Clinical Characteristics and Genetic Background of Congenital Long-QT Syndrome Diagnosed in Fetal, Neonatal, and Infantile Life-Reference-Cited by-同舟云学术

Clinical Characteristics and Genetic Background of Congenital Long-QT Syndrome Diagnosed in Fetal, Neonatal, and Infantile Life

Published:2010-02 Issue:1 Volume:3 Page:10-17
ISSN:1941-3149
Container-title:Circulation: Arrhythmia and Electrophysiology
language:en
Short-container-title:Circ Arrhythm Electrophysiol

Author:

Horigome Hitoshi¹,Nagashima Masami¹,Sumitomo Naokata¹,Yoshinaga Masao¹,Ushinohama Hiroya¹,Iwamoto Mari¹,Shiono Junko¹,Ichihashi Koh¹,Hasegawa Satoshi¹,Yoshikawa Tadahiro¹,Matsunaga Tamotsu¹,Goto Hiroko¹,Waki Kenji¹,Arima Masaki¹,Takasugi Hisashi¹,Tanaka Yasuhiko¹,Tauchi Nobuo¹,Ikoma Masanobu¹,Inamura Noboru¹,Takahashi Hideto¹,Shimizu Wataru¹,Horie Minoru¹

Affiliation:

1. From the Department of Child Health (H.H.), Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan; the Department of Cardiology (M.N.), Aichi Children’s Health and Medical Center, Ohbu, Japan; the Department of Pediatrics and Child Health (N.S.), Nihon University School of Medicine, Tokyo, Japan; the Department of Pediatrics (M.Y.), National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan; the Department of Cardiology (H.U.), Fukuoka Children’s...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference27 articles.

1. Long QT syndrome: from channels to cardiac arrhythmias

2. Association of Long QT Syndrome Loci and Cardiac Events Among Patients Treated With β-Blockers

3. Prenatal findings in patients with prolonged QT interval in the neonatal period.

4. The Long QT Syndrome with Impaired Atrioventricular Conduction: A Malignant Variant in Infants

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