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Annette F Baas

Showing results (41-50 of 71) with videos related to

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Heart Rhythm|August 10, 2023
Phenotypic variability of filamin C-related cardiomyopathy: Insights from a novel Dutch founder variantStephan A C Schoonvelde, Claudine W B Ruijmbeek, Alexander Hirsch, 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 clinicIsabelle P Thierry, Steven A Muller, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosusMagdalena Harakalova, Jasper van der Smagt, Carolien G F de Kovel, et al.
Journal of the American College of Cardiology|May 20, 2023
Individualized Family Screening for Arrhythmogenic Right Ventricular CardiomyopathySteven A Muller, Alessio Gasperetti, Laurens P Bosman, et al.
JACC. Heart Failure|August 11, 2023
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort StudyMark Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
International Journal of Molecular Sciences|February 25, 2023
Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of <i>MYBPC3</i> Founder VariantsMark Jansen, Maike Schuldt, Beau O van Driel, et al.
Human Mutation|June 17, 2018
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disordersEline Overwater, Luisa Marsili, Marieke J H Baars, et al.
Circulation. Genomic and Precision Medicine|December 17, 2024
Recreational and Occupational Physical Activity and Risk of Adverse Events in Truncating <i>MYBPC3</i> Founder Variant CarriersFahima Hassanzada, Mark Jansen, Freyja H M van Lint, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|November 15, 2023
The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overviewLisa M Verheul, Martijn H van der Ree, Sanne A Groeneveld, et al.
International Journal of Cardiology|July 10, 2021
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat-Hamedani, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Heart Rhythm|August 10, 2023
Phenotypic variability of filamin C-related cardiomyopathy: Insights from a novel Dutch founder variantStephan A C Schoonvelde, Claudine W B Ruijmbeek, Alexander Hirsch, 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 clinicIsabelle P Thierry, Steven A Muller, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosusMagdalena Harakalova, Jasper van der Smagt, Carolien G F de Kovel, et al.
Journal of the American College of Cardiology|May 20, 2023
Individualized Family Screening for Arrhythmogenic Right Ventricular CardiomyopathySteven A Muller, Alessio Gasperetti, Laurens P Bosman, et al.
JACC. Heart Failure|August 11, 2023
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort StudyMark Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
International Journal of Molecular Sciences|February 25, 2023
Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of <i>MYBPC3</i> Founder VariantsMark Jansen, Maike Schuldt, Beau O van Driel, et al.
Human Mutation|June 17, 2018
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disordersEline Overwater, Luisa Marsili, Marieke J H Baars, et al.
Circulation. Genomic and Precision Medicine|December 17, 2024
Recreational and Occupational Physical Activity and Risk of Adverse Events in Truncating <i>MYBPC3</i> Founder Variant CarriersFahima Hassanzada, Mark Jansen, Freyja H M van Lint, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|November 15, 2023
The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overviewLisa M Verheul, Martijn H van der Ree, Sanne A Groeneveld, et al.
International Journal of Cardiology|July 10, 2021
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat-Hamedani, et al.
Pageof 8