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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 5
2011 6
2012 5
2013 1
2014 5
2015 5
2016 3
2017 4
2018 1
2019 3
2020 5
2021 9
2022 2
2024 1
2025 6

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106 results

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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
The Two Faces of Pediatric SCA2.
Rive Le Gouard N, G Bah M, Coarelli G, Heinzmann A, Fauret AL, de Sainte-Agathe JM, Cazeneuve C, Gerasimenko A, Gras D, Capri Y, Renaud M, Brais B, Grenenko C, Masurel A, Berquin P, Jobic F, Métreau J, Deiva K, Afenjar A, Gravrand V, Lannuzel A, Anheim M, Geis T, Hehr U, Madan Cohen J, Desnous B, J A Kievit A, Bahi-Buisson N, Rodriguez D, Renaldo F, Cances C, Devos D, Angelini C, Goizet C, Ewenczyk C, Durr A, Mignot C. Rive Le Gouard N, et al. Among authors: cazeneuve c. Eur J Neurol. 2025 Aug;32(8):e70314. doi: 10.1111/ene.70314. Eur J Neurol. 2025. PMID: 40741828 Free PMC article.
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
Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study.
Bogdan T, Wirth T, Iosif A, Schalk A, Montaut S, Bonnard C, Carre G, Lagha-Boukbiza O, Reschwein C, Albugues E, Demuth S, Landsberger H, Einsiedler M, Parratte T, Nguyen A, Lamy F, Durand H, Fahrer P, Voulleminot P, Bigaut K, Chanson JB, Nicolas G, Chelly J, Cazeneuve C, Koenig M, Bund C, Namer IJ, Kremer S, Calmels N, Tranchant C, Anheim M. Bogdan T, et al. Among authors: cazeneuve c. J Neurol. 2022 Dec;269(12):6354-6365. doi: 10.1007/s00415-022-11253-1. Epub 2022 Jul 23. J Neurol. 2022. PMID: 35869996
Amyloidosis and auto-inflammatory syndromes.
Grateau G, Jéru I, Rouaghe S, Cazeneuve C, Ravet N, Duquesnoy P, Cuisset L, Dodé C, Delpech M, Amselem S. Grateau G, et al. Among authors: cazeneuve c. Curr Drug Targets Inflamm Allergy. 2005 Feb;4(1):57-65. doi: 10.2174/1568010053622786. Curr Drug Targets Inflamm Allergy. 2005. PMID: 15720237 Review.
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.
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
106 results