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

Year Number of Results
1989 1
1990 1
1991 1
1993 1
1994 1
2000 2
2002 2
2003 3
2004 3
2005 4
2006 1
2007 3
2008 4
2009 6
2010 5
2011 6
2012 5
2013 6
2014 6
2015 2
2016 4
2017 7
2018 8
2019 11
2020 8
2021 5
2022 5
2023 5
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Search Results

100 results
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Page 1
Targeted therapy in patients with PIK3CA-related overgrowth syndrome.
Venot Q, Blanc T, Rabia SH, Berteloot L, Ladraa S, Duong JP, Blanc E, Johnson SC, Hoguin C, Boccara O, Sarnacki S, Boddaert N, Pannier S, Martinez F, Magassa S, Yamaguchi J, Knebelmann B, Merville P, Grenier N, Joly D, Cormier-Daire V, Michot C, Bole-Feysot C, Picard A, Soupre V, Lyonnet S, Sadoine J, Slimani L, Chaussain C, Laroche-Raynaud C, Guibaud L, Broissand C, Amiel J, Legendre C, Terzi F, Canaud G. Venot Q, et al. Among authors: michot c. Nature. 2018 Jun;558(7711):540-546. doi: 10.1038/s41586-018-0217-9. Epub 2018 Jun 13. Nature. 2018. PMID: 29899452 Free PMC article. Clinical Trial.
Myhre syndrome.
Le Goff C, Michot C, Cormier-Daire V. Le Goff C, et al. Among authors: michot c. Clin Genet. 2014 Jun;85(6):503-13. doi: 10.1111/cge.12365. Epub 2014 Apr 2. Clin Genet. 2014. PMID: 24580733 Review.
Riopel C, Michot C. Riopel C, et al. Among authors: michot c. Ann Pathol. 2007 Feb;27(1):6-15. doi: 10.1016/s0242-6498(07)88679-2. Ann Pathol. 2007. PMID: 17568354 Review. French.
Natural history of Myhre syndrome.
Yang DD, Rio M, Michot C, Boddaert N, Yacoub W, Garcelon N, Thierry B, Bonnet D, Rondeau S, Herve D, Guey S, Angoulvant F, Cormier-Daire V. Yang DD, et al. Among authors: michot c. Orphanet J Rare Dis. 2022 Jul 30;17(1):304. doi: 10.1186/s13023-022-02447-x. Orphanet J Rare Dis. 2022. PMID: 35907855 Free PMC article.
[Huriez syndrome].
Michot C, Girard C, Guillot B, Bessis D. Michot C, et al. Ann Dermatol Venereol. 2005 Aug-Sep;132(8-9 Pt 1):727. doi: 10.1016/s0151-9638(05)79431-x. Ann Dermatol Venereol. 2005. PMID: 16230933 French. No abstract available.
Sleep-disordered breathing in children with pycnodysostosis.
Khirani S, Amaddeo A, Baujat G, Michot C, Couloigner V, Pinto G, Arnaud E, Picard A, Cormier-Daire V, Fauroux B. Khirani S, et al. Among authors: michot c. Am J Med Genet A. 2020 Jan;182(1):122-129. doi: 10.1002/ajmg.a.61393. Epub 2019 Nov 3. Am J Med Genet A. 2020. PMID: 31680459
Growth charts in Kabuki syndrome 1.
Ruault V, Corsini C, Duflos C, Akouete S, Georgescu V, Abaji M, Alembick Y, Alix E, Amiel J, Amouroux C, Barat-Houari M, Baumann C, Bonnard A, Boursier G, Boute O, Burglen L, Busa T, Cordier MP, Cormier-Daire V, Delrue MA, Doray B, Faivre L, Fradin M, Gilbert-Dussardier B, Giuliano F, Goldenberg A, Gorokhova S, Héron D, Isidor B, Jacquemont ML, Jacquette A, Jeandel C, Lacombe D, Le Merrer M, Sang KHLQ, Lyonnet S, Manouvrier S, Michot C, Moncla A, Moutton S, Odent S, Pelet A, Philip N, Pinson L, Reversat J, Roume J, Sanchez E, Sanlaville D, Sarda P, Schaefer E, Till M, Touitou I, Toutain A, Willems M, Gatinois V, Geneviève D. Ruault V, et al. Among authors: michot c. Am J Med Genet A. 2020 Mar;182(3):446-453. doi: 10.1002/ajmg.a.61462. Epub 2019 Dec 26. Am J Med Genet A. 2020. PMID: 31876365
Clinical heterogeneity of NADSYN1-associated VCRL syndrome.
Aubert-Mucca M, Janel C, Porquet-Bordes V, Patat O, Touraine R, Edouard T, Michot C, Tessier A, Cormier-Daire V, Attie-Bitach T, Baujat G. Aubert-Mucca M, et al. Among authors: michot c. Clin Genet. 2023 Mar 23. doi: 10.1111/cge.14328. Online ahead of print. Clin Genet. 2023. PMID: 36951206
[Neonatal renal venous thrombosis in 2008].
Dauger S, Michot C, Garnier A, Hurtaud-Roux MF. Dauger S, et al. Among authors: michot c. Arch Pediatr. 2009 Feb;16(2):132-41. doi: 10.1016/j.arcped.2008.11.014. Epub 2009 Jan 15. Arch Pediatr. 2009. PMID: 19150233 Review. French.
Sleep-disordered breathing in children with mucolipidosis.
Tabone L, Caillaud C, Amaddeo A, Khirani S, Michot C, Couloigner V, Brassier A, Cormier-Daire V, Baujat G, Fauroux B. Tabone L, et al. Among authors: michot c. Am J Med Genet A. 2019 Jul;179(7):1196-1204. doi: 10.1002/ajmg.a.61167. Epub 2019 Apr 30. Am J Med Genet A. 2019. PMID: 31038846
100 results