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 *

185 related articles for article (PubMed ID: 15499693)

  • 21. Isolated cortical vein thrombosis associated with prothrombin gene mutation.
    Giraldo EA; Arora R; Koenigsberg RA
    J Stroke Cerebrovasc Dis; 2014 Apr; 23(4):791-3. PubMed ID: 23834854
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetics of cerebral venous thrombosis.
    Ahmad A
    J Pak Med Assoc; 2006 Nov; 56(11):488-90. PubMed ID: 17183972
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
    Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N
    Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prevalence of the prothrombin gene G20210A mutation in Azerbaijan.
    Togrul J; Rustamov R; Gurgey A; Altay S; Altay C
    Br J Haematol; 2000 Mar; 108(4):887-8. PubMed ID: 10858039
    [No Abstract]   [Full Text] [Related]  

  • 25. [Correlation between single nucleotide polymorphism of prothrombin gene G20210 and deep vein thrombosis after total joint replacement].
    Jiang J; Guan ZP; Lü HS
    Zhonghua Yi Xue Za Zhi; 2009 Mar; 89(11):782-5. PubMed ID: 19595110
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Severe venous thrombosis in an infant heterozygous for the G20210A mutation in the prothrombin gene.
    Martínez-Tallo E; Alonso N; Campo-Sampedro F; Agulla E; Hernandez-Rastrollo R; Galán E
    Acta Paediatr; 2003 Sep; 92(9):1111-3. PubMed ID: 14599081
    [No Abstract]   [Full Text] [Related]  

  • 27. Cerebral venous sinus thrombosis in a neonate with homozygous prothrombin G20210A genotype.
    Klein L; Bhardwaj V; Gebara B
    J Perinatol; 2004 Dec; 24(12):797-9. PubMed ID: 15558004
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.
    Ozyurek E; Balta G; Degerliyurt A; Parlak H; Aysun S; Gürgey A
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):154-60. PubMed ID: 17456624
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Protein C concentrates in a neonate with a cerebral venous thrombosis due to heterozygous type 1 protein C deficiency.
    Tardy-Poncet B; Rayet I; Damon G; Alhenc-Gelas M; Dutour N; Lavocat MP
    Thromb Haemost; 2001 Jun; 85(6):1118-9. PubMed ID: 11434695
    [No Abstract]   [Full Text] [Related]  

  • 30. Prothombin gene G20210A mutation is not a risk factor for ischemic stroke in a South Indian Hyderabadi Population.
    Munshi A; Aliya N; Jyothy A; Kaul S; Alladi S; Shafi G
    Thromb Res; 2009 Jun; 124(2):245-7. PubMed ID: 18995885
    [No Abstract]   [Full Text] [Related]  

  • 31. Cerebral venous thrombosis and the G20210A mutation of factor II.
    Simons PJ; Vanhooren G; Longstreth WT; Colven RM
    Stroke; 2000 Feb; 31(2):543-4. PubMed ID: 10657438
    [No Abstract]   [Full Text] [Related]  

  • 32. Hyperhomocysteinemia and other thrombophilic risk factors in 26 patients with cerebral venous thrombosis.
    Boncoraglio G; Carriero MR; Chiapparini L; Ciceri E; Ciusani E; Erbetta A; Parati EA
    Eur J Neurol; 2004 Jun; 11(6):405-9. PubMed ID: 15171737
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209T.
    Gurgey A; Unal S; Okur H; Duru F; Gumruk F
    Pediatr Hematol Oncol; 2005 Jun; 22(4):309-14. PubMed ID: 16020118
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Distinct association of factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon.
    Bouaziz-Borgi L; Almawi WY; Mtiraoui N; Nsiri B; Keleshian SH; Kreidy R; Louzir B; Hezard N; Mahjoub T
    Am J Hematol; 2006 Aug; 81(8):641-3. PubMed ID: 16823828
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Pregnancy-associated venous thrombosis in women with hereditary heterozygous factor V Leiden and/or factor II gene mutations].
    Samama MM; Rached RA; Conard J; Horellou MH; Elalamy I
    Bull Acad Natl Med; 2004; 188(8):1377-93; discussion 1393-6. PubMed ID: 15918665
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prothrombotic factors in neonates with cerebral thrombosis and intraventricular hemorrhage.
    Aronis S; Bouza H; Pergantou H; Kapsimalis Z; Platokouki H; Xanthou M
    Acta Paediatr Suppl; 2002; 91(438):87-91. PubMed ID: 12477269
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An overview of methods for detection of factor V Leiden and the prothrombin G20210A mutations.
    Cooper PC; Rezende SM
    Int J Lab Hematol; 2007 Jun; 29(3):153-62. PubMed ID: 17474891
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Haplotypes of the EPCR gene, prothrombin levels, and the risk of venous thrombosis in carriers of the prothrombin G20210A mutation.
    Navarro S; Medina P; Mira Y; Estellés A; Villa P; Ferrando F; Vayá A; Bertina RM; España F
    Haematologica; 2008 Jun; 93(6):885-91. PubMed ID: 18403391
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Upper-extremity deep vein thrombosis in a patient on clozapine therapy carrying the prothrombin G20210A mutation.
    Vayá A; Lopez M; Plumé G; Ribes J
    Pathophysiol Haemost Thromb; 2008; 36(2):105-7. PubMed ID: 19127092
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon.
    Taher A; Khalil I; Abou-Merhi R; Shamseddine A; Bazarbachi A
    Thromb Haemost; 2003 May; 89(5):945-6. PubMed ID: 12719795
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.