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

Year Number of Results
1993 2
1999 1
2002 1
2003 3
2004 2
2005 2
2006 5
2007 9
2008 10
2009 7
2010 6
2011 12
2012 10
2013 8
2014 5
2015 8
2016 16
2017 12
2018 19
2019 12
2020 28
2021 18
2022 21
2023 19
2024 9

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209 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, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 Feb 23 [updated 2018 Dec 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301553 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.
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
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 of Rare Variants in ARSA with Parkinson's Disease.
Senkevich K, Beletskaia M, Dworkind A, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Nagornov I, Tyurin A, Miliukhina I, Timofeeva A, Emelyanov A, Trempe JF, Zakharova E, Alcalay RN, Pchelina S, Gan-Or Z. Senkevich K, et al. Among authors: dupre n. Mov Disord. 2023 Oct;38(10):1806-1812. doi: 10.1002/mds.29521. Epub 2023 Jun 28. Mov Disord. 2023. PMID: 37381728
GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease.
Senkevich K, Zorca CE, Dworkind A, Rudakou U, Somerville E, Yu E, Ermolaev A, Nikanorova D, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Grenn FP, Chiang MSR, Sardi SP, Vanderperre B, Blauwendraat C, Trempe JF, Fon EA, Durcan TM, Alcalay RN, Gan-Or Z. Senkevich K, et al. Among authors: dupre n. Brain. 2023 May 2;146(5):1859-1872. doi: 10.1093/brain/awac413. Brain. 2023. PMID: 36370000 Free PMC article.
209 results