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Journal Abstract Search

320 related items for PubMed ID: 27019462

  • 21. Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management.
    Stanciakova L, Kubisz P, Dobrotova M, Stasko J.
    Expert Rev Hematol; 2016 Jul; 9(7):639-48. PubMed ID: 27291795
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  • 22. Cryoprecipitate: no longer the best therapeutic choice in congenital fibrinogen disorders?
    Bevan DH.
    Thromb Res; 2009 Dec; 124 Suppl 2():S12-6. PubMed ID: 20109651
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  • 23. Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects.
    Miesbach W, Scharrer I, Henschen A, Neerman-Arbez M, Spitzer S, Galanakis D.
    Blood Coagul Fibrinolysis; 2010 Jan; 21(1):35-40. PubMed ID: 19923982
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  • 29. [Congenital afibrinogenemia complicated by spontaneous cerebral hemorrhages: a case report].
    Tovone XG, Rasamoelisoa JM, Rakotomalala S, Rabesiaka F, Rakotoarimanana DR, Ramialiharisoa A.
    Arch Inst Pasteur Madagascar; 1999 Jan; 65(1-2):117-9. PubMed ID: 12478976
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  • 30. 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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  • 31. Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation.
    Mukaddam A, Patil R, Jadli A, Chandrakala S, Ghosh K, Shetty S.
    Am J Clin Pathol; 2015 May; 143(5):755-7. PubMed ID: 25873512
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  • 32. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
    Fager Ferrari M, Leinoe E, Rossing M, Norström E, Zetterberg E.
    Blood Coagul Fibrinolysis; 2020 Oct; 31(7):481-484. PubMed ID: 32852326
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  • 34. [Hereditary afibrinogenemia: A literature review and clinical observations].
    Yakovleva EV, Surin VL, Selivanova DS, Sergeeva AM, Gonсharova MV, Demidova EY, Soboleva NP, Makhinya SA, Dezhenkova AV, Likhacheva EA, Zozulya NI.
    Ter Arkh; 2016 Oct; 88(12):120-125. PubMed ID: 28635887
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  • 36. Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
    Richard M, Celeny D, Neerman-Arbez M.
    Semin Thromb Hemost; 2022 Nov; 48(8):889-903. PubMed ID: 35073585
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  • 39. Guideline for diagnosis and management of congenital dysfibrinogenemia.
    Yan J, Liao L, Deng D, Zhou W, Cheng P, Xiang L, Luo M, Lin F.
    Clin Chim Acta; 2024 Jul 15; 561():119680. PubMed ID: 38642629
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