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Identification of transmembrane protein 168 mutation in familial Brugada syndrome.
Shimizu A, Zankov DP, Sato A, Komeno M, Toyoda F, Yamazaki S, Makita T, Noda T, Ikawa M, Asano Y, Miyashita Y, Takashima S, Morita H, Ishikawa T, Makita N, Hitosugi M, Matsuura H, Ohno S, Horie M, Ogita H. Shimizu A, et al. Among authors: ishikawa t. FASEB J. 2020 May;34(5):6399-6417. doi: 10.1096/fj.201902991R. Epub 2020 Mar 16. FASEB J. 2020. PMID: 32175648
Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization.
Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Makiyama T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Kimura A, Maemura K, Watanabe I, Kamakura S, Horie M, Aizawa Y, Shimizu W, Makita N. Watanabe H, et al. Among authors: ishikawa t. Circ Arrhythm Electrophysiol. 2011 Dec;4(6):874-81. doi: 10.1161/CIRCEP.111.963983. Epub 2011 Oct 25. Circ Arrhythm Electrophysiol. 2011. PMID: 22028457
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.
Ishikawa T, Sato A, Marcou CA, Tester DJ, Ackerman MJ, Crotti L, Schwartz PJ, On YK, Park JE, Nakamura K, Hiraoka M, Nakazawa K, Sakurada H, Arimura T, Makita N, Kimura A. Ishikawa T, et al. Circ Arrhythm Electrophysiol. 2012 Dec;5(6):1098-107. doi: 10.1161/CIRCEP.111.969972. Epub 2012 Oct 12. Circ Arrhythm Electrophysiol. 2012. PMID: 23064965
Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.
Abe K, Machida T, Sumitomo N, Yamamoto H, Ohkubo K, Watanabe I, Makiyama T, Fukae S, Kohno M, Harrell DT, Ishikawa T, Tsuji Y, Nogami A, Watabe T, Oginosawa Y, Abe H, Maemura K, Motomura H, Makita N. Abe K, et al. Among authors: ishikawa t. Circ Arrhythm Electrophysiol. 2014 Jun;7(3):511-7. doi: 10.1161/CIRCEP.113.001340. Epub 2014 Apr 24. Circ Arrhythm Electrophysiol. 2014. PMID: 24762805 Free article.
Inherited bradyarrhythmia: A diverse genetic background.
Ishikawa T, Tsuji Y, Makita N. Ishikawa T, et al. J Arrhythm. 2016 Oct;32(5):352-358. doi: 10.1016/j.joa.2015.09.009. Epub 2015 Nov 19. J Arrhythm. 2016. PMID: 27761158 Free PMC article. Review.
Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.
Ishikawa T, Ohno S, Murakami T, Yoshida K, Mishima H, Fukuoka T, Kimoto H, Sakamoto R, Ohkusa T, Aiba T, Nogami A, Sumitomo N, Shimizu W, Yoshiura KI, Horigome H, Horie M, Makita N. Ishikawa T, et al. Heart Rhythm. 2017 May;14(5):717-724. doi: 10.1016/j.hrthm.2017.01.020. Epub 2017 Jan 17. Heart Rhythm. 2017. PMID: 28104484
7,639 results