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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

96 related items for PubMed ID: 12193975

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  • 23. [Dysfibrinogenemia].
    Philippe N.
    Pediatrie; 1972; 27(1):93-100. PubMed ID: 4557225
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  • 24.
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  • 25. Congenital dysfibrinogenemia.
    Rupp C, Beck EA.
    Curr Probl Clin Biochem; 1984; 14():65-130. PubMed ID: 6150812
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  • 26. Dysfibrinogenemia in a patient with primary hepatoma. First observation of an acquired abnormality of fibrin monomer aggregation.
    von Felten A, Straub PW, Frick PG.
    N Engl J Med; 1969 Feb 20; 280(8):405-9. PubMed ID: 4303132
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  • 29. 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 20; 106(3):558-60. PubMed ID: 21725578
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  • 31. Hypofibrinogenemia-dysfibrinogenemia and von Willebrand's disease in the same family.
    Owen CA, Bowie EJ, Fass DN, Perez RA, Cole TL, Stewart M.
    Mayo Clin Proc; 1979 Jun 20; 54(6):375-80. PubMed ID: 312982
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  • 33. The molecular basis of hereditary clotting disorders.
    Ratnoff OD.
    Prog Hemost Thromb; 1972 Jun 20; 1():39-74. PubMed ID: 4571823
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  • 39. 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 20; 21(6):846-51. PubMed ID: 25982359
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  • 40. Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
    Kotlín R, Chytilová M, Suttnar J, Riedel T, Salaj P, Blatný J, Santrůcek J, Klener P, Dyr JE.
    Thromb Res; 2007 Nov 20; 121(1):75-84. PubMed ID: 17408725
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