Patients diagnosed with long QT syndrome after repair of congenital heart disease-Reference-Cited by-同舟云学术

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Patients diagnosed with long QT syndrome after repair of congenital heart disease

Published:2018-10-09 Issue:11 Volume:41 Page:1435-1440
ISSN:0147-8389
Container-title:Pacing and Clinical Electrophysiology
language:en
Short-container-title:Pacing Clin Electrophysiol

Author:

Song Mi Kyoung¹^ORCID,Bae Eun Jung¹,Kim Gi Beom¹,An Hyo Soon²,Ahn Kyung Jin³,Seong Moon-Woo⁴,Park Sung Sup⁴

Affiliation:

1. Department of Pediatrics; Seoul National University Children's Hospital; Seoul Republic of Korea

2. Department of Pediatrics; SMG-SNU Boramae Medical Center; Seoul South Korea

3. Department of Pediatrics; Gachon University Gil Medical Center; Incheon South Korea

4. Department of Laboratory Medicine, Seoul National University Hospital; Seoul National University College of Medicine; Seoul South Korea

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pace.13512/fullpdf

Reference18 articles.

1. Sudden cardiac death in adult congenital heart disease;Koyak;Circulation,2012

2. Arrhythmogenic substrate in young patients with repaired tetralogy of Fallot: Role of an abnormal ventricular repolarization;Sarubbi;Int J Cardiol,1999

3. Depolarization-repolarization inhomogeneity after repair of tetralogy of Fallot. The substrate for malignant ventricular tachycardia;Gatzoulis;Circulation,1997

4. Clinical features of long QT syndrome in children;Sumitomo;Circ J,2016

5. Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired tetralogy of Fallot are associated with the risks of life-threatening events;Chiu;Hum Genet,2012

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Calmodulin mutation in long QT syndrome 15 associated with congenital heart defects further complicated by a functional 2:1 atrioventricular block: Management from foetal life to postpartum;Indian Pacing and Electrophysiology Journal;2024-05

2. Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication;Frontiers in Genetics;2022-07-05

3. Effect of dexmedetomidine on perioperative hemodynamics and organ protection in children with congenital heart disease;Medicine;2021-01-08

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