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

Year Number of Results
1997 1
1998 1
1999 2
2000 4
2002 1
2004 4
2005 3
2006 6
2007 9
2008 9
2009 11
2010 5
2011 5
2012 11
2013 12
2014 7
2015 12
2016 10
2017 9
2018 4
2019 8
2020 6
2021 3
2022 1
2023 2
2025 0

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128 results

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Page 1
New insights into CC2D2A-related Joubert syndrome.
Harion M, Qebibo L, Riquet A, Rougeot C, Afenjar A, Garel C, Louha M, Lacaze E, Audic-Gérard F, Barth M, Berquin P, Bonneau D, Bourdain F, Busa T, Colin E, Cuisset JM, Des Portes V, Dorison N, Francannet C, Héron B, Laroche C, Lebrun M, Métreau J, Odent S, Pasquier L, Trujillo YP, Perrin L, Pinson L, Rivier F, Sigaudy S, Thauvin-Robinet C, Louvier UW, Labayle O, Rodriguez D, Valence S, Burglen L. Harion M, et al. Among authors: cuisset jm. J Med Genet. 2023 Jun;60(6):578-586. doi: 10.1136/jmg-2022-108754. Epub 2022 Nov 1. J Med Genet. 2023. PMID: 36319078
Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1.
Douniol M, Jacquette A, Cohen D, Bodeau N, Rachidi L, Angeard N, Cuisset JM, Vallée L, Eymard B, Plaza M, Héron D, Guilé JM. Douniol M, et al. Among authors: cuisset jm. Dev Med Child Neurol. 2012 Oct;54(10):905-11. doi: 10.1111/j.1469-8749.2012.04379.x. Epub 2012 Aug 3. Dev Med Child Neurol. 2012. PMID: 22861906 Free article. Review.
Delineation of 15q13.3 microdeletions.
Masurel-Paulet A, Andrieux J, Callier P, Cuisset JM, Le Caignec C, Holder M, Thauvin-Robinet C, Doray B, Flori E, Alex-Cordier MP, Beri M, Boute O, Delobel B, Dieux A, Vallee L, Jaillard S, Odent S, Isidor B, Beneteau C, Vigneron J, Bilan F, Gilbert-Dussardier B, Dubourg C, Labalme A, Bidon C, Gautier A, Pernes P, Pinoit JM, Huet F, Mugneret F, Aral B, Jonveaux P, Sanlaville D, Faivre L. Masurel-Paulet A, et al. Among authors: cuisset jm. Clin Genet. 2010 Aug;78(2):149-61. doi: 10.1111/j.1399-0004.2010.01374.x. Epub 2010 Feb 9. Clin Genet. 2010. PMID: 20236110
Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy.
McDonald CM, Meier T, Voit T, Schara U, Straathof CS, D'Angelo MG, Bernert G, Cuisset JM, Finkel RS, Goemans N, Rummey C, Leinonen M, Spagnolo P, Buyse GM; DELOS Study Group. McDonald CM, et al. Among authors: cuisset jm. Neuromuscul Disord. 2016 Aug;26(8):473-80. doi: 10.1016/j.nmd.2016.05.008. Epub 2016 May 12. Neuromuscul Disord. 2016. PMID: 27238057 Free article. Clinical Trial.
Guillain-Barre syndrome, influenzalike illnesses, and influenza vaccination during seasons with and without circulating A/H1N1 viruses.
Grimaldi-Bensouda L, Alpérovitch A, Besson G, Vial C, Cuisset JM, Papeix C, Lyon-Caen O, Benichou J, Rossignol M; Lucien Abenhaim for the GBS-PGRx Study Group. Grimaldi-Bensouda L, et al. Among authors: cuisset jm. Am J Epidemiol. 2011 Aug 1;174(3):326-35. doi: 10.1093/aje/kwr072. Epub 2011 Jun 7. Am J Epidemiol. 2011. PMID: 21652600
[Neuropediatric approach to autism].
Cuisset JM, Joriot S, Auvin S, Gozé O, Medjkane F, Salloum A, Delion P, Vallée L. Cuisset JM, et al. Arch Pediatr. 2005 Dec;12(12):1734-41. doi: 10.1016/j.arcped.2005.09.016. Epub 2005 Oct 10. Arch Pediatr. 2005. PMID: 16219450 Review. French.
[Central manifestations of dystrophinopathies].
Cuisset JM, Rivier F. Cuisset JM, et al. Arch Pediatr. 2015 Dec;22(12 Suppl 1):12S58-62. doi: 10.1016/S0929-693X(16)30010-0. Arch Pediatr. 2015. PMID: 26773588 French.
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.
Caubit X, Gubellini P, Andrieux J, Roubertoux PL, Metwaly M, Jacq B, Fatmi A, Had-Aissouni L, Kwan KY, Salin P, Carlier M, Liedén A, Rudd E, Shinawi M, Vincent-Delorme C, Cuisset JM, Lemaitre MP, Abderrehamane F, Duban B, Lemaitre JF, Woolf AS, Bockenhauer D, Severac D, Dubois E, Zhu Y, Sestan N, Garratt AN, Lydia Kerkerian-Le Goff, Fasano L. Caubit X, et al. Among authors: cuisset jm. Nat Genet. 2016 Nov;48(11):1359-1369. doi: 10.1038/ng.3681. Epub 2016 Sep 26. Nat Genet. 2016. PMID: 27668656 Free PMC article.
128 results