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Journal Abstract Search

361 related items for PubMed ID: 4089808

  • 1. The prevalence of hereditary antithrombin-III deficiency in patients with a history of venous thromboembolism.
    Vikydal R, Korninger C, Kyrle PA, Niessner H, Pabinger I, Thaler E, Lechner K.
    Thromb Haemost; 1985 Dec 17; 54(4):744-5. PubMed ID: 4089808
    [Abstract] [Full Text] [Related]

  • 2. [Familial thromboembolic disease associated with antithrombin III deficiency (author's transl)].
    Bentata-Pessayre M, Aurousseau MH, Josso F, Delzant G.
    Ann Med Interne (Paris); 1980 Dec 17; 131(6):378-82. PubMed ID: 7469244
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
    Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.
    Srp Arh Celok Lek; 1999 Dec 17; 127(1-2):21-7. PubMed ID: 10377836
    [Abstract] [Full Text] [Related]

  • 4. [A family with venous thrombosis and hereditary antithrombin III deficiency].
    Michiels JJ, van Vliet HD.
    Ned Tijdschr Geneeskd; 1986 Jan 04; 130(1):28-31. PubMed ID: 3951576
    [No Abstract] [Full Text] [Related]

  • 5. [Antithrombin III deficiency and tendency to thrombosis (author's transl)].
    Lechner K, Thaler E, Niessner H, Nowotny C, Partsch H.
    Wien Klin Wochenschr; 1977 Apr 01; 89(7):215-22. PubMed ID: 857429
    [Abstract] [Full Text] [Related]

  • 6. Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening.
    Pabinger I, Brücker S, Kyrle PA, Schneider B, Korninger HC, Niessner H, Lechner K.
    Blood Coagul Fibrinolysis; 1992 Oct 01; 3(5):547-53. PubMed ID: 1450321
    [Abstract] [Full Text] [Related]

  • 7. [Factor XII (Hageman factor) deficiency: a risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboembolism and myocardial infarction].
    Halbmayer WM, Mannhalter C, Feichtinger C, Rubi K, Fischer M.
    Wien Med Wochenschr; 1993 Oct 01; 143(2):43-50. PubMed ID: 8488686
    [Abstract] [Full Text] [Related]

  • 8. Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency.
    Luxembourg B, Pavlova A, Geisen C, Spannagl M, Bergmann F, Krause M, Alesci S, Seifried E, Lindhoff-Last E.
    Thromb Haemost; 2014 Feb 01; 111(2):249-57. PubMed ID: 24196373
    [Abstract] [Full Text] [Related]

  • 9. [Familial deficiency of antithrombin III].
    Coget JM, Dendien-Bernard S, Dupuis-Cuny C.
    Phlebologie; 1987 Feb 01; 40(2):381-91. PubMed ID: 3615614
    [Abstract] [Full Text] [Related]

  • 10. [Thromboembolism. The clinical significance of antithrombin III].
    Schramm W.
    Internist (Berl); 1984 Feb 01; 25(2):88-92. PubMed ID: 6368458
    [No Abstract] [Full Text] [Related]

  • 11. Hereditary antithrombin III deficiency and pregnancy: report of two cases and review of the literature.
    Nelson DM, Stempel LE, Brandt JT.
    Obstet Gynecol; 1985 Jun 01; 65(6):848-53. PubMed ID: 4039808
    [Abstract] [Full Text] [Related]

  • 12. [Plasma antithrombin III activity in patients with pulmonary thromboembolism].
    Vertun B, Filipecki S, Szczepański M, Wawrzyńska L, Rózycka J.
    Pol Tyg Lek; 1985 Jun 01; 47(34-35):726-9. PubMed ID: 1488357
    [Abstract] [Full Text] [Related]

  • 13. Familial antithrombin III deficiency.
    Winter JH, Fenech A, Ridley W, Bennett B, Cumming AM, Mackie M, Douglas AS.
    Q J Med; 1982 Jun 01; 51(204):373-95. PubMed ID: 7156320
    [Abstract] [Full Text] [Related]

  • 14. [Etiology and pathogenesis of spontaneous venous thromboembolism].
    Sletnes KE.
    Tidsskr Nor Laegeforen; 1993 Nov 20; 113(28):3457-9. PubMed ID: 8273075
    [Abstract] [Full Text] [Related]

  • 15. Antithrombin III deficiency in a Romanian family. Pathogenic role of concomitantly increased plasma level of clotting factors VII and X.
    Cucuianu M, Comes L, Roman S, Boeru A.
    Med Interne; 1984 Nov 20; 22(1):13-7. PubMed ID: 6710043
    [Abstract] [Full Text] [Related]

  • 16. High incidence of thrombophilia detected in Chinese patients with venous thrombosis.
    Liu HW, Kwong YL, Bourke C, Lam CK, Lie AK, Wei D, Chan LC.
    Thromb Haemost; 1994 Apr 20; 71(4):416-9. PubMed ID: 8052955
    [Abstract] [Full Text] [Related]

  • 17. Inherited antithrombin III deficiency in an Italian family, associated with venous and arterial thrombosis.
    Candrina R, Coppini A, Salvi A, Zuccato F, Del Bono R, Giustina G.
    Haematologica; 1985 Apr 20; 70(5):399-404. PubMed ID: 3937775
    [No Abstract] [Full Text] [Related]

  • 18. Inherited hypercoagulable states in children.
    Whitlock JA, Janco RL, Phillips JA.
    Am J Pediatr Hematol Oncol; 1989 Apr 20; 11(2):170-3. PubMed ID: 2526603
    [Abstract] [Full Text] [Related]

  • 19. [Significance of hereditary thrombophilia for risk of thrombosis with oral contraceptives].
    Bauersachs R, Lindhoff-Last E, Ehrly AM, Kuhl H.
    Zentralbl Gynakol; 1996 Apr 20; 118(5):262-70. PubMed ID: 8701622
    [Abstract] [Full Text] [Related]

  • 20. [Severe pulmonary embolism and recurrent thrombophlebitis caused by hereditary antithrombin III deficiency].
    Rey JL, Delobel J, Claisse JF, Quiret JC, Bor P, Bernasconi P.
    Arch Mal Coeur Vaiss; 1979 Aug 20; 72(8):919-23. PubMed ID: 115439
    [Abstract] [Full Text] [Related]

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