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Journal Abstract Search

306 related items for PubMed ID: 25427968

  • 1. Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency.
    Asselta R, Platè M, Robusto M, Borhany M, Guella I, Soldà G, Afrasiabi A, Menegatti M, Shamsi T, Peyvandi F, Duga S.
    Thromb Haemost; 2015 Mar; 113(3):567-76. PubMed ID: 25427968
    [Abstract] [Full Text] [Related]

  • 2. Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion.
    Platè M, Asselta R, Spena S, Spreafico M, Fagoonee S, Peyvandi F, Tenchini ML, Duga S.
    Blood Cells Mol Dis; 2008 Mar; 41(3):292-7. PubMed ID: 18676163
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  • 3. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.
    Monaldini L, Asselta R, Duga S, Peyvandi F, Karimi M, Malcovati M, Tenchini ML.
    Thromb Haemost; 2007 Apr; 97(4):546-51. PubMed ID: 17393016
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  • 4. 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
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  • 10. The molecular basis of quantitative fibrinogen disorders.
    Asselta R, Duga S, Tenchini ML.
    J Thromb Haemost; 2006 Oct; 4(10):2115-29. PubMed ID: 16999847
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  • 11. 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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  • 17. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
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  • 19. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
    Simurda T, Zolkova J, Snahnicanova Z, Loderer D, Skornova I, Sokol J, Hudecek J, Stasko J, Lasabova Z, Kubisz P.
    Int J Mol Sci; 2017 Dec 29; 19(1):. PubMed ID: 29286337
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