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J Peter van Tintelen

Showing results (21-30 of 232) with videos related to

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JACC. Advances|November 6, 2025
Phenotypic Characterization of Cardiac Involvement in Carriers With Pathogenic TTR Variants Warrants an Evidence-Based ApproachSteven A Muller, Leendert C Kieviet, J Peter van Tintelen, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Influence of Panel Selection on Yield of Clinically Useful Variants in Arrhythmogenic Right Ventricular Cardiomyopathy FamiliesBrittney Murray, Crystal Tichnell, Harikrishna Tandri, et al.
World Neurosurgery|April 29, 2018
Cardiac Arrest During Spine Surgery in the Prone Position: Case Report and Review of the LiteratureVictor E Staartjes, Shiva A Schillevoort, Patricia G Blum, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
Family letters are an effective way to inform relatives about inherited cardiac diseaseWilma P van der Roest, José M Pennings, Marian Bakker, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 21, 2009
Ultrastructural pathology of the nuclear envelope in familial lamin A/C cardiomyopathyGilles F Diercks, J Peter van Tintelen, Rene A Tio, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
The importance of the family history in caring for families with long QT syndrome and dilated cardiomyopathyJolien S Ruiter, Karin Berkenbosch-Nieuwhof, Maarten P van den Berg, et al.
BMJ Open|July 11, 2019
A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|March 27, 2023
Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general populationTetske Dijkstra, Lieke M van den Heuvel, J Peter van Tintelen, et al.
European Journal of Medical Genetics|May 20, 2009
Letter regarding the article: "R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy" by Valenzise et alPaul A van der Zwaag, Jan D H Jongbloed, Maarten P van den Berg, et al.
International Journal of Cardiology|December 18, 2013
Successful treatment of a patient with symptomatic long QT syndrome type 3 using ranolazine combined with a beta-blockerMaarten P van den Berg, Freek van den Heuvel, J Peter van Tintelen, et al.
Pageof 24

Showing results (21-30 of 232) with videos related to

Sort By:
Pageof 24
JACC. Advances|November 6, 2025
Phenotypic Characterization of Cardiac Involvement in Carriers With Pathogenic TTR Variants Warrants an Evidence-Based ApproachSteven A Muller, Leendert C Kieviet, J Peter van Tintelen, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Influence of Panel Selection on Yield of Clinically Useful Variants in Arrhythmogenic Right Ventricular Cardiomyopathy FamiliesBrittney Murray, Crystal Tichnell, Harikrishna Tandri, et al.
World Neurosurgery|April 29, 2018
Cardiac Arrest During Spine Surgery in the Prone Position: Case Report and Review of the LiteratureVictor E Staartjes, Shiva A Schillevoort, Patricia G Blum, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
Family letters are an effective way to inform relatives about inherited cardiac diseaseWilma P van der Roest, José M Pennings, Marian Bakker, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 21, 2009
Ultrastructural pathology of the nuclear envelope in familial lamin A/C cardiomyopathyGilles F Diercks, J Peter van Tintelen, Rene A Tio, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
The importance of the family history in caring for families with long QT syndrome and dilated cardiomyopathyJolien S Ruiter, Karin Berkenbosch-Nieuwhof, Maarten P van den Berg, et al.
BMJ Open|July 11, 2019
A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|March 27, 2023
Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general populationTetske Dijkstra, Lieke M van den Heuvel, J Peter van Tintelen, et al.
European Journal of Medical Genetics|May 20, 2009
Letter regarding the article: "R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy" by Valenzise et alPaul A van der Zwaag, Jan D H Jongbloed, Maarten P van den Berg, et al.
International Journal of Cardiology|December 18, 2013
Successful treatment of a patient with symptomatic long QT syndrome type 3 using ranolazine combined with a beta-blockerMaarten P van den Berg, Freek van den Heuvel, J Peter van Tintelen, et al.
Pageof 24