Gaillard D - Search Results

1

[Increased nuchal translucency and cystic hygroma in the first trimester: prenatal diagnosis and neonatal outcome].

Ducarme G, Graesslin O, Alanio E, Bige V, Gaillard D, Gabriel R. Ducarme G, et al. Among authors: gaillard d. Gynecol Obstet Fertil. 2005 Oct;33(10):750-4. doi: 10.1016/j.gyobfe.2005.07.031. Gynecol Obstet Fertil. 2005. PMID: 16139544 French.

2

Characteristics and outcome of fetal cystic hygroma diagnosed in the first trimester.

Graesslin O, Derniaux E, Alanio E, Gaillard D, Vitry F, Quéreux C, Ducarme G. Graesslin O, et al. Among authors: gaillard d. Acta Obstet Gynecol Scand. 2007;86(12):1442-6. doi: 10.1080/00016340701644843. Epub 2007 Sep 6. Acta Obstet Gynecol Scand. 2007. PMID: 17851808 Free article.

3

Prenatal diagnosis in monozygotic twins with Down syndrome who had different phenotypes.

Grynberg M, Graesslin O, Teyssedre J, Quereux C, Gaillard D, Carré-Pigeon F. Grynberg M, et al. Among authors: gaillard d. Prenat Diagn. 2007 Jun;27(6):552-4. doi: 10.1002/pd.1711. Prenat Diagn. 2007. PMID: 17345584

4

[Sirenomelia. Review of nosology and a case report].

Harika G, Gabriel R, Bory JP, Gaillard D, Quéreux C, Wahl P. Harika G, et al. Among authors: gaillard d. J Gynecol Obstet Biol Reprod (Paris). 1995;24(1):49-51. J Gynecol Obstet Biol Reprod (Paris). 1995. PMID: 7730567 Review. French.

5

Acardiac fetus in a triplet pregnancy: ultrasound pitfalls. A case report.

Abboud P, Garnier R, Mansour G, Gabriel R, Gaillard D, Quéreux C. Abboud P, et al. Among authors: gaillard d. Eur J Obstet Gynecol Reprod Biol. 2000 Mar;89(1):75-80. doi: 10.1016/s0301-2115(99)00170-0. Eur J Obstet Gynecol Reprod Biol. 2000. PMID: 10733028

6

Recurrent prenatally diagnosed isolated bilateral pulmonary agenesis.

Ramanah R, Martin A, Guigue V, Arbez-Gindre F, Piard J, Terrosi P, Alanio E, Favre R, Gaillard D, Riethmuller D. Ramanah R, et al. Among authors: gaillard d. Ultrasound Obstet Gynecol. 2012 Dec;40(6):724-5. doi: 10.1002/uog.11146. Epub 2012 Nov 15. Ultrasound Obstet Gynecol. 2012. PMID: 22374821 Free article. No abstract available.

7

Fryns syndrome phenotype and trisomy 22.

Ladonne JM, Gaillard D, Carré-Pigeon F, Gabriel R. Ladonne JM, et al. Among authors: gaillard d. Am J Med Genet. 1996 Jan 2;61(1):68-70. doi: 10.1002/(SICI)1096-8628(19960102)61:1<68::AID-AJMG13>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8741922

8

Fetal phenotype associated with the 22q11 deletion.

Noël AC, Pelluard F, Delezoide AL, Devisme L, Loeuillet L, Leroy B, Martin A, Bouvier R, Laquerriere A, Jeanne-Pasquier C, Bessieres-Grattagliano B, Mechler C, Alanio E, Leroy C, Gaillard D. Noël AC, et al. Among authors: gaillard d. Am J Med Genet A. 2014 Nov;164A(11):2724-31. doi: 10.1002/ajmg.a.36720. Epub 2014 Aug 8. Am J Med Genet A. 2014. PMID: 25111715

9

Less HLA-G expression in Plasmodium falciparum-infected third trimester placentas is associated with more natural killer cells.

Sartelet H, Schleiermacher D, Le-Hesran JY, Graesslin O, Gaillard D, Fe M, Lechki C, Gaye A, Le Bouteiller P, Birembaut P. Sartelet H, et al. Among authors: gaillard d. Placenta. 2005 Jul;26(6):505-11. doi: 10.1016/j.placenta.2004.08.006. Placenta. 2005. PMID: 15950065

10

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations.

Lefebvre M, Bruel AL, Tisserant E, Bourgon N, Duffourd Y, Collardeau-Frachon S, Attie-Bitach T, Kuentz P, Assoum M, Schaefer E, El Chehadeh S, Antal MC, Kremer V, Girard-Lemaitre F, Mandel JL, Lehalle D, Nambot S, Jean-Marçais N, Houcinat N, Moutton S, Marle N, Lambert L, Jonveaux P, Foliguet B, Mazutti JP, Gaillard D, Alanio E, Poirisier C, Lebre AS, Aubert-Lenoir M, Arbez-Gindre F, Odent S, Quélin C, Loget P, Fradin M, Willems M, Bigi N, Perez MJ, Blesson S, Francannet C, Beaufrere AM, Patrier-Sallebert S, Guerrot AM, Goldenberg A, Brehin AC, Lespinasse J, Touraine R, Capri Y, Saint-Frison MH, Laurent N, Philippe C, Tran Mau-Them F, Thevenon J, Faivre L, Thauvin-Robinet C, Vitobello A. Lefebvre M, et al. Among authors: gaillard d. J Med Genet. 2021 Jun;58(6):400-413. doi: 10.1136/jmedgenet-2020-106867. Epub 2020 Jul 30. J Med Genet. 2021. PMID: 32732226

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