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Journal Abstract Search

222 related items for PubMed ID: 28425010

  • 1. A novel fibrinogen variant: dysfibrinogenemia associated with γAsp185Asn substitution.
    Zhou N, Xu P, Zhou M, Xu Y, Li P, Chen B, Ouyang J, Zhou R.
    J Thromb Thrombolysis; 2017 Jul; 44(1):139-144. PubMed ID: 28425010
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  • 2. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.
    Luo M, Deng D, Xiang L, Cheng P, Liao L, Deng X, Yan J, Lin F.
    Medicine (Baltimore); 2016 Sep; 95(39):e4864. PubMed ID: 27684817
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  • 4. [Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].
    Jiang LL, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2012 Jun; 33(6):475-9. PubMed ID: 22967385
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  • 6. 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; 105(4):506-514. PubMed ID: 27933517
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  • 9. Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.
    Li S, Wang M, Li X, Xu Q, Liu S, Luo S, Chen Y.
    Hamostaseologie; 2020 Dec; 40(5):642-648. PubMed ID: 33374030
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  • 11. [A case of dysfibrinogenemia without hemorrhagic diathesis or thromboembolism linked to a new mutation p.H103N in fibrinogen γ chain].
    Devignes J, Hanss M, Chabaud A, Toussaint-Hacquard M, Mansuy L, De Mazancourt P, Lecompte T.
    Ann Biol Clin (Paris); 2013 Dec; 71(4):489-95. PubMed ID: 23906582
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  • 12. Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
    Kotlín R, Chytilová M, Suttnar J, Riedel T, Salaj P, Blatný J, Santrůcek J, Klener P, Dyr JE.
    Thromb Res; 2007 Dec; 121(1):75-84. PubMed ID: 17408725
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  • 13. A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.
    Luo S, Xu Q, Xie Y, Li X, Jin Y, Yang L, Liu S, Wang M.
    Blood Coagul Fibrinolysis; 2020 Dec; 31(8):569-574. PubMed ID: 32833807
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  • 14. Fibrinogen St. Gallen I (gamma 292 Gly--> Val): evidence for structural alterations causing defective polymerization and fibrinogenolysis.
    Stucki B, Schmutz P, Schmid L, Haeberli A, Lämmle B, Furlan M.
    Thromb Haemost; 1999 Feb; 81(2):268-74. PubMed ID: 10064005
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  • 16. Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region.
    Wei A, Wu Y, Xiang L, Yan J, Cheng P, Deng D, Lin F.
    Hematology; 2021 Dec; 26(1):305-311. PubMed ID: 33663356
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  • 19. A novel fibrinogen variant--Liberec: dysfibrinogenaemia associated with gamma Tyr262Cys substitution.
    Kotlín R, Sobotková A, Suttnar J, Salaj P, Walterová L, Riedel T, Reicheltová Z, Dyr JE.
    Eur J Haematol; 2008 Aug; 81(2):123-9. PubMed ID: 18485115
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