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

Year Number of Results
1999 2
2002 1
2003 1
2004 4
2005 1
2006 1
2007 1
2008 2
2009 2
2010 1
2011 2
2012 2
2013 3
2014 7
2015 5
2016 5
2017 1
2018 5
2019 2
2020 2
2021 5
2022 3
2023 3
2024 1

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52 results

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Page 1
NOTCH2 related disorders: Description and review of the fetal presentation.
Deb W, Joubert M, Cogné B, Vincent M, Ghesh L, Bézieau S, Le Vaillant C, Beneteau C. Deb W, et al. Among authors: le vaillant c. Eur J Med Genet. 2023 Jul;66(7):104769. doi: 10.1016/j.ejmg.2023.104769. Epub 2023 Apr 28. Eur J Med Genet. 2023. PMID: 37121269 Review.
[Monoamniotic twins: diagnosis and management].
Winer N, Caroit Y, Le Vaillant C, Philippe HJ. Winer N, et al. Among authors: le vaillant c. J Gynecol Obstet Biol Reprod (Paris). 2009 Dec;38(8 Suppl):S85-9. doi: 10.1016/S0368-2315(09)73564-1. J Gynecol Obstet Biol Reprod (Paris). 2009. PMID: 20141933 Free article. Review. French.
Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities.
Scala M, Khan K, Beneteau C, Fox RG, von Hardenberg S, Khan A, Joubert M, Fievet L, Musquer M, Le Vaillant C, Holsclaw JK, Lim D, Berking AC, Accogli A, Giacomini T, Nobili L, Striano P, Zara F, Torella A, Nigro V, Cogné B, Salick MR, Kaykas A, Eggan K, Capra V, Bézieau S, Davis EE, Wells MF. Scala M, et al. Among authors: le vaillant c. Genet Med. 2024 Apr;26(4):101057. doi: 10.1016/j.gim.2023.101057. Epub 2023 Dec 27. Genet Med. 2024. PMID: 38158856 Free article.
[Acardiac twins: pronostics markers' study].
Barré M, Le Vaillant C, Boog G, Joubert M, Winer N, Philippe H. Barré M, et al. Among authors: le vaillant c. Gynecol Obstet Fertil. 2012 Feb;40(2):93-8. doi: 10.1016/j.gyobfe.2011.08.011. Epub 2011 Nov 17. Gynecol Obstet Fertil. 2012. PMID: 22099976 Review. French.
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.
Klein J, Buffin-Meyer B, Boizard F, Moussaoui N, Lescat O, Breuil B, Fedou C, Feuillet G, Casemayou A, Neau E, Hindryckx A, Decatte L, Levtchenko E, Raaijmakers A, Vayssière C, Goua V, Lucas C, Perrotin F, Cloarec S, Benachi A, Manca-Pellissier MC, Delmas HL, Bessenay L, Le Vaillant C, Allain-Launay E, Gondry J, Boudailliez B, Simon E, Prieur F, Lavocat MP, Saliou AH, De Parscau L, Bidat L, Noel C, Floch C, Bourdat-Michel G, Favre R, Weingertner AS, Oury JF, Baudouin V, Bory JP, Pietrement C, Fiorenza M, Massardier J, Kessler S, Lounis N, Auriol FC, Marcorelles P, Collardeau-Frachon S, Zürbig P, Mischak H, Magalhães P, Batut J, Blader P, Saulnier Blache JS, Bascands JL, Schaefer F, Decramer S, Schanstra JP; BIOMAN consortium. Klein J, et al. Among authors: le vaillant c. Kidney Int. 2021 Mar;99(3):737-749. doi: 10.1016/j.kint.2020.06.043. Epub 2020 Aug 1. Kidney Int. 2021. PMID: 32750455
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series.
Lesieur-Sebellin M, Till M, Khau Van Kien P, Herve B, Bourgon N, Dupont C, Tabet AC, Barrois M, Coussement A, Loeuillet L, Mousty E, Ea V, El Assal A, Mary L, Jaillard S, Beneteau C, Le Vaillant C, Coutton C, Devillard F, Goumy C, Delabaere A, Redon S, Laurent Y, Lamouroux A, Massardier J, Turleau C, Sanlaville D, Cantagrel V, Sonigo P, Vialard F, Salomon LJ, Malan V. Lesieur-Sebellin M, et al. Among authors: le vaillant c. Prenat Diagn. 2022 Jan;42(1):118-135. doi: 10.1002/pd.6074. Epub 2021 Dec 11. Prenat Diagn. 2022. PMID: 34894355
52 results