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Journal Abstract Search

97 related items for PubMed ID: 23467727

  • 1. Hypodysfibrinogenaemia and thrombosis in association with a new fibrinogen γ chain with two mutations (γ114Tyr→His, and γ320Asp deleted).
    Brennan SO, Chitlur M.
    Thromb Haemost; 2013 Jun; 109(6):1180-2. PubMed ID: 23467727
    [No Abstract] [Full Text] [Related]

  • 2. Congenital hypodysfibrinogenaemia (Fibrinogen Des Moines) due to a gamma320Asp deletion at the Ca2+ binding site.
    Brennan SO, Davis RL, Mosesson MW, Hernandez I, Lowen R, Alexander SJ.
    Thromb Haemost; 2007 Aug; 98(2):467-9. PubMed ID: 17721633
    [No Abstract] [Full Text] [Related]

  • 3. Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.
    Brennan SO, Davis RL, Conard K, Savo A, Furuya KN.
    Liver Int; 2010 Nov; 30(10):1541-7. PubMed ID: 20666993
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  • 6. New fibrinogen substitution (gammaSer313Arg) causes diminished gamma chain expression and hypodysfibrinogenaemia.
    Brennan SO, Davis RL, Chitlur M.
    Thromb Haemost; 2010 Feb; 103(2):478-9. PubMed ID: 20126833
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  • 8. 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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  • 9. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.
    Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML.
    Haematologica; 2002 Aug; 87(8):855-9. PubMed ID: 12161363
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  • 10. A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis.
    Robert-Ebadi H, Le Querrec A, de Moerloose P, Gandon-Laloum S, Borel Derlon A, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2008 Oct; 19(7):697-9. PubMed ID: 18832913
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  • 13. Functionally compromised FGG variant (γ320Asp→Glu) expressed at low level in plasma fibrinogen.
    Brennan SO, Laurie A.
    Thromb Res; 2014 Sep; 134(3):744-6. PubMed ID: 25042726
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  • 15. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
    Neerman-Arbez M, de Moerloose P.
    Hum Mutat; 2007 Jun; 28(6):540-53. PubMed ID: 17295221
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  • 17. Maternal chromosome 4 heterodisomy/isodisomy and Bβ chain Trp323X mutation resulting in severe hypodysfibrinogenaemia.
    Ding Q, Ouyang Q, Xi X, Wang X, Shen Y, Wang H.
    Thromb Haemost; 2012 Oct; 108(4):654-61. PubMed ID: 22955321
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  • 18. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
    Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M.
    Blood Coagul Fibrinolysis; 2006 Jun; 17(4):235-40. PubMed ID: 16651864
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  • 19. Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.
    Castaman G, Giacomelli SH, Duga S, Rodeghiero F.
    Haemophilia; 2008 May; 14(3):630-3. PubMed ID: 18393984
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