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 *

99 related articles for article (PubMed ID: 17920139)

  • 1. A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: combination of prothrombotic gene mutations.
    Botto N; Mariani M; Manfredi S; Andreassi MG
    Int J Cardiol; 2008 Oct; 130(1):e17-9. PubMed ID: 17920139
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Myocardial infarction in a young patient with a previous history of repeated thrombophlebitis: combination of factor V Leiden and prothrombin G20210A gene polymorphisms with coronary artery disease.
    Mugnolo A; Toniolo M; Cicoira M; Vassanelli F; Vassanelli C
    J Cardiovasc Med (Hagerstown); 2010 Feb; 11(2):125-6. PubMed ID: 19829138
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Thrombophilia in young patients with acute myocardial infarction.
    Celik M; Altintas A; Celik Y; Karabulut A; Ayyildiz O
    Saudi Med J; 2008 Jan; 29(1):48-54. PubMed ID: 18176672
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The prevalence of factor V (G1691A), MTHFR (C677T) and PT (G20210A) gene mutations in arterial thrombosis.
    Ozmen F; Ozmen MM; Ozalp N; Akar N
    Ulus Travma Acil Cerrahi Derg; 2009 Mar; 15(2):113-9. PubMed ID: 19353312
    [TBL] [Abstract][Full Text] [Related]  

  • 5. No effect of polymorphisms in prothrombotic genes on the risk of myocardial infarction in young adults without cardiovascular risk factors.
    Martini CH; Doggen CJ; Cavallini C; Rosendaal FR; Mannucci PM
    J Thromb Haemost; 2005 Jan; 3(1):177-9. PubMed ID: 15634285
    [No Abstract]   [Full Text] [Related]  

  • 6. Five prothrombotic polymorphisms and the prevalence of premature myocardial infarction.
    Roldán V; González-Conejero R; Marín F; Pineda J; Vicente V; Corral J
    Haematologica; 2005 Mar; 90(3):421-3. PubMed ID: 15749685
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 18803625
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Acute myocardial infarction following an arthropod bite: is hereditary thrombophilia a contributing factor?
    Kayikcioglu M; Eroglu Z; Kosova B; Olukman M; Karatas A; Can LH; Hasdemir C
    Blood Coagul Fibrinolysis; 2006 Oct; 17(7):581-3. PubMed ID: 16988555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Procarboxypeptidase U (TAFI) contributes to the risk of thrombosis in patients with hereditary thrombophilia.
    Heylen E; Miljic P; Willemse J; Djordjevic V; Radojkovic D; Colovic M; Elezovic I; Hendriks D
    Thromb Res; 2009 Sep; 124(4):427-32. PubMed ID: 19195685
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The prothrombin G20210A polymorphism in patients with myocardial infarction.
    Durante-Mangoni E; Davies GJ; Ahmed N; Ruggiero G; Michaelides K
    Blood Coagul Fibrinolysis; 2002 Oct; 13(7):603-8. PubMed ID: 12439145
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A family history can display a synergistic effect of atherogenic and prothrombotic risk in pregnancy.
    Van Rooijen M; Bremme K
    Acta Obstet Gynecol Scand; 2001 Sep; 80(9):873-4. PubMed ID: 11531643
    [No Abstract]   [Full Text] [Related]  

  • 14. The diagnostic dilemma: dual presentations of clinical mucosal bleeding and venous thrombosis associated with the presence of thrombophilia markers and mild reduction in von Willebrand factor.
    Favaloro EJ; Bonar R; Survela L; McDonald D; Koutts J; Sioufi J; Marsden K
    Lab Hematol; 2007; 13(4):128-34. PubMed ID: 18192144
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Major and potential prothrombotic genotypes in patients with venous thrombosis and in healthy subjects from Slovenia.
    Bedencic M; Bozic M; Peternel P; Stegnar M
    Pathophysiol Haemost Thromb; 2008; 36(2):58-63. PubMed ID: 19127083
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutation.
    Hüdaoglu O; Kurul S; Yis U; Dirik E; Cakmakçi H; Men S
    J Child Neurol; 2007 Mar; 22(3):329-31. PubMed ID: 17621506
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Myocardial infarction and pulmonary embolism in a 45 year-old woman with the prothrombin 20210A mutation--a case report].
    Wozakowska-Kapłon B; Szydziak-Zwierzyńska K
    Kardiol Pol; 2009 Feb; 67(2):162-7. PubMed ID: 19288379
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recurrent arterial thrombosis associated with the antithrombin basel variant and elevated lipoprotein(a) plasma level in an adolescent patient.
    Szilágyi S; Péter A; Magyar MT; Balogh S; Bereczky Z
    J Pediatr Hematol Oncol; 2012 May; 34(4):276-9. PubMed ID: 22134617
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.