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Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 2, 2009
Recurrent and founder mutations in inherited cardiac diseases in the Netherlands
J P van Tintelen, A A M Wilde, J D H Jongbloed
Clinical Genetics
|
August 20, 2010
Desmin-related myopathy
K Y van Spaendonck-Zwarts, L van Hessem, J D H Jongbloed, et al.
Heart Rhythm
|
December 25, 2015
QRS prolongation after premature stimulation is associated with polymorphic ventricular tachycardia in nonischemic cardiomyopathy: Results from the Leiden Nonischemic Cardiomyopathy Study
Sebastiaan R D Piers, Saïd F A Askar, Jeroen Venlet, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 3, 2011
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A van den Wijngaard, P Volders, J P Van Tintelen, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
January 5, 2012
Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D
K Y van Spaendonck-Zwarts, A J van der Kooi, M P van den Berg, et al.
Clinical Genetics
|
June 25, 2010
Haplotype sharing test maps genes for familial cardiomyopathies
P A van der Zwaag, J P van Tintelen, F Gerbens, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 9, 2011
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia
P A van der Zwaag, M G P J Cox, C van der Werf, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 3, 2021
BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants-design and status
M Jansen, I Christiaans, S N van der Crabben, et al.
Journal of Cardiovascular Translational Research
|
June 6, 2023
Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers
Mark Jansen, A F Schmidt, J J M Jans, et al.
International Journal of Cardiology
|
April 13, 2025
Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant
E van Drie, J D H Jongbloed, E Hoorntje, et al.
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Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 2, 2009
Recurrent and founder mutations in inherited cardiac diseases in the Netherlands
J P van Tintelen, A A M Wilde, J D H Jongbloed
Clinical Genetics
|
August 20, 2010
Desmin-related myopathy
K Y van Spaendonck-Zwarts, L van Hessem, J D H Jongbloed, et al.
Heart Rhythm
|
December 25, 2015
QRS prolongation after premature stimulation is associated with polymorphic ventricular tachycardia in nonischemic cardiomyopathy: Results from the Leiden Nonischemic Cardiomyopathy Study
Sebastiaan R D Piers, Saïd F A Askar, Jeroen Venlet, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 3, 2011
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A van den Wijngaard, P Volders, J P Van Tintelen, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
January 5, 2012
Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D
K Y van Spaendonck-Zwarts, A J van der Kooi, M P van den Berg, et al.
Clinical Genetics
|
June 25, 2010
Haplotype sharing test maps genes for familial cardiomyopathies
P A van der Zwaag, J P van Tintelen, F Gerbens, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 9, 2011
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia
P A van der Zwaag, M G P J Cox, C van der Werf, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 3, 2021
BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants-design and status
M Jansen, I Christiaans, S N van der Crabben, et al.
Journal of Cardiovascular Translational Research
|
June 6, 2023
Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers
Mark Jansen, A F Schmidt, J J M Jans, et al.
International Journal of Cardiology
|
April 13, 2025
Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant
E van Drie, J D H Jongbloed, E Hoorntje, et al.
Page
of 2