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Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 8, 2005
The role of genotyping in diagnosing cardiac channelopathies : progress to dateG Michael Vincent, Li ZhangCirculation|June 20, 2007
Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndromeQiuming Gong, Li Zhang, G Michael Vincent, et al.Seminars in Pediatric Neurology|June 3, 2005
The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death in children and young adultsG Michael VincentPacing and Clinical Electrophysiology : PACE|July 16, 2009
Sudden cardiac arrest in the young due to inherited arrhythmias: the importance of family careG Michael VincentHeart Rhythm|March 23, 2011
Nonsense-mediated mRNA decay caused by a frameshift mutation in a large kindred of type 2 long QT syndromeIgnatius Gerardo Zarraga, Li Zhang, Matthew R Stump, et al.Journal of the American College of Cardiology|July 10, 2003
Modulating effects of age and gender on the clinical course of long QT syndrome by genotypeWojciech Zareba, Arthur J Moss, Emanuela H Locati, et al.BMC Medical Genetics|September 24, 2008
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutationsXianqin Zhang, Shenghan Chen, Li Zhang, et al.Journal of Molecular and Cellular Cardiology|February 15, 2008
A splice site mutation in hERG leads to cryptic splicing in human long QT syndromeQiuming Gong, Li Zhang, Arthur J Moss, et al.Neonatology|January 11, 2024
International Cohort of Neonatal Timothy SyndromeAlexandra Matthews, Katherine Timothy, Andy Golden, et al.Journal of the American College of Cardiology|September 5, 2006
Corrected QT variability in serial electrocardiograms in long QT syndrome: the importance of the maximum corrected QT for risk stratificationIlan Goldenberg, Jehu Mathew, Arthur J Moss, et al.Pageof 2,227