Oury JF - Search Results

1

Prenatal diagnosis of propionic acidemia in chorionic villi by direct assay of propionyl CoA carboxylase.

Chadefaux B, Augereau C, Rabier D, Rocchiccioli F, Boué J, Oury JF, Kamoun P. Chadefaux B, et al. Among authors: oury jf. Prenat Diagn. 1988 Feb;8(2):161-4. doi: 10.1002/pd.1970080211. Prenat Diagn. 1988. PMID: 3362779

2

Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experience.

Chadefaux-Vekemans B, Rabier D, Cadoudal N, Lescoat A, Chabli A, Aupetit J, Dumez Y, Oury JF. Chadefaux-Vekemans B, et al. Among authors: oury jf. Prenat Diagn. 2006 Sep;26(9):814-8. doi: 10.1002/pd.1509. Prenat Diagn. 2006. PMID: 16821251

3

First-trimester diagnosis of hypophosphatasia. Importance of gestational age and purity of CV samples.

Muller F, Oury JF, Bussière P, Lewin F, Boué J. Muller F, et al. Among authors: oury jf. Prenat Diagn. 1991 Sep;11(9):725-30. doi: 10.1002/pd.1970110910. Prenat Diagn. 1991. PMID: 1788179

4

Prenatal diagnosis of mucolipidosis type II on first-trimester amniotic fluid.

Poenaru L, Mezard C, Akli S, Oury JF, Dumez Y, Boue J. Poenaru L, et al. Among authors: oury jf. Prenat Diagn. 1990 Apr;10(4):231-5. doi: 10.1002/pd.1970100404. Prenat Diagn. 1990. PMID: 1973293

5

Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.

Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A. Raux-Demay M, et al. Among authors: oury jf. Prenat Diagn. 1989 Jul;9(7):457-66. doi: 10.1002/pd.1970090702. Prenat Diagn. 1989. PMID: 2788885

6

Microvillar enzyme assays in amniotic fluid and fetal tissues at different stages of development.

Muller F, Oury JF, Dumez Y, Boué J, Boué A. Muller F, et al. Among authors: oury jf. Prenat Diagn. 1988 Mar;8(3):189-98. doi: 10.1002/pd.1970080305. Prenat Diagn. 1988. PMID: 2897684

7

Gestational age-related reference values for amniotic fluid amino acids: a useful tool for prenatal diagnosis of aminoacidopathies.

Rabier D, Chadefaux-Vekemans B, Oury JF, Aupetit J, Bardet J, Gasquet M, Merhand E, Parvy P, Kamoun P. Rabier D, et al. Among authors: oury jf. Prenat Diagn. 1996 Jul;16(7):623-8. doi: 10.1002/(SICI)1097-0223(199607)16:7<623::AID-PD921>3.0.CO;2-5. Prenat Diagn. 1996. PMID: 8843471

8

[Prenatal diagnosis of genetic diseases using chorionic villi].

Boué J, Deluchat C, Nicolas H, Oury JF, Dumez Y. Boué J, et al. Among authors: oury jf. J Genet Hum. 1986 Aug;34(3-4):221-33. J Genet Hum. 1986. PMID: 3760827 French.

9

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

10

Prenatal diagnosis of cystic fibrosis: ultrasonography of the gallbladder at 17-19 weeks of gestation.

Duchatel F, Muller F, Oury JF, Mennesson B, Boue J, Boue A. Duchatel F, et al. Among authors: oury jf. Fetal Diagn Ther. 1993 Jan-Feb;8(1):28-36. doi: 10.1159/000263744. Fetal Diagn Ther. 1993. PMID: 8452646

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