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Heart Rhythm|February 6, 2007
Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3Lisa B Cronk, Bin Ye, Toshihiko Kaku, et al.
Mayo Clinic Proceedings|May 6, 2014
Characterization of a phenotype-based genetic test prediction score for unrelated patients with hypertrophic cardiomyopathyJ Martijn Bos, Melissa L Will, Bernard J Gersh, et al.
Congenital Heart Disease|October 26, 2012
Subclinical cardiomyopathy and long QT syndrome: an echocardiographic observationKristina H Haugaa, Jonathan N Johnson, J Martijn Bos, et al.
The Journal of Biological Chemistry|July 21, 2012
A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillationMichelle S Parvatiyar, Andrew P Landstrom, Cicero Figueiredo-Freitas, et al.
Heart Rhythm|September 19, 2021
Role of chronic continuous intravenous lidocaine in the clinical management of patients with malignant type 3 long QT syndromeSahej Bains, Adi Lador, Raquel Neves, et al.
Autonomic Neuroscience : Basic & Clinical|December 26, 2013
Sympathetic nerve activity and simulated diving in healthy humansAbu Shamsuzzaman, Michael J Ackerman, Fatima Sert Kuniyoshi, et al.
Circulation. Arrhythmia and Electrophysiology|April 23, 2019
Mexiletine Shortens the QT Interval in Patients With Potassium Channel-Mediated Type 2 Long QT SyndromeJ Martijn Bos, Lia Crotti, Ram K Rohatgi, et al.
Molecular Genetics and Metabolism|October 21, 2005
Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathyVlad C Vasile, Melissa L Will, Steve R Ommen, et al.
European Heart Journal. Cardiovascular Imaging|November 13, 2013
Deformation patterns in genotyped patients with hypertrophic cardiomyopathyJeffrey B Geske, J Martijn Bos, Bernard J Gersh, et al.
American Heart Journal|June 3, 2008
Relationship between sex, shape, and substrate in hypertrophic cardiomyopathyJ Martijn Bos, Jeanne L Theis, A Jamil Tajik, et al.
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