BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 16439508)

  • 21. Social aspects of genetic testing for factor V Leiden mutation in healthy individuals and their importance for daily practice.
    Bank I; Scavenius MP; Büller HR; Middeldorp S
    Thromb Res; 2004; 113(1):7-12. PubMed ID: 15081560
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical manifestations in thrombotic children with factor V Leiden mutation.
    Gurgey A
    Pediatr Hematol Oncol; 1999; 16(3):233-7. PubMed ID: 10326221
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The prevalence of activated protein C (APC) resistance and factor V Leiden is significantly higher in patients with retinal vein occlusion without general risk factors. Case-control study and meta-analysis.
    Rehak M; Rehak J; Müller M; Faude S; Faude F; Siegemund A; Krcova V; Slavik L; Hasenclever D; Scholz M; Wiedemann P
    Thromb Haemost; 2008 May; 99(5):925-9. PubMed ID: 18449423
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The G1691A mutation of the factor V gene (factor V Leiden) and the G20210A mutation of the prothrombin gene as risk factors in thrombotic microangiopathies.
    Sucker C; Kurschat C; Hetzel GR; Grabensee B; Maruhn-Debowski B; Loncar R; Ostojic L; Scharf RE; Zotz RB
    Clin Appl Thromb Hemost; 2009; 15(3):360-3. PubMed ID: 19448164
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Increased sperm count may account for high population frequency of factor V Leiden.
    Cohn DM; Repping S; Büller HR; Meijers JC; Middeldorp S
    J Thromb Haemost; 2010 Mar; 8(3):513-6. PubMed ID: 20002540
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Thrombophilia-related genetic variations in patients with pulmonary embolism in the main teaching hospital in Jordan.
    Obeidat NM; Awidi A; Sulaiman NA; Abu-Khader IB
    Saudi Med J; 2009 Jul; 30(7):921-5. PubMed ID: 19618008
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Factor V Leiden mutation: a treatable etiology for sporadic and recurrent pregnancy loss.
    Glueck CJ; Gogenini S; Munjal J; Tracy T; Pranikoff J; Wang P
    Fertil Steril; 2008 Feb; 89(2):410-6. PubMed ID: 17582408
    [TBL] [Abstract][Full Text] [Related]  

  • 28. AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
    Miñano A; Ordóñez A; España F; González-Porras JR; Lecumberri R; Fontcuberta J; Llamas P; Marín F; Estellés A; Alberca I; Vicente V; Corral J
    Haematologica; 2008 May; 93(5):729-34. PubMed ID: 18387978
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Factor V Leiden mutation in Arabs in Kuwait by real-time PCR: different values for different Arabs.
    Dashti AA; Jadaon MM; Lewis HL
    J Hum Genet; 2010 Apr; 55(4):232-5. PubMed ID: 20224595
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Role of the factor V Leiden mutation in septic peritonitis assessed in factor V Leiden transgenic mice.
    Brüggemann LW; Schoenmakers SH; Groot AP; Reitsma PH; Spek CA
    Crit Care Med; 2006 Aug; 34(8):2201-6. PubMed ID: 16775574
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Homozygosity for factor V Leiden leads to enhanced thrombosis and atherosclerosis in mice.
    Eitzman DT; Westrick RJ; Shen Y; Bodary PF; Gu S; Manning SL; Dobies SL; Ginsburg D
    Circulation; 2005 Apr; 111(14):1822-5. PubMed ID: 15809370
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Factor V Leiden mutation: a contributory factor for cerebral palsy?
    Reid S; Halliday J; Ditchfield M; Ekert H; Byron K; Glynn A; Petrou V; Reddihough D
    Dev Med Child Neurol; 2006 Jan; 48(1):14-9. PubMed ID: 16359589
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A.
    Lee DH; Walker IR; Teitel J; Poon MC; Ritchie B; Akabutu J; Sinclair GD; Pai M; Wu JW; Reddy S; Carter C; Growe G; Lillicrap D; Lam M; Blajchman MA
    Thromb Haemost; 2000 Mar; 83(3):387-91. PubMed ID: 10744141
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.
    González-Porras JR; García-Sanz R; Alberca I; López ML; Balanzategui A; Gutierrez O; Lozano F; San Miguel J
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):23-8. PubMed ID: 16607075
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Factor V 1691 G-A (Leiden) polymorphism and cancer-related venous thromboembolism: a meta-analysis of published studies.
    Eroglu A; Sertkaya Karasoy D; Eroglu N; Akar N
    J BUON; 2008; 13(1):61-4. PubMed ID: 18404788
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association of inherited thrombophilia with embryonic and postembryonic recurrent pregnancy loss.
    Ivanov PD; Komsa-Penkova RS; Konova EI; Kovacheva KS; Simeonova MN; Popov JD
    Blood Coagul Fibrinolysis; 2009 Mar; 20(2):134-40. PubMed ID: 19786941
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Factor V Leiden and increased risk for arterial thrombotic disease in young Brazilian patients.
    de Paula Sabino A; Ribeiro DD; Carvalho Md; Cardoso J; Dusse LM; Fernandes AP
    Blood Coagul Fibrinolysis; 2006 Jun; 17(4):271-5. PubMed ID: 16651869
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Factor V Leiden mutation and type 1 diabetes mellitus.
    Demirer AN; Alikasifoglu M; Tuncbilek E; Karakus S; Erbas T
    Blood Coagul Fibrinolysis; 2008 Jan; 19(1):70-4. PubMed ID: 18180619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for the Factor V Leiden mutation.
    Procare-GEHT Group
    Br J Haematol; 2006 Dec; 135(5):697-702. PubMed ID: 17107352
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.