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Journal Abstract Search

615 related items for PubMed ID: 23852822

  • 21. Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative.
    Yoda M, Kaido T, Taira C, Higuchi Y, Arai S, Okumura N.
    Thromb Res; 2020 Dec; 196():152-158. PubMed ID: 32871307
    [Abstract] [Full Text] [Related]

  • 22. Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders.
    Castaman G, Giacomelli SH, Biasoli C, Contino L, Radossi P.
    Eur J Haematol; 2019 Oct; 103(4):379-384. PubMed ID: 31314131
    [Abstract] [Full Text] [Related]

  • 23. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
    Fager Ferrari M, Leinoe E, Rossing M, Norström E, Zetterberg E.
    Blood Coagul Fibrinolysis; 2020 Oct; 31(7):481-484. PubMed ID: 32852326
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Congenital fibrinogen disorder caused by digenic mutations of the FGA and FGB genes.
    Wang X, Tang N, Shen N, Lu Y, Li D.
    Hematology; 2020 Dec; 25(1):145-148. PubMed ID: 32228225
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. Cryoprecipitate: no longer the best therapeutic choice in congenital fibrinogen disorders?
    Bevan DH.
    Thromb Res; 2009 Dec; 124 Suppl 2():S12-6. PubMed ID: 20109651
    [Abstract] [Full Text] [Related]

  • 28. 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; 133(5):868-74. PubMed ID: 24560896
    [Abstract] [Full Text] [Related]

  • 29. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
    Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M.
    Blood Coagul Fibrinolysis; 2006 Jun; 17(4):235-40. PubMed ID: 16651864
    [Abstract] [Full Text] [Related]

  • 30. Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains.
    Paraboschi EM, Duga S, Asselta R.
    Int J Mol Sci; 2017 Dec 14; 18(12):. PubMed ID: 29240685
    [Abstract] [Full Text] [Related]

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  • 33. Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation.
    Asselta R, Robusto M, Platé M, Santoro C, Peyvandi F, Duga S.
    Thromb Res; 2015 Jul 14; 136(1):168-74. PubMed ID: 26006300
    [Abstract] [Full Text] [Related]

  • 34. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M.
    Ann N Y Acad Sci; 2001 Jul 14; 936():496-508. PubMed ID: 11460507
    [Abstract] [Full Text] [Related]

  • 35. 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 14; 136(1):144-7. PubMed ID: 25981141
    [Abstract] [Full Text] [Related]

  • 36. Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
    Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F.
    Blood Adv; 2024 Mar 26; 8(6):1392-1404. PubMed ID: 38286442
    [Abstract] [Full Text] [Related]

  • 37. 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 Mar 26; 143(6):529-532. PubMed ID: 32289806
    [Abstract] [Full Text] [Related]

  • 38. [Clinical phenotypes and genotypes of congenital fibrinogen disorder: an analysis of 16 children].
    Wang M, Chen TP, Jiang AS, Zhao YH, Zhu CL, Wei N, Jin YT, Qu LJ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2024 Aug 15; 26(8):840-844. PubMed ID: 39148389
    [Abstract] [Full Text] [Related]

  • 39. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F, Samama M.
    Thromb Haemost; 1995 Jan 15; 73(1):151-61. PubMed ID: 7740487
    [Abstract] [Full Text] [Related]

  • 40. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep 15; 34(9):751-6. PubMed ID: 24103871
    [Abstract] [Full Text] [Related]

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