The survival of factor VIII (antihemophilic globulin) and factor IX (plasma thromboplastin component) in normal humans.
作者信息
ADELSON E, RHEINGOLD J J, PARKER O, STEINER M, KIRBY J C
出版信息
J Clin Invest. 1963 Jul;42(7):1040-7. doi: 10.1172/JCI104789.
Abstract
摘要
相似文献
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The survival of factor VIII (antihemophilic globulin) and factor IX (plasma thromboplastin component) in normal humans.
J Clin Invest. 1963 Jul;42(7):1040-7. doi: 10.1172/JCI104789.
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Antihaemophilic globulin and plasma thromboplastin component deficiencies associated with a qualitative platelet disturbance.
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Purification of plasma thromboplastin factor B (plasma thromboplastin component) and its identification as a beta2 globulin.
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Tobacco and thrombosis.
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Antihaemophilic globulin: preparation by an improved cryoprecipitation method and clinical use.
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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.
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Studies on the response of patients with classic hemophilia to transfusion with concentrates of antihemophilic factor. A difference in the half-life of antihemophilic factor as measured by procoagulant and immunologic techniques.
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The turnover rate of serum albumin in man as measured by I131-tagged albumin.
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