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An immunological investigation of factor VIII associated antigen in combined factor V and factor VIII deficiency.

作者信息

Girolami A, Borsato N, Patrassi G, Sticchi A

出版信息

Blut. 1976 Aug;33(2):97-102. doi: 10.1007/BF00999872.

DOI:10.1007/BF00999872
PMID:822903
Abstract

The behavior of factor VIII associated antigen of three patients with combined factor V and factor VIII deficiency has been evaluated in several immunological systems. Factor VIII associated antigen resulted to be normal or higher than normal in all three patients in the radial immunodiffusion and in the electroimmunoassay systems. In the bidimensional electrophoresis system only one factor VIII precipitate was evident and such factor VIII precipitate showed the same electrophoretic mobility as normal factor VIII antigen. These findings firmly establish the fact that the factor VIII defect in congenital combined factor V and factor VIII deficiency is of the hemophilia type.

摘要

相似文献

1
An immunological investigation of factor VIII associated antigen in combined factor V and factor VIII deficiency.
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引用本文的文献

1
Hemophilia B with associated factor VII deficiency: a distinct variant of hemophilia B with low factor VII activity and normal factor VII antigen.伴有因子VII缺乏的B型血友病:一种具有低因子VII活性和正常因子VII抗原的B型血友病独特变体。
Blut. 1980 Apr;40(4):267-73. doi: 10.1007/BF01080186.

本文引用的文献

1
[Description of a technic simultaneously combining electrophoresis and immunological precipitation in gel: electrosyneresis].[一种在凝胶中同时结合电泳和免疫沉淀的技术描述:电凝缩]
Biochim Biophys Acta. 1959 Jul;34:258-60. doi: 10.1016/0006-3002(59)90261-6.
2
[A micro-method of immuno-electrophoresis].[免疫电泳的微量方法]
Int Arch Allergy Appl Immunol. 1955;7(2):103-10.
3
Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies.在含有抗体的琼脂糖凝胶中通过电泳对蛋白质进行定量估计。
Anal Biochem. 1966 Apr;15(1):45-52. doi: 10.1016/0003-2697(66)90246-6.
4
Quantitative immunoelectrophoresis of human serum proteins.人血清蛋白的定量免疫电泳
Clin Sci. 1968 Oct;35(2):403-13.
5
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.经典血友病(因子Ⅷ缺乏症)和血管性血友病的免疫学分型,以及关于抗血友病因子和加速素(因子Ⅴ)联合缺乏症和一种获得性抗血友病因子循环抗凝剂的观察
J Clin Invest. 1971 Jan;50(1):244-54. doi: 10.1172/JCI106480.
6
The genetic heterogeneity of hemophilia B.乙型血友病的遗传异质性。
N Engl J Med. 1970 Jul 9;283(2):61-4. doi: 10.1056/NEJM197007092830203.
7
Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin.先天性凝血酶原血症:一种人类凝血酶原的遗传性结构紊乱。
J Clin Invest. 1969 Dec;48(12):2251-9. doi: 10.1172/JCI106191.
8
Congenital abnormality of the prothrombin molecule (factor II) in four siblings: prothrombin Barcelona.四名兄弟姐妹中凝血酶原分子(因子II)的先天性异常:凝血酶原巴塞罗那型
Blood. 1971 Jul;38(1):9-16.
9
A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
Br J Haematol. 1970 Aug;19(2):179-92. doi: 10.1111/j.1365-2141.1970.tb01615.x.
10
An investigation of three patients with Christmas disease due to an abnormal type of factor IX.对三名因异常类型的凝血因子IX导致患克里斯马斯病的患者进行的调查。
J Clin Pathol. 1968 Mar;21(2):160-5. doi: 10.1136/jcp.21.2.160.