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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 3
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Search Results

241 results
Results by year
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Page 1
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.
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.
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, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2007 Feb 23 [updated 2018 Dec 6]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301553 Free Books & Documents. 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
Current and Promising Therapies in Autosomal Recessive Ataxias.
Picher-Martel V, Dupre N. Picher-Martel V, et al. Among authors: dupre n. CNS Neurol Disord Drug Targets. 2018;17(3):161-171. doi: 10.2174/1871527317666180419115029. CNS Neurol Disord Drug Targets. 2018. PMID: 29676235 Review.
Assessing non-Mendelian inheritance in inherited axonopathies.
Bis-Brewer DM, Gan-Or Z, Sleiman P; Inherited Neuropathy Consortium, Hakonarson H, Fazal S, Courel S, Cintra V, Tao F, Estiar MA, Tarnopolsky M, Boycott KM, Yoon G, Suchowersky O, Dupré N, Cheng A, Lloyd TE, Rouleau G, Schüle R, Züchner S. Bis-Brewer DM, et al. Among authors: dupre n. Genet Med. 2020 Dec;22(12):2114-2119. doi: 10.1038/s41436-020-0924-0. Epub 2020 Aug 3. Genet Med. 2020. PMID: 32741968 Free PMC article.
Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum.
Gauvreau C, Brisson JD, Dupré N. Gauvreau C, et al. Among authors: dupre n. 2006 Feb 2 [updated 2020 Sep 17]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2006 Feb 2 [updated 2020 Sep 17]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301546 Free Books & Documents. Review.
The Puzzle of Huntington Disease Phenocopies.
Dupré N, Rouleau G. Dupré N, et al. JAMA Neurol. 2016 Sep 1;73(9):1056-8. doi: 10.1001/jamaneurol.2016.2095. JAMA Neurol. 2016. PMID: 27399805 No abstract available.
241 results