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IS DILATED CARDIOMYOPATHY A PRIMARY FEATURE OF ANDERSEN-TAWIL SYNDROME? CHARACTERIZATION OF A NOVEL KCNJ2 MUTATION

Canadian journal of cardiology, 2016-10, Vol.32 (10), p.S213-S213

2016

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UTILITY OF CARDIAC MRI IN THE DIAGNOSIS OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY IN HUTTERITE DSC2 MUTATION CARRIERS

Canadian journal of cardiology, 2014-10, Vol.30 (10), p.S255-S255

2014

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MUTATIONS IN FILAMIN C CAUSE FAMILIAL RESTRICTIVE CARDIOMYOPATHY

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S147-S147

2015

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TRANSGENIC MICE OVEREXPRESSING DSC2 DEVELOP BIVENTRICULAR CARDIOMYOPATHY ASSOCIATED WITH FIBROSIS AND NECROSIS

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S64-S64

2015

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Gendiagnostik bei kardiovaskulären Erkrankungen: Konsensuspapier der Deutschen Gesellschaft für Kardiologie (DGK), der Gesellschaft für Humangenetik (GfH) und der Deutschen Gesellschaft für Pädiatrische Kardiologie (DGPK)

Die Kardiologie, 2023-09, Vol.17 (5), p.300-349

2023

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NOVEL NEXILIN VARIANTS MAY CAUSE DIFFERENT INHERITED CARDIOMYOPATHIES

Canadian journal of cardiology, 2014-10, Vol.30 (10), p.S121-S121

2014

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Non-invasive estimation of left ventricular systolic peak-pressure: a prerequisite to calculate of myocardial work in hypertrophic obstructive cardiomyopathy

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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614 Common Variants in Potassium Channels KCNH2 and KCNE1 Do Not Associate With the Vasovagal Syncope Phenotype

Canadian journal of cardiology, 2012-09, Vol.28 (5), p.S328-S328

2012

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CARDIAC ABNORMALITIES IN RELATIVES OF SUDDEN CARDIAC ARREST VICTIMS: A REPORT FROM THE CASPER REGISTRY

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S118-S118

2015

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EARLY REPOLARIZATION INHERITANCE PATTERN IN CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S119-S119

2015

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T1rho and T2rho based myocardial tissue characterisation in small animals at high-field MRI

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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INFLUENCE OF ASSIGNING A DIAGNOSIS ON ARRHYTHMIA RECURRENCE IN APPARENTLY UNEXPLAINED CARDIAC ARREST PATIENTS (CASPER)

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S118-S119

2015

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THE UTILITY AND INCREMENTAL VALUE OF THE SIGNAL AVERAGED ECG: A NOVEL MODEL FOR STRATIFYING PATIENTS WITH SUSPECTED BRUGADA SYNDROME

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S247-S247

2015

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Quantification of systolic anterior motion of the mitral valve to predict left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Myocardial work in hypertrophic cardiomyopathy - a new non-invasive parameter for segmental myocardial function?

European heart journal cardiovascular imaging, 2022-02, Vol.23 (Supplement_1)

2022

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Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

Nature genetics, 2004-11, Vol.36 (11), p.1162-1164

2004

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Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy

American journal of human genetics, 2006-12, Vol.79 (6), p.1081-1088

2006

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5049Genetic association study suggests involvement of sex-specific serotonin signaling in vasovagal syncope

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

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P1601Mutations in ILK (integrin linked kinase) are associated with human arrhythmogenic cardiomyopathy and decreased survival in zebrafish

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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Mutations of TTN , encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

Nature genetics, 2002-02, Vol.30 (2), p.201-204

2002

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Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients

American journal of medical genetics, 2003-06, Vol.119A (2), p.162-167

2003

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Next-generation sequencing identifies multiple disease associated variants in inherited heart conditions

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2299-P2299

2013

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12-Lead ECG Reliably Identifies Homozygous DSC2 Mutation Carriers in the Hutterite Population

Canadian journal of cardiology, 2013-10, Vol.29 (10), p.S133-S133

2013

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Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15

Circulation (New York, N.Y.), 2004-06, Vol.109 (22), p.2720-2723

2004

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IS DILATED CARDIOMYOPATHY A PRIMARY FEATURE OF ANDERSEN-TAWIL SYNDROME? CHARACTERIZATION OF A NOVEL KCNJ2 MUTATION

UTILITY OF CARDIAC MRI IN THE DIAGNOSIS OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY IN HUTTERITE DSC2 MUTATION CARRIERS

MUTATIONS IN FILAMIN C CAUSE FAMILIAL RESTRICTIVE CARDIOMYOPATHY

TRANSGENIC MICE OVEREXPRESSING DSC2 DEVELOP BIVENTRICULAR CARDIOMYOPATHY ASSOCIATED WITH FIBROSIS AND NECROSIS

Gendiagnostik bei kardiovaskulären Erkrankungen: Konsensuspapier der Deutschen Gesellschaft für Kardiologie (DGK), der Gesellschaft für Humangenetik (GfH) und der Deutschen Gesellschaft für Pädiatrische Kardiologie (DGPK)

NOVEL NEXILIN VARIANTS MAY CAUSE DIFFERENT INHERITED CARDIOMYOPATHIES

Non-invasive estimation of left ventricular systolic peak-pressure: a prerequisite to calculate of myocardial work in hypertrophic obstructive cardiomyopathy

614 Common Variants in Potassium Channels KCNH2 and KCNE1 Do Not Associate With the Vasovagal Syncope Phenotype

CARDIAC ABNORMALITIES IN RELATIVES OF SUDDEN CARDIAC ARREST VICTIMS: A REPORT FROM THE CASPER REGISTRY

EARLY REPOLARIZATION INHERITANCE PATTERN IN CARDIAC ARREST SURVIVORS WITH PRESERVED EJECTION FRACTION REGISTRY (CASPER)

T1rho and T2rho based myocardial tissue characterisation in small animals at high-field MRI

INFLUENCE OF ASSIGNING A DIAGNOSIS ON ARRHYTHMIA RECURRENCE IN APPARENTLY UNEXPLAINED CARDIAC ARREST PATIENTS (CASPER)

THE UTILITY AND INCREMENTAL VALUE OF THE SIGNAL AVERAGED ECG: A NOVEL MODEL FOR STRATIFYING PATIENTS WITH SUSPECTED BRUGADA SYNDROME

Quantification of systolic anterior motion of the mitral valve to predict left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy

Myocardial work in hypertrophic cardiomyopathy - a new non-invasive parameter for segmental myocardial function?

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy

5049Genetic association study suggests involvement of sex-specific serotonin signaling in vasovagal syncope

P1601Mutations in ILK (integrin linked kinase) are associated with human arrhythmogenic cardiomyopathy and decreased survival in zebrafish

Mutations of TTN , encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients

Next-generation sequencing identifies multiple disease associated variants in inherited heart conditions

12-Lead ECG Reliably Identifies Homozygous DSC2 Mutation Carriers in the Hutterite Population

Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15

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