Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Peter van Tintelen

Showing results (161-170 of 232) with videos related to

Pageof 24
Sort By:
Clinical Genetics|January 4, 2020
Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patientLuisa Marsili, Eline Overwater, Nadine Hanna, 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.
Circulation Research|January 19, 2018
Mutations in <i>CYB561</i> Causing a Novel Orthostatic Hypotension SyndromeMaarten P van den Berg, Rowida Almomani, Italo Biaggioni, 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|April 16, 2020
Diagnosing arrhythmogenic right ventricular cardiomyopathy by 2010 Task Force Criteria: clinical performance and simplified practical implementationLaurens P Bosman, Julia Cadrin-Tourigny, Mimount Bourfiss, et al.
European Heart Journal|March 7, 2014
The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleusHendrik Milting, Bärbel Klauke, Alex Hoerby Christensen, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular CardiomyopathyRobert W Roudijk, Lisa Verheul, Laurens P Bosman, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Circulation. Cardiovascular Genetics|June 10, 2014
Outcome in phospholamban R14del carriers: results of a large multicentre cohort studyIngrid A W van Rijsingen, Paul A van der Zwaag, Judith A Groeneweg, et al.
European Heart Journal. Cardiovascular Imaging|April 11, 2018
Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imagingWouter P Te Rijdt, Judith N Ten Sande, Thomas M Gorter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.
Pageof 24

Showing results (161-170 of 232) with videos related to

Sort By:
Pageof 24
Clinical Genetics|January 4, 2020
Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patientLuisa Marsili, Eline Overwater, Nadine Hanna, 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.
Circulation Research|January 19, 2018
Mutations in <i>CYB561</i> Causing a Novel Orthostatic Hypotension SyndromeMaarten P van den Berg, Rowida Almomani, Italo Biaggioni, 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|April 16, 2020
Diagnosing arrhythmogenic right ventricular cardiomyopathy by 2010 Task Force Criteria: clinical performance and simplified practical implementationLaurens P Bosman, Julia Cadrin-Tourigny, Mimount Bourfiss, et al.
European Heart Journal|March 7, 2014
The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleusHendrik Milting, Bärbel Klauke, Alex Hoerby Christensen, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular CardiomyopathyRobert W Roudijk, Lisa Verheul, Laurens P Bosman, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Circulation. Cardiovascular Genetics|June 10, 2014
Outcome in phospholamban R14del carriers: results of a large multicentre cohort studyIngrid A W van Rijsingen, Paul A van der Zwaag, Judith A Groeneweg, et al.
European Heart Journal. Cardiovascular Imaging|April 11, 2018
Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imagingWouter P Te Rijdt, Judith N Ten Sande, Thomas M Gorter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.
Pageof 24