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M Barge

Showing results (111-120 of 133) with videos related to

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Human Molecular Genetics|October 21, 2022
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetranceJaël S Copier, Marianne Bootsma, Chai A Ng, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|September 3, 2017
A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defectsI H M van der Linde, Y L Hiemstra, R Bökenkamp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2022
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohortLisa M van den Bersselaar, Judith M A Verhagen, Jos A Bekkers, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|July 28, 2023
The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variantThomas A Bos, Sebastiaan R D Piers, Marja W Wessels, et al.
Astrobiology|January 16, 2024
Future of the Search for Life: Workshop ReportMarc Neveu, Richard Quinn, Laura M Barge, 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.
Circulation. Genomic and Precision Medicine|May 18, 2023
Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular ArrhythmiasCaroline Pham, Karolina Andrzejczyk, Sean J Jurgens, et al.
Circulation. Genomic and Precision Medicine|September 30, 2022
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk StratificationMarijke H van der Meulen, Johanna C Herkert, Susanna L den Boer, et al.
Astrobiology|October 23, 2018
The NASA Roadmap to Ocean WorldsAmanda R Hendrix, Terry A Hurford, Laura M Barge, et al.
Astrobiology|December 20, 2015
A Strategy for Origins of Life ResearchCaleb Scharf, Nathaniel Virgo, H James Cleaves, et al.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
Human Molecular Genetics|October 21, 2022
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetranceJaël S Copier, Marianne Bootsma, Chai A Ng, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|September 3, 2017
A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defectsI H M van der Linde, Y L Hiemstra, R Bökenkamp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2022
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohortLisa M van den Bersselaar, Judith M A Verhagen, Jos A Bekkers, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|July 28, 2023
The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variantThomas A Bos, Sebastiaan R D Piers, Marja W Wessels, et al.
Astrobiology|January 16, 2024
Future of the Search for Life: Workshop ReportMarc Neveu, Richard Quinn, Laura M Barge, 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.
Circulation. Genomic and Precision Medicine|May 18, 2023
Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular ArrhythmiasCaroline Pham, Karolina Andrzejczyk, Sean J Jurgens, et al.
Circulation. Genomic and Precision Medicine|September 30, 2022
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk StratificationMarijke H van der Meulen, Johanna C Herkert, Susanna L den Boer, et al.
Astrobiology|October 23, 2018
The NASA Roadmap to Ocean WorldsAmanda R Hendrix, Terry A Hurford, Laura M Barge, et al.
Astrobiology|December 20, 2015
A Strategy for Origins of Life ResearchCaleb Scharf, Nathaniel Virgo, H James Cleaves, et al.
Pageof 14