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Journal Abstract Search

212 related items for PubMed ID: 16999847

  • 41.
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  • 42. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.
    Neerman-Arbez M, de Moerloose P, Bridel C, Honsberger A, Schönbörner A, Rossier C, Peerlinck K, Claeyssens S, Di Michele D, d'Oiron R, Dreyfus M, Laubriat-Bianchin M, Dieval J, Antonarakis SE, Morris MA.
    Blood; 2000 Jul 01; 96(1):149-52. PubMed ID: 10891444
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  • 46. A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family.
    Xie X, Du J, Geng S, Yi B, Li Q, Zuo J.
    Hereditas; 2024 Feb 20; 161(1):9. PubMed ID: 38374144
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  • 47. Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders.
    Szanto T, Lassila R, Lemponen M, Lehtinen E, Neerman-Arbez M, Casini A.
    Int J Mol Sci; 2021 Feb 25; 22(5):. PubMed ID: 33668986
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  • 50. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M.
    Ann N Y Acad Sci; 2001 Feb 25; 936():496-508. PubMed ID: 11460507
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  • 51. Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation.
    Asselta R, Duga S, Simonic T, Malcovati M, Santagostino E, Giangrande PL, Mannucci PM, Tenchini ML.
    Blood; 2000 Oct 01; 96(7):2496-500. PubMed ID: 11001902
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  • 52. [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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  • 54. Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations (gamma Ala341Thr, Bbeta Tyr326Cys and Aalpha Asp496Asn).
    Hanss M, Chevreaud C, French P, Négrier C, de Mazancourt P.
    Thromb Haemost; 2007 Sep 15; 98(3):689-91. PubMed ID: 17849064
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  • 55. Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications.
    Amri Y, Kallel C, Becheur M, Dabboubi R, Elloumi M, Belaaj H, Kammoun S, Messaoud T, de Moerloose P, Toumi Nel H.
    Clin Chim Acta; 2016 Sep 01; 460():55-62. PubMed ID: 27343352
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  • 58. Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the ERSD-associated gamma-G284R mutant.
    Duga S, Braidotti P, Asselta R, Maggioni M, Santagostino E, Pellegrini C, Coggi G, Malcovati M, Tenchini ML.
    J Thromb Haemost; 2005 Apr 01; 3(4):724-32. PubMed ID: 15842357
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