D85N, a KCNE1 Polymorphism, Is a Disease-Causing Gene Variant in Long QT Syndrome
Nishio, Yukiko, MD, Makiyama, Takeru, MD, PhD, Itoh, Hideki, MD, PhD, Sakaguchi, Tomoko, MD, PhD, Ohno, Seiko, MD, PhD, Gong, Yin-Zhi, MD, PhD, Yamamoto, Satoshi, MD, Ozawa, Tomoya, MD, PhD, Ding, Wei-Guang, MD, PhD, Toyoda, Futoshi, PhD, Kawamura, Mihoko, MD, Akao, Masaharu, MD, PhD, Matsuura, Hiroshi, MD, PhD, Kimura, Takeshi, MD, PhD, Kita, Toru, MD, PhD, Horie, Minoru, MD, PhD
Published in Journal of the American College of Cardiology (25.08.2009)
Published in Journal of the American College of Cardiology (25.08.2009)
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A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation
Makiyama, Takeru, MD, PhD, Akao, Masaharu, MD, PhD, Shizuta, Satoshi, MD, Doi, Takahiro, MD, Nishiyama, Kei, MD, Oka, Yuko, MD, Ohno, Seiko, MD, PhD, Nishio, Yukiko, MD, Tsuji, Keiko, MS, Itoh, Hideki, MD, PhD, Kimura, Takeshi, MD, PhD, Kita, Toru, MD, PhD, Horie, Minoru, MD, PhD
Published in Journal of the American College of Cardiology (14.10.2008)
Published in Journal of the American College of Cardiology (14.10.2008)
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Journal Article
Autotaxin, Pruritus and Primary Biliary Cholangitis (PBC)
Sun, Ying, Zhang, Weici, Evans, Jilly F, Floreani, Annarosa, Zou, Zhengsheng, Nishio, Yukiko, Qi, Ruizhao, Leung, Patrick S.C, Bowlus, Christopher L, Gershwin, M. Eric
Published in Autoimmunity reviews (01.08.2016)
Published in Autoimmunity reviews (01.08.2016)
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Journal Article
Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT Syndrome
Itoh, Hideki, Sakaguchi, Tomoko, Ding, Wei-Guang, Watanabe, Eiichi, Watanabe, Ichiro, Nishio, Yukiko, Makiyama, Takeru, Ohno, Seiko, Akao, Masaharu, Higashi, Yukei, Zenda, Naoko, Kubota, Tomoki, Mori, Chikara, Okajima, Katsunori, Haruna, Tetsuya, Miyamoto, Akashi, Kawamura, Mihoko, Ishida, Katsuya, Nagaoka, Iori, Oka, Yuko, Nakazawa, Yuko, Yao, Takenori, Jo, Hikari, Sugimoto, Yoshihisa, Ashihara, Takashi, Hayashi, Hideki, Ito, Makoto, Imoto, Keiji, Matsuura, Hiroshi, Horie, Minoru
Published in Circulation. Arrhythmia and electrophysiology (01.10.2009)
Published in Circulation. Arrhythmia and electrophysiology (01.10.2009)
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Mutation Analysis of the Glycerol-3 Phosphate Dehydrogenase-1 Like (GPD1L) Gene in Japanese Patients With Brugada Syndrome
Makiyama, Takeru, Akao, Masaharu, Haruna, Yoshisumi, Tsuji, Keiko, Doi, Takahiro, Ohno, Seiko, Nishio, Yukiko, Kita, Toru, Horie, Minoru
Published in Circulation Journal (2008)
Published in Circulation Journal (2008)
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Atrioventricular Block-Induced Torsades de Pointes With Clinical and Molecular Backgrounds Similar to Congenital Long QT Syndrome
Oka, Yuko, Itoh, Hideki, Ding, Wei-Guang, Shimizu, Wataru, Makiyama, Takeru, Ohno, Seiko, Nishio, Yukiko, Sakaguchi, Tomoko, Miyamoto, Akashi, Kawamura, Mihoko, Matsuura, Hiroshi, Horie, Minoru
Published in Circulation Journal (2010)
Published in Circulation Journal (2010)
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Measurements of baseline and follow-up concentrations of cardiac troponin-T and brain natriuretic peptide in patients with heart failure from various etiologies
Taniguchi, Ryoji, Sato, Yukihito, Nishio, Yukiko, Kimura, Takeshi, Kita, Toru
Published in Heart and vessels (01.11.2006)
Published in Heart and vessels (01.11.2006)
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Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia
Kawamura, Mihoko, Nagaoka, Iori, Dohchi, Kenichi, Nishio, Yukiko, Itoh, Hideki, Kimura, Hiromi, Miyamoto, Akashi, Mizusawa, Yuka, Jito, Yuko, Ishida, Katsuya, Ito, Makoto, Makiyama, Takeru, Ohno, Seiko, Sumitomo, Naokata, Oyama, Kotaro, Horie, Minoru
Published in Journal of arrhythmia (2011)
Published in Journal of arrhythmia (2011)
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Investigating Lifestyle Changes to Improve Metabolic Syndrome in Thorough Health Check-up Examinees
Yoshioka, Takayuki, Yamadori, Takako, Nishio, Yukiko, Inoue, Tugumi, Matsuda, Kouhei, Yoshida, Kimihisa, Inoue, Nobutaka
