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Results by year

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

Year Number of Results
1991 1
1993 3
1995 3
1996 4
1997 4
1998 4
1999 4
2000 5
2001 5
2002 8
2003 11
2004 10
2005 7
2006 7
2007 11
2008 8
2009 8
2010 17
2011 9
2012 18
2013 13
2014 11
2015 17
2016 17
2017 16
2018 9
2019 9
2020 16
2021 15
2022 22
2023 11
2024 3

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PubMed for id: 1639

279 results

Results by year

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Page 1
Perry disease in an Argentine family due to the DCTN1 p.G67D variant.
Silva E, Itzcovich T, Niikado M, Caride A, Fernández E, Vázquez JC, Romorini L, Marazita M, Sevlever G, Martinetto H, Surace EI. Silva E, et al. Parkinsonism Relat Disord. 2022 Apr;97:63-64. doi: 10.1016/j.parkreldis.2022.03.009. Epub 2022 Mar 21. Parkinsonism Relat Disord. 2022. PMID: 35325666 No abstract available.
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB.
Procopio R, Gagliardi M, D'Amelio M, Brighina L, Nicoletti G, Morelli M, Bonapace G, Quattrone A, Annesi G. Procopio R, et al. Neurobiol Aging. 2020 Sep;93:143.e5-143.e7. doi: 10.1016/j.neurobiolaging.2020.04.006. Epub 2020 Apr 15. Neurobiol Aging. 2020. PMID: 32402491
DCTN1-related neurodegeneration: Perry syndrome and beyond.
Konno T, Ross OA, Teive HAG, Sławek J, Dickson DW, Wszolek ZK. Konno T, et al. Parkinsonism Relat Disord. 2017 Aug;41:14-24. doi: 10.1016/j.parkreldis.2017.06.004. Epub 2017 Jun 12. Parkinsonism Relat Disord. 2017. PMID: 28625595 Free PMC article. Review.
279 results