Oury JF - 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: oury jf. Prenat Diagn. 2008 Aug;28(8):699-703. doi: 10.1002/pd.2051. Prenat Diagn. 2008. PMID: 18615544

2

Down syndrome maternal serum marker screening after 18 weeks' gestation.

Muller F, Dreux S, Oury JF, Luton D, Uzan S, Uzan M, Levardon M, Dommergues M. Muller F, et al. Among authors: oury jf. Prenat Diagn. 2002 Nov;22(11):1001-4. doi: 10.1002/pd.451. Prenat Diagn. 2002. PMID: 12424764

3

Second-trimester Down syndrome maternal serum screening in twin pregnancies: impact of chorionicity.

Muller F, Dreux S, Dupoizat H, Uzan S, Dubin MF, Oury JF, Dingeon B, Dommergues M. Muller F, et al. Among authors: oury jf. Prenat Diagn. 2003 Apr;23(4):331-5. doi: 10.1002/pd.594. Prenat Diagn. 2003. PMID: 12673641

4

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: oury jf. Prenat Diagn. 2008 Dec;28(12):1105-9. doi: 10.1002/pd.2145. Prenat Diagn. 2008. PMID: 19003979

5

Second-trimester maternal serum screening for Down syndrome in twin-to-twin transfusion syndrome.

Sermondade N, Dreux S, Oury JF, Muller F. Sermondade N, et al. Among authors: oury jf. Prenat Diagn. 2009 Aug;29(8):814-5. doi: 10.1002/pd.2285. Prenat Diagn. 2009. PMID: 19418465 No abstract available.

6

Outcome of prenatally detected bilateral higher urinary tract obstruction or megacystis: sex-related study on a series of 709 cases.

Al-Hazmi H, Dreux S, Delezoide AL, Dommergues M, Lortat-Jacob S, Oury JF, El-Ghoneimi A, Muller F. Al-Hazmi H, et al. Among authors: oury jf. Prenat Diagn. 2012 Jul;32(7):649-54. doi: 10.1002/pd.3877. Epub 2012 Apr 30. Prenat Diagn. 2012. PMID: 22544566

7

Outcome and etiologies of fetal megacystis according to the gestational age at diagnosis.

Bornes M, Spaggiari E, Schmitz T, Dreux S, Czerkiewicz I, Delezoide AL, El-Ghoneimi A, Oury JF, Muller F. Bornes M, et al. Among authors: oury jf. Prenat Diagn. 2013 Dec;33(12):1162-6. doi: 10.1002/pd.4215. Epub 2013 Sep 3. Prenat Diagn. 2013. PMID: 23939878

8

Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone.

Rachid ML, Dreux S, Pean de Ponfilly G, Vargas-Poussou R, Czerkiewicz I, Chevenne D, Oury JF, Deschênes G, Muller F. Rachid ML, et al. Among authors: oury jf. Prenat Diagn. 2016 Jan;36(1):88-91. doi: 10.1002/pd.4717. Epub 2015 Dec 1. Prenat Diagn. 2016. PMID: 26528764

9

Bartter syndrome prenatal diagnosis based on amniotic fluid biochemical analysis.

Garnier A, Dreux S, Vargas-Poussou R, Oury JF, Benachi A, Deschênes G, Muller F. Garnier A, et al. Among authors: oury jf. Pediatr Res. 2010 Mar;67(3):300-3. doi: 10.1203/PDR.0b013e3181ca038d. Pediatr Res. 2010. PMID: 19915517

10

Sonographic measurement of corpus spongiosum in male fetuses.

Vuillard E, Chitrit Y, Dreux S, Elghoneimi A, Oury JF, Muller F. Vuillard E, et al. Among authors: oury jf. Prenat Diagn. 2011 Dec;31(12):1160-3. doi: 10.1002/pd.2854. Epub 2011 Sep 26. Prenat Diagn. 2011. PMID: 21953058 Clinical Trial.

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