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Journal Abstract Search

168 related items for PubMed ID: 21453389

  • 1. Arg 304 Gln (FVII Padua) and Ala 294 Val mutations are equally present in patients with FVII deficiency and thrombosis.
    Girolami A, Candeo N, Bonamigo E, Fabris F.
    Eur J Haematol; 2011 Jul; 87(1):92-4. PubMed ID: 21453389
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  • 2. The paradoxical association between inherited factor VII deficiency and venous thrombosis.
    Marty S, Barro C, Chatelain B, Fimbel B, Tribout B, Reynaud J, Schved JF, Giansily-Blaizot M.
    Haemophilia; 2008 May; 14(3):564-70. PubMed ID: 18282149
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  • 3. [Significant decrease in factor VII activity by tissue thromboplastin derived from rabbit brain in a patient with congenital factor VII deficiency (FVII Padua)].
    Sekiya A, Morishita E, Maruyama K, Asakura H, Nakao S, Ohtake S.
    Rinsho Ketsueki; 2012 Mar; 53(3):357-60. PubMed ID: 22499055
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  • 4. Molecular analysis in a patient with severe factor VII deficiency and an inhibitor: report of a novel mutation (S103G).
    Pruthi RK, Rodriguez V, Allen C, Slaby JA, Schmidt KA, Plumhoff EA.
    Eur J Haematol; 2007 Oct; 79(4):354-9. PubMed ID: 17692102
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  • 5. Pathogenetic role of Factor VII deficiency and thrombosis in cross-reactive material positive patients.
    Girolami A, Sambado L, Bonamigo E, Ferrari S, Lombardi AM.
    Lab Hematol; 2013 Dec; 19(4):17-21. PubMed ID: 24370871
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  • 6. Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s).
    Furlan Freguia C, Toso R, Pollak ES, Arruda VR, Pinotti M, Bernardi F.
    Haematologica; 2004 Dec; 89(12):1504-9. PubMed ID: 15590402
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  • 10. Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain.
    Borensztajn K, Chafa O, Le Bonniec B, Wajcman H, Reghis A, Fischer AM, Tapon-Bretaudière J.
    Thromb Res; 2005 Dec; 116(2):115-20. PubMed ID: 15907525
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  • 16. Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain.
    D'Andrea G, Bossone A, Lupone MR, Peyvandi F, Maisto G, Perricone F, Grandone E, Margaglione M.
    Haematologica; 2004 Aug; 89(8):979-84. PubMed ID: 15339682
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  • 17. [Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].
    Jin YH, Wang MS, Zheng FX, Xie YS, Xie HX, Xu PF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):404-7. PubMed ID: 22875495
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  • 18. Characterization of a Cys329Gly mutation causing hereditary factor VII deficiency.
    Wu Y, Tu X, Lian Y, Chen F, Lan F, Zhu Z.
    Acta Haematol; 2006 Aug; 116(2):96-100. PubMed ID: 16914903
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