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Journal Abstract Search

86 related items for PubMed ID: 9184429

  • 1. Characterisation of Fibrinogen Oslo IV by electrospray mass spectrometry.
    Brennan SO, Ridgway H, Stormorken H, Brosstad F, George PM.
    Thromb Haemost; 1997 May; 77(5):1040-1. PubMed ID: 9184429
    [No Abstract] [Full Text] [Related]

  • 2. A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.
    Margaglione M, Vecchione G, Santacroce R, D'Angelo F, Casetta B, Papa ML, Grandone E, Di Minno G.
    Thromb Haemost; 2001 Dec; 86(6):1483-8. PubMed ID: 11776317
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  • 3. Fibrinogen Saint-Germain II: hypofibrinogenemia due to heterozygous gamma N345S mutation.
    de Raucourt E, de Mazancourt P, Maghzal GJ, Brennan SO, Mosesson MW.
    Thromb Haemost; 2005 Nov; 94(5):965-8. PubMed ID: 16363237
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  • 4. A new dysfibrinogenemia: fibrinogen Oslo IV.
    Stormorken H, Brosstad F, Seim H.
    Thromb Haemost; 1983 Apr 28; 49(2):120-2. PubMed ID: 6868008
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  • 7. Fibrinogen Cordoba I: A gammaArg 275 His substitution associated with defective polymerization.
    Guglielmone HA, Minoldo S, Jarchum GD, Daga DA, Bocco JL.
    Thromb Res; 2007 Apr 28; 121(3):429-30. PubMed ID: 17604827
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  • 8. Fibrinogen St. Gallen I (gamma 292 Gly--> Val): evidence for structural alterations causing defective polymerization and fibrinogenolysis.
    Stucki B, Schmutz P, Schmid L, Haeberli A, Lämmle B, Furlan M.
    Thromb Haemost; 1999 Feb 28; 81(2):268-74. PubMed ID: 10064005
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  • 9. Novel fibrinogen mutation (gamma 313 Ser-->Asn) associated with hypofibrinogenemia in two unrelated families.
    Meyer M, Bergmann F, Brennan SO.
    Blood Coagul Fibrinolysis; 2006 Jan 28; 17(1):63-7. PubMed ID: 16607083
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  • 10. Abnormal fibrinogen Zlín (γThr21Ile) with missense mutation causing hypofibrinogenemia.
    Riedelová-Reicheltová Z, Riedel T, Májek P, Kotlin R, Geierová V, Suttnar J, Dyr JE.
    Acta Haematol; 2014 Jan 28; 132(2):140-3. PubMed ID: 24556703
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  • 11. Adjacent substitutions (γ352Gly→Cys and 353Thr→Pro) in fibrinogen Ilam cause diminished γ chain expression.
    Brennan SO, Oliver J, Davis RL.
    Thromb Haemost; 2011 Feb 28; 105(2):379-81. PubMed ID: 21057694
    [No Abstract] [Full Text] [Related]

  • 12. A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.
    Iida H, Ishii E, Nakahara M, Urata M, Wakiyama M, Kurihara M, Watanabe K, Kai T, Ihara K, Kinoshita S, Hamasaki N.
    Thromb Haemost; 2000 Jul 28; 84(1):49-53. PubMed ID: 10928469
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  • 13. Fibrinogen Foxton: a novel BbetaA277V mutation causing low normal plasma fibrinogen concentration.
    Davis RL, Baker B, Brennan SO.
    Thromb Haemost; 2008 Oct 28; 100(4):708-10. PubMed ID: 18841297
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  • 14. Substitution (γ335Trp→Arg) in fibrinogen Fremantle causes diminished γ chain expression and increased sialic acid content.
    Brennan SO, Davis RL.
    Thromb Haemost; 2010 Dec 28; 104(6):1274-6. PubMed ID: 20838743
    [No Abstract] [Full Text] [Related]

  • 15. Exon skipping and aberrant signal peptide cleavage produce novel fibrinogen with an Aα chain lacking the first 42 residues.
    Brennan SO, Laurie AD, McRae S.
    Thromb Haemost; 2016 Aug 30; 116(3):581-5. PubMed ID: 27277572
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  • 17. Fibrinogen Milano IV (A alpha 16 Arg-->His): characterization of its abnormal interaction with human alpha-thrombin.
    De Cristofaro R, Furlan M, Landolfi R.
    Biochem J; 1994 Sep 01; 302 ( Pt 2)(Pt 2):623-4. PubMed ID: 8093017
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  • 18. Fibrinogen Baltimore I: polymerization defect associated with a gamma 292Gly----Val (GGC----GTC) mutation.
    Bantia S, Mane SM, Bell WR, Dang CV.
    Blood; 1990 Dec 01; 76(11):2279-83. PubMed ID: 2257302
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  • 20. Novel gamma230 Asn-->Asp substitution in fibrinogen Middlemore associated hypofibrinogenaemia.
    Brennan SO, Sheen CR, George PM.
    Thromb Haemost; 2005 Jun 01; 93(6):1196-7. PubMed ID: 15968409
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