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Bull World Health Organ. 1997;75(3):177-89.
2
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Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population.汉族人群中蛋白S缺乏与静脉血栓栓塞风险
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本文引用的文献

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Thrombotic risk during pregnancy and puerperium in women with APC-resistance--effective subcutaneous heparin prophylaxis in a pregnant patient.
Thromb Haemost. 1995 Aug;74(2):793-4.
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Optimal duration of oral anticoagulant therapy: a randomized trial comparing four weeks with three months of warfarin in patients with proximal deep vein thrombosis.
Thromb Haemost. 1995 Aug;74(2):606-11.
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A review of mutations causing deficiencies of antithrombin, protein C and protein S.
Thromb Haemost. 1995 Jul;74(1):81-9.
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Treatment of coumarin-induced skin necrosis with a monoclonal antibody purified protein C concentrate.用单克隆抗体纯化蛋白C浓缩物治疗香豆素诱导的皮肤坏死。
Arch Dermatol. 1993 Jun;129(6):753-6.
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High levels of histidine-rich glycoprotein and thrombotic diathesis. Report of two unrelated families.高浓度富含组氨酸糖蛋白与血栓形成素质。两个非亲缘家族的报告。
Thromb Res. 1993 Feb 1;69(3):297-305. doi: 10.1016/0049-3848(93)90027-l.
6
Anticoagulant protein C pathway defective in majority of thrombophilic patients.大多数血栓形成倾向患者的抗凝蛋白C途径存在缺陷。
Blood. 1993 Oct 1;82(7):1989-93.
7
Resistance to activated protein C as a basis for venous thrombosis.对活化蛋白C的抵抗作为静脉血栓形成的基础。
N Engl J Med. 1994 Feb 24;330(8):517-22. doi: 10.1056/NEJM199402243300801.
8
Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S.蛋白S德岛:一种异常分子,在蛋白S的第二个表皮生长因子样结构域中,第155位赖氨酸被谷氨酸替代。
Blood. 1994 Feb 1;83(3):683-90.
9
Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.抗凝血酶III突变数据库:首次更新。由国际血栓与止血协会科学与标准化委员会凝血酶及其抑制剂小组委员会发布。
Thromb Haemost. 1993 Aug 2;70(2):361-9.
10
The weight-based heparin dosing nomogram compared with a "standard care" nomogram. A randomized controlled trial.基于体重的肝素剂量计算图与“标准护理”剂量计算图的比较。一项随机对照试验。
Ann Intern Med. 1993 Nov 1;119(9):874-81. doi: 10.7326/0003-4819-119-9-199311010-00002.

遗传性血栓形成倾向:世界卫生组织/国际血栓与止血学会联合会议纪要

Inherited thrombophilia: memorandum from a joint WHO/International Society on Thrombosis and Haemostasis meeting.

出版信息

Bull World Health Organ. 1997;75(3):177-89.

PMID:9277004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2486958/
Abstract

Inherited thrombophilias are common disorders with a worldwide distribution, including antithrombin, protein C, and protein S deficiencies as well as resistance to activated protein C. Increased understanding of these disorders suggests that thrombophilia can arise from interaction between defective genes and environmental factors. WHO and the international Society on Thrombosis and Haemostasis (ISTH) discussed the problems of inherited thrombophilia at a joint meeting held in Geneva on 6-8 November 1995. The present article reports on the various possibilities for controlling the disorder and makes a series of recommendations for diagnosis, treatment, and research into the condition.

摘要

遗传性血栓形成倾向是一种在全球范围内普遍存在的疾病,包括抗凝血酶、蛋白C和蛋白S缺乏症以及对活化蛋白C的抵抗。对这些疾病的进一步了解表明,血栓形成倾向可能源于缺陷基因与环境因素之间的相互作用。世界卫生组织(WHO)和国际血栓与止血学会(ISTH)于1995年11月6日至8日在日内瓦举行的一次联合会议上讨论了遗传性血栓形成倾向的问题。本文报告了控制该疾病的各种可能性,并就该疾病的诊断、治疗和研究提出了一系列建议。