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PUBMED FOR HANDHELDS

Journal Abstract Search

106 related items for PubMed ID: 15968409

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  • 3. Hypofibrinogenaemia associated with a novel heterozygous gamma289 Ala -->Val substitution (fibrinogen Dorfen).
    Dear A, Brennan SO, Dempfle CE, Kirschstein W, George PM.
    Thromb Haemost; 2004 Dec; 92(6):1291-5. PubMed ID: 15583736
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  • 4. 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 Dec; 121(3):429-30. PubMed ID: 17604827
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  • 6. Familial hypofibrinogenaemia associated with heterozygous substitution of a conserved arginine residue; Bbeta255 Arg-->His (Fibrinogen Merivale).
    Maghzal GJ, Brennan SO, Fellowes AP, Spearing R, George PM.
    Biochim Biophys Acta; 2003 Feb 21; 1645(2):146-51. PubMed ID: 12573244
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  • 8. Hypofibrinogenemia due to novel 316 Asp --> Tyr substitution in the fibrinogen Bbeta chain.
    Brennan SO, Wyatt JM, May S, De Caigney S, George PM.
    Thromb Haemost; 2001 Mar 21; 85(3):450-3. PubMed ID: 11307813
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  • 10. 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 21; 17(1):63-7. PubMed ID: 16607083
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  • 11. Novel fibrinogen truncation with deletion of Bbeta chain residues 440-461 causes hypofibrinogenaemia.
    Homer VM, Brennan SO, Ockelford P, George PM.
    Thromb Haemost; 2002 Sep 21; 88(3):427-31. PubMed ID: 12353071
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  • 13. 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 21; 81(2):268-74. PubMed ID: 10064005
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  • 14. Fibrinogen Nottingham II: a novel Bbeta Arg264gly substitution causing hypofibrinogenaemia.
    Hill MB, Brennan SO, Dear A, Strong J, Nejim T, Dolan G.
    Thromb Haemost; 2006 Sep 21; 96(3):378-80. PubMed ID: 16953282
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  • 15. Fibrinogen Columbus: a novel gamma Gly200Val mutation causing hypofibrinogenemia in a family with associated thrombophilia.
    Davis RL, Mosesson MW, Kerlin BA, Canner JA, Ruymann FB, Brennan SO.
    Haematologica; 2007 Aug 21; 92(8):1151-2. PubMed ID: 17650452
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  • 16. 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 21; 84(1):49-53. PubMed ID: 10928469
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  • 17. Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene.
    Monaldini L, Asselta R, Duga S, Peyvandi F, Ghosh K, Malcovati M, Tenchini ML.
    Haematologica; 2006 May 21; 91(5):628-33. PubMed ID: 16670068
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  • 20. Fibrinogen Tolaga Bay: a novel gammaAla341Val mutation causing hypofibrinogenaemia.
    Davis RL, Brennan SO.
    Thromb Haemost; 2007 Nov 21; 98(5):1136-8. PubMed ID: 18000621
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