Leporrier N - Search Results

1

Maternal serum screening in cases of mosaic and translocation Down syndrome.

Dreux S, Olivier C, Dupont JM, Leporrier N; Study Group; Oury JF, Muller F. Dreux S, et al. Among authors: leporrier n. Prenat Diagn. 2008 Aug;28(8):699-703. doi: 10.1002/pd.2051. Prenat Diagn. 2008. PMID: 18615544

2

Second-trimester Down syndrome maternal serum marker screening: a prospective study of 11 040 twin pregnancies.

Garchet-Beaudron A, Dreux S, Leporrier N, Oury JF, Muller F; ABA Study Group; Clinical Study Group. Garchet-Beaudron A, et al. Among authors: leporrier n. Prenat Diagn. 2008 Dec;28(12):1105-9. doi: 10.1002/pd.2145. Prenat Diagn. 2008. PMID: 19003979

3

Screening for fetal Down syndrome with maternal serum hCG and oestriol: a prospective study.

Herrou M, Leporrier N, Leymarie P. Herrou M, et al. Among authors: leporrier n. Prenat Diagn. 1992 Nov;12(11):887-92. doi: 10.1002/pd.1970121106. Prenat Diagn. 1992. PMID: 1494541

4

Maternal serum pregnancy-associated plasma protein A (PAPP-A) but not pregnancy-specific beta1-glycoprotein (SP1) is a useful second-trimester marker for fetal trisomy 18.

Bersinger NA, Leporrier N, Herrou M, Leymarie P. Bersinger NA, et al. Among authors: leporrier n. Prenat Diagn. 1999 Jun;19(6):537-41. Prenat Diagn. 1999. PMID: 10416969

5

Prenatal diagnosis of a mosaic 46,XY/47,X,i(Xq)Y.

Alliet J, Leporrier N, Lebris C, Gourdier D. Alliet J, et al. Among authors: leporrier n. Prenat Diagn. 1989 Jan;9(1):61-5. doi: 10.1002/pd.1970090109. Prenat Diagn. 1989. PMID: 2748552

6

[Maternal serum markers and prenatal screening for trisomy 21].

Leymarie P, Leporrier N. Leymarie P, et al. Among authors: leporrier n. Arch Fr Pediatr. 1993 May;50(5):455-7. Arch Fr Pediatr. 1993. PMID: 8239901 French. No abstract available.

7

Shift of the fetal sex ratio in hCG selected pregnancies at risk for Down syndrome.

Leporrier N, Herrou M, Leymarie P. Leporrier N, et al. Prenat Diagn. 1992 Aug;12(8):703-4. doi: 10.1002/pd.1970120813. Prenat Diagn. 1992. PMID: 1438064 No abstract available.

8

Chromosomal prenatal diagnosis: study of 936 cases of intrauterine abnormalities after ultrasound assessment.

Eydoux P, Choiset A, Le Porrier N, Thépot F, Szpiro-Tapia S, Alliet J, Ramond S, Viel JF, Gautier E, Morichon N, et al. Eydoux P, et al. Prenat Diagn. 1989 Apr;9(4):255-69. doi: 10.1002/pd.1970090405. Prenat Diagn. 1989. PMID: 2654910

9

Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases.

Gruchy N, Vialard F, Blondeel E, Le Meur N, Joly-Hélas G, Chambon P, Till M, Herbaut-Graux M, Vigouroux-Castera A, Coussement A, Lespinasse J, Amblard F, Jimenez M, Lebel Roy Camille L, Carré-Pigeon F, Flori E, Mugneret F, Jaillard S, Yardin C, Harbuz R, Collonge Rame M, Vago P, Valduga M, Leporrier N. Gruchy N, et al. Among authors: leporrier n. Prenat Diagn. 2014 Dec;34(12):1133-8. doi: 10.1002/pd.4439. Epub 2014 Jul 22. Prenat Diagn. 2014. PMID: 24961405

10

Hyperechogenic fetal bowel: a large French collaborative study of 682 cases.

Simon-Bouy B, Satre V, Ferec C, Malinge MC, Girodon E, Denamur E, Leporrier N, Lewin P, Forestier F, Muller F; French Collaborative Group. Simon-Bouy B, et al. Among authors: leporrier n. Am J Med Genet A. 2003 Sep 1;121A(3):209-13. doi: 10.1002/ajmg.a.20168. Am J Med Genet A. 2003. PMID: 12923859

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