These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 23157044)

  • 1. Impact of Factor V Leiden, prothrombin and methylenetetrahydrofolate reductase gene mutations on infant birth weight in women with recurrent fetal loss and women with successful pregnancies.
    Canda MT; Demir N; Sezer O
    Clin Exp Obstet Gynecol; 2012; 39(3):359-61. PubMed ID: 23157044
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 23342883
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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. PubMed ID: 18333414
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The association of factor V G1961A (factor V Leiden), prothrombin G20210A, MTHFR C677T and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Bosnian women.
    Jusić A; Balić D; Avdić A; Pođanin M; Balić A
    Med Glas (Zenica); 2018 Aug; 15(2):158-163. PubMed ID: 29703881
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 19906129
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 24779247
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Effects of inherited thrombophilia in women with recurrent pregnancy loss.
    Habibovic Z; Zeybek B; Sanhal C; Eroglu Z; Karaca E; Ulukus M
    Clin Exp Obstet Gynecol; 2011; 38(4):347-50. PubMed ID: 22268272
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages.
    Foka ZJ; Lambropoulos AF; Saravelos H; Karas GB; Karavida A; Agorastos T; Zournatzi V; Makris PE; Bontis J; Kotsis A
    Hum Reprod; 2000 Feb; 15(2):458-62. PubMed ID: 10655323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited thrombophilia screening in Greek women with recurrent fetal loss.
    Mougiou A; Androutsopoulos G; Karakantza M; Theodori E; Decavalas G; Zoumbos N
    Clin Exp Obstet Gynecol; 2008; 35(3):172-4. PubMed ID: 18754285
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Factor V Leiden and G20210A prothrombin mutations in patients with recurrent pregnancy loss: data from the southeast of Turkey.
    Altintas A; Pasa S; Akdeniz N; Cil T; Yurt M; Ayyildiz O; Batun S; Isi H
    Ann Hematol; 2007 Oct; 86(10):727-31. PubMed ID: 17572893
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.
    Carp H; Salomon O; Seidman D; Dardik R; Rosenberg N; Inbal A
    Hum Reprod; 2002 Jun; 17(6):1633-7. PubMed ID: 12042290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thrombophilic polymorphisms--factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations--and preterm birth.
    Resch B; Gallistl S; Kutschera J; Mannhalter C; Muntean W; Mueller WD
    Wien Klin Wochenschr; 2004 Sep; 116(17-18):622-6. PubMed ID: 15515881
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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. PubMed ID: 22047507
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Incidence of hereditary thrombophilia in women with pregnancy loss in multi-center studies in Poland].
    Skrzypczak J; Rajewski M; Wirstlein P; Goździewicz T; Breborowicz G; Leszczyńska-Gorzelak B; Ludwikowski G; Preis K; Wołczyński S; Zimmer M
    Ginekol Pol; 2012 May; 83(5):330-6. PubMed ID: 22708328
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions.
    Pauer HU; Voigt-Tschirschwitz T; Hinney B; Burfeind P; Wolf C; Emons G; Neesen J
    Acta Obstet Gynecol Scand; 2003 Oct; 82(10):942-7. PubMed ID: 12956845
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of factor V Leiden, prothrombin and methylenetetrahydrofolate reductase gene mutations in patients with severe pregnancy complications in northern Finland.
    Jarvenpaa J; Pakkila M; Savolainen ER; Perheentupa A; Jarvela I; Ryynanen M
    Gynecol Obstet Invest; 2006; 62(1):28-32. PubMed ID: 16514238
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The role of 1691G>A (Leiden) mutation in Factor V gene, 20210G>A in prothrombin gene and 677C>T in MTHFR gene in etiology of early pregnancy loss].
    Slezak R; Łaczmański Ł; Karpiński P; Reszczyńska-Slezak D
    Ginekol Pol; 2011 Jun; 82(6):446-50. PubMed ID: 21853935
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.
    Farahmand K; Totonchi M; Hashemi M; Reyhani Sabet F; Kalantari H; Gourabi H; Mohseni Meybodi A
    J Matern Fetal Neonatal Med; 2016; 29(8):1269-73. PubMed ID: 26135458
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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. PubMed ID: 16635210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the factor V, prothrombin and MTHFR genes are not risk factors for recurrent fetal loss.
    Dilley A; Benito C; Hooper WC; Austin H; Miller C; El-Jamil M; Cottrell S; Benson J; Evatt BL; Patterson-Bamett A; Eller D; Philipp C
    J Matern Fetal Neonatal Med; 2002 Mar; 11(3):176-82. PubMed ID: 12380673
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.