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Circulation|April 23, 2008
Long-QT syndrome after age 40Ilan Goldenberg, Arthur J Moss, James Bradley, et al.Circulation. Heart Failure|September 14, 2010
Ventricular remodeling and survival are more favorable for myocarditis than for idiopathic dilated cardiomyopathy in childhood: an outcomes study from the Pediatric Cardiomyopathy RegistrySusan R Foerster, Charles E Canter, Amy Cinar, et al.Cancer|August 19, 2021
Cardiac remodeling after anthracycline and radiotherapy exposure in adult survivors of childhood cancer: A report from the St Jude Lifetime Cohort StudyJohn L Jefferies, Wojciech M Mazur, Carrie R Howell, et al.Circulation|January 11, 2000
Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypesL Zhang, K W Timothy, G M Vincent, et al.Journal of the American College of Cardiology|November 21, 2009
Genotype-phenotype aspects of type 2 long QT syndromeWataru Shimizu, Arthur J Moss, Arthur A M Wilde, et al.Journal of the American College of Cardiology|January 24, 2007
Long QT syndrome in adultsAndrew J Sauer, Arthur J Moss, Scott McNitt, et al.JAMA Cardiology|February 28, 2017
The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet StudyCarolyn Y Ho, Sharlene M Day, Steven D Colan, et al.Circulation|June 9, 2004
Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseasesBarry J Maron, Bernard R Chaitman, Michael J Ackerman, et al.Circulation|September 8, 2005
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in childrenZhao Yang, Colin J McMahon, Liana R Smith, et al.Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.Pageof 44