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Congenital familial deficiency of the stable prothrombin conversion factor; restudy of case originally reported as idiopathic hypoprothrombinemia.

作者信息

FRICK P G, HAGEN P S

出版信息

J Lab Clin Med. 1953 Aug;42(2):212-23.

PMID:13069867
Abstract
摘要

相似文献

1
Congenital familial deficiency of the stable prothrombin conversion factor; restudy of case originally reported as idiopathic hypoprothrombinemia.先天性家族性稳定凝血酶原转化因子缺乏症；对最初报告为特发性低凝血酶原血症病例的重新研究。
J Lab Clin Med. 1953 Aug;42(2):212-23.
2
[Contribution to the study of idiopathic hypoprothrombinemia. (Clinical case)].[特发性低凝血酶原血症的研究贡献。（临床病例）]
Haematologica. 1961;46:1062-72.
3
BLOOD COAGULATION. VII. COAGULATION II.血液凝固。VII. 凝固II。
Memphis Mid South Med J. 1963 Jan;38:19-22.
4
Idiopathic hypoprothrombinemia associated with hemorrhagic diathesis, and the effect of vitamin K.
Blood. 1951 Aug;6(8):740-55.
5
[Hemorrhagic diathesis and hypoprothrombinemia].[出血素质与低凝血酶原血症]
Med Glas. 1950 Jun;4(6):135-7.
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Deficiency of prothrombin and proconvertin after therapy with propylthiouracil.丙硫氧嘧啶治疗后凝血酶原和凝血酶原转变加速因子缺乏
J Am Med Assoc. 1959 Dec 26;171:2315-8. doi: 10.1001/jama.1959.73010350009007c.
7
[Idiopathic hemorrhagic disease due to factor VII and prothrombin deficiency].[因凝血因子VII和凝血酶原缺乏所致的特发性出血性疾病]
Klin Wochenschr. 1954 Dec 1;32(45-46):1078-82. doi: 10.1007/BF01467105.
8
Congenital idiopathic hypoprothrombinemia.先天性特发性低凝血酶原血症
Acta Paediatr Suppl (Upps). 1954;43(100):245-55. doi: 10.1111/j.1651-2227.1954.tb15475.x.
9
Hypoprothrombinemia and hypoproconvertinemia during pregnancy.妊娠期低凝血酶原血症和低凝血因子转化素血症。
J Lab Clin Med. 1955 Feb;45(2):308-12.
10
[Use of lyophilized blood plasma fractions for the in vitro correction of the deficit of thromboplastin generation; observations induced from an observed hemorrhagic syndrome due to combined deficit of PTC, factor VII and prothrombin].[使用冻干血浆组分进行体外纠正凝血活酶生成不足；对因凝血活酶原复合物（PTC）、因子 VII 和凝血酶原联合缺乏导致的出血综合征的观察]
Pediatria (Napoli). 1956 May-Jun;64(3):365-73.

引用本文的文献

1
Familial haemophilia and factor VII deficiency.家族性血友病和凝血因子VII缺乏症。
J Clin Pathol. 1958 Sep;11(5):412-6. doi: 10.1136/jcp.11.5.412.
2
[Congenital familial hypoproconverteinemia].[先天性家族性低前转化素血症]
Blut. 1957 May;3(3):135-47. doi: 10.1007/BF01630688.
3
The laboratory detection of heterozygotes.杂合子的实验室检测。
Am J Hum Genet. 1957 Jun;9(2):98-116.
4
Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency.斯图尔特凝血缺陷。I. 从迄今为止称为稳定因子（血清凝血酶原转变加速素、前转变素、因子VII）缺乏的异质性组中分离出一种遗传性出血状态。
J Clin Invest. 1957 Mar;36(3):485-96. doi: 10.1172/JCI103446.
5
Congenital factor VII deficiency; a review with a report of a case in an Indian infant.先天性因子VII缺乏症；附一例印度婴儿病例报告的综述
Arch Dis Child. 1956 Aug;31(158):293-7. doi: 10.1136/adc.31.158.293.
6
Genetics of human blood coagulation.人类血液凝固的遗传学
J Med Genet. 1965 Dec;2(4):254-303. doi: 10.1136/jmg.2.4.254.