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Gain-of-function KCNH2 mutations in patients with Brugada syndrome.
Wang QI, Ohno S, Ding WG, Fukuyama M, Miyamoto A, Itoh H, Makiyama T, Wu J, Bai J, Hasegawa K, Shinohara T, Takahashi N, Shimizu A, Matsuura H, Horie M. Wang QI, et al. Among authors: fukuyama m. J Cardiovasc Electrophysiol. 2014 May;25(5):522-530. doi: 10.1111/jce.12361. Epub 2014 Jan 30. J Cardiovasc Electrophysiol. 2014. PMID: 24400717
Brugada syndrome in spinal and bulbar muscular atrophy.
Araki A, Katsuno M, Suzuki K, Banno H, Suga N, Hashizume A, Mano T, Hijikata Y, Nakatsuji H, Watanabe H, Yamamoto M, Makiyama T, Ohno S, Fukuyama M, Morimoto S, Horie M, Sobue G. Araki A, et al. Among authors: fukuyama m. Neurology. 2014 May 20;82(20):1813-21. doi: 10.1212/WNL.0000000000000434. Epub 2014 Apr 23. Neurology. 2014. PMID: 24759840
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: fukuyama m. 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: fukuyama m. Intern Med. 2016;55(3):259-62. doi: 10.2169/internalmedicine.55.6014. Epub 2016 Feb 1. Intern Med. 2016. PMID: 26831020 Free article.
301 results