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Variable manifestations of plasma thromboplastin component deficiency.

作者信息

RAMOT B, ANGELOPOULOS B, SINGER K

出版信息

J Lab Clin Med. 1955 Jul;46(1):80-8.

PMID:14392402
Abstract
摘要

相似文献

1
Variable manifestations of plasma thromboplastin component deficiency.血浆凝血活酶成分缺乏的多种表现
J Lab Clin Med. 1955 Jul;46(1):80-8.
2
[Case of sporadic hemophilia caused by deficiency of plasma thromboplastin antecedent and plasma thromboplastin component].[由血浆凝血活酶前体和血浆凝血活酶成分缺乏引起的散发性血友病病例]
G Clin Med. 1956 Nov;37(11):1557-80.
3
[Case of hemophilia caused by deficiency of plasma thromboplastin component, or hemophilia B].[血浆凝血活酶成分缺乏所致血友病病例，即血友病B]
Prog Med (Napoli). 1954 Aug 15;10(15):454-62.
4
[Studies on hemorrhagic disease due to plasma thromboplastin component deficiency].[血浆凝血活酶成分缺乏所致出血性疾病的研究]
Pediatria (Napoli). 1953 Nov-Dec;61(11-12):889-900.
5
[Semi-diagnostic value of lyophilized plasma fractions (containing antihemophilic globulin and plasma thromboplastin component) and serum fractions (containing plasma thromboplastin component) in hemorrhagic syndromes of the hemophilic type].
Quad Clin Ostet Ginecol. 1954;9:87-92.
6
[Deficiency of plasma component of thromboplastin; hemorrhagic diseases recently differentiated].[凝血活酶血浆成分缺乏；近期鉴别出的出血性疾病]
Rev Med Chil. 1953 Dec;81(12):737-45.
7
[Studies on a new hemorrhagic diseases similar to hemophilia; plasma thromboplastin component deficiency].[关于一种类似血友病的新型出血性疾病的研究；血浆凝血活酶成分缺乏症]
Pediatria (Napoli). 1953 May-Jun;61(5-6):336-50.
8
[Preparation from normal plasma of a partially purified plasma thromboplastin component and activity of the latter in vitro in some hemorrhagic diseases].[从正常血浆制备部分纯化的血浆凝血致活酶成分及其在某些出血性疾病中的体外活性]
Quad Clin Ostet Ginecol. 1954;9:17-34.
9
[Case of severe hemorrhagic disease due to combined antihemophilic globulin deficiency and plasma thromboplastin deficiency].[联合抗血友病球蛋白缺乏症和血浆凝血活酶原缺乏症所致严重出血性疾病病例]
Prog Med (Napoli). 1954 Jul 31;10(14):425-40.
10
[Laboratory tests in differential diagnosis of hemorrhagic syndromes due to the deficiency of thromboplastin factors].[凝血活酶因子缺乏所致出血综合征鉴别诊断中的实验室检查]
Pediatria (Napoli). 1954;62(5-6):313-37.

引用本文的文献

1
The Inheritance of "Vascular Hemophilia": A New and Interesting Problem in Human Genetics.“血管性血友病”的遗传：人类遗传学中一个新的有趣问题。
Am J Hum Genet. 1959 Jun;11(2 Pt 2):385-96.
2
Sex chromatin and gene action in the mammalian X-chromosome.哺乳动物X染色体中的性染色质与基因作用
Am J Hum Genet. 1962 Jun;14(2):135-48.
3
Demonstrable deficiency of Christmas factor in two sisters.两名姐妹中可证实的克里斯马斯因子缺乏。
Br Med J. 1960 Feb 13;1(5171):479-82. doi: 10.1136/bmj.1.5171.479.
4
The laboratory detection of heterozygotes.杂合子的实验室检测。
Am J Hum Genet. 1957 Jun;9(2):98-116.
5
Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state.斯图尔特凝血缺陷。二、一种新的出血状态的遗传学方面。
J Clin Invest. 1957 Mar;36(3):497-503. doi: 10.1172/JCI103447.
6
A laboratory study of the carrier state in classic hemophilia.经典血友病携带者状态的实验室研究。
J Clin Invest. 1956 Nov;35(11):1316-23. doi: 10.1172/JCI103387.
7
Biochemical genetics of blood coagulation.血液凝固的生化遗传学
Am J Hum Genet. 1956 Jun;8(2):63-79.
8
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.