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85 related items for PubMed ID: 10994543

  • 1. Design of a prospective neonatal cohort study of homozygous and double heterozygous factor V Leiden and factor II G20210A.
    Hundsdoerfer P, Vetter B, Stöver B, Bassir C, Mönch E, Ziemer S, Kulozik AE.
    Klin Padiatr; 2000; 212(4):159-62. PubMed ID: 10994543
    [Abstract] [Full Text] [Related]

  • 2. Risk of recurrent venous thrombosis in homozygous carriers and double heterozygous carriers of factor V Leiden and prothrombin G20210A.
    Lijfering WM, Middeldorp S, Veeger NJ, Hamulyák K, Prins MH, Büller HR, van der Meer J.
    Circulation; 2010 Apr 20; 121(15):1706-12. PubMed ID: 20368522
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  • 3. Homozygous and double heterozygous Factor V Leiden and Factor II G20210A genotypes predispose infants to thromboembolism but are not associated with an increase of foetal loss.
    Hundsdoerfer P, Vetter B, Stöver B, Bassir C, Scholz T, Grimmer I, Mönch E, Ziemer S, Rossi R, Kulozik AE.
    Thromb Haemost; 2003 Oct 20; 90(4):628-35. PubMed ID: 14515183
    [Abstract] [Full Text] [Related]

  • 4. Concomitant heterozygous factor V Leiden mutation and homozygous prothrombin gene variant (G20210A) in patient with cerebral venous thrombosis.
    Kurkowska-Jastrzebska I, Wicha W, Dowzenko A, Vertun-Baranowska B, Pytlewski A, Bogusławska R, Członkowska A.
    Med Sci Monit; 2003 May 20; 9(5):CS41-5. PubMed ID: 12761462
    [Abstract] [Full Text] [Related]

  • 5. Molecular characterization of factor V leiden G1691A and prothrombin G20210A mutations in Saudi newborns with stroke.
    Gawish GE.
    Biochem Genet; 2011 Oct 20; 49(9-10):601-10. PubMed ID: 21461667
    [Abstract] [Full Text] [Related]

  • 6. Factor V Leiden and prothrombin G20210A mutations in Thai patients awaiting kidney transplant.
    Arnutti P, Nathalang O, Cowawintaweewat S, Prayoonwiwat W, Choovichian P.
    Southeast Asian J Trop Med Public Health; 2002 Dec 20; 33(4):869-71. PubMed ID: 12757241
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  • 7. 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 20; 28(5):699-703. PubMed ID: 17984931
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  • 8. Thrombophilia in infancy: factor V Leiden and MTHFR or factor II double heterozygocity as a risk factor.
    Koren A, Levin C, Hujirat Y, El-Hasid R, Kutai M, Lanir N, Shalev S, Brenner B.
    Pediatr Hematol Oncol; 2003 Oct 20; 20(3):219-27. PubMed ID: 12637218
    [Abstract] [Full Text] [Related]

  • 9. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.
    Emmerich J, Rosendaal FR, Cattaneo M, Margaglione M, De Stefano V, Cumming T, Arruda V, Hillarp A, Reny JL.
    Thromb Haemost; 2001 Sep 20; 86(3):809-16. PubMed ID: 11583312
    [Abstract] [Full Text] [Related]

  • 10. 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 20; 21(1):11-5. PubMed ID: 19474699
    [Abstract] [Full Text] [Related]

  • 11. 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 20; 17(1):23-8. PubMed ID: 16607075
    [Abstract] [Full Text] [Related]

  • 12. Family history is a poor screen for prothrombotic genes in children with stroke.
    Johal SC, Garg BP, Heiny ME, Williams LS, Saha C, Walsh LE, Golomb MR.
    J Pediatr; 2006 Jan 20; 148(1):68-71. PubMed ID: 16423600
    [Abstract] [Full Text] [Related]

  • 13. Rapid multiplex analysis for the factor V Leiden and prothrombin G20210A mutations associated with hereditary thrombophilia.
    Linfert DR, Rezuke WN, Tsongalis GJ.
    Conn Med; 1998 Sep 20; 62(9):519-25. PubMed ID: 9785636
    [Abstract] [Full Text] [Related]

  • 14. 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 20; 13(4):435-8. PubMed ID: 17911197
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  • 17. Two common genetic thrombotic risk factors: factor V Leiden and prothrombin G20210A in adult Turkish patients with thrombosis.
    Gurgey A, Haznedaroglu IC, Egesel T, Buyukasik Y, Ozcebe OI, Sayinalp N, Dundar SV, Bayraktar Y.
    Am J Hematol; 2001 Jun 20; 67(2):107-11. PubMed ID: 11343382
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  • 18. 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 20; 71(4):300-5. PubMed ID: 12447960
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  • 20. The impact of heterozygosity for the factor V Leiden and factor II G20210A mutations on the risk of thrombosis in Greek patients.
    Hatzaki A, Anagnostopoulou E, Metaxa-Mariatou V, Melissinos C, Philalithis P, Iliadis K, Kontaxis A, Liberatos K, Pangratis N, Nasioulas G.
    Int Angiol; 2003 Mar 20; 22(1):79-82. PubMed ID: 12771861
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