Bussières L - Search Results

1

Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophy.

Mouawia H, Saker A, Jais JP, Benachi A, Bussières L, Lacour B, Bonnefont JP, Frydman R, Simpson JL, Paterlini-Brechot P. Mouawia H, et al. Among authors: bussieres l. Reprod Biomed Online. 2012 Nov;25(5):508-20. doi: 10.1016/j.rbmo.2012.08.002. Epub 2012 Aug 31. Reprod Biomed Online. 2012. PMID: 23000084

2

Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21: A Randomized Clinical Trial.

Malan V, Bussières L, Winer N, Jais JP, Baptiste A, Le Lorc'h M, Elie C, O'Gorman N, Fries N, Houfflin-Debarge V, Sentilhes L, Vekemans M, Ville Y, Salomon LJ; SAFE 21 Study Group. Malan V, et al. Among authors: bussieres l. JAMA. 2018 Aug 14;320(6):557-565. doi: 10.1001/jama.2018.9396. JAMA. 2018. PMID: 30120476 Free PMC article. Clinical Trial.

3

[Cell-free fetal DNA screening tests for trisomy 21].

Malan V, Bussières L, Salomon LJ. Malan V, et al. Among authors: bussieres l. Gynecol Obstet Fertil. 2016 Dec;44(12):675-678. doi: 10.1016/j.gyobfe.2016.10.002. Epub 2016 Nov 7. Gynecol Obstet Fertil. 2016. PMID: 27839716 Review. French. No abstract available.

4

Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysis.

Le Bras A, Salomon LJ, Bussières L, Malan V, Elie C, Mahallati H, Ville Y, Vekemans M, Durand-Zaleski I. Le Bras A, et al. Among authors: bussieres l. Ultrasound Obstet Gynecol. 2019 Nov;54(5):596-603. doi: 10.1002/uog.20301. Ultrasound Obstet Gynecol. 2019. PMID: 31006923 Free article.

5

A standardized approach for the assessment of the lower uterine segment at first trimester by transvaginal ultrasound: a flash study.

Kuleva M, Castaing O, Fries N, Bernard JP, Bussières L, Fontanges M, Moeglin D, Salomon LJ. Kuleva M, et al. Among authors: bussieres l. J Matern Fetal Neonatal Med. 2016;29(9):1376-81. doi: 10.3109/14767058.2015.1051956. Epub 2015 Jun 5. J Matern Fetal Neonatal Med. 2016. PMID: 26043645 Clinical Trial.

6

Assessment of human placental perfusion by intravoxel incoherent motion MR imaging.

Siauve N, Hayot PH, Deloison B, Chalouhi GE, Alison M, Balvay D, Bussières L, Clément O, Salomon LJ. Siauve N, et al. Among authors: bussieres l. J Matern Fetal Neonatal Med. 2019 Jan;32(2):293-300. doi: 10.1080/14767058.2017.1378334. Epub 2017 Oct 3. J Matern Fetal Neonatal Med. 2019. PMID: 28974131 Clinical Trial.

7

Women's Attitudes Toward Invasive and Noninvasive Testing When Facing a High Risk of Fetal Down Syndrome.

Seror V, L'Haridon O, Bussières L, Malan V, Fries N, Vekemans M, Salomon LJ, Ville Y; SAFE 21 Study Group. Seror V, et al. Among authors: bussieres l, l haridon o. JAMA Netw Open. 2019 Mar 1;2(3):e191062. doi: 10.1001/jamanetworkopen.2019.1062. JAMA Netw Open. 2019. PMID: 30924894 Free PMC article.

8

Down syndrome screening using first-trimester combined tests and contingent use of femur length at routine anomaly scan.

Salomon LJ, Chevret S, Bussieres L, Ville Y, Rozenberg P. Salomon LJ, et al. Among authors: bussieres l. Prenat Diagn. 2010 Aug;30(8):783-9. doi: 10.1002/pd.2550. Prenat Diagn. 2010. PMID: 20575148

9

Timing of delivery following selective laser photocoagulation for twin-to-twin transfusion syndrome.

Stirnemann JJ, Quibel T, Essaoui M, Salomon LJ, Bussieres L, Ville Y. Stirnemann JJ, et al. Among authors: bussieres l. Am J Obstet Gynecol. 2012 Aug;207(2):127.e1-6. doi: 10.1016/j.ajog.2012.06.042. Epub 2012 Jun 23. Am J Obstet Gynecol. 2012. PMID: 22840722

10

Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.

Alberti A, Salomon LJ, Le Lorc'h M, Couloux A, Bussières L, Goupil S, Malan V, Pelletier E, Hyon C, Vialard F, Rozenberg P, Bouhanna P, Oury JF, Schmitz T, Romana S, Weissenbach J, Vekemans M, Ville Y. Alberti A, et al. Among authors: bussieres l. Prenat Diagn. 2015 May;35(5):471-6. doi: 10.1002/pd.4561. Prenat Diagn. 2015. PMID: 25643828

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