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- Long QT syndrome (LQTS) is usually a lifelong condition. 通常而言，LQTS是一种伴随终生的疾病。
- Congenital long QT syndrome is a group of familial inherited disease. 先天性Q-T间期延长综合征是一组家族遗传性疾病。
- A novel SCN5A gene mutation (del D1790) associated with congenital long QT syndrome. 遗传性长QT综合征SCN5A基因delD1790新突变
- Andersen-Tawil syndrome. also called Andersen syndrome and Long QT syndrome 7 is a form of long QT syndrome. 什么是'安徒生-泰维勒综合征-先天性长QT综合征'?
- Abstract:Two novel mutations that have been described in human MINKgene are corresponding for Long QT Syndrome (LQTS). 摘要人类MINK基因的两种突变导致长QT综合征（LQTS）。
- QT dispersions in the pediatric patients with idiopathic long QT Syndrome are increased significantly, and no decreased after beta-blockade treatment. 长QT间期综合征患儿心电图QT离散度明显延长。
- Objective: To analyse EKG QT dispersion in pediatric patients with idiopathic long QT Syndrome and its change after treatment. 目的分析特发性长QT间期综合征患儿心电图QT间期离散度及其治疗后的改变。
- The protein that HERG gene encodes is very important in cardiac repolarization, and HERG gene mutation will lead to inherited long QT syndrome. HERG基因编码的蛋白在心室复极过程中很重要,HERG基因突变导致遗传性长QT综合征。
- As molecular genetic research proceeds, the molecular mechanism whereby HERG gene mutation causes long QT syndrome is being gradually revealed. 随着分子遗传学的进展,HERG基因突变如何导致长QT综合征的分子机制正逐步被揭示。
- Individualized therapy according to the clinical situation and ECG patterns should be provided to the patients with long QT syndrome. 结论：针对长QT综合征病人的临床特征采取相应的治疗，疗效尚可。
- Objective To assess the feasibility, safety and effectiveness of video-assisted thoracoscopic sympathectomy (VATS) for the treatment of congenital long QT syndrome. 目的探讨经电视胸腔镜切除左胸交感神经治疗先天性QT间期延长综合征的方法和效果。
- Rubart M,Pressler ML,Pride HP,et al.Electrophysiological mechanism in a canine model of eryhromycin-associated long QT syndrome[J].Circulation,1993,88(part 4):1832. 邓万俊.;红霉素与双异丙吡胺之间可能致命的相互作用[J]
- To study the clinical manifestations and therapy of Chinese long QT syndrome (LQTS) patients. According to the criteria by Schwartz 1993, 76 patients who came from 18 provinces were diagnosed as LQTS. 为研究我国长QT综合征 (LQTS)患者的整体发病和治疗情况 ,选择按照 1993年Schwartz等提出的LQTS诊断标准确诊为本病的家系 76个。
- New Findings on Long QT Syndrome 长QT综合征的研究进展
- Current outcome of treating long QT syndrome 长QT综合征治疗进展
- Keywords Long QT syndrome;Genes;Mutation; QT延长综合征;基因;突变;
- Keywords long QT syndrome syncope gene mutation; 长QT综合征;晕厥;基因;突变;
- Keywords Syncopy;Gene;Mutations;Long QT syndrome; 晕厥;基因;突变;长QT综合征;
- Keywords Long QT syndrome;HERG mutation;Ikr; QT延长综合征;HERG基因突变;钾通道;
- Keywords long QT syndrome;KCNQ1 gene;eukaryotic expression vector; 长QT综合征;KCNQ1基因;真核表达载体;
