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Journal Abstract Search

207 related items for PubMed ID: 23962069

  • 1. Successful living-related kidney transplantation in a boy with inherited dysfibrinogenemia.
    Imamura H, Akioka Y, Asano T, Sugawara N, Ishizuka K, Chikamoto H, Taki M, Terasawa F, Okumura N, Hattori M.
    Pediatr Transplant; 2013 Nov; 17(7):E161-4. PubMed ID: 23962069
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  • 2. Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects.
    Miesbach W, Scharrer I, Henschen A, Neerman-Arbez M, Spitzer S, Galanakis D.
    Blood Coagul Fibrinolysis; 2010 Jan; 21(1):35-40. PubMed ID: 19923982
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  • 3. Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders.
    Castaman G, Giacomelli SH, Biasoli C, Contino L, Radossi P.
    Eur J Haematol; 2019 Oct; 103(4):379-384. PubMed ID: 31314131
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  • 4. The dilemma of inherited dysfibrinogenemia during pregnancy.
    Munoz J, Schering J, Lambing A, Neal S, Goyert G, Green PM, Hanbali A, Raman S, Kuriakose P.
    Blood Coagul Fibrinolysis; 2012 Dec; 23(8):775-7. PubMed ID: 23135383
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  • 6. 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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  • 7. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
    Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M.
    Blood Coagul Fibrinolysis; 2006 Jun; 17(4):235-40. PubMed ID: 16651864
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  • 10. [Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA].
    Zhang YL, Liu SY, Zhang ZL, Tao XY, Peng XX, Kong YY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct; 25(5):1514-1517. PubMed ID: 29070135
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  • 12. 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; 21(7):640-8. PubMed ID: 20829681
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  • 13. Fibrinogen Bonn (p. Arg510Cys) in the Aα-Chain Is Associated with High Risk of Venous Thrombosis.
    Ivaškevičius V, Biswas A, Singh S, Stulpinaitė U, Reda S, Rühl H, Pezeshkpoor B, Pavlova A, Oldenburg J.
    Hamostaseologie; 2023 Dec; 43(6):440-446. PubMed ID: 37442158
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  • 16. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
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  • 17. [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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  • 18. Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerization.
    Zhou J, Ding Q, Wu W, Ouyang Q, Xie Y, Wu X, Lu Y, Dai J, Liang Q, Wang H, Wang X, Hu Y.
    J Clin Pathol; 2017 Feb; 70(2):145-153. PubMed ID: 27555433
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  • 20. Congenital fibrinogen disorders: an update.
    de Moerloose P, Casini A, Neerman-Arbez M.
    Semin Thromb Hemost; 2013 Sep; 39(6):585-95. PubMed ID: 23852822
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