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Congenital Heart Disease|May 8, 2013
Sudden cardiac arrest in a young patient with hypertrophic cardiomyopathy and zero canonical risk factors: the inherent limitations of risk stratification in hypertrophic cardiomyopathyJohn J Kohorst, J Martijn Bos, Donald J Hagler, et al.
Pediatrics|May 22, 2013
Maternal mosaicism confounds the neonatal diagnosis of type 1 Timothy syndromeKeith A Dufendach, John R Giudicessi, Nicole J Boczek, et al.
Biochemical and Biophysical Research Communications|May 23, 2006
A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathyVlad C Vasile, Steve R Ommen, William D Edwards, et al.
Circulation|May 16, 2007
Diagnostic miscues in congenital long-QT syndromeNathaniel W Taggart, Carla M Haglund, David J Tester, et al.
The Journal of Hand Surgery|November 6, 2022
Classic Timothy Syndrome Associated With Bilateral Border Digit Syndactyly: A Case SeriesEugene E Zheng, Francisco R Avila, Michael J Ackerman, et al.
Heart Rhythm|September 2, 2018
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channelDan Ye, David J Tester, Wei Zhou, et al.
Heart Rhythm O2|October 20, 2021
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndromeJohn R Giudicessi, Joseph J Maleszewski, David J Tester, et al.
International Journal of Cardiology|September 17, 2018
Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapseJohn R Giudicessi, Ram K Rohatgi, Johan M Bos, et al.
Mayo Clinic Proceedings|August 19, 2022
Outcomes of Athletes With Genetic Heart Diseases and Implantable Cardioverter-Defibrillators Who Chose to Return to PlayKathryn E Tobert, J Martijn Bos, Bryan C Cannon, et al.
Heart Rhythm|May 4, 2018
Beyond the length and look of repolarization: Defining the non-QTc electrocardiographic profiles of patients with congenital long QT syndromeConor M Lane, J Martijn Bos, Ram K Rohatgi, et al.
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