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Journal Abstract Search

409 related items for PubMed ID: 7886560

  • 1. Experience with factor VIII: C inhibitors and acquired von Willebrand's disease in an adult at Ramathibodi Hospital.
    Angchaisuksiri P, Atichartakarn V, Pathepchotiwong K, Jootar S, Ungkanont A, Chuncharunee S.
    Southeast Asian J Trop Med Public Health; 1993; 24 Suppl 1():152-8. PubMed ID: 7886560
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  • 2. Hemophilia in Sweden. Studies on demography of hemophilia and surgery in hemophilia and von Willebrand's disease.
    Larsson SA.
    Acta Med Scand Suppl; 1984; 684():1-72. PubMed ID: 6611018
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  • 3. [Report of 2 cases with acquired von Willebrand disease and one with acquired hemophilia A].
    Martínez-Murillo C, Quintana González S, Ambriz Fernández R, Domínguez García V, Rodríguez Moyado H, Arias Aranda A, Collazo Jaloma J, Gutiérrez Romero M.
    Rev Invest Clin; 1995; 47(3):211-6. PubMed ID: 7569365
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  • 5. Hemophilia and von Willebrand's disease: 1. Diagnosis, comprehensive care and assessment. Association of Hemophilia Clinic Directors of Canada.
    CMAJ; 1995 Jul 01; 153(1):19-25. PubMed ID: 7796372
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  • 7. Recent advances in hemophilia.
    Tann G.
    Southeast Asian J Trop Med Public Health; 1979 Jun 01; 10(2):218-28. PubMed ID: 524146
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  • 11. Immunologic studies in von Willebrand's disease: alteration of factor VIII/von Willebrand protein after transfusion with plasma concentrates in patients with von Willebrand's disease.
    Sultan Y, Simeon J, Maisonneuve P, Caen JP.
    Thromb Haemost; 1976 Feb 29; 35(1):110-9. PubMed ID: 1085498
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  • 12. Acquired von Willebrand's syndrome: a single institution experience.
    Kumar S, Pruthi RK, Nichols WL.
    Am J Hematol; 2003 Apr 29; 72(4):243-7. PubMed ID: 12666134
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  • 13. [Acquired von Willebrand's syndrome associated with malignant lymphoma].
    Schneider P, Tran-Thang C, Maillard M, Bachmann F.
    Schweiz Med Wochenschr; 1979 Sep 29; 109(37):1390. PubMed ID: 314665
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  • 14. Efficacy and safety of factor VIII/von Willebrand's factor concentrate (Haemate-P) in preventing bleeding during surgery or invasive procedures in patients with von Willebrand disease.
    Franchini M, Rossetti G, Tagliaferri A, Pattacini C, Pozzoli D, Lippi G, Manzato F, Bertuzzo D, Gandini G.
    Haematologica; 2003 Nov 29; 88(11):1279-83. PubMed ID: 14607757
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  • 15. [Immunosuppressive treatment of a spontaneous inhibitor hemophilia A using cyclophosphamide, vincristine and prednisone following prior Factor VIII stimulation].
    Dürig J, de Wit M, Fiedler W, Marx G, Hossfeld DK.
    Schweiz Med Wochenschr; 1996 Nov 23; 126(47):2026-31. PubMed ID: 8984611
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  • 16. Acquired hemophilia in the patient suffering from rheumatoid arthritis: case report.
    Drobiecki A, Pasiarski M, Hus I, Sokołowska B, Wątek M.
    Blood Coagul Fibrinolysis; 2013 Dec 23; 24(8):874-80. PubMed ID: 24042266
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  • 18. An inhibitor to factor VIII:C in a patient with possible combined haemophilia A and von Willebrand's disease.
    Taylor LD, Dean FL, Tiedemann K, Ekert H.
    Thromb Haemost; 1986 Apr 30; 55(2):158-61. PubMed ID: 3087000
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  • 19. Hemophilia with factor VIII and factor IX inhibitors, incidence, bleeding problems and management.
    Mahasandana C, Patharathienskul D, Suvatte V.
    Southeast Asian J Trop Med Public Health; 1993 Apr 30; 24 Suppl 1():106-12. PubMed ID: 7886549
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  • 20. Acquired von Willebrand syndromes: clinical features, aetiology, pathophysiology, classification and management.
    Michiels JJ, Budde U, van der Planken M, van Vliet HH, Schroyens W, Berneman Z.
    Best Pract Res Clin Haematol; 2001 Jun 30; 14(2):401-36. PubMed ID: 11686107
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