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Journal Abstract Search

372 related items for PubMed ID: 21245743

  • 1. A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family.
    Levrat E, Aboukhamis I, de Moerloose P, Farho J, Chamaa S, Reber G, Fort A, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2011 Mar; 22(2):148-50. PubMed ID: 21245743
    [Abstract] [Full Text] [Related]

  • 2. A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.
    Robert-Ebadi H, de Moerloose P, El Khorassani M, El Khattab M, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2009 Jul; 20(5):385-7. PubMed ID: 19417632
    [Abstract] [Full Text] [Related]

  • 3. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
    Fang Y, Dai BT, Wang XF, Fu QH, Dai J, Xie F, Cai XH, Wang HL, Wang ZY.
    Haemophilia; 2006 Nov; 12(6):615-20. PubMed ID: 17083511
    [Abstract] [Full Text] [Related]

  • 4. 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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  • 8. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.
    Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML.
    Haematologica; 2002 Aug; 87(8):855-9. PubMed ID: 12161363
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  • 9. A novel fibrinogen B beta chain frameshift mutation causes congenital afibrinogenaemia.
    Zhang J, Zhao X, Wang Z, Yu Z, Cao L, Zhang W, Bai X, Ruan C.
    Thromb Haemost; 2013 Jul; 110(1):76-82. PubMed ID: 23740095
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  • 11. [Congenital afibrinogenemia associated with a novel nonsense mutation in the FGA gene].
    Wu SY, Wang ZY, Dong NZ, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):133-6. PubMed ID: 15946522
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  • 12. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
    Neerman-Arbez M, de Moerloose P.
    Hum Mutat; 2007 Jun; 28(6):540-53. PubMed ID: 17295221
    [Abstract] [Full Text] [Related]

  • 13. Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia.
    Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA.
    J Clin Invest; 1999 Jan; 103(2):215-8. PubMed ID: 9916133
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  • 14. [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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  • 15. 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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  • 16. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M.
    Ann N Y Acad Sci; 2001 Apr; 936():496-508. PubMed ID: 11460507
    [Abstract] [Full Text] [Related]

  • 17. Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients.
    Abdel Wahab M, de Moerloose P, Fish RJ, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2010 Mar; 21(2):164-7. PubMed ID: 20051841
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  • 18. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
    Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P.
    Thromb Res; 2016 Jul; 143():11-6. PubMed ID: 27164460
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  • 19. 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 Jul; 41(3):292-7. PubMed ID: 18676163
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  • 20. 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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