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Page 1
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: dochi 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.
Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan.
Kawamura M, Ohno S, Naiki N, Nagaoka I, Dochi K, Wang Q, Hasegawa K, Kimura H, Miyamoto A, Mizusawa Y, Itoh H, Makiyama T, Sumitomo N, Ushinohama H, Oyama K, Murakoshi N, Aonuma K, Horigome H, Honda T, Yoshinaga M, Ito M, Horie M. Kawamura M, et al. Among authors: dochi k. Circ J. 2013;77(7):1705-13. doi: 10.1253/circj.cj-12-1460. Epub 2013 Apr 18. Circ J. 2013. PMID: 23595086 Free article. Clinical Trial.
Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan.
Kawamura M, Ohno S, Naiki N, Nagaoka I, Dochi K, Wang Q, Hasegawa K, Kimura H, Miyamoto A, Mizusawa Y, Itoh H, Makiyama T, Sumitomo N, Ushinohama H, Oyama K, Murakoshi N, Aonuma K, Horigome H, Honda T, Yoshinaga M, Ito M, Horie M. Kawamura M, et al. Among authors: dochi k. Circ J. 2020;84(11):2124-2126. doi: 10.1253/circj.CJ-66-0186. Circ J. 2020. PMID: 33100286 Free article. No abstract available.
11 results