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The Journal of Pediatrics|August 31, 2014
Compound heterozygous mutations in the SCN5A-encoded Nav1.5 cardiac sodium channel resulting in atrial standstill and His-Purkinje system diseaseShankar Baskar, Michael J Ackerman, Diane Clements, et al.
Computers in Biology and Medicine|December 6, 2005
Using UMLS metathesaurus concepts to describe medical images: dermatology vocabularyJames W Woods, Charles A Sneiderman, Kamran Hameed, et al.
Heart Rhythm O2|August 8, 2022
COVID-19 vaccination in patients with long QT syndromeCheng-I Wu, Peter J Schwartz, Michael J Ackerman, et al.
Pediatric Cardiology|December 16, 2014
Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: a case seriesNupoor Narula, David J Tester, Anna Paulmichl, et al.
Circulation|February 13, 2018
Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic TestingJohn R Giudicessi, Dan M Roden, Arthur A M Wilde, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 9, 2007
Mechanical dysfunction in extreme QT prolongationHimeshkumar Vyas, Patrick W O'Leary, Michael G Earing, et al.
Circulation. Cardiovascular Genetics|October 8, 2017
Genomic Triangulation and Coverage Analysis in Whole-Exome Sequencing-Based Molecular AutopsiesGarrett W Shanks, David J Tester, Sneha Nishtala, et al.
JACC. Clinical Electrophysiology|September 5, 2025
Diagnostic and Prognostic Significance of Exercise Stress Testing in Desmosomal Arrhythmogenic CardiomyopathyMatteo Castrichini, Raquel Neves, Ramin Garmany, et al.
Journal of Cardiovascular Electrophysiology|January 29, 2021
Efficacy of intentional permanent atrial pacing in the long-term management of congenital long QT syndromeGurukripa N Kowlgi, John R Giudicessi, Walid Barake, et al.
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