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American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
Communications Medicine|May 23, 2022
Implementation of a fully remote randomized clinical trial with cardiac monitoringJacob J Mayfield, Neal A Chatterjee, Peter A Noseworthy, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Circulation|August 28, 2016
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter StudyArthur A M Wilde, Arthur J Moss, Elizabeth S Kaufman, et al.
Heart Rhythm|December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndromeChristian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
Nature Genetics|July 3, 2007
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyBhaswati Pandit, Anna Sarkozy, Len A Pennacchio, et al.
Journal of the American College of Cardiology|March 19, 2013
Prevention of sudden cardiac death with implantable cardioverter-defibrillators in children and adolescents with hypertrophic cardiomyopathyBarry J Maron, Paolo Spirito, Michael J Ackerman, et al.
Gastroenterology|March 12, 2014
Loss-of-function of the voltage-gated sodium channel NaV1.5 (channelopathies) in patients with irritable bowel syndromeArthur Beyder, Amelia Mazzone, Peter R Strege, et al.
Mayo Clinic Proceedings|March 6, 2016
Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic ExperienceKonstantinos N Lazaridis, Kimberly A Schahl, Margot A Cousin, et al.
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