• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Diagnosis and management of inherited and acquired thrombophilias.

作者信息

Spencer F A, Becker R C

机构信息

Cardiovascular Thrombosis Research Center, University of Massachusetts Medical School, Worcester, Massachusetts 01655,USA.

出版信息

J Thromb Thrombolysis. 1999 Apr;7(2):91-104. doi: 10.1023/a:1008817116524.

DOI:10.1023/a:1008817116524
PMID:10364773
Abstract
摘要

相似文献

1
Diagnosis and management of inherited and acquired thrombophilias.遗传性和获得性血栓形成倾向的诊断与管理
J Thromb Thrombolysis. 1999 Apr;7(2):91-104. doi: 10.1023/a:1008817116524.
2
Laboratory Diagnostics in Thrombophilia.血栓形成倾向的实验室诊断。
Hamostaseologie. 2019 Feb;39(1):49-61. doi: 10.1055/s-0039-1677840. Epub 2019 Jan 31.
3
Practice bulletin no. 124: inherited thrombophilias in pregnancy.实践公告第 124 号：妊娠期遗传性血栓形成倾向。
Obstet Gynecol. 2011 Sep;118(3):730-740. doi: 10.1097/AOG.0b013e3182310c6f.
4
Inherited thrombophilia and stillbirth.遗传性血栓形成倾向与死产
Semin Perinatol. 2002 Feb;26(1):51-69. doi: 10.1053/sper.2002.29858.
5
Protein C deficiency as the major cause of thrombophilias in childhood.蛋白C缺乏是儿童期血栓形成倾向的主要原因。
Pediatr Int. 2013 Jun;55(3):267-71. doi: 10.1111/ped.12102.
6
[Hereditary thrombophilia testing and its therapeutic impact on venous thromboembolism disease: Results from a retrospective single-center study of 162 patients].[遗传性血栓形成倾向检测及其对静脉血栓栓塞性疾病的治疗影响：一项对162例患者的回顾性单中心研究结果]
Rev Med Interne. 2016 Oct;37(10):661-666. doi: 10.1016/j.revmed.2016.01.001. Epub 2016 May 27.
7
Hunting for the mutation in inherited thrombophilia.寻找遗传性血栓形成倾向中的突变。
Blood Coagul Fibrinolysis. 2004 Mar;15(2):125-7. doi: 10.1097/00001721-200403000-00002.
8
The investigation and management of neonatal haemostasis and thrombosis.新生儿止血与血栓形成的调查与处理
Br J Haematol. 2002 Nov;119(2):295-309. doi: 10.1046/j.1365-2141.2002.03674.x.
9
Unraveling the thrombophilia paradox: from hypercoagulability to the prothrombotic state.解析血栓形成倾向悖论：从高凝状态到血栓前状态。
J Thromb Haemost. 2010 Feb;8(2):228-33. doi: 10.1111/j.1538-7836.2009.03702.x. Epub 2009 Nov 23.
10
Screening for inherited thrombophilia: indications and therapeutic implications.遗传性血栓形成倾向的筛查：指征及治疗意义
Haematologica. 2002 Oct;87(10):1095-108.

引用本文的文献

1
Association of oral estradiol dose/levels with coagulation measures in early/late postmenopausal women.口服雌二醇剂量/水平与绝经后早期/晚期女性凝血指标的相关性。
Climacteric. 2020 Jun;23(3):273-278. doi: 10.1080/13697137.2019.1703939. Epub 2020 Jan 15.

本文引用的文献

1
INHERITED ANTITHROMBIN DEFICIENCY CAUSING THROMBOPHILIA.遗传性抗凝血酶缺乏导致血栓形成倾向。
Thromb Diath Haemorrh. 1965 Jun 15;13:516-30.
2
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.凝血酶原基因的20210 A等位基因是瑞典确诊为深静脉血栓形成的门诊患者中的常见危险因素。
Thromb Haemost. 1997 Sep;78(3):990-2.
3
Molecular characterization of a type I quantitative factor V deficiency in a thrombosis patient that is "pseudo homozygous" for activated protein C resistance.
一名血栓形成患者中 I 型定量因子 V 缺乏症的分子特征，该患者对活化蛋白 C 抵抗呈“假纯合子”状态。
Thromb Haemost. 1997 Feb;77(2):252-7.
4
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease.5,10-亚甲基四氢叶酸还原酶（MTHFR）基因多态性作为冠状动脉疾病的一个危险因素
Circulation. 1997 Apr 15;95(8):2032-6. doi: 10.1161/01.cir.95.8.2032.
5
Antiphospholipid thrombosis syndromes: etiology, pathophysiology, diagnosis and management.
Int J Hematol. 1997 Apr;65(3):193-213. doi: 10.1016/s0925-5710(96)00550-6.
6
Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women.凝血因子V莱顿突变（对活化蛋白C的抵抗）会增加年轻女性患心肌梗死的风险。
Blood. 1997 Apr 15;89(8):2817-21.
7
Age-specific incidence rates of venous thromboembolism among heterozygous carriers of factor V Leiden mutation.凝血因子V莱顿突变杂合子携带者中静脉血栓栓塞的年龄特异性发病率。
Ann Intern Med. 1997 Apr 1;126(7):528-31. doi: 10.7326/0003-4819-126-7-199704010-00005.
8
Management of deep vein thrombosis and pulmonary embolism. A statement for healthcare professionals. Council on Thrombosis (in consultation with the Council on Cardiovascular Radiology), American Heart Association.
Circulation. 1996 Jun 15;93(12):2212-45. doi: 10.1161/01.cir.93.12.2212.
9
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.凝血酶原基因3'非翻译区的一种常见基因变异与血浆凝血酶原水平升高及静脉血栓形成增加有关。
Blood. 1996 Nov 15;88(10):3698-703.
10
Guidelines for the management of thrombophilia. Department of Haematology, The Royal London Hospital, Whitechapel, London, UK.血栓形成倾向管理指南。英国伦敦白教堂区皇家伦敦医院血液科
Postgrad Med J. 1996 Feb;72(844):87-94. doi: 10.1136/pgmj.72.844.87.