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Loss-of-Function of the Voltage-Gated Sodium Channel NaV1.5 (Channelopathies) in Patients With Irritable Bowel Syndrome

Gastroenterology (New York, N.Y. 1943), 2014-06, Vol.146 (7), p.1659-1668

2014

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Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies: A Scientific Statement From the American Heart Association and American College of Cardiology

Journal of the American College of Cardiology, 2015-12, Vol.66 (21), p.2424-2428

2015

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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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Dravet syndrome—From epileptic encephalopathy to channelopathy

Epilepsia (Copenhagen), 2014-07, Vol.55 (7), p.979-984

2014

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Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies: A Scientific Statement From the American Heart Association and American College of Cardiology

Circulation (New York, N.Y.), 2015-12, Vol.132 (22), p.e326-e329

2015

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Gene mutations in comorbidity of epilepsy and arrhythmia

Journal of neurology, 2023-03, Vol.270 (3), p.1229-1248

2023

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Prevalence study of genetically defined skeletal muscle channelopathies in England

Neurology, 2013-04, Vol.80 (16), p.1472

2013

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The prevalence and significance of a short QT interval in 18 825 low-risk individuals including athletes

British journal of sports medicine, 2016-01, Vol.50 (2), p.124-129

2016

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Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis

Neurology, 2016-02, Vol.86 (5), p.410

2016

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1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants

Human genomics, 2022-08, Vol.16 (1), p.30-30, Article 30

2022

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Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics

Circulation. Arrhythmia and electrophysiology, 2014-06, Vol.7 (3), p.511-517

2014

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Primary ventricular tachycardia in paediatric population in a tertiary centre

Archives of disease in childhood, 2017-12, Vol.102 (12), p.1137

2017

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Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors

Journal of human genetics, 2017-06, Vol.62 (6), p.615-620

2017

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Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?

Epilepsia (Copenhagen), 2010-02, Vol.51 (2), p.293-296

2010

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Rare neurological channelopathies--networks to study patients, pathogenesis and treatment

Nature reviews. Neurology, 2016-04, Vol.12 (4), p.195

2016

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Congenital long QT syndrome presenting with a history of epilepsy: Misdiagnosis or relationship between channelopathies of the heart and brain?

Epilepsia (Copenhagen), 2010-02, Vol.51 (2), p.289-292

2010

Volltextzugriff (PDF)

Clinical evaluation of unselected cardiac arrest survivors in a tertiary center over a 1-year period (the LAZARUZ study)

Journal of electrocardiology, 2016-09, Vol.49 (5), p.707-713

2016

Volltextzugriff (PDF)

Drowning and sudden cardiac death

Archives of Disease in Childhood, 2011-01, Vol.96 (1), p.5-8

2011

Volltextzugriff (PDF)

EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias

European journal of neurology, 2010-05, Vol.17 (5), p.641-648

2010

Volltextzugriff (PDF)

Channelopathies in Children and Adults

Pacing and clinical electrophysiology, 2008-02, Vol.31 (s1), p.S41-S45

WILDE, ARTHUR A.M.

2008

Volltextzugriff (PDF)

Primary electrical diseases diagnosis, genetic and management

Minerva cardioangiologica, 2010-08, Vol.58 (4), p.449

2010

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Causes of sudden cardiac death in young athletes and non-athletes: systematic review and meta-analysis: Sudden cardiac death in the young

Trends in cardiovascular medicine, 2022-07, Vol.32 (5), p.299-308

2022

Volltextzugriff (PDF)

Arrhythmias and COVID-19: A Review

JACC. Clinical electrophysiology, 2020-09, Vol.6 (9), p.1193-1204

2020

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Sudden unexplained death versus nonautopsied possible sudden cardiac death: Findings in relatives

Journal of cardiovascular electrophysiology, 2022-02, Vol.33 (2), p.254-261

2022

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Loss-of-Function of the Voltage-Gated Sodium Channel NaV1.5 (Channelopathies) in Patients With Irritable Bowel Syndrome

Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies: A Scientific Statement From the American Heart Association and American College of Cardiology

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

Dravet syndrome—From epileptic encephalopathy to channelopathy

Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies: A Scientific Statement From the American Heart Association and American College of Cardiology

Gene mutations in comorbidity of epilepsy and arrhythmia

Prevalence study of genetically defined skeletal muscle channelopathies in England

The prevalence and significance of a short QT interval in 18 825 low-risk individuals including athletes

Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis

1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants

Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics

Primary ventricular tachycardia in paediatric population in a tertiary centre

Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors

Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?

Rare neurological channelopathies--networks to study patients, pathogenesis and treatment

Congenital long QT syndrome presenting with a history of epilepsy: Misdiagnosis or relationship between channelopathies of the heart and brain?

Clinical evaluation of unselected cardiac arrest survivors in a tertiary center over a 1-year period (the LAZARUZ study)

Drowning and sudden cardiac death

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias

Channelopathies in Children and Adults

Primary electrical diseases diagnosis, genetic and management

Causes of sudden cardiac death in young athletes and non-athletes: systematic review and meta-analysis: Sudden cardiac death in the young

Arrhythmias and COVID-19: A Review

Sudden unexplained death versus nonautopsied possible sudden cardiac death: Findings in relatives

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