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Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|January 21, 2022
School-based routine screenings of electrocardiograms for the diagnosis of long QT syndromeMegumi Fukuyama, Minoru Horie, Hisaaki Aoki, et al.
Pediatric Cardiology|May 9, 2019
Post-Extubation Inhaled Nitric Oxide Therapy via High-Flow Nasal Cannula After Fontan ProcedureYuji Tominaga, Shigemitsu Iwai, Sanae Yamauchi, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 28, 2023
Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and InfancyMegumi Fukuyama, Minoru Horie, Koichi Kato, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada SyndromeKeisuke Suzuki, Keiko Sonoda, Hisaaki Aoki, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|August 18, 2022
Control of Heart Rate in Infant and Child Tachyarrhythmia With Reduced Cardiac Function Using Landiolol (HEARTFUL) - Results of a Prospective, Multicenter, Uncontrolled Clinical StudyKoichi Sagawa, Tsugutoshi Suzuki, Kohta Takei, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 18, 2021
Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndromeSayako Hirose, Takashi Murayama, Naoyuki Tetsuo, et al.
Heart Rhythm|October 21, 2016
A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsades de pointes ventricular arrhythmiaYusuke Fujii, Hideki Itoh, Seiko Ohno, et al.
International Journal of Cardiology. Congenital Heart Disease|May 27, 2026
Registry-based estimation of cardiac event-free survival in congenital heart disease complicated by pulmonary hypertension: A nationwide registry study from JapanTaku Ishii, Tatsuhiko Anzai, Keiko Uchida, et al.
Circulation. Arrhythmia and Electrophysiology|March 3, 2023
Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived CardiomyocytesJingshan Gao, Takeru Makiyama, Yuta Yamamoto, et al.
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