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Cardiology
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November 14, 2012
Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation
Jasper J van der Smagt, Paul A van der Zwaag, J Peter van Tintelen, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
July 10, 2024
Diagnostic value of late gadolinium enhancement at cardiovascular magnetic resonance to distinguish arrhythmogenic right ventricular cardiomyopathy from differentials
Lian Y Rekker, Steven A Muller, Alessio Gasperetti, et al.
Heart Rhythm
|
December 29, 2012
Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?
Judith A Groeneweg, Paul A van der Zwaag, Jan D H Jongbloed, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
January 20, 2025
Yield of family screening for dilated cardiomyopathy: 10-year experience at a multidisciplinary cardiogenetic outpatient clinic
Isabelle P Thierry, Steven A Muller, Annette F Baas, et al.
Circulation. Arrhythmia and Electrophysiology
|
December 13, 2024
Performance of ARVC Risk Calculators in (Likely) Pathogenic Plakophilin-2 Variant Carriers Without Definite ARVC Diagnosis
Steven A Muller, Babken Asatryan, Brittney Murray, et al.
Circulation. Arrhythmia and Electrophysiology
|
July 2, 2026
Yield of Family Screening in Arrhythmogenic Right Ventricular Cardiomyopathy Without a Validated Genetic Cause
Steven A Muller, Brittney Murray, Crystal Tichnell, et al.
Plos One
|
April 6, 2012
Inflammation aggravates disease severity in Marfan syndrome patients
Teodora Radonic, Piet de Witte, Maarten Groenink, et al.
JACC. Clinical Electrophysiology
|
May 16, 2018
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset Disease
Anneline S J M Te Riele, Cynthia A James, Abhishek C Sawant, et al.
European Heart Journal
|
December 19, 2009
The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening
Imke Christiaans, Erwin Birnie, Irene M van Langen, et al.
Circulation. Arrhythmia and Electrophysiology
|
October 22, 2009
New ECG criteria in arrhythmogenic right ventricular dysplasia/cardiomyopathy
Moniek G P J Cox, Jasper J van der Smagt, Arthur A M Wilde, et al.
Page
of 24
Search research articles
Search
Showing results (111-120 of 232) with videos related to
Sort By:
Page
of 24
Cardiology
|
November 14, 2012
Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation
Jasper J van der Smagt, Paul A van der Zwaag, J Peter van Tintelen, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
July 10, 2024
Diagnostic value of late gadolinium enhancement at cardiovascular magnetic resonance to distinguish arrhythmogenic right ventricular cardiomyopathy from differentials
Lian Y Rekker, Steven A Muller, Alessio Gasperetti, et al.
Heart Rhythm
|
December 29, 2012
Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?
Judith A Groeneweg, Paul A van der Zwaag, Jan D H Jongbloed, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
January 20, 2025
Yield of family screening for dilated cardiomyopathy: 10-year experience at a multidisciplinary cardiogenetic outpatient clinic
Isabelle P Thierry, Steven A Muller, Annette F Baas, et al.
Circulation. Arrhythmia and Electrophysiology
|
December 13, 2024
Performance of ARVC Risk Calculators in (Likely) Pathogenic Plakophilin-2 Variant Carriers Without Definite ARVC Diagnosis
Steven A Muller, Babken Asatryan, Brittney Murray, et al.
Circulation. Arrhythmia and Electrophysiology
|
July 2, 2026
Yield of Family Screening in Arrhythmogenic Right Ventricular Cardiomyopathy Without a Validated Genetic Cause
Steven A Muller, Brittney Murray, Crystal Tichnell, et al.
Plos One
|
April 6, 2012
Inflammation aggravates disease severity in Marfan syndrome patients
Teodora Radonic, Piet de Witte, Maarten Groenink, et al.
JACC. Clinical Electrophysiology
|
May 16, 2018
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset Disease
Anneline S J M Te Riele, Cynthia A James, Abhishek C Sawant, et al.
European Heart Journal
|
December 19, 2009
The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening
Imke Christiaans, Erwin Birnie, Irene M van Langen, et al.
Circulation. Arrhythmia and Electrophysiology
|
October 22, 2009
New ECG criteria in arrhythmogenic right ventricular dysplasia/cardiomyopathy
Moniek G P J Cox, Jasper J van der Smagt, Arthur A M Wilde, et al.
Page
of 24