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Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome

Journal of the American College of Cardiology, 2014-07, Vol.64 (1), p.66-79

2014

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Acquired short QT syndrome in a cancer patient treated with Toad

Pacing and clinical electrophysiology, 2019-09, Vol.42 (9), p.1273-1275

2019

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Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome

Journal of molecular and cellular cardiology, 2014-03, Vol.68, p.20-28

2014

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Hypertension as a sequela in patients of SARS-CoV-2 infection

PloS one, 2021-04, Vol.16 (4), p.e0250815-e0250815

2021

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Maximum Diastolic Potential of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Depends Critically on IKr

PloS one, 2012-07, Vol.7 (7), p.e40288

2012

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Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation

Heart rhythm, 2012-01, Vol.9 (1), p.125-131

2012

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Lidocaine-Induced Brugada Syndrome Phenotype Linked to a Novel Double Mutation in the Cardiac Sodium Channel

Circulation research, 2008-08, Vol.103 (4), p.396-404

2008

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Effect of Wenxin Keli and quinidine to suppress arrhythmogenesis in an experimental model of Brugada syndrome

Heart rhythm, 2013-07, Vol.10 (7), p.1054-1062

2013

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The potential anti-arrhythmic effect of SGLT2 inhibitors

Cardiovascular diabetology, 2024-07, Vol.23 (1), p.252-17, Article 252

2024

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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

Journal of the American Heart Association, 2016-07, Vol.5 (7), p.n/a

2016

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Mechanisms underlying atrial-selective block of sodium channels by Wenxin Keli: Experimental and theoretical analysis

International journal of cardiology, 2016-03, Vol.207, p.326-334

2016

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Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome

Heart rhythm, 2016-06, Vol.13 (6), p.1326-1334

2016

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SCN5A Genetic Polymorphisms Associated With Increased Defibrillator Shocks in Brugada Syndrome

Journal of the American Heart Association, 2017-06, Vol.6 (6)

2017

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Ionic and Cellular Mechanisms Underlying the Development of Acquired Brugada Syndrome in Patients Treated with Antidepressants

Journal of cardiovascular electrophysiology, 2012-04, Vol.23 (4), p.423-432

2012

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Clinical and Functional Genetic Characterization of the Role of Cardiac Calcium Channel Variants in the Early Repolarization Syndrome

Frontiers in cardiovascular medicine, 2021-06, Vol.8, p.680819-680819

2021

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Mechanisms underlying the antiarrhythmic effect of ARumenamide-787 in experimental models of the J wave syndromes and hypothermia

PloS one, 2023-05, Vol.18 (5), p.e0281977-e0281977

2023

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Acacetin suppresses the electrocardiographic and arrhythmic manifestations of the J wave syndromes

PloS one, 2020-11, Vol.15 (11), p.e0242747

2020

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A carvedilol analogue, VK‐II‐86, prevents hypokalaemia‐induced ventricular arrhythmia through novel multi‐channel effects

British journal of pharmacology, 2022-06, Vol.179 (11), p.2713-2732

2022

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Editorial: Arrhythmias in women

Frontiers in cardiovascular medicine, 2024, Vol.11, p.1348878-1348878

2024

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Neuronal Nav1.8 Channels as a Novel Therapeutic Target of Acute Atrial Fibrillation Prevention

Journal of the American Heart Association, 2016-11, Vol.5 (11), p.n/a

2016

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Erratum to: Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

Journal of translational medicine, 2017-05, Vol.15 (1), p.101-101, Article 101

2017

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The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome

JACC. Clinical electrophysiology, 2017-07, Vol.3 (7), p.727-743

2017

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A temporal window of vulnerability for development of atrial fibrillation with advancing heart failure

European journal of heart failure, 2014-03, Vol.16 (3), p.271-280

2014

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Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

International journal of molecular sciences, 2021-07, Vol.22 (13), p.7108

2021

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Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome

Acquired short QT syndrome in a cancer patient treated with Toad

Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome

Hypertension as a sequela in patients of SARS-CoV-2 infection

Maximum Diastolic Potential of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Depends Critically on IKr

Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation

Lidocaine-Induced Brugada Syndrome Phenotype Linked to a Novel Double Mutation in the Cardiac Sodium Channel

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

Effect of Wenxin Keli and quinidine to suppress arrhythmogenesis in an experimental model of Brugada syndrome

The potential anti-arrhythmic effect of SGLT2 inhibitors

Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

Mechanisms underlying atrial-selective block of sodium channels by Wenxin Keli: Experimental and theoretical analysis

Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome

SCN5A Genetic Polymorphisms Associated With Increased Defibrillator Shocks in Brugada Syndrome

Ionic and Cellular Mechanisms Underlying the Development of Acquired Brugada Syndrome in Patients Treated with Antidepressants

Clinical and Functional Genetic Characterization of the Role of Cardiac Calcium Channel Variants in the Early Repolarization Syndrome

Mechanisms underlying the antiarrhythmic effect of ARumenamide-787 in experimental models of the J wave syndromes and hypothermia

Acacetin suppresses the electrocardiographic and arrhythmic manifestations of the J wave syndromes

A carvedilol analogue, VK‐II‐86, prevents hypokalaemia‐induced ventricular arrhythmia through novel multi‐channel effects

Editorial: Arrhythmias in women

Neuronal Nav1.8 Channels as a Novel Therapeutic Target of Acute Atrial Fibrillation Prevention

Erratum to: Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome

A temporal window of vulnerability for development of atrial fibrillation with advancing heart failure

Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

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