• 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

Role of factor V Leiden polymorphism or G20210A prothrombin variant in patients with sudden sensorineural hearing loss: a meta-analysis of the literature.

作者信息

Spiezia Luca, Vasques Francesco, Bovo Roberto, Martini Alessandro, Simioni Paolo

机构信息

Department of Medicine (DIMED), University of Padua, Padua, Italy.

Otolaryngology and Otosurgery Unit, Department of Neurosciences, University of Padua, Padua, Italy.

出版信息

Thromb Res. 2015 Mar;135(3):565-7. doi: 10.1016/j.thromres.2014.12.011. Epub 2014 Dec 13.

DOI:10.1016/j.thromres.2014.12.011
PMID:25538030
Abstract
摘要

相似文献

1
Role of factor V Leiden polymorphism or G20210A prothrombin variant in patients with sudden sensorineural hearing loss: a meta-analysis of the literature.因子V莱顿多态性或凝血酶原G20210A变异在突发性感音神经性听力损失患者中的作用：文献荟萃分析
Thromb Res. 2015 Mar;135(3):565-7. doi: 10.1016/j.thromres.2014.12.011. Epub 2014 Dec 13.
2
The role of factor V Leiden and prothrombin G20210A mutations in sudden sensorineural hearing loss.凝血因子V莱顿突变和凝血酶原G20210A突变在突发性感音神经性听力损失中的作用。
Otol Neurotol. 2005 Jul;26(4):599-601. doi: 10.1097/01.mao.0000178120.46290.6c.
3
A preliminary study on the role of inherited prothrombotic risk factors in Taiwanese patients with sudden sensorineural hearing loss.遗传性促血栓形成风险因素在台湾突发性感觉神经性听力损失患者中的作用初步研究。
Eur Arch Otorhinolaryngol. 2011 Jun;268(6):817-22. doi: 10.1007/s00405-010-1457-y. Epub 2010 Dec 19.
4
Role of genetic and acquired prothrombotic risk factors in genesis of sudden sensorineural hearing loss.遗传和后天获得性血栓形成风险因素在突发性感音神经性听力损失发病机制中的作用。
Audiol Neurootol. 2011;16(3):185-90. doi: 10.1159/000319310. Epub 2010 Aug 25.
5
Association between the prothrombin G20210A mutation and sudden sensorineural hearing loss in European population: a meta-analysis.
Thromb Res. 2015 Jan;135(1):73-7. doi: 10.1016/j.thromres.2014.10.032. Epub 2014 Nov 6.
6
[A Meta-analysis of prothrombin G20210A polymorphism and its risk for sudden sensorineural hearing loss].[凝血酶原G20210A多态性及其与突发性感音神经性听力损失风险的Meta分析]
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 May;48(5):417-21.
7
Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy Jordanians.表面健康的约旦人中因子V G1691A（莱顿）和凝血酶原G20210A基因多态性的患病率。
Neuro Endocrinol Lett. 2007 Oct;28(5):699-703.
8
Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.复发性流产人群中因子V G1691A（因子V莱顿）和凝血酶原G20210A基因突变的患病率。
Am J Hematol. 2002 Dec;71(4):300-5. doi: 10.1002/ajh.10223.
9
Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.凝血因子V G1691A、凝血酶原G20210A及亚甲基四氢叶酸还原酶基因多态性C677T与伊朗西部的冠状动脉疾病和2型糖尿病无关。
Blood Coagul Fibrinolysis. 2009 Jun;20(4):252-6. doi: 10.1097/MBC.0b013e3283255487.
10
Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages.复发性特发性流产病史女性不良妊娠结局与母体凝血因子V G1691A（莱顿）和凝血酶原G20210A基因型之间的关联。
Am J Hematol. 2005 Sep;80(1):12-9. doi: 10.1002/ajh.20419.

引用本文的文献

1
Evaluation of Serum Endocan Levels in Sensorineural Hearing Loss.感音神经性听力损失患者血清内脂素水平的评估。
J Int Adv Otol. 2019 Apr;15(1):83-86. doi: 10.5152/iao.2018.5051.