Diagnosis and Management of Inherited Arrhythmias: Long- and Short-QT Syndromes, Catecholaminergic Polymorphic Ventricular Tachycardia, and Brugada Syndrome
Author:
Affiliation:
1. Uonuma Institute of Community Medicine, Niigata University Medical and Dental Hospital
Publisher
The Japanese Society of Pediatric Cardiology and Cardiac Surgery
Subject
Polymers and Plastics,General Environmental Science
Link
https://www.jstage.jst.go.jp/article/jspccs/35/4/35_2019-0006/_pdf
Reference60 articles.
1. 1) Schwartz PJ, Stramba-Badiale M, Crotti L, et al: Prevalence of the congenital long-QT syndrome. Circulation 2009; 120: 1761–1767
2. 2) Yoshinaga M, Ushinohama H, Sato S, et al: Electrocardiographic screening of 1-month-old infants for identifying prolonged QT intervals. Circ Arrhythm Electrophysiol 2013; 6: 932–938
3. 3) Mitani Y, Ohta K, Ichida F, et al: Circumstances and outcomes of Out-of-Hospital cardiac arrest in elementary and middle school students in the era of public-access defibrillation. Circ J 2014; 78: 701–707
4. 4) Fukuyama M, Wang Q, Kato K, et al: Long QT syndrome type 8: Novel CACNA1C mutations causing QT prolongation and variant phenotypes. Europace 2014; 16: 1828–1837
5. 5) Harada M, Suzuki H, Ohno S, et al: Dynamic QT Changes in Long QT Syndrome Type 8. Circ J 2019; 83: 1614 [Epub ahead of print]
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