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Matteo Vatta

Showing results (71-80 of 124) with videos related to

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Molecular Genetics and Metabolism|December 15, 2005
Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethoninJ Martijn Bos, Rainer N Poley, Melissa Ny, et al.
American Journal of Nephrology|January 23, 2019
Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing HemodialysisTae-Hwi Schwantes-An, Sai Liu, Margaret Stedman, et al.
Journal of Cardiovascular Electrophysiology|March 19, 2004
Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:Kui Hong, Antonio Berruezo-Sanchez, Naravat Poungvarin, et al.
Journal of Thrombosis and Thrombolysis|February 11, 2014
Factor XIII Val34Leu polymorphism and recurrent myocardial infarction in patients with coronary artery diseaseRolf P Kreutz, Abbas Bitar, Janelle Owens, et al.
Pediatric Cardiology|October 29, 2021
Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic ConditionsDana B Gal, Ana Morales, Susan Rojahn, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Calibrated Functional Data Decreases Clinical Uncertainty for Tier 1 Monogenic Disease: Application to Long QT SyndromeChai-Ann Ng, Matthew J O'Neill, Samskruthi R Padigepati, et al.
Biochemical and Biophysical Research Communications|November 14, 2006
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathyJeanne L Theis, J Martijn Bos, Virginia B Bartleson, et al.
Circulation. Genomic and Precision Medicine|February 19, 2025
Analysis of <i>TTN</i> Truncating Variants in >74 000 Cases Reveals New Clinically Relevant Gene RegionsMatteo Vatta, Ellen Regalado, Michael Parfenov, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 9, 2018
Angiotensin-related genetic determinants of cardiovascular disease in patients undergoing hemodialysisSharon M Moe, Jin Long, Tae-Hwi Linus Schwantes-An, et al.
Journal of Cardiac Failure|March 24, 2018
Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice GuidelineRay E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Molecular Genetics and Metabolism|December 15, 2005
Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethoninJ Martijn Bos, Rainer N Poley, Melissa Ny, et al.
American Journal of Nephrology|January 23, 2019
Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing HemodialysisTae-Hwi Schwantes-An, Sai Liu, Margaret Stedman, et al.
Journal of Cardiovascular Electrophysiology|March 19, 2004
Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:Kui Hong, Antonio Berruezo-Sanchez, Naravat Poungvarin, et al.
Journal of Thrombosis and Thrombolysis|February 11, 2014
Factor XIII Val34Leu polymorphism and recurrent myocardial infarction in patients with coronary artery diseaseRolf P Kreutz, Abbas Bitar, Janelle Owens, et al.
Pediatric Cardiology|October 29, 2021
Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic ConditionsDana B Gal, Ana Morales, Susan Rojahn, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Calibrated Functional Data Decreases Clinical Uncertainty for Tier 1 Monogenic Disease: Application to Long QT SyndromeChai-Ann Ng, Matthew J O'Neill, Samskruthi R Padigepati, et al.
Biochemical and Biophysical Research Communications|November 14, 2006
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathyJeanne L Theis, J Martijn Bos, Virginia B Bartleson, et al.
Circulation. Genomic and Precision Medicine|February 19, 2025
Analysis of <i>TTN</i> Truncating Variants in >74 000 Cases Reveals New Clinically Relevant Gene RegionsMatteo Vatta, Ellen Regalado, Michael Parfenov, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 9, 2018
Angiotensin-related genetic determinants of cardiovascular disease in patients undergoing hemodialysisSharon M Moe, Jin Long, Tae-Hwi Linus Schwantes-An, et al.
Journal of Cardiac Failure|March 24, 2018
Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice GuidelineRay E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Pageof 13