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Journal Abstract Search

146 related items for PubMed ID: 35949040

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  • 2. Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature.
    Yan J, Deng D, Luo M, Cheng P, Chi B, Yuan Y, Liao L, Lin F.
    Clin Chim Acta; 2015 Jul 20; 447():86-9. PubMed ID: 26057201
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  • 4. A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report.
    Cai R, Li Y, Wang W, Gao X, Liu M, Diao Y, Tang Y, Feng Q.
    Medicine (Baltimore); 2018 Oct 20; 97(40):e12697. PubMed ID: 30290666
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  • 6. Combined use of Clauss and prothrombin time-derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia.
    Xiang L, Luo M, Yan J, Liao L, Zhou W, Deng X, Deng D, Cheng P, Lin F.
    J Clin Lab Anal; 2018 May 20; 32(4):e22322. PubMed ID: 28922493
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  • 10. 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 20; 182():133-140. PubMed ID: 31479941
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  • 11. Management of dysfibrinogenemia in pregnancy: A case report.
    Yan J, Deng D, Cheng P, Liao L, Luo M, Lin F.
    J Clin Lab Anal; 2018 Mar 20; 32(3):. PubMed ID: 28948631
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  • 14. [Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].
    Luo J, Duan SR, Wang H.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2022 Jan 20; 53(1):171-174. PubMed ID: 35048620
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  • 15. Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method.
    Arai S, Kamijo T, Hayashi F, Shinohara S, Arai N, Sugano M, Uehara T, Honda T, Okumura N.
    Int J Lab Hematol; 2021 Apr 20; 43(2):281-289. PubMed ID: 33030793
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  • 17. 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 20; 143():11-6. PubMed ID: 27164460
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  • 18. Congenital hypofibrinogenemia and recurrent placental abruption.
    Ness PM, Budzynski AZ, Olexa SA, Rodvien R.
    Obstet Gynecol; 1983 Apr 20; 61(4):519-23. PubMed ID: 6828283
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  • 19. [Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
    Fang Y, Wang X, Qi H, Wu W, Ding Q, Dai J, Zhou R, Wang W, Xie S, Wang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 20; 22(2):201-3. PubMed ID: 15793786
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  • 20. Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
    Hua B, Li K, Lee A, Poon MC, Zhao Y.
    Haemophilia; 2015 Nov 20; 21(6):846-51. PubMed ID: 25982359
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