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Journal Abstract Search

403 related items for PubMed ID: 307953

  • 41. Development of an inhibitor specific to factor VIII: coagulant activity in a patient with platelet-type von Willebrand's disease.
    Castella A, Miller JL, Neuberg RW, Gawryl MS, Hoyer LW.
    Am J Clin Pathol; 1983 Nov; 80(5):745-9. PubMed ID: 6416054
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  • 43. [Multimeric composition of factor VIII-related protein following DDAVP infusion in normal subjects and patients with hemophilia A and von Willebrand's disease].
    Takase T, Nishino M, Yasui M, Shima M, Yoshikawa N, Fukui H.
    Nihon Ketsueki Gakkai Zasshi; 1985 Nov; 48(7):1571-8. PubMed ID: 3937410
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  • 47. Dissociation between factor VIII (activity and antigen) and ristocetin-induced platelet aggregation in von Willebrand's disease.
    Barbui T, Dini E.
    Acta Haematol; 1975 Nov; 53(1):44-8. PubMed ID: 807074
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  • 48. Von Willebrand's disease.
    Holmberg L, Nilsson IM.
    Annu Rev Med; 1975 Nov; 26():33-44. PubMed ID: 1096769
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  • 49. Von Willebrand's disease and pregnancy.
    Krishnamurthy M, Miotti AB.
    Obstet Gynecol; 1977 Feb; 49(2):244-7. PubMed ID: 299933
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  • 51. [Advances in hematology. Willebrand's disease and hemophilia A in the light of latest studies of the factor VIII].
    Zawilska K.
    Pol Arch Med Wewn; 1976 Aug; 56(8):179-84. PubMed ID: 787944
    [No Abstract] [Full Text] [Related]

  • 52. Acquired von Willebrand syndrome with inhibitors both to factor VIII clotting activity and ristocetin-induced platelet aggregation.
    Stableforth P, Tamagnini GL, Dormandy KM.
    Br J Haematol; 1976 Aug; 33(4):565-73. PubMed ID: 1087568
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  • 53. Familial incidence of precipitating antibodies in von Willebrand's disease: a study of four cases.
    Ruggeri ZM, Ciavarella N, Mannucci PM, Molinari A, Dammacco F, Lavergne JM, Meyer D.
    J Lab Clin Med; 1979 Jul; 94(1):60-75. PubMed ID: 112210
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  • 54. Classic hemophilia A in a female.
    Joist JH, Bouhasin JD, Roodman S.
    Acta Haematol; 1977 Jul; 58(2):94-102. PubMed ID: 409025
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  • 55. Abnormal factor VIII related antigen (FVIIIRAG) in von Willebrand's disease (vWd): decreased precipitation by concanavalin A.
    Peake IR, Bloom AL.
    Thromb Haemost; 1977 Apr 30; 37(2):361-2. PubMed ID: 301669
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  • 56. In vivo dissociation of factor VII (AHF) activity and factor VII-related antigen in von Willebrand's disease.
    Lian EC, Deykin D.
    Am J Hematol; 1976 Apr 30; 1(1):71-8. PubMed ID: 1086597
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  • 57. [Differential diagnosis of hemophilia A and Willebrand's disease].
    Iurlov VM, Promakhina EK.
    Probl Gematol Pereliv Krovi; 1978 Jul 30; (7):21-4. PubMed ID: 307759
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  • 58. An in vivo study of a new factor VIII high purity preparation.
    Thorell L, Blombäck M, Blombäck B.
    Thromb Res; 1983 Jul 15; 31(2):375-85. PubMed ID: 6415854
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  • 59. Letter: Enhanced factor VIII activity in von Willebrand's disease.
    Mannucci PM, Pareti FI, Ruggeri ZM.
    N Engl J Med; 1974 May 30; 290(22):1259. PubMed ID: 4545219
    [No Abstract] [Full Text] [Related]

  • 60. [Coagulation tests in von Willebrand's disease(author's transl)].
    Schöndorf TH, Heene DL.
    Dtsch Med Wochenschr; 1975 Mar 21; 100(12):596-600. PubMed ID: 1091430
    [Abstract] [Full Text] [Related]

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