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Journal Abstract Search

213 related items for PubMed ID: 28948631

  • 1. Management of dysfibrinogenemia in pregnancy: A case report.
    Yan J, Deng D, Cheng P, Liao L, Luo M, Lin F.
    J Clin Lab Anal; 2018 Mar; 32(3):. PubMed ID: 28948631
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  • 5. Epidemiology and treatment of congenital fibrinogen deficiency.
    Peyvandi F.
    Thromb Res; 2012 Dec; 130 Suppl 2():S7-11. PubMed ID: 23439004
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  • 6. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
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  • 9. 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
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  • 12. Misdiagnosis of a patient with congenital dysfibrinogenemia: A case report and literature review.
    Chen X, Yan J, Xiang L, Lin F.
    J Clin Lab Anal; 2022 Sep; 36(9):e24624. PubMed ID: 35949040
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  • 13. Successful living-related kidney transplantation in a boy with inherited dysfibrinogenemia.
    Imamura H, Akioka Y, Asano T, Sugawara N, Ishizuka K, Chikamoto H, Taki M, Terasawa F, Okumura N, Hattori M.
    Pediatr Transplant; 2013 Nov; 17(7):E161-4. PubMed ID: 23962069
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  • 15. Congenital fibrinogen disorders.
    de Moerloose P, Neerman-Arbez M.
    Semin Thromb Hemost; 2009 Jun; 35(4):356-66. PubMed ID: 19598064
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  • 17. 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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  • 19. Congenital fibrinogen disorders: an update.
    de Moerloose P, Casini A, Neerman-Arbez M.
    Semin Thromb Hemost; 2013 Sep; 39(6):585-95. PubMed ID: 23852822
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