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PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 17886104

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  • 3. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
    Xu XC, Zhou RF, Wu JS, Fang Y, Wang XF, Zhai ZM, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):137-9. PubMed ID: 15946523
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  • 5. Molecular basis of congenital afibrinogenaemia in a Dutch family.
    Remijn JA, van Wijk R, Nieuwenhuis HK, de Groot PG, van Solinge WW.
    Blood Coagul Fibrinolysis; 2003 Apr; 14(3):299-302. PubMed ID: 12695755
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  • 9. The molecular basis of inherited afibrinogenaemia.
    Neerman-Arbez M.
    Thromb Haemost; 2001 Jul; 86(1):154-63. PubMed ID: 11487003
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  • 13. Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene.
    Spena S, Duga S, Asselta R, Peyvandi F, Mahasandana C, Malcovati M, Tenchini ML.
    Eur J Hum Genet; 2004 Nov; 12(11):891-8. PubMed ID: 15489905
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  • 15. Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy.
    Brennan SO, Mosesson MW, Lowen R, Siebenlist KR, Matsunaga A.
    Thromb Haemost; 2006 Apr; 95(4):738-9. PubMed ID: 16601848
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  • 16. 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; 98(3):689-91. PubMed ID: 17849064
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  • 18. 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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  • 19. Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
    Vu D, Di Sanza C, Caille D, de Moerloose P, Scheib H, Meda P, Neerman-Arbez M.
    Hum Mol Genet; 2005 Nov 01; 14(21):3271-80. PubMed ID: 16195396
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  • 20. 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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