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

Year Number of Results
1987 1
1991 2
1992 1
1994 1
1996 4
1997 1
1998 1
1999 5
2001 1
2002 2
2003 2
2004 1
2005 1
2006 2
2007 3
2008 2
2009 1
2010 3
2011 4
2012 5
2013 6
2014 6
2015 11
2016 12
2017 11
2018 16
2019 25
2020 16
2021 18
2022 14
2023 17
2024 8

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173 results

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Page 1
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).
Fiot E, Alauze B, Donadille B, Samara-Boustani D, Houang M, De Filippo G, Bachelot A, Delcour C, Beyler C, Bois E, Bourrat E, Bui Quoc E, Bourcigaux N, Chaussain C, Cohen A, Cohen-Solal M, Da Costa S, Dossier C, Ederhy S, Elmaleh M, Iserin L, Lengliné H, Poujol-Robert A, Roulot D, Viala J, Albarel F, Bismuth E, Bernard V, Bouvattier C, Brac A, Bretones P, Chabbert-Buffet N, Chanson P, Coutant R, de Warren M, Demaret B, Duranteau L, Eustache F, Gautheret L, Gelwane G, Gourbesville C, Grynberg M, Gueniche K, Jorgensen C, Kerlan V, Lebrun C, Lefevre C, Lorenzini F, Manouvrier S, Pienkowski C, Reynaud R, Reznik Y, Siffroi JP, Tabet AC, Tauber M, Vautier V, Tauveron I, Wambre S, Zenaty D, Netchine I, Polak M, Touraine P, Carel JC, Christin-Maitre S, Léger J. Fiot E, et al. Among authors: bourrat e. Orphanet J Rare Dis. 2022 Jul 12;17(Suppl 1):261. doi: 10.1186/s13023-022-02423-5. Orphanet J Rare Dis. 2022. PMID: 35821070 Free PMC article.
Childhood pilomatricomas: Associated anomalies.
Richet C, Maza A, Dreyfus I, Bourrat E, Mazereeuw-Hautier J. Richet C, et al. Among authors: bourrat e. Pediatr Dermatol. 2018 Sep;35(5):548-551. doi: 10.1111/pde.13564. Epub 2018 Jul 1. Pediatr Dermatol. 2018. PMID: 29962097 Review.
French national diagnostic and care protocol for Kawasaki disease.
Galeotti C, Bajolle F, Belot A, Biscardi S, Bosdure E, Bourrat E, Cimaz R, Darbon R, Dusser P, Fain O, Hentgen V, Lambert V, Lefevre-Utile A, Marsaud C, Meinzer U, Morin L, Piram M, Richer O, Stephan JL, Urbina D, Kone-Paut I; collaborators. Galeotti C, et al. Among authors: bourrat e. Rev Med Interne. 2023 Jul;44(7):354-380. doi: 10.1016/j.revmed.2023.06.002. Epub 2023 Jun 20. Rev Med Interne. 2023. PMID: 37349225 Review.
Genetics of Inherited Ichthyoses and Related Diseases.
Fischer J, Bourrat E. Fischer J, et al. Among authors: bourrat e. Acta Derm Venereol. 2020 Mar 25;100(7):adv00096. doi: 10.2340/00015555-3432. Acta Derm Venereol. 2020. PMID: 32147747 Free PMC article. Review.
Self-application of aminoglycoside-based creams to treat cutaneous leishmaniasis in travelers.
Mouri O, Melenotte C, Guéry R, Cotteret C, Schweitzer-Chaput A, Perignon A, Thellier M, Bourrat E, Kaguelidou F, Siriez JY, Malvy D, Gangneux JP, Duvignaud A, Ravel C, Cisternino S, Ransom J, Caumes E, Lortholary O, Grogl M, Buffet P. Mouri O, et al. Among authors: bourrat e. PLoS Negl Trop Dis. 2023 Aug 10;17(8):e0011492. doi: 10.1371/journal.pntd.0011492. eCollection 2023 Aug. PLoS Negl Trop Dis. 2023. PMID: 37561802 Free PMC article.
[Genetics of complex and syndromic palmoplantar keratoderma].
Sperelakis-Beedham B, Lopez M, Girodon E, Hickman G, Bourrat E, Bienvenu T. Sperelakis-Beedham B, et al. Among authors: bourrat e. Ann Biol Clin (Paris). 2021 Dec 1;79(6):551-565. doi: 10.1684/abc.2021.1688. Ann Biol Clin (Paris). 2021. PMID: 34961738 Review. French.
Treatment of heterotopic ossifications secondary to pseudohypoparathyroid.
Guigonis V, Bahans C, Ea K, Bourrat E, Lienhardt A, Chabre O, Jost J, Mutar H, Ratsimbazafy V, Linglart A. Guigonis V, et al. Among authors: bourrat e. Ann Endocrinol (Paris). 2015 May;76(2):183-4. doi: 10.1016/j.ando.2015.03.012. Epub 2015 Apr 24. Ann Endocrinol (Paris). 2015. PMID: 25916756 Review. No abstract available.
Expanding the phenotype of GTF2E2-associated trichothiodystrophy.
Sperelakis-Beedham B, Ruaud L, Vial Y, Rachid M, Ageorges F, Goujon L, Verloes A, Tabet AC, Bourrat E, Lévy J. Sperelakis-Beedham B, et al. Among authors: bourrat e. J Eur Acad Dermatol Venereol. 2024 Mar;38(3):e222-e226. doi: 10.1111/jdv.19545. Epub 2023 Oct 16. J Eur Acad Dermatol Venereol. 2024. PMID: 37793898 No abstract available.
Acrogeria, an exceptional cause of acro-osteolysis.
Valayer S, Hickman G, Petit A, Solal MC, De Sandre Giovannoli A, Bourrat E. Valayer S, et al. Among authors: bourrat e. Clin Exp Dermatol. 2024 Jan 25;49(2):206-208. doi: 10.1093/ced/llad360. Clin Exp Dermatol. 2024. PMID: 37889144 No abstract available.
Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.
Faivre L, Crépin JC, Réda M, Nambot S, Carmignac V, Abadie C, Mirault T, Faure-Conter C, Mazereeuw-Hautier J, Maza A, Puzenat E, Collonge-Rame MA, Bursztejn AC, Philippe C, Thauvin-Robinet C, Chevarin M, Abasq-Thomas C, Amiel J, Arpin S, Barbarot S, Baujat G, Bessis D, Bourrat E, Boute O, Chassaing N, Coubes C, Demeer B, Edery P, El Chehadeh S, Goldenberg A, Hadj-Rabia S, Haye D, Isidor B, Jacquemont ML, Van Kien PK, Lacombe D, Lehalle D, Lambert L, Martin L, Maruani A, Morice-Picard F, Petit F, Phan A, Pinson L, Rossi M, Touraine R, Vanlerberghe C, Vincent M, Vincent-Delorme C, Whalen S, Willems M, Marle N, Verkarre V, Devalland C, Devouassoux-Shisheboran M, Abad M, Rioux-Leclercq N, Bonniaud B, Duffourd Y, Martel J, Binquet C, Kuentz P, Vabres P. Faivre L, et al. Among authors: bourrat e. Clin Genet. 2023 Nov;104(5):554-563. doi: 10.1111/cge.14410. Epub 2023 Aug 14. Clin Genet. 2023. PMID: 37580112
173 results