord. 2022 Jan;32(1):1-4. doi: 10.1016/j.nmd.2022.01.003. Neuromuscul Disord. 2022. PMID: 35144754 No abstract available.
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.
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
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.
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.
[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.
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.
Hereditary myosin myopathies.
Oldfors A. Oldfors A. Neuromuscul Disord. 2007 May;17(5):355-67. doi: 10.1016/j.nmd.2007.02.008. Epub 2007 Apr 16. Neuromuscul Disord. 2007. PMID: 17434305 Review.
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.
152 results