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

Year Number of Results
1996 1
1997 1
2002 4
2003 4
2004 10
2005 23
2006 9
2007 8
2008 18
2009 15
2010 13
2011 11
2012 16
2013 23
2014 19
2015 14
2016 23
2017 14
2018 21
2019 33
2020 37
2021 49
2022 2
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325 results
Results by year
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Page 1
Coding mutations in NUS1 contribute to Parkinson's disease.
Guo JF, Zhang L, Li K, Mei JP, Xue J, Chen J, Tang X, Shen L, Jiang H, Chen C, Guo H, Wu XL, Sun SL, Xu Q, Sun QY, Chan P, Shang HF, Wang T, Zhao GH, Liu JY, Xie XF, Jiang YQ, Liu ZH, Zhao YW, Zhu ZB, Li JD, Hu ZM, Yan XX, Fang XD, Wang GH, Zhang FY, Xia K, Liu CY, Zhu XW, Yue ZY, Li SC, Cai HB, Zhang ZH, Duan RH, Tang BS. Guo JF, et al. Proc Natl Acad Sci U S A. 2018 Nov 6;115(45):11567-11572. doi: 10.1073/pnas.1809969115. Epub 2018 Oct 22. Proc Natl Acad Sci U S A. 2018. PMID: 30348779 Free PMC article.
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.
Huang XJ, Wang SG, Guo XN, Tian WT, Zhan FX, Zhu ZY, Yin XM, Liu Q, Yin KL, Liu XR, Zhang Y, Liu ZG, Liu XL, Zheng L, Wang T, Wu L, Rong TY, Wang Y, Zhang M, Bi GH, Tang WG, Zhang C, Zhong P, Wang CY, Tang JG, Lu W, Zhang RX, Zhao GH, Li XH, Li H, Chen T, Li HY, Luo XG, Song YY, Tang HD, Luan XH, Zhou HY, Tang BS, Chen SD, Cao L. Huang XJ, et al. Mov Disord. 2020 Aug;35(8):1428-1437. doi: 10.1002/mds.28061. Epub 2020 May 11. Mov Disord. 2020. PMID: 32392383
First annual report of Chinese haemovigilance network.
Yin Y, Tian X, Li L, Kong Y, Wang J, Lin F, Song N, Chen Q, Gan J, Peng T, Li X, Wu Y, Ge H, Wang H, Jiang J, Bai L, Ji H, Zhao G, Huang Y, Liu Z; Chinese Haemovigilance Network. Yin Y, et al. Among authors: zhao g. Vox Sang. 2021 Jul;116(6):718-724. doi: 10.1111/vox.13059. Epub 2021 Jan 10. Vox Sang. 2021. PMID: 33423307
325 results