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[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.
Oroesophageal motor disorders in Pierre Robin syndrome.
Baujat G, Faure C, Zaouche A, Viarme F, Couly G, Abadie V. Baujat G, et al. Among authors: abadie v. J Pediatr Gastroenterol Nutr. 2001 Mar;32(3):297-302. doi: 10.1097/00005176-200103000-00012. J Pediatr Gastroenterol Nutr. 2001. PMID: 11345179
Pierre Robin sequence: a series of 117 consecutive cases.
Holder-Espinasse M, Abadie V, Cormier-Daire V, Beyler C, Manach Y, Munnich A, Lyonnet S, Couly G, Amiel J. Holder-Espinasse M, et al. Among authors: abadie v. J Pediatr. 2001 Oct;139(4):588-90. doi: 10.1067/mpd.2001.117784. J Pediatr. 2001. PMID: 11598609
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.
Benko S, Fantes JA, Amiel J, Kleinjan DJ, Thomas S, Ramsay J, Jamshidi N, Essafi A, Heaney S, Gordon CT, McBride D, Golzio C, Fisher M, Perry P, Abadie V, Ayuso C, Holder-Espinasse M, Kilpatrick N, Lees MM, Picard A, Temple IK, Thomas P, Vazquez MP, Vekemans M, Roest Crollius H, Hastie ND, Munnich A, Etchevers HC, Pelet A, Farlie PG, Fitzpatrick DR, Lyonnet S. Benko S, et al. Among authors: abadie v. Nat Genet. 2009 Mar;41(3):359-64. doi: 10.1038/ng.329. Epub 2009 Feb 22. Nat Genet. 2009. PMID: 19234473
Identification of novel craniofacial regulatory domains located far upstream of SOX9 and disrupted in Pierre Robin sequence.
Gordon CT, Attanasio C, Bhatia S, Benko S, Ansari M, Tan TY, Munnich A, Pennacchio LA, Abadie V, Temple IK, Goldenberg A, van Heyningen V, Amiel J, FitzPatrick D, Kleinjan DA, Visel A, Lyonnet S. Gordon CT, et al. Among authors: abadie v. Hum Mutat. 2014 Aug;35(8):1011-20. doi: 10.1002/humu.22606. Hum Mutat. 2014. PMID: 24934569 Free PMC article.
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