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Journal Abstract Search

79 related items for PubMed ID: 12193971

  • 1. [Fibrinolysis in dysfibrinogenemia].
    Witt I.
    Hamostaseologie; 2002 May; 22(2):11-2. PubMed ID: 12193971
    [No Abstract] [Full Text] [Related]

  • 2. Fibrinogen Valencia. A new case of congenital dysfibrinogenemia.
    Aznar J, Fernandez-Pavón A, Regañón E, Vila V, Orellana F.
    Thromb Diath Haemorrh; 1974 Dec 31; 32(2-3):564-77. PubMed ID: 4217955
    [No Abstract] [Full Text] [Related]

  • 3. [Aortocoronary venous bypass in dysfibrinogenemia].
    Neidhardt B, Schricker KT, Weniger J.
    Med Welt; 1983 Jan 28; 34(4):119-22. PubMed ID: 6600811
    [No Abstract] [Full Text] [Related]

  • 4. [Congenital dysfibrinogenemia. Apropos of 13 cases].
    Corrihons G, Soria J, Soria C, Conard J, Horellou MH, Samama M.
    Sem Hop; 1983 Oct 13; 59(36):2517-23. PubMed ID: 6316508
    [Abstract] [Full Text] [Related]

  • 5. Fibrinogen Foxton: a novel BbetaA277V mutation causing low normal plasma fibrinogen concentration.
    Davis RL, Baker B, Brennan SO.
    Thromb Haemost; 2008 Oct 13; 100(4):708-10. PubMed ID: 18841297
    [No Abstract] [Full Text] [Related]

  • 6. [Familial dysfibrinogenemia with abnormal nonomer aggregation. Paris III fibrinogen].
    Soria J, Soria C.
    Pathol Biol (Paris); 1974 Nov 13; 22 suppl():72-9. PubMed ID: 4620099
    [No Abstract] [Full Text] [Related]

  • 7. [Molecular variants of fibrinogen].
    Plendl H, Caliebe A, Grote W.
    Hamostaseologie; 2002 May 13; 22(2):36-41. PubMed ID: 12193975
    [Abstract] [Full Text] [Related]

  • 8. Defective alpha-polymerization in the conversion of fibrinogen Baltimore to fibrin.
    Brown CH, Crowe MF.
    J Clin Invest; 1975 Jun 13; 55(6):1190-4. PubMed ID: 1133167
    [Abstract] [Full Text] [Related]

  • 9. Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
    Hua B, Li K, Lee A, Poon MC, Zhao Y.
    Haemophilia; 2015 Nov 13; 21(6):846-51. PubMed ID: 25982359
    [Abstract] [Full Text] [Related]

  • 10. Dysfibrinogenemia (fibrinogen Dusard) associated with impaired fibrin-enhanced plasminogen activation.
    Lijnen HR, Soria J, Soria C, Collen D, Caen JP.
    Thromb Haemost; 1984 Feb 28; 51(1):108-9. PubMed ID: 6539000
    [Abstract] [Full Text] [Related]

  • 11. Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III.
    Pietrys D, Balwierz W, Iwaniec T, Vorjohann S, Neerman-Arbez M, Undas A.
    Thromb Haemost; 2011 Sep 28; 106(3):558-60. PubMed ID: 21725578
    [No Abstract] [Full Text] [Related]

  • 12. "Fibrinogen Tokyo II". An abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules.
    Matsuda M, Baba M, Morimoto K, Nakamikawa C.
    J Clin Invest; 1983 Sep 28; 72(3):1034-41. PubMed ID: 6886002
    [Abstract] [Full Text] [Related]

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  • 16. [Congenital dysfibrinogenemia. Report on a new family (fibrinogen "Wiesbaden")].
    Winckelmann G.
    Thromb Diath Haemorrh Suppl; 1973 Sep 28; 55():345-56. PubMed ID: 4216115
    [No Abstract] [Full Text] [Related]

  • 17. Two novel mutations in the fibrinogen γ nodule.
    Kotlín R, Pastva O, Stikarová J, Hlaváčková A, Suttnar J, Chrastinová L, Riedel T, Salaj P, Dyr JE.
    Thromb Res; 2014 Oct 28; 134(4):901-8. PubMed ID: 25074738
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  • 20. A new dysfibrinogenemia: fibrinogen Oslo IV.
    Stormorken H, Brosstad F, Seim H.
    Thromb Haemost; 1983 Apr 28; 49(2):120-2. PubMed ID: 6868008
    [Abstract] [Full Text] [Related]

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