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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 10, 2024. (Total: 231322Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Torsades de Pointes and SCN5A[original query]
Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
Journal of the American College of Cardiology 2004 Mar 43 (5): 826-30.
Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P
Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes.
American heart journal 2006 Dec 152 (6): 1116-22.
Mank-Seymour Amy R, Richmond Jodi L, Wood Linda S, Reynolds Jennifer M, Fan Yu-Ti, Warnes Gregory R, Milos Patrice M, Thompson John
Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.
The Canadian journal of cardiology 2010 Apr 26 (4): 208-12.
Subbiah Rajesh N, Gollob Michael H, Gula Lorne J, Davies Robert W, Leong-Sit Peter, Skanes Allan C, Yee Raymond, Klein George J, Krahn Andrew
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.
Circulation. Arrhythmia and electrophysiology 2013 Aug .
Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW
Influence of Pregnancy in Patients With Congenital Long QT Syndrome.
Cardiology in review 2016 Mar .
Garg Lohit, Garg Jalaj, Krishnamoorthy Parasuram, Ahnert Amy, Shah Neeraj, Dusaj Raman S, Bozorgnia Bab
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