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

Year Number of Results
1986 1
1987 1
1989 1
1991 1
1992 2
1993 4
1994 3
1995 3
1996 4
1997 3
1998 4
1999 6
2000 4
2001 4
2002 7
2003 5
2004 5
2005 8
2006 7
2007 11
2008 19
2009 23
2010 14
2011 14
2012 13
2013 8
2014 11
2015 7
2016 11
2017 12
2018 10
2019 8
2020 10
2021 12
2022 3
2024 0

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PubMed for id: 2643

223 results

Results by year

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Page 1
GCH1 mutations in hereditary spastic paraplegia.
Varghaei P, Yoon G, Estiar MA, Veyron S, Leveille E, Dupré N, Trempe JF, Rouleau GA, Gan-Or Z. Varghaei P, et al. Clin Genet. 2021 Jul;100(1):51-58. doi: 10.1111/cge.13955. Epub 2021 Mar 18. Clin Genet. 2021. PMID: 33713342
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
Pan HX, Zhao YW, Mei JP, Fang ZH, Wang Y, Zhou X, Zhou YJ, Zhang R, Zhang KL, Jiang L, Zeng Q, He Y, Wang Z, Liu ZH, Xu Q, Sun QY, Yang Y, Hu YC, Chen YS, Du J, Lei LF, Zhang HN, Wang CY, Yan XX, Shen L, Jiang H, Tan JQ, Li JC, Tang BS, Guo JF. Pan HX, et al. Transl Neurodegener. 2020 Aug 4;9(1):31. doi: 10.1186/s40035-020-00212-3. Transl Neurodegener. 2020. PMID: 32746945 Free PMC article.
223 results