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Journal Abstract Search

194 related items for PubMed ID: 38286442

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  • 5. Mutational Epidemiology of Congenital Fibrinogen Disorders.
    Casini A, Blondon M, Tintillier V, Goodyer M, Sezgin ME, Gunes AM, Hanss M, de Moerloose P, Neerman-Arbez M.
    Thromb Haemost; 2018 Nov; 118(11):1867-1874. PubMed ID: 30332696
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  • 8. [Clinical phenotypes and genotypes of congenital fibrinogen disorder: an analysis of 16 children].
    Wang M, Chen TP, Jiang AS, Zhao YH, Zhu CL, Wei N, Jin YT, Qu LJ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2024 Aug 15; 26(8):840-844. PubMed ID: 39148389
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  • 9. Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.
    Neerman-Arbez M, de Moerloose P, Casini A.
    Semin Thromb Hemost; 2016 Jun 15; 42(4):356-65. PubMed ID: 27019463
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  • 11. Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
    Casini A, Brungs T, Lavenu-Bombled C, Vilar R, Neerman-Arbez M, de Moerloose P.
    J Thromb Haemost; 2017 May 15; 15(5):876-888. PubMed ID: 28211264
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  • 12. Diagnosis of congenital fibrinogen disorders.
    Lebreton A, Casini A.
    Ann Biol Clin (Paris); 2016 Aug 01; 74(4):405-12. PubMed ID: 27492693
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  • 18. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 01; 14(6):1151-8. PubMed ID: 19141154
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