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A molecular mechanism for adrenergic-induced long QT syndrome.
Wu J, Naiki N, Ding WG, Ohno S, Kato K, Zang WJ, Delisle BP, Matsuura H, Horie M. Wu J, et al. Among authors: kato k. J Am Coll Cardiol. 2014 Mar 4;63(8):819-27. doi: 10.1016/j.jacc.2013.08.1648. Epub 2013 Oct 30. J Am Coll Cardiol. 2014. PMID: 24184248 Free article.
A Common Mutation of Long QT Syndrome Type 1 in Japan.
Itoh H, Dochi K, Shimizu W, Denjoy I, Ohno S, Aiba T, Kimura H, Kato K, Fukuyama M, Hasagawa K, Schulze-Bahr E, Guicheney P, Horie M. Itoh H, et al. Among authors: kato k. Circ J. 2015;79(9):2026-30. doi: 10.1253/circj.CJ-15-0342. Epub 2015 Jun 29. Circ J. 2015. PMID: 26118460 Free article. Clinical Trial.
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family.
Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Kimura H, Itoh H, Hayashi H, Horie M. Ichikawa M, et al. Among authors: kato k. Intern Med. 2016;55(3):259-62. doi: 10.2169/internalmedicine.55.6014. Epub 2016 Feb 1. Intern Med. 2016. PMID: 26831020 Free article.
Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry.
Nakajima K, Aiba T, Makiyama T, Nishiuchi S, Ohno S, Kato K, Yamamoto Y, Doi T, Shizuta S, Onoue K, Yagihara N, Ishikawa T, Watanabe I, Kawakami H, Oginosawa Y, Murakoshi N, Nogami A, Aonuma K, Saito Y, Kimura T, Yasuda S, Makita N, Shimizu W, Horie M, Kusano K. Nakajima K, et al. Among authors: kato k. Circ J. 2018 Oct 25;82(11):2707-2714. doi: 10.1253/circj.CJ-18-0339. Epub 2018 Aug 4. Circ J. 2018. PMID: 30078822 Free article. Clinical Trial.
9,659 results