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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 20
Text availability
Article attribute
Article type
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Search Results

255 results
Results by year
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Page 1
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, 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, 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.
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
Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7.
Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E, Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Dion PA, Suchowersky O, Trempe JF, Rouleau GA, Gan-Or Z. Estiar MA, et al. Among authors: dupre n. Mov Disord. 2021 Jul;36(7):1664-1675. doi: 10.1002/mds.28528. Epub 2021 Feb 17. Mov Disord. 2021. PMID: 33598982
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.
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.
Therapies for ataxias.
Martineau L, Noreau A, Dupré N. Martineau L, et al. Among authors: dupre n. Curr Treat Options Neurol. 2014 Jul;16(7):300. doi: 10.1007/s11940-014-0300-y. Curr Treat Options Neurol. 2014. PMID: 24832479
Oligogenicity, C9orf72 expansion, and variant severity in ALS.
Ross JP, Leblond CS, Laurent SB, Spiegelman D, Dionne-Laporte A, Camu W, Dupré N, Dion PA, Rouleau GA. Ross JP, et al. Among authors: dupre n. Neurogenetics. 2020 Jul;21(3):227-242. doi: 10.1007/s10048-020-00612-7. Epub 2020 May 8. Neurogenetics. 2020. PMID: 32385536
255 results