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- 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 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;
- Keywords Long QT syndrome;KCNE1 gene;Clone;Eukaryotic expression vector; 长QT综合征;KCNE1基因;克隆;真核表达载体;
- Keywords Long QT syndrome;Pinacidil;Early afterdepolarization;Torsade de pointes;Rabbit; 长QT综合征;钾通道开放剂;吡那地尔;早期后去极化;尖端扭转型室性心动过速;兔;
- Keywords long QT syndrome（LQTS）;HERG;eukaryotic expression vector;gene transfection; 遗传性长QT综合征;HERG;真核表达载体;基因转染;
- Keywords Long QT syndrome;Surface electrocardiogram;Pedigree analysis;Propranolol; 长QT综合征;体表心电图;系谱分析;普萘洛尔;
- Keywords Long QT syndrome;Transmembrane action potentials;Transmural electrocardiogram;Isoproterenol; 长QT综合征;跨壁动作电位;跨壁心电图;异丙肾上腺素;
- 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。
