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Journal Abstract Search

208 related items for PubMed ID: 20640913

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  • 4. 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; 95(39):e4864. PubMed ID: 27684817
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  • 5. Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications.
    Amri Y, Kallel C, Becheur M, Dabboubi R, Elloumi M, Belaaj H, Kammoun S, Messaoud T, de Moerloose P, Toumi Nel H.
    Clin Chim Acta; 2016 Sep 01; 460():55-62. PubMed ID: 27343352
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  • 7. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
    Simurda T, Zolkova J, Snahnicanova Z, Loderer D, Skornova I, Sokol J, Hudecek J, Stasko J, Lasabova Z, Kubisz P.
    Int J Mol Sci; 2017 Dec 29; 19(1):. PubMed ID: 29286337
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  • 8. Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen.
    Kotlín R, Reicheltová Z, Malý M, Suttnar J, Sobotková A, Salaj P, Hirmerová J, Riedel T, Dyr JE.
    Thromb Haemost; 2009 Sep 29; 102(3):479-86. PubMed ID: 19718467
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  • 12. Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region.
    Wei A, Wu Y, Xiang L, Yan J, Cheng P, Deng D, Lin F.
    Hematology; 2021 Dec 29; 26(1):305-311. PubMed ID: 33663356
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  • 13. Comparison of molecular structure and fibrin polymerization between two Bβ-chain N-terminal region fibrinogen variants, Bβp.G45C and Bβp.R74C.
    Kaido T, Yoda M, Kamijo T, Taira C, Higuchi Y, Okumura N.
    Int J Hematol; 2020 Sep 29; 112(3):331-340. PubMed ID: 32562089
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  • 16. 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 Sep 29; 121(1):75-84. PubMed ID: 17408725
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  • 17. Hypofibrinogenemia caused by a nonsense mutation in the fibrinogen Bbeta chain gene.
    Mimuro J, Hamano A, Tanaka T, Madoiwa KS, Sugo T, Matsuda M, Sakata Y.
    J Thromb Haemost; 2003 Nov 29; 1(11):2356-9. PubMed ID: 14629469
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  • 18. Heterozygous Bβ-chain C-terminal 12 amino acid elongation variant, BβX462W (Kyoto VI), showed dysfibrinogenemia.
    Okumura N, Terasawa F, Takezawa Y, Hirota-Kawadobora M, Inaba T, Fujita N, Saito M, Sugano M, Honda T.
    Blood Coagul Fibrinolysis; 2012 Jan 29; 23(1):87-90. PubMed ID: 22001526
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