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

Year Number of Results
1985 2
1986 2
1988 2
1989 3
1990 3
1991 3
1992 4
1993 6
1995 7
1996 3
1997 3
1998 5
1999 4
2000 6
2001 5
2002 10
2003 9
2004 11
2005 6
2006 9
2007 8
2008 15
2009 18
2010 21
2011 17
2012 21
2013 18
2014 13
2015 7
2016 10
2017 10
2018 13
2019 9
2020 6
2021 3
2022 3
2023 4
2024 0

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262 results

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Page 1
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.
Coutelier M, Hammer MB, Stevanin G, Monin ML, Davoine CS, Mochel F, Labauge P, Ewenczyk C, Ding J, Gibbs JR, Hannequin D, Melki J, Toutain A, Laugel V, Forlani S, Charles P, Broussolle E, Thobois S, Afenjar A, Anheim M, Calvas P, Castelnovo G, de Broucker T, Vidailhet M, Moulignier A, Ghnassia RT, Tallaksen C, Mignot C, Goizet C, Le Ber I, Ollagnon-Roman E, Pouget J, Brice A, Singleton A, Durr A; Spastic Paraplegia and Ataxia Network. Coutelier M, et al. Among authors: broussolle e. JAMA Neurol. 2018 May 1;75(5):591-599. doi: 10.1001/jamaneurol.2017.5121. JAMA Neurol. 2018. PMID: 29482223 Free PMC article.
LRP10 in α-synucleinopathies.
Tesson C, Brefel-Courbon C, Corvol JC, Lesage S, Brice A; French Parkinson's Disease Genetics Study Group. Tesson C, et al. Lancet Neurol. 2018 Dec;17(12):1034. doi: 10.1016/S1474-4422(18)30400-9. Epub 2018 Nov 13. Lancet Neurol. 2018. PMID: 30507386 Free article. No abstract available.
Jules Froment (1878-1946).
Broussolle E, Rethy MP, Thobois S. Broussolle E, et al. J Neurol. 2009 Sep;256(9):1581-2. doi: 10.1007/s00415-009-5214-3. Epub 2009 Jun 30. J Neurol. 2009. PMID: 19565178 No abstract available.
Table tennis dystonia.
Le Floch A, Vidailhet M, Flamand-Rouvière C, Grabli D, Mayer JM, Gonce M, Broussolle E, Roze E. Le Floch A, et al. Among authors: broussolle e. Mov Disord. 2010 Feb 15;25(3):394-7. doi: 10.1002/mds.22968. Mov Disord. 2010. PMID: 20108363
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability.
Fevga C, Tesson C, Carreras Mascaro A, Courtin T, van Coller R, Sakka S, Ferraro F, Farhat N, Bardien S, Damak M, Carr J, Ferrien M, Boumeester V, Hundscheid J, Grillenzoni N, Kessissoglou IA, Kuipers DJS, Quadri M; French and Mediterranean Parkinson disease Genetics Study Group; International Parkinsonism Genetics Network; Corvol JC, Mhiri C, Hassan BA, Breedveld GJ, Lesage S, Mandemakers W, Brice A, Bonifati V. Fevga C, et al. Brain. 2023 Apr 19;146(4):1496-1510. doi: 10.1093/brain/awac326. Brain. 2023. PMID: 36073231 Free PMC article.
Wilson's disease, 100 years later….
Trocello JM, Broussolle E, Girardot-Tinant N, Pelosse M, Lachaux A, Lloyd C, Woimant F. Trocello JM, et al. Among authors: broussolle e. Rev Neurol (Paris). 2013 Dec;169(12):936-43. doi: 10.1016/j.neurol.2013.05.002. Epub 2013 Oct 9. Rev Neurol (Paris). 2013. PMID: 24119853 Review.
Differences in Survival across Monogenic Forms of Parkinson's Disease.
Lanore A, Casse F, Tesson C, Courtin T, Menon PJ, Sambin S, Mangone G, Mariani LL, Lesage S, Brice A, Elbaz A, Corvol JC; French Clinicians Network for Parkinson's Disease Genetics (the PDG Group). Lanore A, et al. Ann Neurol. 2023 Jul;94(1):123-132. doi: 10.1002/ana.26636. Epub 2023 Mar 27. Ann Neurol. 2023. PMID: 36905164
Adrafinil-induced orofacial dyskinesia.
Thobois S, Xie J, Mollion H, Benatru I, Broussolle E. Thobois S, et al. Among authors: broussolle e. Mov Disord. 2004 Aug;19(8):965-6. doi: 10.1002/mds.20154. Mov Disord. 2004. PMID: 15300665
Functional imaging of non-motor signs in Parkinson's disease.
Ballanger B, Poisson A, Broussolle E, Thobois S. Ballanger B, et al. Among authors: broussolle e. J Neurol Sci. 2012 Apr 15;315(1-2):9-14. doi: 10.1016/j.jns.2011.11.008. Epub 2011 Dec 9. J Neurol Sci. 2012. PMID: 22154188 Review.
262 results