Inherited Arrhythmic Disorders in Japan
Author:
Affiliation:
1. Department of Cardiovascular Diseases, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan
Publisher
Wiley
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1540-8167.2003.02435.x
Reference25 articles.
1. Hereditary QT Prolongation Syndrome in Japan : Genetic Analysis and Pathological Findings of the Conducting System : II. Heart Diseases Mostly Ascertained at Later Stage : SYMPOSIUM ON GENE-ENVIRONMENT INTERACTION IN CARDIOVASCULAR DISEASES
2. The QT prolongation syndrome: Long‐term follow‐up study of 13 families with Romano‐Ward syndrome;Hashiba K;Heart Vessels,1987
3. Effect of age and overweight on the QT interval and the prevalence of long QT syndrome in children
4. Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome
5. Four Novel KVLQT1 and Four Novel HERG Mutations in Familial Long-QT Syndrome
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2. Genetic analysis of cardiac SCN5A Gene in Iranian patients with hereditary cardiac arrhythmias;The Anatolian Journal of Cardiology;2015-08-21
3. Clinical impact of the number of extrastimuli in programmed electrical stimulation in patients with Brugada type 1 electrocardiogram;Heart Rhythm;2012-02
4. Genotyping Has a Minor Role in Selecting Therapy for Congenital Long-QT Syndromes at Present;Circulation: Arrhythmia and Electrophysiology;2008-08
5. Phenotypic Variability in Caucasian and Japanese Patients with Matched LQT1 Mutations;Annals of Noninvasive Electrocardiology;2008-07
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