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

Year Number of Results
1960 1
1961 1
1962 4
1963 2
1967 2
1968 1
1969 1
1976 1
1979 1
1983 1
1993 2
1999 3
2001 1
2002 2
2003 3
2004 3
2005 2
2006 8
2007 13
2008 14
2009 10
2010 8
2011 14
2012 14
2013 13
2014 11
2015 10
2016 19
2017 14
2018 23
2019 16
2020 36
2021 22
2022 22
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Article attribute
Article type
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Search Results

257 results
Results by year
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Page 1
SYNE1 Deficiency.
Beaudin M, Gamache PL, Gros-Louis F, Dupré N. Beaudin M, et al. Among authors: dupre n. 2007 Feb 23 [updated 2018 Dec 6]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2007 Feb 23 [updated 2018 Dec 6]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301553 Free Books & Documents. Review.
Spastic ataxias.
Bereznyakova O, Dupré N. Bereznyakova O, et al. Among authors: dupre n. Handb Clin Neurol. 2018;155:191-203. doi: 10.1016/B978-0-444-64189-2.00012-3. Handb Clin Neurol. 2018. PMID: 29891058 Review.
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. Among authors: dupre n. Clin Genet. 2021 Jul;100(1):51-58. doi: 10.1111/cge.13955. Epub 2021 Mar 18. Clin Genet. 2021. PMID: 33713342
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease.
Saini P, Rudakou U, Yu E, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Espay AJ, Rouleau GA, Alcalay RN, Fon EA, Postuma RB, Gan-Or Z. Saini P, et al. Among authors: dupre n. Neurobiol Aging. 2021 Apr;100:119.e7-119.e13. doi: 10.1016/j.neurobiolaging.2020.10.019. Epub 2020 Oct 31. Neurobiol Aging. 2021. PMID: 33239198 Free PMC article.
The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force.
Beaudin M, Matilla-Dueñas A, Soong BW, Pedroso JL, Barsottini OG, Mitoma H, Tsuji S, Schmahmann JD, Manto M, Rouleau GA, Klein C, Dupre N. Beaudin M, et al. Among authors: dupre n. Cerebellum. 2019 Dec;18(6):1098-1125. doi: 10.1007/s12311-019-01052-2. Cerebellum. 2019. PMID: 31267374 Free PMC article. Review.
Moyamoya Disease Susceptibility Gene RNF213 Regulates Endothelial Barrier Function.
Roy V, Ross JP, Pépin R, Cortez Ghio S, Brodeur A, Touzel Deschênes L, Le-Bel G, Phillips DE, Milot G, Dion PA, Guérin S, Germain L, Berthod F, Auger FA, Rouleau GA, Dupré N, Gros-Louis F. Roy V, et al. Among authors: dupre n. Stroke. 2022 Apr;53(4):1263-1275. doi: 10.1161/STROKEAHA.120.032691. Epub 2022 Jan 7. Stroke. 2022. PMID: 34991336
257 results