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Journal Abstract Search

223 related items for PubMed ID: 32228225

  • 1. 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
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  • 3. 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
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  • 4. 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
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  • 5. 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; 108(3):237-40. PubMed ID: 11354637
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  • 6. 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
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  • 7. 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
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  • 8. 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
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  • 9. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M.
    Ann N Y Acad Sci; 2001 Oct; 936():496-508. PubMed ID: 11460507
    [Abstract] [Full Text] [Related]

  • 10. Molecular basis of fibrinogen deficiency.
    Neerman-Arbez M.
    Pathophysiol Haemost Thromb; 2006 Oct; 35(1-2):187-98. PubMed ID: 16855369
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  • 11. 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; 27(6):1022-1027. PubMed ID: 34460979
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  • 12. Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
    Richard M, Celeny D, Neerman-Arbez M.
    Semin Thromb Hemost; 2022 Nov; 48(8):889-903. PubMed ID: 35073585
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  • 13. 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
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  • 14. 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
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  • 16. 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
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  • 17. 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
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