These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

141 related items for PubMed ID: 16894470

  • 1. Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.
    Sheen CR, Brennan SO, Jabado N, George PM.
    Thromb Haemost; 2006 Aug; 96(2):231-2. PubMed ID: 16894470
    [No Abstract] [Full Text] [Related]

  • 2. Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion.
    Vu D, de Moerloose P, Batorova A, Lazur J, Palumbo L, Neerman-Arbez M.
    J Med Genet; 2005 Sep; 42(9):e57. PubMed ID: 16141000
    [Abstract] [Full Text] [Related]

  • 3. 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; 96(3):378-80. PubMed ID: 16953282
    [No Abstract] [Full Text] [Related]

  • 4. Fibrinogen Tolaga Bay: a novel gammaAla341Val mutation causing hypofibrinogenaemia.
    Davis RL, Brennan SO.
    Thromb Haemost; 2007 Nov; 98(5):1136-8. PubMed ID: 18000621
    [No Abstract] [Full Text] [Related]

  • 5. 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
    [No Abstract] [Full Text] [Related]

  • 6. Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia.
    Tirefort Y, Alson OR, de Moerloose P, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2012 Sep; 23(6):556-8. PubMed ID: 22732251
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Expression of four mutant fibrinogen gammaC domains in Pichia pastoris confirms them as causes of hypofibrinogenaemia.
    Sheen CR, Dear A, Brennan SO.
    Protein Expr Purif; 2010 Oct; 73(2):184-8. PubMed ID: 20580674
    [Abstract] [Full Text] [Related]

  • 10. 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
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Fibrinogen Gdansk: hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro).
    Mital A, Undas A, Neerman-Arbez M, Hellmann A.
    Thromb Res; 2012 Sep; 130(3):e196-7. PubMed ID: 22795623
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121Arg.
    Zhang H, Luo S, Fang W, Liu S, Su K, Yang L, Jin Y, Wang M.
    Blood Coagul Fibrinolysis; 2019 Jul; 30(5):233-238. PubMed ID: 31259773
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. To aggregate or not to aggregate..
    Neerman-Arbez M.
    J Thromb Haemost; 2007 Oct 21; 5(10):1997-8. PubMed ID: 17883695
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.