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Correction of the platelet abnormality in von Willebrand's disease by cryoprecipitate.
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Antihemophilic factor release by perfused liver and spleen: relationship to hemophilia.
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Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor.
J Clin Invest. 1971 Jan;50(1):244-54
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The treatment of haemorrhage in von Willebrand's disease and the blood level of factor VIII (AHG).
Br J Haematol. 1963 Apr;9:203-14
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Factor 8 on the vascular intima: possible importance in haemostasis and thrombosis.
Nat New Biol. 1973 Feb 14;241(111):217-9
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Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria.
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Kidney antihemophilic factor. Partial purification and some properties.
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Hemophilia: role of organ homografts.
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Characterization of the coagulant activity of cultured human fibroblasts.
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Nature. 1967 Mar 18;213(5081):1146-7
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Acute poststreptococcal glomerulonephritis: immune deposit disease.
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Changes in antihemophilic factor (AHF, factor 8) procoagulant activity and AHF-like antigen in normal pregnancy, and following exercise and pneumoencephalography.
J Lab Clin Med. 1972 Aug;80(2):256-63
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Studies of the metabolism and distribution of fibrinogen in healthy men with autologous 125-I-labeled fibrinogen.
J Clin Invest. 1966 Jan;45(1):103-11
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Role of the lymphocyte in antihemophilic globulin production: a rise in antihemophilic globulin levels in a hemophilic subject with acute lymphoblastic leukemia.
J Lab Clin Med. 1971 Jul;78(1):122-9
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Immunological characterization of purified anti-haemophilic factor A (factor VIII) which corrects abnormal platelet retention in Von Willebrand's disease.
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Immunologic identification of tissue factor (thromboplastin) synthesized by cultured fibroblasts.
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Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.
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Factor 8 detection by hemagglutination inhibition: hemophilia A and von Willebrand's disease.
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Purification of human antihemophilic factor (factor VIII) by gel chromatography.
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Localization of immunological complexes fixing beta1C (C3) in germinal centers of lymph nodes.
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Storage, release, and synthesis of coagulation factors in isolated perfused organs.
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Von Willebrand's disease and its correction with human plasma fraction 1-0.
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Plasma factor VIII synthesis and control as revealed by canine organ transplantation.
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Tissue factor (thromboplastin): localization to plasma membranes by peroxidase-conjugated antibodies.
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Transfusion studies in von Willebrand's disease: effect on bleeding time and factor VIII.
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Factor VIII (antihaemophilic factor) in tissues detected by antibody neutralization.
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In vitro abnormality of the blood in von Willebrand's disease correctable by normal plasma.
Nature. 1963 Feb 9;197:601-2
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Tissue factor activity in lymphocyte cultures from normal individuals and patients with hemophilia A.
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Analytical pathology. IV. The role of localized antibodies in the pathogenesis of nephrotoxic nephritis in the rat.
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Immunoglobulin class and pattern of nuclear fluorescence in systemic lupus erythematosus.
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The role of the splenic macrophage in antihemophilic factor (factor VIII) synthesis.
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