凝血因子 VIII 免疫测定：使用全血对几种方法的评估 - Suppr

Suppr

超能文献

Factor VIII immunological assay. An evaluation of several methods using whole plasma.

作者信息

Girolami A, Sticchi A, Barbui T, Bareggi G

出版信息

Blut. 1974 Nov;29(5):309-16. doi: 10.1007/BF01634015.

DOI:10.1007/BF01634015

PMID:4214574

Abstract

摘要

相似文献

Factor VIII immunological assay. An evaluation of several methods using whole plasma.

Blut. 1974 Nov;29(5):309-16. doi: 10.1007/BF01634015.

[Diagnosis of von Willebrand's disease by means of the quantitative immunological assay of factor VIII-related antigen (author's transl)].

Dtsch Med Wochenschr. 1974 Aug 2;99(31):1593-5. doi: 10.1055/s-0028-1107991.

Immunological studies of factor VIII in haemophilia and von Willebrand's disease.

Nat New Biol. 1973 Aug 29;244(139):281-2. doi: 10.1038/newbio244281a0.

[Development of a competitive enzyme immunoassay for factor VIII-related antigen].

Folia Haematol Int Mag Klin Morphol Blutforsch. 1984;111(1):72-83.

Immunological characterization of purified anti-haemophilic factor A (factor VIII) which corrects abnormal platelet retention in Von Willebrand's disease.

Nat New Biol. 1972 Mar 29;236(65):104-6. doi: 10.1038/newbio236104a0.

The cold-insoluble globulin of plasma and its relationship to factor VIII.

J Lab Clin Med. 1974 Aug;84(2):258-63.

Unsuitability of laser nephelometer in the evaluation of factor VIII antigen.

Folia Haematol Int Mag Klin Morphol Blutforsch. 1989;116(2):269-75.

Factor VIII competitive enzyme assay: observations in von Willebrand's variants and hemophiliacs.

Clin Physiol Biochem. 1984;2(6):298-303.

Haemophilia A and von Willebrand's disease in a Swedish family.

Acta Paediatr Scand. 1972 Sep;61(5):517-25. doi: 10.1111/j.1651-2227.1972.tb15938.x.

Anti-haemophilic factor, normal and abnormal.

Br J Haematol. 1974 Jan;26(1):1-7. doi: 10.1111/j.1365-2141.1974.tb00444.x.

引用本文的文献

Relationship between ristocetin-induced platelet aggregation and factor VIII (activity and antigen) in v. Willebrand's disease.

Blut. 1974 Oct;29(4):260-4. doi: 10.1007/BF01635547.

Increased factor VIII/vWf levels in patients with reduced platelet number.

Blut. 1987 May;54(5):281-8. doi: 10.1007/BF00320876.

Combined deficiency of factor V and factor VIII. A report of another case.

Blut. 1976 Jun;32(6):415-22. doi: 10.1007/BF01013881.

Platelet adhesiveness and aggregation in congenital afibrinogenemia. An investigation of three patients with post-transfusion, cross-correction studies between two of them.

Blut. 1975 Feb;30(2):87-100. doi: 10.1007/BF01633963.

The effect of heparin on platelet aggregation by common inductors and by ristocetin in congenital bleeding disorders due to factor VIII or fibrinogen defects.

Blut. 1975 Oct;31(4):219-26. doi: 10.1007/BF01633505.

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

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

Factor X Friuli: An immunological study in plasma and in serum using several methods.

Blut. 1975 Mar;30(3):203-12. doi: 10.1007/BF01633955.

[Current aspects on evaluation of assays of factor-VIII activity, factor-VIII associated protein and factor-VIII neutralizing antibody (author's transl)].

Blut. 1978 Feb;36(2):95-107. doi: 10.1007/BF00996836.

本文引用的文献

[Description of a technic simultaneously combining electrophoresis and immunological precipitation in gel: electrosyneresis].

Biochim Biophys Acta. 1959 Jul;34:258-60. doi: 10.1016/0006-3002(59)90261-6.

[A micro-method of immuno-electrophoresis].

Int Arch Allergy Appl Immunol. 1955;7(2):103-10.

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies.

Anal Biochem. 1966 Apr;15(1):45-52. doi: 10.1016/0003-2697(66)90246-6.

Quantitative immunoelectrophoresis of human serum proteins.

Clin Sci. 1968 Oct;35(2):403-13.

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. doi: 10.1172/JCI106480.

The genetic heterogeneity of hemophilia B.

N Engl J Med. 1970 Jul 9;283(2):61-4. doi: 10.1056/NEJM197007092830203.

Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin.

J Clin Invest. 1969 Dec;48(12):2251-9. doi: 10.1172/JCI106191.

Congenital abnormality of the prothrombin molecule (factor II) in four siblings: prothrombin Barcelona.

Blood. 1971 Jul;38(1):9-16.

Prothrombin level and activity in the abnormal factor X (factor X Friuli) hemorrhagic disorder.

Thromb Diath Haemorrh. 1971;25(1):147-56.

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.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验