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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 4
2016 3
2017 4
2018 1
2019 3
2020 4
2021 5
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92 results
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Page 1
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
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
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
Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg disease.
Berrechid AG, Bendjebara M, Bouteiller D, Nasri A, Peuvion JN, Marie Y, Baulac S, Mrabet S, Ribierre T, Cazeneuve C, Imenkacem, Leguern E, Gouider R. Berrechid AG, et al. Among authors: cazeneuve c. Epileptic Disord. 2019 Aug 1;21(4):359-365. doi: 10.1684/epd.2019.1078. Epileptic Disord. 2019. PMID: 31368437 Free article.
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.
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
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.
92 results
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