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Journal Abstract Search

234 related items for PubMed ID: 35054908

  • 21. Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.
    Castaman G, Giacomelli SH, Duga S, Rodeghiero F.
    Haemophilia; 2008 May; 14(3):630-3. PubMed ID: 18393984
    [No Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release.
    Yan J, Luo M, Cheng P, Liao L, Deng X, Deng D, Lin F.
    Int J Hematol; 2017 Apr 08; 105(4):506-514. PubMed ID: 27933517
    [Abstract] [Full Text] [Related]

  • 24. A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family.
    Zhu L, Wang M, Xie H, Jin Y, Yang L, Xu P.
    Blood Coagul Fibrinolysis; 2013 Sep 08; 24(6):642-4. PubMed ID: 23492915
    [Abstract] [Full Text] [Related]

  • 25. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 08; 14(6):1151-8. PubMed ID: 19141154
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  • 31. Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens.
    Kotlín R, Blažek B, Suttnar J, Malý M, Kvasnička J, Dyr JE.
    Blood Coagul Fibrinolysis; 2010 Oct 08; 21(7):640-8. PubMed ID: 20829681
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  • 32. A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys-Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia.
    Zhou W, Luo M, Yan J, Xiang L, Wei A, Deng X, Liao L, Cheng P, Deng D, Lin F.
    Thromb Res; 2018 Dec 08; 172():128-134. PubMed ID: 30412834
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  • 33. Functionally compromised FGG variant (γ320Asp→Glu) expressed at low level in plasma fibrinogen.
    Brennan SO, Laurie A.
    Thromb Res; 2014 Sep 08; 134(3):744-6. PubMed ID: 25042726
    [No Abstract] [Full Text] [Related]

  • 34. Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
    Simurda T, Brunclikova M, Asselta R, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P.
    Int J Mol Sci; 2020 Jun 29; 21(13):. PubMed ID: 32610551
    [Abstract] [Full Text] [Related]

  • 35. Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.
    Brennan SO, Davis RL, Conard K, Savo A, Furuya KN.
    Liver Int; 2010 Nov 29; 30(10):1541-7. PubMed ID: 20666993
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  • 36. Congenital fibrinogen disorders: an update.
    de Moerloose P, Casini A, Neerman-Arbez M.
    Semin Thromb Hemost; 2013 Sep 29; 39(6):585-95. PubMed ID: 23852822
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  • 37. [Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].
    Fang Y, Wang HL, Wang XF, Fu QH, Wang WB, Xie S, Zhou RF, Dai J, Wang ZY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Dec 29; 13(6):1086-9. PubMed ID: 16403286
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  • 38. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.
    Castaman G, Rimoldi V, Giacomelli SH, Duga S.
    Thromb Res; 2015 Jul 29; 136(1):144-7. PubMed ID: 25981141
    [Abstract] [Full Text] [Related]

  • 39. 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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  • 40. 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]

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