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Journal Abstract Search

218 related items for PubMed ID: 28211264

  • 1. Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
    Casini A, Brungs T, Lavenu-Bombled C, Vilar R, Neerman-Arbez M, de Moerloose P.
    J Thromb Haemost; 2017 May; 15(5):876-888. PubMed ID: 28211264
    [Abstract] [Full Text] [Related]

  • 2. Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
    Wypasek E, Klukowska A, Zdziarska J, Zawilska K, Treliński J, Iwaniec T, Mital A, Pietrys D, Sydor W, Neerman-Arbez M, Undas A.
    Thromb Res; 2019 Oct; 182():133-140. PubMed ID: 31479941
    [Abstract] [Full Text] [Related]

  • 3. Diagnosis of congenital fibrinogen disorders.
    Lebreton A, Casini A.
    Ann Biol Clin (Paris); 2016 Aug 01; 74(4):405-12. PubMed ID: 27492693
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  • 4. Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications.
    Amri Y, Kallel C, Becheur M, Dabboubi R, Elloumi M, Belaaj H, Kammoun S, Messaoud T, de Moerloose P, Toumi Nel H.
    Clin Chim Acta; 2016 Sep 01; 460():55-62. PubMed ID: 27343352
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  • 5. 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 01; 113(3):567-76. PubMed ID: 25427968
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  • 6. 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 01; 196():152-158. PubMed ID: 32871307
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  • 7. Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder.
    Ceznerová E, Kaufmanová J, Sovová Ž, Štikarová J, Loužil J, Kotlín R, Suttnar J.
    Int J Mol Sci; 2022 Jan 10; 23(2):. PubMed ID: 35054908
    [Abstract] [Full Text] [Related]

  • 8. Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
    Tavasoli B, Safa M, Dorgalaleh A, Ghasemi JB, Rezaei Makhouri F, Rezvani MR, Ahmadi A, Tabibian S, Jazebi M, Baghaipour MR, Zaker F.
    Int J Lab Hematol; 2020 Oct 10; 42(5):619-627. PubMed ID: 32639687
    [Abstract] [Full Text] [Related]

  • 9. Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature review.
    Li Y, Ding B, Wang X, Ding Q.
    Thromb Res; 2022 Sep 10; 217():36-47. PubMed ID: 35853369
    [Abstract] [Full Text] [Related]

  • 10. Congenital fibrinogen disorders: an update.
    de Moerloose P, Casini A, Neerman-Arbez M.
    Semin Thromb Hemost; 2013 Sep 10; 39(6):585-95. PubMed ID: 23852822
    [Abstract] [Full Text] [Related]

  • 11. Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.
    Asselta R, Robusto M, Braidotti P, Peyvandi F, Nastasio S, D'Antiga L, Perisic VN, Maggiore G, Caccia S, Duga S.
    J Thromb Haemost; 2015 Aug 10; 13(8):1459-67. PubMed ID: 26039544
    [Abstract] [Full Text] [Related]

  • 12. Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens.
    Kaido T, Yoda M, Kamijo T, Taira C, Higuchi Y, Okumura N.
    Int J Lab Hematol; 2020 Apr 10; 42(2):190-197. PubMed ID: 31957968
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  • 15. 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 10; 31(7):481-484. PubMed ID: 32852326
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  • 18. 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 10; 98(3):689-91. PubMed ID: 17849064
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  • 20. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.
    Luo M, Deng D, Xiang L, Cheng P, Liao L, Deng X, Yan J, Lin F.
    Medicine (Baltimore); 2016 Sep 10; 95(39):e4864. PubMed ID: 27684817
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