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Journal Abstract Search

156 related items for PubMed ID: 3413737

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  • 2. AT III Barcelona: a familial quantitative-qualitative AT III deficiency.
    Grau E, Fontcuberta J, Félez J, de Diego I, Soto R, Rutllant ML.
    Thromb Haemost; 1988 Feb 25; 59(1):13-7. PubMed ID: 3363529
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  • 3. Antithrombin III Pescara: a defective AT III variant with no alterations of plasma crossed immunoelectrophoresis, but with an abnormal crossed immunoelectrofocusing pattern.
    Leone G, De Stefano V, Di Donfrancesco A, Ferrelli R, Traisci G, Bizzi B.
    Br J Haematol; 1987 Feb 25; 65(2):187-91. PubMed ID: 3828226
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  • 7. Antithrombin III Toyama: a hereditary abnormal antithrombin III of a patient with recurrent thrombophlebitis.
    Sakuragawa N, Takahashi K, Kondo S, Koide T.
    Thromb Res; 1983 Jul 15; 31(2):305-17. PubMed ID: 6636045
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  • 8. Antithrombin III molecular variants with defective binding to heparin or to serine proteases: evidence of two different abnormal patterns identified by crossed immunoelectrofocusing.
    Leone G, De Stefano V, Ferrelli R, Teofili L, Tengborn L, Vahtera E, Bizzi B.
    Thromb Haemost; 1988 Aug 30; 60(1):8-12. PubMed ID: 3187949
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  • 9. An abnormal antithrombin III (AT III) with low heparin affinity: AT III Clichy.
    Aiach M, François D, Priollet P, Capron L, Roncato M, Alhenc-Gelas M, Fiessinger JN.
    Br J Haematol; 1987 Aug 30; 66(4):515-22. PubMed ID: 3663508
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  • 10. Antithrombin III Geneva: a hereditary abnormal AT III with defective heparin cofactor activity.
    de Moerloose PA, Reber G, Vernet P, Minazio P, Bouvier CA.
    Thromb Haemost; 1987 Apr 07; 57(2):154-7. PubMed ID: 3603409
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  • 11. Homozygous variant of antithrombin III: AT III Fontainebleau.
    Boyer C, Wolf M, Vedrenne J, Meyer D, Larrieu MJ.
    Thromb Haemost; 1986 Aug 20; 56(1):18-22. PubMed ID: 3775688
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  • 14. Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene.
    Bock SC, Harris JF, Schwartz CE, Ward JH, Hershgold EJ, Skolnick MH.
    Am J Hum Genet; 1985 Jan 20; 37(1):32-41. PubMed ID: 2983542
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  • 16. Molecular genetics of inherited antithrombin III deficiencies.
    Prochownik EV.
    Am J Med; 1989 Sep 11; 87(3B):15S-18S. PubMed ID: 2572168
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  • 17. Antithrombin III Kumamoto II; a single mutation at Arg393-His increased the affinity of antithrombin III for heparin.
    Okajima K, Abe H, Wagatsuma M, Okabe H, Takatsuki K.
    Am J Hematol; 1995 Jan 11; 48(1):12-8. PubMed ID: 7832187
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  • 19. Identification and characterization of a new antithrombin III familial variant (AT Dublin) with possible increased frequency in children with cancer.
    Daly M, O'Meara A, Hallinan FM.
    Br J Haematol; 1987 Apr 11; 65(4):457-62. PubMed ID: 3472589
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