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

Year Number of Results
1994 2
1995 5
1997 1
1998 2
1999 7
2000 7
2001 2
2002 1
2003 6
2004 1
2005 4
2006 3
2007 1
2008 4
2009 8
2010 4
2011 6
2012 5
2013 1
2014 5
2015 5
2016 3
2017 4
2018 1
2019 3
2020 4
2021 8
2022 0
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Search Results

94 results
Results by year
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Page 1
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
Depienne C, Trouillard O, Saint-Martin C, Gourfinkel-An I, Bouteiller D, Carpentier W, Keren B, Abert B, Gautier A, Baulac S, Arzimanoglou A, Cazeneuve C, Nabbout R, LeGuern E. Depienne C, et al. Among authors: cazeneuve c. J Med Genet. 2009 Mar;46(3):183-91. doi: 10.1136/jmg.2008.062323. Epub 2008 Oct 17. J Med Genet. 2009. PMID: 18930999
Pre-symptomatic diagnosis in ALS.
Corcia P, Lumbroso S, Cazeneuve C, Mouzat K, Camu W, Vourc'h P; on Behalf the FILSLAN network. Corcia P, et al. Among authors: cazeneuve c. Rev Neurol (Paris). 2020 Mar;176(3):166-169. doi: 10.1016/j.neurol.2019.07.027. Epub 2020 Jan 10. Rev Neurol (Paris). 2020. PMID: 31932031
Autosomal dominant cerebellar ataxias.
Marelli C, Cazeneuve C, Brice A, Stevanin G, Dürr A. Marelli C, et al. Among authors: cazeneuve c. Rev Neurol (Paris). 2011 May;167(5):385-400. doi: 10.1016/j.neurol.2011.01.015. Epub 2011 May 5. Rev Neurol (Paris). 2011. PMID: 21546047 Review.
SOD1-related ALS with anticipation in a large family from Martinique.
Giguet-Valard AG, Bellance R, Jeannin S, Duclos S, Olive P, Allard-Saint-Albin O, Cazeneuve C, Clot F, Sophie PV, Barnetche T, Smith-Ravin J, Goizet C. Giguet-Valard AG, et al. Among authors: cazeneuve c. Amyotroph Lateral Scler Frontotemporal Degener. 2021 Nov;22(7-8):545-551. doi: 10.1080/21678421.2021.1900870. Epub 2021 Mar 23. Amyotroph Lateral Scler Frontotemporal Degener. 2021. PMID: 33754899
Deciphering the natural history of SCA7 in children.
Bah MG, Rodriguez D, Cazeneuve C, Mochel F, Devos D, Suppiej A, Roubertie A, Meunier I, Gitiaux C, Curie A, Klapczynski F, Allani-Essid N, Carneiro M, Van Minkelen R, Kievit A, Fluss J, Leheup B, Ratbi L, Héron D, Gras D, Do Cao J, Pichard S, Strubi-Villaume I, Audo I, Lesca G, Charles P, Dubois F, Comet-Didierjean P, Capri Y, Barondiot C, Barathon M, Ewenczyk C, Durr A, Mignot C. Bah MG, et al. Among authors: cazeneuve c. Eur J Neurol. 2020 Nov;27(11):2267-2276. doi: 10.1111/ene.14405. Epub 2020 Jul 23. Eur J Neurol. 2020. PMID: 32558018
Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis.
Teyssou E, Muratet F, Amador MD, Ferrien M, Lautrette G, Machat S, Boillée S, Larmonier T, Saker S, Leguern E, Cazeneuve C, Marie Y, Guegan J, Gyorgy B, Cintas P, Meininger V, Le Forestier N, Salachas F, Couratier P, Camu W, Seilhean D, Millecamps S. Teyssou E, et al. Among authors: cazeneuve c. Neurobiol Aging. 2021 Mar;99:102.e11-102.e20. doi: 10.1016/j.neurobiolaging.2020.10.015. Epub 2020 Oct 23. Neurobiol Aging. 2021. PMID: 33218681
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration.
Barbier M, Camuzat A, Hachimi KE, Guegan J, Rinaldi D, Lattante S, Houot M, Sánchez-Valle R, Sabatelli M, Antonell A, Molina-Porcel L, Clot F, Couratier P, van der Ende E, van der Zee J, Manzoni C, Camu W, Cazeneuve C, Sellal F, Didic M, Golfier V, Pasquier F, Duyckaerts C, Rossi G, Bruni AC, Alvarez V, Gómez-Tortosa E, de Mendonça A, Graff C, Masellis M, Nacmias B, Oumoussa BM, Jornea L, Forlani S; French clinical and genetic Research network on FTLD/FTLD-ALS and PREVDEMALS, The International Frontotemporal Dementia Genomics Consortium, The European Early Onset Dementia (EU -EOD) Consortium, Brainbank Neuro-CEB Neuropathology Network, Neurological Tissue Bank of the Biobank Hospital Clinic-IDIBAPS, Van Deerlin V, Rohrer JD, Gelpi E, Rademakers R, Van Swieten J, Le Guern E, Van Broeckhoven C, Ferrari R, Génin E, Brice A, Le Ber I. Barbier M, et al. Among authors: cazeneuve c. Brain. 2021 Oct 22;144(9):2798-2811. doi: 10.1093/brain/awab171. Brain. 2021. PMID: 34687211
94 results