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170 related items for PubMed ID: 31725541

  • 21. Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
    Nojehdeh ST, Mojbafan M, Masoodifard M, Amini M, Zeinali S.
    Blood Coagul Fibrinolysis; 2021 Jul 01; 32(5):323-327. PubMed ID: 33901106
    [Abstract] [Full Text] [Related]

  • 22. 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 01; 97(4):546-51. PubMed ID: 17393016
    [Abstract] [Full Text] [Related]

  • 23. A novel missense mutation in the FGB gene (p.Gly302Arg) leading to afibrinogenemia. Predicted structure and function consequences.
    Ivaškevičius V, Rühl H, Detarsio G, Biswas A, Gupta S, Davoli M, Quartara A, Pérez S, Raviola M, Oldenburg J.
    Hamostaseologie; 2016 Nov 08; 36(Suppl. 2):S34-S38. PubMed ID: 27824214
    [Abstract] [Full Text] [Related]

  • 24. Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
    Shen MC, Wang JD, Tsai W, Lin CY, Lin JS, Kuo SF, Lin PT, Huang YC, Hung MH.
    Haemophilia; 2021 Nov 08; 27(6):1022-1027. PubMed ID: 34460979
    [Abstract] [Full Text] [Related]

  • 25. Hereditary Hypofibrinogenemia with Hepatic Storage.
    Asselta R, Paraboschi EM, Duga S.
    Int J Mol Sci; 2020 Oct 22; 21(21):. PubMed ID: 33105716
    [Abstract] [Full Text] [Related]

  • 26. A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia.
    Wu S, Wang Z, Dong N, Bai X, Ruan C.
    Blood Coagul Fibrinolysis; 2005 Apr 22; 16(3):221-6. PubMed ID: 15795544
    [Abstract] [Full Text] [Related]

  • 27. Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management.
    Stanciakova L, Kubisz P, Dobrotova M, Stasko J.
    Expert Rev Hematol; 2016 Jul 22; 9(7):639-48. PubMed ID: 27291795
    [Abstract] [Full Text] [Related]

  • 28. 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 22; 28(6):540-53. PubMed ID: 17295221
    [Abstract] [Full Text] [Related]

  • 29. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
    Neerman-Arbez M, Germanos-Haddad M, Tzanidakis K, Vu D, Deutsch S, David A, Morris MA, de Moerloose P.
    Blood; 2004 Dec 01; 104(12):3618-23. PubMed ID: 15284111
    [Abstract] [Full Text] [Related]

  • 30. [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 01; 26(3):133-6. PubMed ID: 15946522
    [Abstract] [Full Text] [Related]

  • 31. 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 01; 87(8):855-9. PubMed ID: 12161363
    [Abstract] [Full Text] [Related]

  • 32. 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 01; 21(2):164-7. PubMed ID: 20051841
    [Abstract] [Full Text] [Related]

  • 33. Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature.
    Zdziarska J, Wypasek E, Iwaniec T, Vilar R, Neerman-Arbez M, Undas A.
    Haemophilia; 2021 Jan 01; 27(1):26-32. PubMed ID: 33245842
    [Abstract] [Full Text] [Related]

  • 34. Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population.
    Özkan DT, Sarper N, Akar N.
    Acta Haematol; 2020 Jan 01; 143(6):529-532. PubMed ID: 32289806
    [Abstract] [Full Text] [Related]

  • 35. 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 01; 12(6):615-20. PubMed ID: 17083511
    [Abstract] [Full Text] [Related]

  • 36. [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 01; 26(3):137-9. PubMed ID: 15946523
    [Abstract] [Full Text] [Related]

  • 37. siRNA down-regulation of FGA mRNA in HepG2 cells demonstrated that heterozygous abnormality of the Aα-chain gene does not affect the plasma fibrinogen level.
    Takezawa Y, Matsuda K, Terasawa F, Sugano M, Honda T, Okumura N.
    Thromb Res; 2013 Apr 01; 131(4):342-8. PubMed ID: 23414568
    [Abstract] [Full Text] [Related]

  • 38. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations.
    Casini A, Lukowski S, Quintard VL, Crutu A, Zak M, Regazzoni S, de Moerloose P, Neerman-Arbez M.
    Thromb Res; 2014 May 01; 133(5):868-74. PubMed ID: 24560896
    [Abstract] [Full Text] [Related]

  • 39. 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 01; 23(6):556-8. PubMed ID: 22732251
    [Abstract] [Full Text] [Related]

  • 40. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.
    Castaman G, Rimoldi V, Giacomelli SH, Duga S.
    Thromb Res; 2015 Jul 01; 136(1):144-7. PubMed ID: 25981141
    [Abstract] [Full Text] [Related]

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