Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a <i>Ryanodine Receptor Type 2</i> Missense Mutation-Reference-Cited by-同舟云学术

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Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation

Published:2020-01-24 Issue:2 Volume:84 Page:226-234
ISSN:1346-9843
Container-title:Circulation Journal
language:en
Short-container-title:Circ J

Author:

Nozaki Yoshihiro¹,Kato Yoshiaki¹,Uike Kiyoshi²,Yamamura Kenichiro²,Kikuchi Masahiro³,Yasuda Maki³,Ohno Seiko⁴,Horie Minoru⁴,Murayama Takashi⁵,Kurebayashi Nagomi⁵,Horigome Hitoshi¹

Affiliation:

1. Department of Child Health, Faculty of Medicine, University of Tsukuba

2. Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University

3. Department of Pediatrics, Hitachi General Hospital

4. Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science

5. Department of Cellular and Molecular Pharmacology, Juntendo University Graduate School of Medicine

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/circj/84/2/84_CJ-19-0720/_pdf

Reference39 articles.

1. 1. Jenni R, Oechslin E, Schneider J, Attenhofer Jost C, Kaufmann PA. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: A step towards classification as a distinct cardiomyopathy. Heart 2001; 86: 666–671.

2. 2. Brescia ST, Rossano JW, Pignatelli R, Jefferies JL, Price JF, Decker JA, et al. Mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center. Circulation 2013; 127: 2202–2208.

3. 3. Finsterer J. Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction. Pediatr Cardiol 2009; 30: 659–681.

4. 4. Miller EM, Hinton RB, Czosek R, Lorts A, Parrott A, Shikany AR, et al. Genetic testing in pediatric left ventricular noncompaction. Circ Cardiovasc Genet 2017; 10: e001735.

5. 5. Priori SG, Napolitano C, Memmi M, Colombi B, Drago F, Gasparini M, et al. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. Circulation 2002; 106: 69–74.

Cited by 24 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. An inherited life-threatening arrhythmia model established by screening randomly mutagenized mice;Proceedings of the National Academy of Sciences;2024-04-15

2. RYR2 receptor gene mutation associated with catecholaminergic polymorphic ventricular tachycardia in children: a case report & literature review;Translational Pediatrics;2024-02

3. Ventricular Non-compaction in Children;Pediatric Cardiology;2024

4. Clinical and genetic characteristics of catecholaminergic polymorphic ventricular tachycardia combined with left ventricular non-compaction;Cardiology in the Young;2023-11-29

5. Screening for Novel Type 2 Ryanodine Receptor Inhibitors by Endoplasmic Reticulum Ca²⁺Monitoring;Molecular Pharmacology;2023-09-07

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