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Journal Abstract Search

174 related items for PubMed ID: 35853369

  • 1. Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature review.
    Li Y, Ding B, Wang X, Ding Q.
    Thromb Res; 2022 Sep; 217():36-47. PubMed ID: 35853369
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  • 2. 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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  • 4. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.
    Casini A, Neerman-Arbez M, Ariëns RA, de Moerloose P.
    J Thromb Haemost; 2015 Jun 01; 13(6):909-19. PubMed ID: 25816717
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  • 5. 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 Jun 01; 121(1):75-84. PubMed ID: 17408725
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  • 6. Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization.
    Amri Y, Jouini H, Becheur M, Dabboubi R, Mahjoub B, Messaoud T, Sfar MT, Casini A, de Moerloose P, Toumi NEH.
    Haemophilia; 2017 Jul 01; 23(4):e340-e347. PubMed ID: 28594476
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  • 7. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F, Samama M.
    Thromb Haemost; 1995 Jan 01; 73(1):151-61. PubMed ID: 7740487
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  • 8. A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release.
    Yan J, Luo M, Cheng P, Liao L, Deng X, Deng D, Lin F.
    Int J Hematol; 2017 Apr 01; 105(4):506-514. PubMed ID: 27933517
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  • 9. 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 01; 95(39):e4864. PubMed ID: 27684817
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  • 10. 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 01; 112(3):331-340. PubMed ID: 32562089
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  • 11. Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
    Simurda T, Brunclikova M, Asselta R, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P.
    Int J Mol Sci; 2020 Jun 29; 21(13):. PubMed ID: 32610551
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  • 12. Congenital structural and functional fibrinogen disorders: a primer for internists.
    Undas A, Casini A.
    Pol Arch Intern Med; 2019 Dec 23; 129(12):913-920. PubMed ID: 31797863
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  • 15. Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens.
    Kaido T, Yoda M, Kamijo T, Taira C, Higuchi Y, Okumura N.
    Int J Lab Hematol; 2020 Apr 23; 42(2):190-197. PubMed ID: 31957968
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  • 18. Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature.
    Yan J, Luo M, Xiang L, Wu Y, Lin F.
    Clin Chim Acta; 2022 Mar 01; 528():1-5. PubMed ID: 35063457
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