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Items: 1 to 20 of 131

1.

Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.

Ozdemir O, Yenicesu GI, Silan F, Köksal B, Atik S, Ozen F, Göl M, Cetin A.

Genet Test Mol Biomarkers. 2012 Apr;16(4):279-86. doi: 10.1089/gtmb.2011.0191. Epub 2011 Nov 2.

PMID:
22047507
2.

A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.

Yenicesu GI, Cetin M, Ozdemir O, Cetin A, Ozen F, Yenicesu C, Yildiz C, Kocak N.

Am J Reprod Immunol. 2010 Feb;63(2):126-36. doi: 10.1111/j.1600-0897.2009.00770.x. Epub 2009 Nov 10.

PMID:
19906129
3.

Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.

Coulam CB, Jeyendran RS, Fishel LA, Roussev R.

Am J Reprod Immunol. 2006 May;55(5):360-8.

PMID:
16635210
4.

The association between inherited thrombophilia and recurrent pregnancy loss in Turkish women.

Isaoglu U, Ulug P, Delibas IB, Yilmaz M, Kumtepe Y, Dogan H, Tasdemir S.

Clin Exp Obstet Gynecol. 2014;41(2):177-81.

PMID:
24779247
5.

[Inherited thrombophilic factors in women with secondary infertility].

Ivanov P, Gecheva S, Tsvyatkovska T, Georgieva G, Komsa-Penkova R, Konova E, Simeonova M, Tanchev S.

Akush Ginekol (Sofiia). 2012;51(4):3-7. Bulgarian.

PMID:
23234018
6.

Combined germline variations of thrombophilic genes promote genesis of lung cancer.

Ozen F, Polat F, Arslan S, Ozdemir O.

Asian Pac J Cancer Prev. 2013;14(9):5449-54.

7.

Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss?

Goodman CS, Coulam CB, Jeyendran RS, Acosta VA, Roussev R.

Am J Reprod Immunol. 2006 Oct;56(4):230-6.

PMID:
16938111
8.

Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.

Pietropolli A, Giuliani E, Bruno V, Patrizi L, Piccione E, Ticconi C.

J Obstet Gynaecol. 2014 Apr;34(3):229-34. doi: 10.3109/01443615.2013.836476. Epub 2014 Jan 31.

PMID:
24484533
9.

Analysis of inherited thrombophilic mutations and natural anticoagulant deficiency in patients with idiopathic portal hypertension.

Bayan K, Tüzün Y, Yilmaz S, Canoruc N, Dursun M.

J Thromb Thrombolysis. 2009 Jul;28(1):57-62. doi: 10.1007/s11239-008-0244-8. Epub 2008 Aug 7.

PMID:
18685811
10.

A comprehensive analysis of 12 thrombophilic mutations and related parameters in patients with inflammatory bowel disease: data from Turkey.

Yilmaz S, Bayan K, Tüzün Y, Batun S, Altintaş A.

J Thromb Thrombolysis. 2006 Dec;22(3):205-12.

PMID:
17111197
11.

Plasminogen activator inhibitor 1 and methylenetetrahydrofolate reductase gene mutations in iranian women with polycystic ovary syndrome.

Idali F, Zareii S, Mohammad-Zadeh A, Reihany-Sabet F, Akbarzadeh-Pasha Z, Khorram-Khorshid HR, Zarnani AH, Jeddi-Tehrani M.

Am J Reprod Immunol. 2012 Nov;68(5):400-7. doi: 10.1111/aji.12002. Epub 2012 Aug 6.

PMID:
22882325
12.

Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.

Coulam CB, Wallis D, Weinstein J, DasGupta DS, Jeyendran RS.

Am J Reprod Immunol. 2008 Nov;60(5):426-31. doi: 10.1111/j.1600-0897.2008.00640.x.

PMID:
18803625
13.

Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?

Gokalp D, Tuzcu A, Bahceci M, Ayyildiz O, Yurt M, Celik Y, Alpagat G.

Pituitary. 2011 Jun;14(2):168-73. doi: 10.1007/s11102-010-0276-x.

PMID:
21107737
14.

Lack of association between thrombophilic gene variants and recurrent pregnancy loss.

Dutra CG, Fraga LR, Nácul AP, Passos EP, Gonçalves RO, Nunes OL, De Godoy BA, Leistner-Segal S, Vianna FS, Schüler-Faccini L, Sanseverino MT.

Hum Fertil (Camb). 2014 Jun;17(2):99-105. doi: 10.3109/14647273.2014.882022. Epub 2014 Feb 24.

PMID:
24564524
15.

The association between thrombophilic gene mutations and recurrent pregnancy loss.

Poursadegh Zonouzi A, Chaparzadeh N, Ghorbian S, Sadaghiani MM, Farzadi L, Ghasemzadeh A, Kafshdooz T, Sakhinia M, Sakhinia E.

J Assist Reprod Genet. 2013 Oct;30(10):1353-9. doi: 10.1007/s10815-013-0071-5. Epub 2013 Aug 29.

16.

Inherited thrombophilia with recurrent pregnancy loss in Turkish women--a real phenomenon?

Yildiz G, Yavuzcan A, Yildiz P, Süer N, Tandoğan N.

Ginekol Pol. 2012 Aug;83(8):598-603.

PMID:
23342883
17.

[Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].

Kovacheva K, Ivanov P, Konova E, Simeonova M, Komsa-Penkova R.

Akush Ginekol (Sofiia). 2007;46(7):10-6. Bulgarian.

PMID:
18333414
18.

[Combined thrombophilic factors among women with late recurrent spontaneous abortions].

Ivanov P, Komsa-Penkova R, Konova E, Gecheva S, Ivanov I, Kovacheva K, Simeonova M, Tanchev S.

Akush Ginekol (Sofiia). 2011;50(3):8-12. Bulgarian.

PMID:
21916309
19.

Genetic thrombophilic mutations among couples with recurrent miscarriage.

Jivraj S, Rai R, Underwood J, Regan L.

Hum Reprod. 2006 May;21(5):1161-5. Epub 2006 Jan 23.

20.

-455G/A beta-fibrinogen gene polymorphism, factor V Leiden, prothrombin G20210A mutation and MTHFR C677T, and placental vascular complications.

Camilleri RS, Peebles D, Portmann C, Everington T, Cohen H.

Blood Coagul Fibrinolysis. 2004 Mar;15(2):139-47.

PMID:
15091001
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