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Diagnostic lacunae and implications of an automated implantable cardioverter defibrillator implantation in a child with type 3 Long QT (LQT3) syndrome

Annals of cardiac anaesthesia, 2022-04, Vol.25 (2), p.210-213

2022

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Diagnosis, management and therapeutic strategies for congenital long QT syndrome

Heart (British Cardiac Society), 2022-03, Vol.108 (5), p.332

2022

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Long QT syndrome and current exercise recommendations: do we speak an infinite deal of… nothing?

European journal of preventive cardiology, 2023-03, Vol.30 (5), p.e25

2023

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Validating QT-Interval Measurement Using the Apple Watch ECG to Enable Remote Monitoring During the COVID-19 Pandemic

Circulation (New York, N.Y.), 2020-07, Vol.142 (4), p.416-418

2020

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Beyond the One Gene–One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders

Circulation (New York, N.Y.), 2019-08, Vol.140 (7), p.595-610

2019

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The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy

European heart journal, 2013-10, Vol.34 (40), p.3109-3116

2013

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The genetic architecture of long QT syndrome: A critical reappraisal

Trends in cardiovascular medicine, 2018-10, Vol.28 (7), p.453-464

2018

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Genetics in medicine, 2021-01, Vol.23 (1), p.47-58

2021

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Andersen-Tawil syndrome: A long QT syndrome with variable expression

Medicina clinica, 2024-03, Vol.162 (6), p.309

2024

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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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Artificial Intelligence-Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device

Circulation (New York, N.Y.), 2021-03, Vol.143 (13), p.1274-1286

2021

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Long-QT Syndrome: From Genetics to Management

Circulation. Arrhythmia and electrophysiology, 2012-08, Vol.5 (4), p.868-877

2012

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Towards Precision Medicine With Human iPSCs for Cardiac Channelopathies

Circulation research, 2019-08, Vol.125 (6), p.653-658

2019

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A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome

Circulation research, 2017-01, Vol.120 (1), p.39-48

2017

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Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing

Circulation (New York, N.Y.), 2018-02, Vol.137 (6), p.619-630

2018

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Translational Models and Tools to Reduce Clinical Trials and Improve Regulatory Decision Making for QTc and Proarrhythmia Risk (ICH E14/S7B Updates)

Clinical pharmacology and therapeutics, 2021-02, Vol.109 (2), p.319-333

2021

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Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue

Heart rhythm, 2015-11, Vol.12 (11), p.2325-2331

Ackerman, Michael J., MD, PhD

2015

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Which QT Correction Formulae to Use for QT Monitoring?

Journal of the American Heart Association, 2016-06, Vol.5 (6), p.n/a

2016

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Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Circulation (New York, N.Y.), 2013-03, Vol.127 (9), p.1009-1017

2013

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Guidance on Minimizing Risk of Drug-Induced Ventricular Arrhythmia During Treatment of COVID-19: A Statement from the Canadian Heart Rhythm Society

Canadian journal of cardiology, 2020-06, Vol.36 (6), p.948-951

2020

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Effects of hydroxychloroquine treatment on QT interval

Heart rhythm, 2020-11, Vol.17 (11), p.1930-1935

2020

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Independent validation and clinical implications of the risk prediction model for long QT syndrome (1-2-3-LQTS-Risk)

Europace (London, England), 2022-04, Vol.24 (4), p.614-619

2022

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Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

European heart journal, 2023-09, Vol.44 (35), p.3357-3370

2023

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In Vivo Base Editing of Scn5a Rescues Type 3 Long QT Syndrome in Mice

Circulation (New York, N.Y.), 2024-01, Vol.149 (4), p.317

2024

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A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome

International journal of cardiology, 2018-09, Vol.266, p.89-94

2018

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Diagnostic lacunae and implications of an automated implantable cardioverter defibrillator implantation in a child with type 3 Long QT (LQT3) syndrome

Diagnosis, management and therapeutic strategies for congenital long QT syndrome

Long QT syndrome and current exercise recommendations: do we speak an infinite deal of… nothing?

Validating QT-Interval Measurement Using the Apple Watch ECG to Enable Remote Monitoring During the COVID-19 Pandemic

Beyond the One Gene–One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders

The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy

The genetic architecture of long QT syndrome: A critical reappraisal

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Andersen-Tawil syndrome: A long QT syndrome with variable expression

Genetic and Clinical Advances in Congenital Long QT Syndrome

Artificial Intelligence-Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device

Long-QT Syndrome: From Genetics to Management

Towards Precision Medicine With Human iPSCs for Cardiac Channelopathies

A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome

Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing

Translational Models and Tools to Reduce Clinical Trials and Improve Regulatory Decision Making for QTc and Proarrhythmia Risk (ICH E14/S7B Updates)

Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue

Which QT Correction Formulae to Use for QT Monitoring?

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Guidance on Minimizing Risk of Drug-Induced Ventricular Arrhythmia During Treatment of COVID-19: A Statement from the Canadian Heart Rhythm Society

Effects of hydroxychloroquine treatment on QT interval

Independent validation and clinical implications of the risk prediction model for long QT syndrome (1-2-3-LQTS-Risk)

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

In Vivo Base Editing of Scn5a Rescues Type 3 Long QT Syndrome in Mice

A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome

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