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The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
Makita N, Behr E, Shimizu W, Horie M, Sunami A, Crotti L, Schulze-Bahr E, Fukuhara S, Mochizuki N, Makiyama T, Itoh H, Christiansen M, McKeown P, Miyamoto K, Kamakura S, Tsutsui H, Schwartz PJ, George AL Jr, Roden DM. Makita N, et al. Among authors: miyamoto k. J Clin Invest. 2008 Jun;118(6):2219-29. doi: 10.1172/JCI34057. J Clin Invest. 2008. PMID: 18451998 Free PMC article.
Significance of non-type 1 anterior early repolarization in patients with inferolateral early repolarization syndrome.
Kamakura T, Kawata H, Nakajima I, Yamada Y, Miyamoto K, Okamura H, Noda T, Satomi K, Aiba T, Takaki H, Aihara N, Kamakura S, Kimura T, Shimizu W. Kamakura T, et al. Among authors: miyamoto k. J Am Coll Cardiol. 2013 Oct 22;62(17):1610-8. doi: 10.1016/j.jacc.2013.05.081. Epub 2013 Jul 10. J Am Coll Cardiol. 2013. PMID: 23850930 Free article.
Electrocardiographic predictors of response to cardiac resynchronization therapy in patients with intraventricular conduction delay.
Takaya Y, Noda T, Nakajima I, Yamada Y, Miyamoto K, Okamura H, Satomi K, Aiba T, Kusano KF, Kanzaki H, Anzai T, Ishihara M, Yasuda S, Ogawa H, Kamakura S, Shimizu W. Takaya Y, et al. Among authors: miyamoto k. Circ J. 2014;78(1):71-7. doi: 10.1253/circj.cj-12-1569. Epub 2013 Oct 25. Circ J. 2014. PMID: 24162927 Free article. Clinical Trial.
Risk stratification in patients with Brugada syndrome without previous cardiac arrest – prognostic value of combined risk factors.
Okamura H, Kamakura T, Morita H, Tokioka K, Nakajima I, Wada M, Ishibashi K, Miyamoto K, Noda T, Aiba T, Nishii N, Nagase S, Shimizu W, Yasuda S, Ogawa H, Kamakura S, Ito H, Ohe T, Kusano KF. Okamura H, et al. Among authors: miyamoto k. Circ J. 2015;79(2):310-7. doi: 10.1253/circj.CJ-14-1059. Epub 2014 Nov 26. Circ J. 2015. PMID: 25428522 Free article. Clinical Trial.
3,558 results