Published in Official Journal of Japan Society of Ningen Dock (2019)
Published in Official Journal of Japan Society of Ningen Dock (2019)
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Journal Article
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents
HATTORI, Tetsuhisa, MAKIYAMA, Takeru, KITA, Toru, HORIE, Minoru, KIMURA, Takeshi, AKAO, Masaharu, EHARA, Eiji, OHNO, Seiko, IGUCHI, Moritake, NISHIO, Yukiko, SASAKI, Kenichi, ITOH, Hideki, YOKODE, Masayuki
Published in Cardiovascular research (15.03.2012)
Published in Cardiovascular research (15.03.2012)
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Journal Article
Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia
Kawamura, Mihoko, Nagaoka, Iori, Dohchi, Kenichi, Nishio, Yukiko, Itoh, Hideki, Kimura, Hiromi, Miyamoto, Akashi, Mizusawa, Yuka, Jito, Yuko, Ishida, Katsuya, Ito, Makoto, Makiyama, Takeru, Ohno, Seiko, Sumitomo, Naokata, Oyama, Kotaro, Horie, Minoru
Published in Japanese Journal of Electrocardiology (2010)
Published in Japanese Journal of Electrocardiology (2010)
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Malignant link between chronic heart failure and acute cardiac decompensation in patients with persistently increased serum concentrations of cardiac troponin
Sato, Yukihito, Kuwabara, Yasuhide, Taniguchi, Ryoji, Nishio, Yukiko, Miyamoto, Tadashi, Fujiwara, Hisayoshi, Takatsu, Yoshiki
Published in International journal of cardiology (23.05.2008)
Published in International journal of cardiology (23.05.2008)
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Journal Article
Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome
Haruna, Yoshisumi, Kobori, Atsushi, Makiyama, Takeru, Yoshida, Hidetada, Akao, Masaharu, Doi, Takahiro, Tsuji, Keiko, Ono, Seiko, Nishio, Yukiko, Shimizu, Wataru, Inoue, Takehiko, Murakami, Tomoaki, Tsuboi, Naoya, Yamanouchi, Hideo, Ushinohama, Hiroya, Nakamura, Yoshihide, Yoshinaga, Masao, Horigome, Hitoshi, Aizawa, Yoshifusa, Kita, Toru, Horie, Minoru
Published in Human mutation (01.02.2007)
Published in Human mutation (01.02.2007)
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Complex myxoma detected by syncope: a case report
Ejima, Koichiro, Uchida, Tatsuro, Hen, Yasuki, Nishio, Yukiko, Nomoto, Fumiko, Uchida, Yoshie, Mun, Jebon, Satoh, Takahiro, Fujimori, Kanichi, Tanino, Shunsuke, Hirosawa, Koshichiro, Agematsu, Kota, Nanaumi, Miwa, Sugimoto, Koichi, Koizumi, Junichi, Ohkado, Akihiko, Shiikawa, Akira
Published in Journal of cardiology (01.02.2003)
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Published in Journal of cardiology (01.02.2003)
Journal Article
Prognostic utility of T-wave alternans in a real-world population of patients with left ventricular dysfunction: the PREVENT-SCD study
Shizuta, Satoshi, Ando, Kenji, Nobuyoshi, Masakiyo, Ikeda, Takanori, Yoshino, Hideaki, Hiramatsu, Shinichi, Kazatani, Yukio, Yamashiro, Kohei, Okajima, Katsunori, Kajiya, Teishi, Kobayashi, Yoshinori, Kato, Takao, Fujii, Satoki, Mitsudo, Kazuaki, Inoue, Koichi, Ito, Hiroshi, Haruna, Yoshisumi, Doi, Takahiro, Nishio, Yukiko, Ozasa, Neiko, Nishiyama, Kei, Kita, Toru, Morimoto, Takeshi, Kimura, Takeshi
Published in Clinical research in cardiology (01.02.2012)
Published in Clinical research in cardiology (01.02.2012)
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Journal Article
Malignant Acanthosis Nigricans with Enhanced Expression of Fibroblast Growth Factor Receptor 3
HIDA, Yasutoshi, KUBO, Yoshiaki, NISHIO, Yukiko, MURAKAMI, Shinji, FUKUMOTO, Daisuke, SAYAMA, Koji, HASHIMOTO, Koji, ARASE, Seiji
Published in Acta dermato-venereologica (2009)
Published in Acta dermato-venereologica (2009)
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Journal Article
Abstract 1523: A Novel SCN5A Gain-of-Function Mutation M1875T Associated with Familial Atrial Fibrillation
Makiyama, Takeru, Akao, Masaharu, Shizuta, Satoshi, Doi, Takahiro, Nishiyama, Kei, Yuko, Oka, Nishio, Yukiko, Tsuji, Keiko, Itoh, Hideki, Kimura, Takeshi, Kita, Toru, Horie, Minoru
Published in Circulation (New York, N.Y.) (28.10.2008)
Published in Circulation (New York, N.Y.) (28.10.2008)
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