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Page 1
Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.
Ranza E, Le Gouez M, Guimier A, Dunlop NK, Beaudoin S, Malan V, Michot C, Baujat G, Rio M, Cormier-Daire V, Abadie V, Sarnacki S, Delacourt C, Lyonnet S, Attié-Bitach T, Pingault V, Rousseau V, Amiel J. Ranza E, et al. Among authors: sarnacki s. Am J Med Genet A. 2023 Jan;191(1):77-83. doi: 10.1002/ajmg.a.62989. Epub 2022 Oct 21. Am J Med Genet A. 2023. PMID: 36271508
An overview of isolated and syndromic oesophageal atresia.
Geneviève D, de Pontual L, Amiel J, Sarnacki S, Lyonnet S. Geneviève D, et al. Among authors: sarnacki s. Clin Genet. 2007 May;71(5):392-9. doi: 10.1111/j.1399-0004.2007.00798.x. Clin Genet. 2007. PMID: 17489843 Review.
Neonatal outcome of gastroschisis is mainly influenced by nutritional management.
Walter-Nicolet E, Rousseau V, Kieffer F, Fusaro F, Bourdaud N, Oucherif S, Benachi A, Sarnacki S, Mitanchez D. Walter-Nicolet E, et al. Among authors: sarnacki s. J Pediatr Gastroenterol Nutr. 2009 May;48(5):612-7. doi: 10.1097/MPG.0b013e31818c5281. J Pediatr Gastroenterol Nutr. 2009. PMID: 19367181 Clinical Trial.
Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
Cognet M, Nougayrede A, Malan V, Callier P, Cretolle C, Faivre L, Genevieve D, Goldenberg A, Heron D, Mercier S, Philip N, Sigaudy S, Verloes A, Sarnacki S, Munnich A, Vekemans M, Lyonnet S, Etchevers H, Amiel J, de Pontual L. Cognet M, et al. Among authors: sarnacki s. Eur J Hum Genet. 2011 May;19(5):602-6. doi: 10.1038/ejhg.2010.225. Epub 2011 Jan 12. Eur J Hum Genet. 2011. PMID: 21224895 Free PMC article.
EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia.
Gordon CT, Petit F, Oufadem M, Decaestecker C, Jourdain AS, Andrieux J, Malan V, Alessandri JL, Baujat G, Baumann C, Boute-Benejean O, Caumes R, Delobel B, Dieterich K, Gaillard D, Gonzales M, Lacombe D, Escande F, Manouvrier-Hanu S, Marlin S, Mathieu-Dramard M, Mehta SG, Simonic I, Munnich A, Vekemans M, Porchet N, de Pontual L, Sarnacki S, Attie-Bitach T, Lyonnet S, Holder-Espinasse M, Amiel J. Gordon CT, et al. Among authors: sarnacki s. J Med Genet. 2012 Dec;49(12):737-46. doi: 10.1136/jmedgenet-2012-101173. J Med Genet. 2012. PMID: 23188108
[Anorectal malformations].
Cretolle C, Rousseau V, Lottmann H, Irtan S, Lortat-Jacob S, Alova I, Michel JL, Aigrain Y, Podevin G, Lehur PA, Sarnacki S. Cretolle C, et al. Among authors: sarnacki s. Arch Pediatr. 2013 Sep;20 Suppl 1:S19-27. doi: 10.1016/S0929-693X(13)71405-2. Arch Pediatr. 2013. PMID: 23992833 French.
Segmental volvulus in the neonate: A particular clinical entity.
Khen-Dunlop N, Beaudoin S, Marion B, Rousseau V, Giuseppi A, Nicloux M, Grevent D, Salomon LJ, Aigrain Y, Lapillonne A, Sarnacki S. Khen-Dunlop N, et al. Among authors: sarnacki s. J Pediatr Surg. 2017 Mar;52(3):454-457. doi: 10.1016/j.jpedsurg.2016.10.002. Epub 2016 Oct 13. J Pediatr Surg. 2017. PMID: 28443816
238 results