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307 related items for PubMed ID: 32639687

  • 1. 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; 42(5):619-627. PubMed ID: 32639687
    [Abstract] [Full Text] [Related]

  • 2. Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
    Mohsenian S, Seidizadeh O, Mirakhorli M, Jazebi M, Azarkeivan A.
    Transfus Apher Sci; 2021 Dec; 60(6):103203. PubMed ID: 34275736
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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]

  • 6. 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 01; 25(1):145-148. PubMed ID: 32228225
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 27(6):1022-1027. PubMed ID: 34460979
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
    Neerman-Arbez M, Vu D, Abu-Libdeh B, Bouchardy I, Morris MA.
    Blood; 2003 May 01; 101(9):3492-4. PubMed ID: 12511408
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 182():133-140. PubMed ID: 31479941
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 13(8):1459-67. PubMed ID: 26039544
    [Abstract] [Full Text] [Related]

  • 11. Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
    Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M.
    Blood; 2003 Dec 15; 102(13):4413-5. PubMed ID: 12893758
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 136(1):168-74. PubMed ID: 26006300
    [Abstract] [Full Text] [Related]

  • 13. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 15; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 14. Mutational Epidemiology of Congenital Fibrinogen Disorders.
    Casini A, Blondon M, Tintillier V, Goodyer M, Sezgin ME, Gunes AM, Hanss M, de Moerloose P, Neerman-Arbez M.
    Thromb Haemost; 2018 Nov 15; 118(11):1867-1874. PubMed ID: 30332696
    [Abstract] [Full Text] [Related]

  • 15. The molecular basis of quantitative fibrinogen disorders.
    Asselta R, Duga S, Tenchini ML.
    J Thromb Haemost; 2006 Oct 15; 4(10):2115-29. PubMed ID: 16999847
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Congenital fibrinogen disorders: an update.
    de Moerloose P, Casini A, Neerman-Arbez M.
    Semin Thromb Hemost; 2013 Sep 01; 39(6):585-95. PubMed ID: 23852822
    [Abstract] [Full Text] [Related]

  • 18. Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.
    Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML.
    Blood; 2000 Feb 15; 95(4):1336-41. PubMed ID: 10666208
    [Abstract] [Full Text] [Related]

  • 19. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
    Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg JY, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis SE, Morris MA.
    Hum Genet; 2001 Mar 15; 108(3):237-40. PubMed ID: 11354637
    [Abstract] [Full Text] [Related]

  • 20. 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; 15(5):876-888. PubMed ID: 28211264
    [Abstract] [Full Text] [Related]

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