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Journal Abstract Search

102 related items for PubMed ID: 8093017

  • 1. Fibrinogen Milano IV (A alpha 16 Arg-->His): characterization of its abnormal interaction with human alpha-thrombin.
    De Cristofaro R, Furlan M, Landolfi R.
    Biochem J; 1994 Sep 01; 302 ( Pt 2)(Pt 2):623-4. PubMed ID: 8093017
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  • 2. Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogen.
    Seydewitz HH, Gram J, Bruhn HD, Witt I.
    Blood Coagul Fibrinolysis; 1991 Aug 01; 2(4):501-6. PubMed ID: 1768762
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  • 3. Fibrinogens Bern IV, Bern V and Milano XI: three dysfunctional variants with amino acid substitutions in the thrombin cleavage site of the Aalpha-chain.
    Stucki B, Zenhäusern R, Biedermann B, Baudo F, Redaelli R, Lämmle B, Furlan M.
    Blood Coagul Fibrinolysis; 1999 Mar 01; 10(2):93-9. PubMed ID: 10192658
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  • 4. Fibrinogen Sapporo: dysfibrinogenemia characterized by the replacement of A alpha arginine-16 by histidine resulting in the delayed release of fibrinopeptide A by thrombin.
    Asakura S, Terukina S, Yamazumi K, Matsuda M, Murayama H, Higuchi A, Musashi M, Sakurada K, Miyazaki T.
    Nihon Ketsueki Gakkai Zasshi; 1989 Sep 01; 52(6):1094-104. PubMed ID: 2588959
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  • 6. Fibrinogen Milano. VI: A heterozygous dysfibrinogenemia (A alpha 16 Arg----His) with bleeding tendency.
    Bögli C, Cofrancesco E, Cortellaro M, Della Volpe A, Hofer A, Furlan M, Zanussi C.
    Eur J Haematol; 1990 Jul 01; 45(1):26-30. PubMed ID: 2379562
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  • 7. Fibrinogen Milano IV, another case of congenital dysfibrinogenemia with an abnormal fibrinopeptide A release (A alpha 16 Arg----His).
    Bögli C, Hofer A, Baudo F, Redaelli R, Furlan M.
    Haemostasis; 1992 Jul 01; 22(1):7-11. PubMed ID: 1521828
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  • 8. Fibrinogen Stony Brook II: partial characterization of a heterozygously transmitted peptide A anomaly.
    Galanakis DK, Hultin M.
    Blood Coagul Fibrinolysis; 1990 Oct 01; 1(4-5):567-70. PubMed ID: 2133235
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  • 13. Novel fibrinogen (B β401Gly→Val) presents as dys- or hypodysfibrinogenaemia due to alterations in sialic acid content.
    Brennan SO, Roncolato F.
    Thromb Haemost; 2011 Sep 01; 106(3):551-3. PubMed ID: 21713329
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  • 14. Unusual A alpha 16Arg-->Cys dysfibrinogenaemic family: absence of normal A alpha-chains in fibrinogen from two of four heterozygous siblings.
    Galanakis D, Spitzer S, Scharrer I.
    Blood Coagul Fibrinolysis; 1993 Feb 01; 4(1):67-71. PubMed ID: 8457654
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  • 15. Fibrinogen Mitaka II: a hereditary dysfibrinogen with defective thrombin binding caused by an A alpha Glu-11 to Gly substitution.
    Niwa K, Yaginuma A, Nakanishi M, Wada Y, Sugo T, Asakura S, Watanabe N, Matsuda M.
    Blood; 1993 Dec 15; 82(12):3658-63. PubMed ID: 7903170
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  • 16. Fibrinogen Matsumoto V: a variant with Aalpha19 Arg-->Gly (AGG-->GGG). Comparison between fibrin polymerization stimulated by thrombin or reptilase and fibrin monomer polymerization.
    Tanaka H, Terasawa F, Ito T, Tokunaga S, Ishida F, Kitano K, Kiyosawa K, Okumura N.
    Thromb Haemost; 2001 Jan 15; 85(1):108-13. PubMed ID: 11204560
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