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Results by year

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

Year Number of Results
1976 1
1979 1
1981 1
1982 1
1983 3
1984 1
1985 2
1989 3
1990 2
1993 2
1995 3
1996 1
1997 24
1998 14
1999 16
2000 17
2001 19
2002 12
2003 14
2004 15
2005 16
2006 14
2007 15
2008 22
2009 13
2010 15
2011 28
2012 20
2013 24
2014 24
2015 27
2016 22
2017 18
2018 15
2019 20
2020 15
2021 18
2022 22
2023 29
2024 12

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PubMed for id: 342591

500 results

Results by year

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Page 1
Phenotypic spectrum of inclusion body myositis.
Roy B, Dimachkie MM, Naddaf E. Roy B, et al. Clin Exp Rheumatol. 2024 Feb;42(2):445-453. doi: 10.55563/clinexprheumatol/fhrx3q. Epub 2024 Feb 28. Clin Exp Rheumatol. 2024. PMID: 38436356 Free article. Review.
Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy.
Donkervoort S, Mohassel P, O'Leary M, Bonner DE, Hartley T, Acquaye N, Brull A, Mozaffar T, Saporta MA, Dyment DA, Sampson JB, Pajusalu S, Austin-Tse C, Hurth K, Cohen JS, McWalter K, Warman-Chardon J, Crunk A, Foley AR; Undiagnosed Diseases Network; Mammen AL, Wheeler MT, O'Donnell-Luria A, Bönnemann CG. Donkervoort S, et al. Ann Clin Transl Neurol. 2024 Mar;11(3):629-640. doi: 10.1002/acn3.51983. Epub 2024 Feb 4. Ann Clin Transl Neurol. 2024. PMID: 38311799 Free PMC article.
Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 2.
Kleefeld F, Horvath R, Pinal-Fernandez I, Mammen AL, Casal-Dominguez M, Hathazi D, Melchert S, Hahn K, Sickmann A, Muselmann-Genschow C, Hentschel A, Preuße C, Roos A, Schoser B, Stenzel W. Kleefeld F, et al. Acta Neuropathol. 2024 Jan 19;147(1):19. doi: 10.1007/s00401-023-02673-y. Acta Neuropathol. 2024. PMID: 38240888 Free PMC article.
500 results