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Journal Abstract Search

175 related items for PubMed ID: 33419567

  • 1. Heterogeneity of congenital afibrinogenemia, from epidemiology to clinical consequences and management.
    Casini A, Neerman-Arbez M, de Moerloose P.
    Blood Rev; 2021 Jul; 48():100793. PubMed ID: 33419567
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  • 8. Can the phenotype of inherited fibrinogen disorders be predicted?
    Casini A, de Moerloose P.
    Haemophilia; 2016 Sep; 22(5):667-75. PubMed ID: 27293018
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  • 9. 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
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  • 13. A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.
    Aydin Köker S, Köker A, Neerman-Arbez M, Ö Tunçer G, Akbas Y, Kara TT, Coban Y.
    J Pediatr Hematol Oncol; 2020 Mar; 42(2):e98-e99. PubMed ID: 31725541
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  • 19. Congenital afibrinogenemia.
    al-Mondhiry H, Ehmann WC.
    Am J Hematol; 1994 Aug; 46(4):343-7. PubMed ID: 8037188
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