Blood coagulation factor VIII (antihemophilic factor): with comments on von Willebrand's disease and Christmas disease.

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作者信息

Barrow E M, Graham J B

出版信息

Physiol Rev. 1974 Jan;54(1):23-74. doi: 10.1152/physrev.1974.54.1.23.

DOI:10.1152/physrev.1974.54.1.23

PMID:4594032

Abstract

摘要

相似文献

Blood coagulation factor VIII (antihemophilic factor): with comments on von Willebrand's disease and Christmas disease.

Physiol Rev. 1974 Jan;54(1):23-74. doi: 10.1152/physrev.1974.54.1.23.

[Factor VIII in hemophilia and von Willebrand's disease].[血友病和血管性血友病中的凝血因子VIII]

Rev Med Liege. 1978 Apr 15;33(8):284-95.

Von Willebrand's disease, hemophilia A, and factor VIII.血管性血友病、甲型血友病和凝血因子VIII。

Hum Pathol. 1974 May;5(3):277-89. doi: 10.1016/s0046-8177(74)80112-7.

Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。

J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.

Properties of post-infusion factor VIII in von Willebrand's disease.

Thromb Res. 1974 Aug;5(2):111-23. doi: 10.1016/0049-3848(74)90062-0.

The spectrum of von Willebrand's disease.血管性血友病的谱系

Southeast Asian J Trop Med Public Health. 1979 Jun;10(2):229-33.

Stabilization of factor VIII in plasma by the von Willebrand factor. Studies on posttransfusion and dissociated factor VIII and in patients with von Willebrand's disease.血管性血友病因子对血浆中凝血因子VIII的稳定作用。关于输血后及解离的凝血因子VIII的研究以及血管性血友病患者的研究。

J Clin Invest. 1977 Aug;60(2):390-404. doi: 10.1172/JCI108788.

The effects of epinephrine infusion in patients with von Willebrand's disease.肾上腺素输注对血管性血友病患者的影响。

J Clin Invest. 1976 Jun;57(6):1618-25. doi: 10.1172/JCI108432.

Detection of heterozygotes for recessive von Willebrand's disease by the assay of antihemophilic-factor-like antigen.通过抗血友病因子样抗原检测法对隐性血管性血友病杂合子的检测。

N Engl J Med. 1973 Oct 25;289(17):882-5. doi: 10.1056/NEJM197310252891703.

[Congenital coagulation disorders in children (II) (Willebrand's disease, Christmas disease, factor IX, XI, XII, I, II, VII and V deficiencies)].儿童先天性凝血障碍（II）（血管性血友病、克里斯马斯病、因子IX、XI、XII、I、II、VII和V缺乏症）

Rev Pediatr Obstet Ginecol Pediatr. 1987 Apr-Jun;36(2):123-36.

引用本文的文献

Genetic causes of haemophilia in women and girls.女性和女童血友病的遗传学病因。

Haemophilia. 2021 Mar;27(2):e164-e179. doi: 10.1111/hae.14186. Epub 2020 Dec 13.

Hemophilia A or von Willebrand disease?甲型血友病还是血管性血友病？

Ann Hematol. 1994 Dec;69(6):317-9. doi: 10.1007/BF01696562.

Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.关于撒丁岛甲型血友病的研究，涉及复等位基因、携带者检测以及两性间差异突变率等问题。

Am J Hum Genet. 1984 Jan;36(1):44-71.

The defect in hemophilic and von Willebrand's disease plasmas studied by a recombination technique.通过重组技术研究血友病和血管性血友病血浆中的缺陷。

J Clin Invest. 1974 Nov;54(5):1093-9. doi: 10.1172/JCI107853.

Medical staff conference: recent chapters in the factor VIII saga--perils of a protein. Fifth annual Paul M. Aggeler Memorial Lecture.医务人员会议：第八因子传奇的新篇章——一种蛋白质的风险。第五届年度保罗·M·阿格勒纪念讲座。

West J Med. 1975 May;122(5):406-16.

The phenotypic range of hemophilia A carriers.甲型血友病携带者的表型范围。

Am J Hum Genet. 1976 Sep;28(5):482-8.

Effect of phospholipases on factor-VIII activity.

Hum Genet. 1978 Jan 19;40(2):185-91. doi: 10.1007/BF00272299.

Factor VIII coagulant activity and factor VIII-related antigen released from isolated perfused human spleens.

Blut. 1977 Jan;34(1):27-30. doi: 10.1007/BF00997035.

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