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Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Circulation Journal, 2020/10/23, Vol.84(11), pp.2123

2020

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Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Circulation Journal, 2013, Vol.77(6), pp.1534-1542

2013

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Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

Circulation Journal, 2013, Vol.77(7), pp.1705-1713

2013

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Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

Circulation Journal, 2020/10/23, Vol.84(11), pp.2124-2126

2020

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Association of Atrial Arrhythmia and Sinus Node Dysfunction in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation Journal, 2007, Vol.71(10), pp.1606-1609

2007

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Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2009-10, Vol.2 (5), p.511-523

2009

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Age- and Genotype-Specific Triggers for Life-Threatening Arrhythmia in the Genotyped Long QT Syndrome

Journal of cardiovascular electrophysiology, 2008-08, Vol.19 (8), p.794-799

2008

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Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome

Circulation Journal, 2008, Vol.72(5), pp.694-699

2008

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Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go–Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation

Journal of Pharmacological Sciences, 2008, Vol.108(4), pp.462-471

2008

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Novel Mutation of Plakophilin-2 Associated With Arrhythmogenic Right Ventricular Cardiomyopathy

Circulation Journal, 2006, Vol.70(7), pp.933-935

2006

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Genetic Background of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Time to Start Asian Registry

Journal of Arrhythmia, 2008-01, Vol.24 (4), p.195-199

2008

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Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia

Journal of arrhythmia, 2011, Vol.27 (Supplement), p.JEBP1

2011

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A novel KCNH2 mutation as a modifier for short QT interval

International journal of cardiology, 2009-09, Vol.137 (1), p.83-85

2009

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An Autopsy Case of ARVC Caused by a PKP2 Mutation

Shindenzu, 2015, Vol.35 (1), p.31-38

2015

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A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome

International journal of cardiology, 2007-10, Vol.121 (3), p.239-248

2007

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APJ-1 Genetic Background for Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (ARVC/D) in Japan

Journal of Arrhythmia, 2012-05, Vol.28 (suppl), p.188-188

2012

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Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndrome

Europace (London, England), 2010-11, Vol.12 (11), p.1623-1629

2010

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Abstract 2636: Age-Related Triggers for Life-Threatning Arrhythmia in the Genotyped Long QT Syndrome

Circulation (New York, N.Y.), 2007-10, Vol.116 (suppl_16)

2007

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Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go-Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation

Journal of Pharmacological Sciences, 2008-12, Vol.108 (4), p.462-471

2008

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Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation

Journal of pharmacological sciences, 2008-12, Vol.108 (4), p.462

2008

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JEBP1 Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia

Journal of Arrhythmia, 2011-09, Vol.27 (suppl), p.187-187

2011

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A novel KCNH2 mutation as a modifier for short QT interval

International journal of cardiology, 2009, Vol.137 (1), p.83-85

2009

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Design of Variable Bit-Width Arithmetic Unit Using Single Flux Quantum Device

2022 IEEE International Symposium on Circuits and Systems (ISCAS), 2022, p.3547-3551

2022

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XQsim: modeling cross-technology control processors for 10+K qubit quantum computers

Proceedings of the 49th Annual International Symposium on Computer Architecture, 2022, p.366-382

2022

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ESTIMATION OF EFFECTIVE SHEAR STRESS WORKING ON FLAT SHEET MEMBRANE USING FLUIDIZED MEDIA IN MBRs

Journal of Japan Society of Civil Engineers, Ser. G (Environmental Research), 2011, Vol.67 (4), p.170-177

2011

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Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

Association of Atrial Arrhythmia and Sinus Node Dysfunction in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT Syndrome

Age- and Genotype-Specific Triggers for Life-Threatening Arrhythmia in the Genotyped Long QT Syndrome

Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome

Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go–Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation

Novel Mutation of Plakophilin-2 Associated With Arrhythmogenic Right Ventricular Cardiomyopathy

Genetic Background of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Time to Start Asian Registry

Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia

A novel KCNH2 mutation as a modifier for short QT interval

An Autopsy Case of ARVC Caused by a PKP2 Mutation

A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome

APJ-1 Genetic Background for Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (ARVC/D) in Japan

Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndrome

Abstract 2636: Age-Related Triggers for Life-Threatning Arrhythmia in the Genotyped Long QT Syndrome

Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go-Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation

Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation

JEBP1 Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia

A novel KCNH2 mutation as a modifier for short QT interval

Design of Variable Bit-Width Arithmetic Unit Using Single Flux Quantum Device

XQsim: modeling cross-technology control processors for 10+K qubit quantum computers

ESTIMATION OF EFFECTIVE SHEAR STRESS WORKING ON FLAT SHEET MEMBRANE USING FLUIDIZED MEDIA IN MBRs

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