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Journal Abstract Search

615 related items for PubMed ID: 23852822

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

  • 2. Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.
    Neerman-Arbez M, de Moerloose P, Casini A.
    Semin Thromb Hemost; 2016 Jun; 42(4):356-65. PubMed ID: 27019463
    [Abstract] [Full Text] [Related]

  • 3. Congenital fibrinogen disorders.
    de Moerloose P, Neerman-Arbez M.
    Semin Thromb Hemost; 2009 Jun; 35(4):356-66. PubMed ID: 19598064
    [Abstract] [Full Text] [Related]

  • 4. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Diagnosis of congenital fibrinogen disorders.
    Lebreton A, Casini A.
    Ann Biol Clin (Paris); 2016 Aug 01; 74(4):405-12. PubMed ID: 27492693
    [Abstract] [Full Text] [Related]

  • 8. Molecular basis of fibrinogen deficiency.
    Neerman-Arbez M.
    Pathophysiol Haemost Thromb; 2006 Aug 01; 35(1-2):187-98. PubMed ID: 16855369
    [Abstract] [Full Text] [Related]

  • 9. 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 Aug 01; 41(3):292-7. PubMed ID: 18676163
    [Abstract] [Full Text] [Related]

  • 10. Congenital structural and functional fibrinogen disorders: a primer for internists.
    Undas A, Casini A.
    Pol Arch Intern Med; 2019 Dec 23; 129(12):913-920. PubMed ID: 31797863
    [Abstract] [Full Text] [Related]

  • 11. 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 23; 42(5):619-627. PubMed ID: 32639687
    [Abstract] [Full Text] [Related]

  • 12. Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
    Richard M, Celeny D, Neerman-Arbez M.
    Semin Thromb Hemost; 2022 Nov 23; 48(8):889-903. PubMed ID: 35073585
    [Abstract] [Full Text] [Related]

  • 13. Epidemiology and treatment of congenital fibrinogen deficiency.
    Peyvandi F.
    Thromb Res; 2012 Dec 23; 130 Suppl 2():S7-11. PubMed ID: 23439004
    [Abstract] [Full Text] [Related]

  • 14. Clinical Features and Management of Congenital Fibrinogen Deficiencies.
    Casini A, de Moerloose P, Neerman-Arbez M.
    Semin Thromb Hemost; 2016 Jun 23; 42(4):366-74. PubMed ID: 27019462
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. 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 29; 15(5):876-888. PubMed ID: 28211264
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 08; 22(2):148-50. PubMed ID: 21245743
    [Abstract] [Full Text] [Related]

  • 20. 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 08; 143():11-6. PubMed ID: 27164460
    [Abstract] [Full Text] [Related]

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