BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

940 related articles for article (PubMed ID: 16635210)

  • 21. Risk factors for clinical manifestations in carriers of Factor V Leiden and prothrombin gene mutations.
    DeSancho MT; Berlus N; Christos PJ; Rand J
    Blood Coagul Fibrinolysis; 2010 Jan; 21(1):11-5. PubMed ID: 19474699
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent--the Nîmes Obstetricians and Haematologists Study5 (NOHA5).
    Gris JC; Quéré I; Monpeyroux F; Mercier E; Ripart-Neveu S; Tailland ML; Hoffet M; Berlan J; Daurès JP; Marès P
    Thromb Haemost; 1999 Jun; 81(6):891-9. PubMed ID: 10404763
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Inherited thrombophilia in infertile women: implication in unexplained infertility.
    Casadei L; Puca F; Privitera L; Zamaro V; Emidi E
    Fertil Steril; 2010 Jul; 94(2):755-7. PubMed ID: 19939360
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
    Borsi E; Potre O; Ionita I; Samfireag M; Secosan C; Potre C
    Medicina (Kaunas); 2024 Mar; 60(4):. PubMed ID: 38674167
    [No Abstract]   [Full Text] [Related]  

  • 25. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z; Nomani H; Mozafari H; Vaisi-Raygani A; Madani H; Malek-Khosravi S; Parsian A
    Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic prothrombotic risk factors in women with unexplained pregnancy loss.
    Sottilotta G; Oriana V; Latella C; Luise F; Piromalli A; Ramirez F; Mammì C; Santoro R; Iannaccaro P; Muleo G; Lombardo VT
    Thromb Res; 2006; 117(6):681-4. PubMed ID: 16014310
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary thrombophilia, anti-beta2 glycoprotein 1 IgM, and anti-annexin V antibodies in recurrent pregnancy loss.
    Karata S; Aydin Y; Ocer F; Buyru A; Balci H
    Am J Reprod Immunol; 2012 Mar; 67(3):251-5. PubMed ID: 22103678
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
    Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
    Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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. PubMed ID: 24484533
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Impact of inherited thrombophilia on the development of some pregnancy complications].
    Koleva R; Dimitrova V; Chernev T; Savov A; Karag'ozova Zh; Mazneŭkova V; Kremenski I
    Akush Ginekol (Sofiia); 2005; 44(5):18-26. PubMed ID: 16313049
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multifactorial thrombophilia in a pregnancy: a case report.
    Gumus II; Uslu H; Bavbek N; Turhan N
    Clin Appl Thromb Hemost; 2008 Jan; 14(1):112-5. PubMed ID: 17895510
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The C677T MTHFR gene mutation is not predictive of risk for recurrent fetal loss.
    Holmes ZR; Regan L; Chilcott I; Cohen H
    Br J Haematol; 1999 Apr; 105(1):98-101. PubMed ID: 10233370
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Patients with inherited trombophilia and recurrent pregnancy loss: incidence].
    Flores-Alatriste JD; Jacobo-Nájera S; Segura-Rodríguez R; Stern-Colin y Nunes JJ
    Ginecol Obstet Mex; 2014 Jun; 82(6):383-8. PubMed ID: 25016897
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Thrombophilic gene mutations in women with repeated spontaneous miscarriage.
    Mohamed MA; El Moaty MA; El Kholy AF; Mohamed SA; Ali AI
    Genet Test Mol Biomarkers; 2010 Oct; 14(5):593-7. PubMed ID: 20707730
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages.
    Mahjoub T; Mtiraoui N; Tamim H; Hizem S; Finan RR; Nsiri B; Almawi WY
    Am J Hematol; 2005 Sep; 80(1):12-9. PubMed ID: 16138341
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The factor V Leiden mutation, high factor VIII, and high plasminogen activator inhibitor activity: etiologies for sporadic miscarriage.
    Glueck CJ; Pranikoff J; Aregawi D; Haque M; Zhu B; Tracy T; Wang P
    Metabolism; 2005 Oct; 54(10):1345-9. PubMed ID: 16154434
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Prothrombotic gene mutations in women with recurrent abortions and intrauterine fetal death].
    Santoro R; Iannaccaro P; Sottilotta G
    Minerva Ginecol; 2005 Aug; 57(4):447-50. PubMed ID: 16170289
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage.
    Karatas A; Eroz R; Albayrak M; Ozlu T; Cakmak B; Keskin F
    Afr Health Sci; 2014 Mar; 14(1):216-22. PubMed ID: 26060483
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause.
    Brenner B; Sarig G; Weiner Z; Younis J; Blumenfeld Z; Lanir N
    Thromb Haemost; 1999 Jul; 82(1):6-9. PubMed ID: 10456445
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 47.