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 (31-40 of 232) with videos related to

Pageof 24
Sort By:
Current Opinion in Cardiology|April 7, 2007
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?J Peter van Tintelen, Robert Mw Hofstra, Ans Cp Wiesfeld, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|June 3, 2008
Prophylactic aortic root surgery in patients with Marfan syndrome: 10 years' experience with a protocol based on body surface areaJan J J Aalberts, Tjalling W Waterbolk, J Peter van Tintelen, et al.
European Journal of Heart Failure|October 19, 2010
Familial dilated cardiomyopathy: another risk factor for anthracycline-induced cardiotoxicity?Maarten P van den Berg, Karin Y van Spaendonck-Zwarts, Dirk J van Veldhuisen, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Clinical utility gene card for: dilated cardiomyopathy (CMD)Anna Posafalvi, Johanna C Herkert, Richard J Sinke, et al.
Stem Cell Research|March 5, 2022
Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family membersNishka Mittal, Jaydev Dave, Magdalena Harakalova, et al.
European Journal of Human Genetics : EJHG|June 6, 2013
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)Wouter P Te Rijdt, Jan Dh Jongbloed, Rudolf A de Boer, et al.
Cardiovascular Research|September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesisEdgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variantEline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 8, 2019
[Hypertrophic cardiomyopathy]Beau van Driel, Folkert W Asselbergs, Rudolf A de Boer, et al.
European Journal of Human Genetics : EJHG|November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
Pageof 24

Showing results (31-40 of 232) with videos related to

Sort By:
Pageof 24
Current Opinion in Cardiology|April 7, 2007
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?J Peter van Tintelen, Robert Mw Hofstra, Ans Cp Wiesfeld, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|June 3, 2008
Prophylactic aortic root surgery in patients with Marfan syndrome: 10 years' experience with a protocol based on body surface areaJan J J Aalberts, Tjalling W Waterbolk, J Peter van Tintelen, et al.
European Journal of Heart Failure|October 19, 2010
Familial dilated cardiomyopathy: another risk factor for anthracycline-induced cardiotoxicity?Maarten P van den Berg, Karin Y van Spaendonck-Zwarts, Dirk J van Veldhuisen, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Clinical utility gene card for: dilated cardiomyopathy (CMD)Anna Posafalvi, Johanna C Herkert, Richard J Sinke, et al.
Stem Cell Research|March 5, 2022
Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family membersNishka Mittal, Jaydev Dave, Magdalena Harakalova, et al.
European Journal of Human Genetics : EJHG|June 6, 2013
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)Wouter P Te Rijdt, Jan Dh Jongbloed, Rudolf A de Boer, et al.
Cardiovascular Research|September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesisEdgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variantEline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 8, 2019
[Hypertrophic cardiomyopathy]Beau van Driel, Folkert W Asselbergs, Rudolf A de Boer, et al.
European Journal of Human Genetics : EJHG|November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
Pageof 24