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Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia.
Jamshidi Y, Nolte IM, Dalageorgou C, Zheng D, Johnson T, Bastiaenen R, Ruddy S, Talbott D, Norris KJ, Snieder H, George AL, Marshall V, Shakir S, Kannankeril PJ, Munroe PB, Camm AJ, Jeffery S, Roden DM, Behr ER. Jamshidi Y, et al. Among authors: roden dm. J Am Coll Cardiol. 2012 Aug 28;60(9):841-50. doi: 10.1016/j.jacc.2012.03.031. Epub 2012 Jun 6. J Am Coll Cardiol. 2012. PMID: 22682551 Free PMC article.
Congenital and acquired long QT syndrome.
Camm AJ, Janse MJ, Roden DM, Rosen MR, Cinca J, Cobbe SM. Camm AJ, et al. Among authors: roden dm. Eur Heart J. 2000 Aug;21(15):1232-7. doi: 10.1053/euhj.2000.2222. Eur Heart J. 2000. PMID: 10924312 Review. No abstract available.
Novel Brugada SCN5A mutation causing sudden death in children.
Todd SJ, Campbell MJ, Roden DM, Kannankeril PJ. Todd SJ, et al. Among authors: roden dm. Heart Rhythm. 2005 May;2(5):540-3. doi: 10.1016/j.hrthm.2005.01.029. Heart Rhythm. 2005. PMID: 15840483 No abstract available.
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Among authors: roden dm. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
804 results