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Journal Abstract Search

169 related items for PubMed ID: 31542854

  • 1. Congenital fibrinogen disorders with repeated thrombosis.
    Zhang X, Zhang C, Wang B, Chen N, Sun G, Guo X.
    J Thromb Thrombolysis; 2020 Feb; 49(2):312-315. PubMed ID: 31542854
    [Abstract] [Full Text] [Related]

  • 2. Combined use of Clauss and prothrombin time-derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia.
    Xiang L, Luo M, Yan J, Liao L, Zhou W, Deng X, Deng D, Cheng P, Lin F.
    J Clin Lab Anal; 2018 May; 32(4):e22322. PubMed ID: 28922493
    [Abstract] [Full Text] [Related]

  • 3. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.
    Casini A, Neerman-Arbez M, Ariëns RA, de Moerloose P.
    J Thromb Haemost; 2015 Jun; 13(6):909-19. PubMed ID: 25816717
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  • 4. Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method.
    Arai S, Kamijo T, Hayashi F, Shinohara S, Arai N, Sugano M, Uehara T, Honda T, Okumura N.
    Int J Lab Hematol; 2021 Apr; 43(2):281-289. PubMed ID: 33030793
    [Abstract] [Full Text] [Related]

  • 5. Comparison of the fibrinogen Clauss assay and the fibrinogen PT derived method in patients with dysfibrinogenemia.
    Miesbach W, Schenk J, Alesci S, Lindhoff-Last E.
    Thromb Res; 2010 Dec; 126(6):e428-33. PubMed ID: 20947138
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  • 6. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F, Samama M.
    Thromb Haemost; 1995 Jan; 73(1):151-61. PubMed ID: 7740487
    [Abstract] [Full Text] [Related]

  • 7. Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders.
    Castaman G, Giacomelli SH, Biasoli C, Contino L, Radossi P.
    Eur J Haematol; 2019 Oct; 103(4):379-384. PubMed ID: 31314131
    [Abstract] [Full Text] [Related]

  • 8. Use of Fibrinogen Determination Methods in Differential Diagnosis of Hypofibrinogenemia and Dysfibrinogenemia.
    Skornova I, Simurda T, Stasko J, Horvath D, Zolkova J, Holly P, Brunclikova M, Samos M, Bolek T, Schnierer M, Slavik L, Kubisz P.
    Clin Lab; 2021 Apr 01; 67(4):. PubMed ID: 33865248
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 134(4):901-8. PubMed ID: 25074738
    [Abstract] [Full Text] [Related]

  • 10. The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia.
    Jacquemin M, Vanlinthout I, Van Horenbeeck I, Debasse M, Toelen J, Schoeters J, Lavend'homme R, Freson K, Peerlinck K.
    Int J Lab Hematol; 2017 Jun 01; 39(3):301-307. PubMed ID: 28318107
    [Abstract] [Full Text] [Related]

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  • 12. 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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  • 14. Treatment of patients with dysfibrinogenemia and a history of abortions during pregnancy.
    Miesbach W, Galanakis D, Scharrer I.
    Blood Coagul Fibrinolysis; 2009 Jul 01; 20(5):366-70. PubMed ID: 19357502
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  • 16. Laboratory testing for fibrinogen abnormalities.
    Verhovsek M, Moffat KA, Hayward CP.
    Am J Hematol; 2008 Dec 01; 83(12):928-31. PubMed ID: 18951466
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  • 19. Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature review.
    Li Y, Ding B, Wang X, Ding Q.
    Thromb Res; 2022 Sep 01; 217():36-47. PubMed ID: 35853369
    [Abstract] [Full Text] [Related]

  • 20. [Dysfibrinogenemia and thrombosis. A case report].
    Kraiem I, Guermazi S, Ben Abid H, Meddeb B.
    Tunis Med; 2010 Oct 01; 88(10):757-60. PubMed ID: 20890827
    [Abstract] [Full Text] [Related]

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