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Recent advances in genetic testing and counseling for inherited arrhythmias

Journal of arrhythmia, 2016-10, Vol.32 (5), p.389-397

Mizusawa, Yuka, MD

2016

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Genetic and Clinical Advances in Congenital Long QT Syndrome

Circulation Journal, 2014/11/25, Vol.78(12), pp.2827-2833

2014

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The Prognostic Significance of Fever-Induced Brugada Syndrome

Heart rhythm, 2016-07, Vol.13 (7), p.1515-1520

2016

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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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Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

European journal of human genetics : EJHG, 2016-08, Vol.24 (8), p.1160-1166

2016

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A refined protocol of flecainide testing in Brugada syndrome: From ambiguous assessment toward definite diagnosis

Heart rhythm, 2015-02, Vol.12 (2), p.358-359

2015

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QT Prolongation and Mortality in Hospital Settings: Identifying Patients at High Risk

Mayo Clinic proceedings, 2013-04, Vol.88 (4), p.309-311

2013

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Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome

Circulation Journal, 2012, Vol.76(9), pp.2112-2118

2012

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Risk Determinants in Individuals With a Spontaneous Type 1 Brugada ECG

Circulation Journal, 2011, Vol.75(4), pp.844-851

2011

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Channelopathies - Emerging Trends in The Management of Inherited Arrhythmias

Indian pacing and electrophysiology journal, 2015, Vol.15 (1), p.43-54

2015

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Sodium Current Disorders

Cardiac electrophysiology clinics, 2014-12, Vol.6 (4), p.819-824

2014

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Brugada Syndrome

Circulation. Arrhythmia and electrophysiology, 2012-06, Vol.5 (3), p.606-616

2012

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Nature genetics, 2013-09, Vol.45 (9), p.1044-1049

2013

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Bidirectional Ventricular Tachycardia Caused by a Reentrant Mechanism With Left Bundle Branch Block Configuration on Electrocardiography

Circulation Journal, 2008, Vol.72(8), pp.1373-1377

2008

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Mayo Clinic Proceedings: QT prolongation and mortality in hospital settings: identifying patients at high risk

Mayo Clinic proceedings, 2013-04, Vol.88 (4), p.309

2013

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Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome

Journal of the American College of Cardiology, 2019-04, Vol.73 (14), p.1756-1765

2019

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Carvedilol, a Non-Selective β-with α1-Blocker is Effective in Long QT Syndrome Type 2

Journal of arrhythmia, 2011-12, Vol.27 (4), p.324-331

2011

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Fever-related arrhythmic events in the multicenter Survey on Arrhythmic Events in Brugada Syndrome

Heart rhythm, 2018-09, Vol.15 (9), p.1394-1401

2018

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Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients

Heart rhythm, 2018-10, Vol.15 (10), p.1457-1465

2018

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Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

Heart rhythm, 2018-05, Vol.15 (5), p.716-724

2018

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Effect of Cigarette Smoking on the Risk of Atrial Fibrillation Recurrence after Pulmonary Vein Isolation

Journal of Arrhythmia, 2010-01, Vol.26 (1), p.21-29

2010

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Multiple Clinical Manifestations of a Single SCN5A Mutation

Journal of arrhythmia, 2011, Vol.27 (Supplement), p.YIAB_3

2011

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Recent advances in genetic testing and counseling for inherited arrhythmias

Genetic and Clinical Advances in Congenital Long QT Syndrome

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

The Prognostic Significance of Fever-Induced Brugada Syndrome

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

A refined protocol of flecainide testing in Brugada syndrome: From ambiguous assessment toward definite diagnosis

QT Prolongation and Mortality in Hospital Settings: Identifying Patients at High Risk

Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome

Risk Determinants in Individuals With a Spontaneous Type 1 Brugada ECG

Channelopathies - Emerging Trends in The Management of Inherited Arrhythmias

Sodium Current Disorders

Brugada Syndrome

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Bidirectional Ventricular Tachycardia Caused by a Reentrant Mechanism With Left Bundle Branch Block Configuration on Electrocardiography

Mayo Clinic Proceedings: QT prolongation and mortality in hospital settings: identifying patients at high risk

Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome

Carvedilol, a Non-Selective β-with α1-Blocker is Effective in Long QT Syndrome Type 2

Fever-related arrhythmic events in the multicenter Survey on Arrhythmic Events in Brugada Syndrome

Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients

Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

Effect of Cigarette Smoking on the Risk of Atrial Fibrillation Recurrence after Pulmonary Vein Isolation

Multiple Clinical Manifestations of a Single SCN5A Mutation

Rationale and design of the PRAETORIAN trial: A Prospective, RAndomizEd comparison of subcuTaneOus and tRansvenous ImplANtable cardioverter-defibrillator therapy

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