Mercier E - Search Results

1

JAK2 V617F mutation in unexplained loss of first pregnancy.

Mercier E, Lissalde-Lavigne G, Gris JC. Mercier E, et al. N Engl J Med. 2007 Nov 8;357(19):1984-5. doi: 10.1056/NEJMc071528. N Engl J Med. 2007. PMID: 17989398 No abstract available.

2

The association between hereditary thrombophilias and pregnancy loss.

Lissalde-Lavigne G, Cochery-Nouvellon E, Mercier E, Quéré I, Dauzat M, Marès P, Gris JC. Lissalde-Lavigne G, et al. Among authors: mercier e. Haematologica. 2005 Sep;90(9):1223-30. Haematologica. 2005. PMID: 16154846 Review.

3

High frequency of protein Z deficiency in patients with unexplained early fetal loss.

Gris JC, Quéré I, Dechaud H, Mercier E, Pinçon C, Hoffet M, Vasse M, Marès P. Gris JC, et al. Among authors: mercier e. Blood. 2002 Apr 1;99(7):2606-8. doi: 10.1182/blood.v99.7.2606. Blood. 2002. PMID: 11895801 Free article.

4

[Is haemostasis assessment mandatory in case of pregnancy loss?].

Gris JC, Cochery-Nouvellon E, Mercier E. Gris JC, et al. Among authors: mercier e. Rev Med Suisse. 2011 Feb 9;7(281):361-4. Rev Med Suisse. 2011. PMID: 21416716 French.

5

Antiphospholipid/antiprotein antibodies, hemostasis-related autoantibodies, and plasma homocysteine as risk factors for a first early pregnancy loss: a matched case-control study.

Gris JC, Perneger TV, Quéré I, Mercier E, Fabbro-Peray P, Lavigne-Lissalde G, Hoffet M, Déchaud H, Boyer JC, Ripart-Neveu S, Tailland ML, Daurès JP, Marès P, Dauzat M. Gris JC, et al. Among authors: mercier e. Blood. 2003 Nov 15;102(10):3504-13. doi: 10.1182/blood-2003-01-0320. Epub 2003 Jul 17. Blood. 2003. PMID: 12869511 Free article.

6

Association of factor V gene polymorphisms (Leiden; Cambridge; Hong Kong and HR2 haplotype) with recurrent idiopathic pregnancy loss in Tunisia. A case-control study.

Zammiti W, Mtiraoui N, Mercier E, Abboud N, Saidi S, Mahjoub T, Almawi WY, Gris JC. Zammiti W, et al. Among authors: mercier e. Thromb Haemost. 2006 Apr;95(4):612-7. Thromb Haemost. 2006. PMID: 16601830

7

Interleukin 10 gene promoter polymorphisms in women with pregnancy loss: preferential association with embryonic wastage.

Cochery-Nouvellon E, Nguyen P, Attaoua R, Cornillet-Lefebvre P, Mercier E, Vitry F, Gris JC. Cochery-Nouvellon E, et al. Among authors: mercier e. Biol Reprod. 2009 Jun;80(6):1115-20. doi: 10.1095/biolreprod.108.072215. Epub 2009 Feb 4. Biol Reprod. 2009. PMID: 19208551

8

The A6936G polymorphism of the endothelial protein C receptor gene is associated with the risk of unexplained foetal loss in Mediterranean European couples.

Cochery-Nouvellon E, Chauleur C, Demattei C, Mercier E, Fabbro-Peray P, Marès P, Mismetti P, Lissalde-Lavigne G, Gris JC. Cochery-Nouvellon E, et al. Among authors: mercier e. Thromb Haemost. 2009 Oct;102(4):656-67. doi: 10.1160/TH-09-04-0224. Thromb Haemost. 2009. PMID: 19806250

9

Novel genes and mutations in patients affected by recurrent pregnancy loss.

Quintero-Ronderos P, Mercier E, Fukuda M, González R, Suárez CF, Patarroyo MA, Vaiman D, Gris JC, Laissue P. Quintero-Ronderos P, et al. Among authors: mercier e. PLoS One. 2017 Oct 10;12(10):e0186149. doi: 10.1371/journal.pone.0186149. eCollection 2017. PLoS One. 2017. PMID: 29016666 Free PMC article.

10

THBD sequence variants potentially related to recurrent pregnancy loss.

Quintero-Ronderos P, Mercier E, Gris JC, Esteban-Perez C, Moreno-Ortiz H, Fonseca DJ, Lucena E, Vaiman D, Laissue P. Quintero-Ronderos P, et al. Among authors: mercier e. Reprod Biol Endocrinol. 2017 Dec 1;15(1):92. doi: 10.1186/s12958-017-0311-0. Reprod Biol Endocrinol. 2017. PMID: 29195508 Free PMC article.

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