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Journal Abstract Search

398 related items for PubMed ID: 19718467

  • 21. Fibrinogen Milano II: a congenital dysfibrinogenaemia associated with juvenile arterial and venous thrombosis.
    Haverkate F, Koopman J, Kluft C, D'Angelo A, Cattaneo M, Mannucci PM.
    Thromb Haemost; 1986 Feb 28; 55(1):131-5. PubMed ID: 3705000
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  • 22. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.
    Luo M, Deng D, Xiang L, Cheng P, Liao L, Deng X, Yan J, Lin F.
    Medicine (Baltimore); 2016 Sep 28; 95(39):e4864. PubMed ID: 27684817
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  • 23. Fibrinogen Guarenas, an abnormal fibrinogen with an Aalpha-chain truncation due to a nonsense mutation at Aalpha 467 Glu (GAA)-->stop (TAA).
    Marchi R, Carvajal Z, Meyer M, Soria J, Ruiz-Saez A, Arocha-Piñango CL, Weisel JW.
    Thromb Res; 2006 Sep 28; 118(5):637-50. PubMed ID: 16406498
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  • 24. Heterozygous abnormal fibrinogen Osaka III with the replacement of gamma arginine-275 by histidine has an apparently higher molecular weight gamma-chain variant.
    Yoshida N, Imaoka S, Hirata H, Matsuda M, Asakura S.
    Thromb Haemost; 1992 Nov 10; 68(5):534-8. PubMed ID: 1455400
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  • 25. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F, Samama M.
    Thromb Haemost; 1995 Jan 10; 73(1):151-61. PubMed ID: 7740487
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  • 26. Biophysical characterization of fibrinogen Caracas I with an Aalpha-chain truncation at Aalpha-466 Ser: identification of the mutation and biophysical characterization of properties of clots from plasma and purified fibrinogen.
    Marchi R, Meyer M, de Bosch N, Soria J, Arocha-Piñango CL, Weisel JW.
    Blood Coagul Fibrinolysis; 2004 Jun 10; 15(4):285-93. PubMed ID: 15166913
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  • 27. Fibrinogen Seoul (FGG Ala341Asp): a novel mutation associated with hypodysfibrinogenemia.
    Song KS, Park NJ, Choi JR, Doh HJ, Chung KH.
    Clin Appl Thromb Hemost; 2006 Jul 10; 12(3):338-43. PubMed ID: 16959688
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  • 30. Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens.
    Kotlín R, Blažek B, Suttnar J, Malý M, Kvasnička J, Dyr JE.
    Blood Coagul Fibrinolysis; 2010 Oct 10; 21(7):640-8. PubMed ID: 20829681
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  • 32. A novel mutation (deletion of Aalpha-Asn 80) in an abnormal fibrinogen: fibrinogen Caracas VI. Consequences of disruption of the coiled coil for the polymerization of fibrin: peculiar clot structure and diminished stiffness of the clot.
    Marchi RC, Meyer MH, de Bosch NB, Arocha-Piñango CL, Weisel JW.
    Blood Coagul Fibrinolysis; 2004 Oct 10; 15(7):559-67. PubMed ID: 15389122
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  • 33. A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.
    Margaglione M, Vecchione G, Santacroce R, D'Angelo F, Casetta B, Papa ML, Grandone E, Di Minno G.
    Thromb Haemost; 2001 Dec 10; 86(6):1483-8. PubMed ID: 11776317
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  • 37. A novel fibrinogen variant--Praha I: hypofibrinogenemia associated with gamma Gly351Ser substitution.
    Kotlín R, Chytilová M, Suttnar J, Salaj P, Riedel T, Santrůcek J, Klener P, Dyr JE.
    Eur J Haematol; 2007 May 10; 78(5):410-6. PubMed ID: 17331136
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  • 38. Homophenotypic Aalpha R16H fibrinogen (Kingsport): uniquely altered polymerization associated with slower fibrinopeptide A than fibrinopeptide B release.
    Galanakis DK, Neerman-Arbez M, Scheiner T, Henschen A, Hubbs D, Nagaswami C, Weisel JW.
    Blood Coagul Fibrinolysis; 2007 Dec 10; 18(8):731-7. PubMed ID: 17982313
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