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Results by year

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

Year Number of Results
1986 1
1987 1
1988 1
1989 1
1991 1
1992 2
1993 5
1994 3
1995 2
1996 4
1997 2
1998 3
1999 5
2000 8
2001 7
2002 3
2003 5
2004 3
2005 5
2006 3
2007 4
2008 6
2009 5
2010 5
2011 2
2012 3
2013 8
2014 3
2015 6
2016 8
2017 7
2018 6
2019 1
2020 7
2021 10
2022 5
2023 2
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141 results
Results by year
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Page 1
Pierre Robin sequence: A comprehensive narrative review of the literature over time.
Giudice A, Barone S, Belhous K, Morice A, Soupre V, Bennardo F, Boddaert N, Vazquez MP, Abadie V, Picard A. Giudice A, et al. Among authors: abadie v. J Stomatol Oral Maxillofac Surg. 2018 Nov;119(5):419-428. doi: 10.1016/j.jormas.2018.05.002. Epub 2018 May 17. J Stomatol Oral Maxillofac Surg. 2018. PMID: 29777780 Review.
IL-15, gluten and HLA-DQ8 drive tissue destruction in coeliac disease.
Abadie V, Kim SM, Lejeune T, Palanski BA, Ernest JD, Tastet O, Voisine J, Discepolo V, Marietta EV, Hawash MBF, Ciszewski C, Bouziat R, Panigrahi K, Horwath I, Zurenski MA, Lawrence I, Dumaine A, Yotova V, Grenier JC, Murray JA, Khosla C, Barreiro LB, Jabri B. Abadie V, et al. Nature. 2020 Feb;578(7796):600-604. doi: 10.1038/s41586-020-2003-8. Epub 2020 Feb 12. Nature. 2020. PMID: 32051586 Free PMC article.
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Chopra M, McEntagart M, Clayton-Smith J, Platzer K, Shukla A, Girisha KM, Kaur A, Kaur P, Pfundt R, Veenstra-Knol H, Mancini GMS, Cappuccio G, Brunetti-Pierri N, Kortüm F, Hempel M, Denecke J, Lehman A; CAUSES Study; Kleefstra T, Stuurman KE, Wilke M, Thompson ML, Bebin EM, Bijlsma EK, Hoffer MJV, Peeters-Scholte C, Slavotinek A, Weiss WA, Yip T, Hodoglugil U, Whittle A, diMonda J, Neira J, Yang S, Kirby A, Pinz H, Lechner R, Sleutels F, Helbig I, McKeown S, Helbig K, Willaert R, Juusola J, Semotok J, Hadonou M, Short J; Genomics England Research Consortium; Yachelevich N, Lala S, Fernández-Jaen A, Pelayo JP, Klöckner C, Kamphausen SB, Abou Jamra R, Arelin M, Innes AM, Niskakoski A, Amin S, Williams M, Evans J, Smithson S, Smedley D, de Burca A, Kini U, Delatycki MB, Gallacher L, Yeung A, Pais L, Field M, Martin E, Charles P, Courtin T, Keren B, Iascone M, Cereda A, Poke G, Abadie V, Chalouhi C, Parthasarathy P, Halliday BJ, Robertson SP, Lyonnet S, Amiel J, Gordon CT. Chopra M, et al. Among authors: abadie v. Am J Hum Genet. 2021 Jun 3;108(6):1138-1150. doi: 10.1016/j.ajhg.2021.04.007. Epub 2021 Apr 27. Am J Hum Genet. 2021. PMID: 33909992 Free PMC article.
A Mouse Model of Celiac Disease.
Abadie V, Khosla C, Jabri B. Abadie V, et al. Curr Protoc. 2022 Aug;2(8):e515. doi: 10.1002/cpz1.515. Curr Protoc. 2022. PMID: 35994521
Managing infants with craniofacial malformations - Where to go next?
Poets CF, Abadie V, Breugem C, Wallis C, Abel F, Chalouhi C, Kruisinga F, Sorg AL, Wiechers C. Poets CF, et al. Among authors: abadie v. Semin Fetal Neonatal Med. 2021 Dec;26(6):101289. doi: 10.1016/j.siny.2021.101289. Epub 2021 Sep 17. Semin Fetal Neonatal Med. 2021. PMID: 34548245 Review.
[Neonatal trismus].
Abadie V, Chéron G, Madjiidi A, Couly G. Abadie V, et al. Arch Pediatr. 1994 Jun;1(6):568-72. Arch Pediatr. 1994. PMID: 7994348 French.
[Infantile rumination].
Thouvenin B, d'Arc BF, Baujat G, Brousse V, Abadie V. Thouvenin B, et al. Among authors: abadie v. Arch Pediatr. 2005 Sep;12(9):1368-71. doi: 10.1016/j.arcped.2005.03.048. Arch Pediatr. 2005. PMID: 15921903 French.
B Lymphocytes Contribute to Celiac Disease Pathogenesis.
Lejeune T, Meyer C, Abadie V. Lejeune T, et al. Among authors: abadie v. Gastroenterology. 2021 Jun;160(7):2608-2610.e4. doi: 10.1053/j.gastro.2021.02.063. Epub 2021 Mar 2. Gastroenterology. 2021. PMID: 33667487 Free PMC article. No abstract available.
Congenital feeding and swallowing disorders.
Abadie V, Couly G. Abadie V, et al. Handb Clin Neurol. 2013;113:1539-49. doi: 10.1016/B978-0-444-59565-2.00024-1. Handb Clin Neurol. 2013. PMID: 23622377 Review.
141 results