Hereditary disorders of blood coagulation due to defective and deficient synthesis of protein.
作者信息
Jackson D P
出版信息
Trans Am Clin Climatol Assoc. 1971;82:114-23.
Abstract
摘要
相似文献
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Hereditary disorders of blood coagulation due to defective and deficient synthesis of protein.由于蛋白质合成缺陷和不足导致的遗传性血液凝固障碍。
Trans Am Clin Climatol Assoc. 1971;82:114-23.
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本文引用的文献
1
[ON THE IMMUNOLOGICAL DETERMINATION OF FACTOR 8-PROTEIN IN THE BLOOD PLASMA AND ITS SIGNIFICANCE FOR THE UNDERSTANDING OF HEMOPHILIA A].
Thromb Diath Haemorrh. 1964 Jul 31;11:423-43.
2
[ANTI-FACTOR VIII CIRCULATING ANTICOAGULANTS DURING HEMOPHILIA A. (NATURE AND MECHANISM OF ACTION)].[血友病A患者体内的抗凝血因子VIII循环抗凝物质。（性质及作用机制）]
Nouv Rev Fr Hematol. 1963 Nov-Dec;3:703-22.
3
[CONGENITAL AFIBRINOGENEMIA].
Helv Paediatr Acta. 1963 Sep;18:208-29.
4
[Congenital hypofibrinogenemia with fibrinoasthenia].[先天性低纤维蛋白原血症伴纤维蛋白无力症]
Helv Paediatr Acta. 1958 Oct;13(4):380-99.
5
Investigation of a haemorrhagic disease due to beta-prothromboplastin deficiency complicated by a specific inhibitor of thromboplastin formation.β-凝血活酶原缺乏所致出血性疾病并伴有凝血活酶形成特异性抑制剂的研究
Australas Ann Med. 1956 Aug;5(3):163-76. doi: 10.1111/imj.1956.5.3.163.
6
Congenital afibrinogenemia.
Pediatrics. 1954 Jan;13(1):44-58.
7
Genetic variants of hemophilia B: detection by means of a specific PTC inhibitor.B型血友病的基因变异：通过一种特定的PTC抑制剂进行检测。
J Clin Invest. 1968 Feb;47(2):360-5. doi: 10.1172/JCI105732.
8
[Hemorrhagic diathesis with dominant heredity, caused by an abnormal fibrinogen (fibrinogen Baltimore)].[由异常纤维蛋白原（巴尔的摩纤维蛋白原）引起的显性遗传出血素质]
Schweiz Med Wochenschr. 1966 Sep 17;96(37):1196-9.
9
Familial disturbance of fibrin monomer aggregation.
Br J Haematol. 1966 Nov;12(6):667-77. doi: 10.1111/j.1365-2141.1966.tb00152.x.
10
Congenital disorders of fibrinogen.
Fed Proc. 1965 Jul-Aug;24(4):816-21.
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