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

Year Number of Results
1981 1
1994 2
1996 1
1997 3
1998 3
2001 1
2004 1
2006 2
2007 1
2008 5
2009 7
2010 6
2011 7
2012 14
2013 13
2014 10
2015 12
2016 10
2017 15
2018 6
2019 4
2020 2
2021 3
2022 2
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106 results
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Page 1
Hodel J, Outteryck O, Verclytte S, Deramecourt V, Lacour A, Pruvo JP, Vermersch P, Leclerc X. Hodel J, et al. Among authors: lacour a. AJNR Am J Neuroradiol. 2016 Feb;37(2):E12. doi: 10.3174/ajnr.A4634. Epub 2015 Dec 3. AJNR Am J Neuroradiol. 2016. PMID: 26635281 Free PMC article. No abstract available.
[Current issues in hereditary neuropathies].
Lacour A. Lacour A. Rev Neurol (Paris). 2013 Dec;169(12):1001-3. doi: 10.1016/j.neurol.2013.05.005. Epub 2013 Nov 11. Rev Neurol (Paris). 2013. PMID: 24230477 Review. French.
Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France.
Davion JB, Bocquillon P, Cassim F, Frezel N, Lacour A, Dhaenens CM, Maurage CA, Gibier JB, Hachulla E, Nguyen The Tich S, Defebvre L, Merle PE, Tard C. Davion JB, et al. Among authors: lacour a. Rev Neurol (Paris). 2021 Nov;177(9):1160-1167. doi: 10.1016/j.neurol.2021.02.392. Epub 2021 Jul 10. Rev Neurol (Paris). 2021. PMID: 34253345
Quick, "imputation-free" meta-analysis with proxy-SNPs.
Meesters C, Leber M, Herold C, Angisch M, Mattheisen M, Drichel D, Lacour A, Becker T. Meesters C, et al. Among authors: lacour a. BMC Bioinformatics. 2012 Sep 12;13:231. doi: 10.1186/1471-2105-13-231. BMC Bioinformatics. 2012. PMID: 22971100 Free PMC article.
Integrated genome-wide pathway association analysis with INTERSNP.
Herold C, Mattheisen M, Lacour A, Vaitsiakhovich T, Angisch M, Drichel D, Becker T. Herold C, et al. Among authors: lacour a. Hum Hered. 2012;73(2):63-72. doi: 10.1159/000336196. Epub 2012 Mar 7. Hum Hered. 2012. PMID: 22399020 Free article.
A one-degree-of-freedom test for supra-multiplicativity of SNP effects.
Herold C, Ramirez A, Drichel D, Lacour A, Vaitsiakhovich T, Nöthen MM, Jessen F, Maier W, Becker T. Herold C, et al. Among authors: lacour a. PLoS One. 2013 Oct 30;8(10):e78038. doi: 10.1371/journal.pone.0078038. eCollection 2013. PLoS One. 2013. PMID: 24205078 Free PMC article.
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies.
Villar-Quiles RN, Donkervoort S, de Becdelièvre A, Gartioux C, Jobic V, Foley AR, McCarty RM, Hu Y, Menassa R, Michel L, Gousse G, Lacour A, Petiot P, Streichenberger N, Choumert A, Declerck L, Urtizberea JA, Sole G, Furby A, Cérino M, Krahn M, Campana-Salort E, Ferreiro A, Eymard B, Bönnemann CG, Bharucha-Goebel D, Sumner CJ, Connolly AM, Richard P, Allamand V, Métay C, Stojkovic T. Villar-Quiles RN, et al. Among authors: lacour a. J Neuromuscul Dis. 2021;8(4):633-645. doi: 10.3233/JND-200577. J Neuromuscul Dis. 2021. PMID: 33749658
Confounding clinical presentation and different disease progression in CMT4B1.
Guimarães-Costa R, Villar-Quiles RN, Latour P, Sole G, Husson I, Lacour A, Leonard-Louis S, Stojkovic T. Guimarães-Costa R, et al. Among authors: lacour a. Neuromuscul Disord. 2020 Jul;30(7):576-582. doi: 10.1016/j.nmd.2020.05.003. Epub 2020 May 16. Neuromuscul Disord. 2020. PMID: 32586600
106 results