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 *

1121 related articles for article (PubMed ID: 19349859)

  • 21. The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.
    Eroglu A; Egin Y; Cam R; Akar N
    Ann Hematol; 2009 Jan; 88(1):73-6. PubMed ID: 18682947
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Role of thrombotic risk factors in end-stage renal disease.
    Tripathi G; Sankhwar SN; Sharma RK; Baburaj VP; Agrawal S
    Clin Appl Thromb Hemost; 2010 Apr; 16(2):132-40. PubMed ID: 19520684
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Mutation frequencies of the thrombophilic state genes in Uzbekistan].
    Sadikova ShE; Karimov KhIa; Muminov ShM; Tulakov RP; Boboev KT
    Tsitol Genet; 2008; 42(6):50-4. PubMed ID: 19253755
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.
    Hessner MJ; Luhm RA; Pearson SL; Endean DJ; Friedman KD; Montgomery RR
    Thromb Haemost; 1999 May; 81(5):733-8. PubMed ID: 10365746
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Risk of thrombophilia in carriers of thrombophilic genetic factors in unsuccessful assisted reproduction].
    Ivanov P; Komsa-Penkova R; Kovacheva K; Konova E; Todorova K; Simeonova M; Ivanov I; Stoĭkov S; Popov I; Tanchev S; Bozhinova S
    Akush Ginekol (Sofiia); 2007; 46(6):3-8. PubMed ID: 17974163
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The factor V G1691A, factor V H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease.
    Ciftdoğan DY; Coşkun S; Ulman C; Tikiz H
    Coron Artery Dis; 2009 Nov; 20(7):435-9. PubMed ID: 19609209
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia.
    Fawaz NA; Bashawery L; Al-Sheikh I; Qatari A; Al-Othman SS; Almawi WY
    Am J Hematol; 2004 Jul; 76(3):307-9. PubMed ID: 15224376
    [TBL] [Abstract][Full Text] [Related]  

  • 28. PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events in central Iran.
    Pourgheysari B; Boroujeni HR; Hasheminia AM; Drees F
    Blood Coagul Fibrinolysis; 2013 Jul; 24(5):471-6. PubMed ID: 23358226
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.
    Behjati R; Modarressi MH; Jeddi-Tehrani M; Dokoohaki P; Ghasemi J; Zarnani AH; Aarabi M; Memariani T; Ghaffari M; Akhondi MA
    Ann Hematol; 2006 Apr; 85(4):268-71. PubMed ID: 16450127
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
    Almawi WY; Tamim H; Kreidy R; Timson G; Rahal E; Nabulsi M; Finan RR; Irani-Hakime N
    J Thromb Thrombolysis; 2005 Jun; 19(3):189-96. PubMed ID: 16082606
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Relationship between three thrombophilic gene mutations and unexplained recurrent early spontaneous abortion].
    Xu L; Liu XM; Zhang HY; Zhao J; Qi QW; Chang YF
    Zhonghua Fu Chan Ke Za Zhi; 2007 Mar; 42(3):180-3. PubMed ID: 17537304
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
    Gerhardt A; Scharf RE; Beckmann MW; Struve S; Bender HG; Pillny M; Sandmann W; Zotz RB
    N Engl J Med; 2000 Feb; 342(6):374-80. PubMed ID: 10666427
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy Jordanians.
    Nusier MK; Radaideh AM; Ababneh NA; Qaqish BM; Alzoubi R; Khader Y; Mersa JY; Irshaid NM; El-Khateeb M
    Neuro Endocrinol Lett; 2007 Oct; 28(5):699-703. PubMed ID: 17984931
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Factor V Leiden, prothrombin G20210A and MTHFR gene mutations in inflammatory bowel disease.
    Törüner M; Erkan O; Soykan I; Bozdayi M; Cetinkaya H; Yurdaydin C; Uzunalimoğlu O; Ozden A
    Turk J Gastroenterol; 2004 Dec; 15(4):250-2. PubMed ID: 16249980
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.
    Finan RR; Tamim H; Ameen G; Sharida HE; Rashid M; Almawi WY
    Am J Hematol; 2002 Dec; 71(4):300-5. PubMed ID: 12447960
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia.
    Dávalos IP; Moran MC; Martínez-Abundis E; González-Ortiz M; Flores-Martínez SE; Machorro V; Sandoval L; Figuera LE; Mena JP; Oliva JM; Tlacuilo-Parra JA; Sánchez-Corona J; Salazar-Páramo M
    Blood Cells Mol Dis; 2005; 35(1):66-9. PubMed ID: 15905108
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
    Ben Salem-Berrabah O; Fekih-Mrissa N; N'siri B; Ben Hamida A; Benammar-Elgaaied A; Gritli N; Mrissa R
    J Clin Neurosci; 2012 Sep; 19(9):1326-7. PubMed ID: 22721898
    [TBL] [Abstract][Full Text] [Related]  

  • 38. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
    Cruciani F; Moramarco A; Curto T; Labate A; Recupero V; Conti L; Gandolfo GM; Balacco Gabrieli C
    Clin Ter; 2003; 154(5):299-303. PubMed ID: 14994919
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).
    Freitas AI; Mendonça I; Guerra G; Brión M; Reis RP; Carracedo A; Brehm A
    Thromb Res; 2008; 122(5):648-56. PubMed ID: 18384842
    [TBL] [Abstract][Full Text] [Related]  

  • 40. No association of factor V Leiden, prothrombin G20210A, and MTHFR C677T gene polymorphisms with kidney allograft survival: a multicenter study.
    Meyer M; Laux G; Scherer S; Tran TH; Opelz G; Mytilineos J
    Transplantation; 2007 Apr; 83(8):1055-8. PubMed ID: 17452895
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 57.