Works by Horie, Minoru


Results: 157
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    Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome.

    Published in:
    EP: Europace, 2023, v. 25, n. 4, p. 1491, doi. 10.1093/europace/euac269
    By:
    • Aizawa, Takanori;
    • Wada, Yuko;
    • Hasegawa, Kanae;
    • Huang, Hai;
    • Imamura, Tomohiko;
    • Gao, Jingshan;
    • Kashiwa, Asami;
    • Kohjitani, Hirohiko;
    • Fukuyama, Megumi;
    • Kato, Koichi;
    • Kato, Eri Toda;
    • Hisamatsu, Takashi;
    • Ohno, Seiko;
    • Makiyama, Takeru;
    • Kimura, Takeshi;
    • Horie, Minoru
    Publication type:
    Article
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    Author reply.

    Published in:
    EP: Europace, 2014, v. 16, n. 12, p. 1864, doi. 10.1093/europace/euu061
    By:
    • Ohno, Seiko;
    • Horie, Minoru
    Publication type:
    Article
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    Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.

    Published in:
    2013
    By:
    • Priori, Silvia G;
    • Wilde, Arthur A;
    • Horie, Minoru;
    • Cho, Yongkeun;
    • Behr, Elijah R;
    • Berul, Charles;
    • Blom, Nico;
    • Brugada, Josep;
    • Chiang, Chern-En;
    • Huikuri, Heikki;
    • Kannankeril, Prince;
    • Krahn, Andrew;
    • Leenhardt, Antoine;
    • Moss, Arthur;
    • Schwartz, Peter J;
    • Shimizu, Wataru;
    • Tomaselli, Gordon;
    • Tracy, Cynthia;
    • Ackerman, Michael;
    • Belhassen, Bernard
    Publication type:
    Journal Article
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    Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.

    Published in:
    EP: Europace, 2013, v. 15, n. 10, p. 1389
    By:
    • Priori, Silvia G.;
    • Wilde, Arthur A.;
    • Horie, Minoru;
    • Cho, Yongkeun;
    • Behr, Elijah R.;
    • Berul, Charles;
    • Blom, Nico;
    • Brugada, Josep;
    • Chiang, Chern-En;
    • Huikuri, Heikki;
    • Kannankeril, Prince;
    • Krahn, Andrew;
    • Leenhardt, Antoine;
    • Moss, Arthur;
    • Schwartz, Peter J.;
    • Shimizu, Wataru;
    • Tomaselli, Gordon;
    • Tracy, Cynthia;
    • Ackerman, Michael;
    • Belhassen, Bernard
    Publication type:
    Article
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    Gain-of-Function KCNH2 Mutations in Patients with Brugada Syndrome.

    Published in:
    Journal of Cardiovascular Electrophysiology, 2014, v. 25, n. 5, p. 522, doi. 10.1111/jce.12361
    By:
    • WANG, QI;
    • OHNO, SEIKO;
    • DING, WEI‐GUANG;
    • FUKUYAMA, MEGUMI;
    • MIYAMOTO, AKASHI;
    • ITOH, HIDEKI;
    • MAKIYAMA, TAKERU;
    • WU, JIE;
    • BAI, JIAYU;
    • HASEGAWA, KANAE;
    • SHINOHARA, TETSUJI;
    • TAKAHASHI, NAOHIKO;
    • SHIMIZU, AKIHIKO;
    • MATSUURA, HIROSHI;
    • HORIE, MINORU
    Publication type:
    Article
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    Clinical efficacy of thrombus aspiration on 5-year clinical outcomes in patients with ST-segment elevation acute myocardial infarction undergoing percutaneous coronary intervention.

    Published in:
    2015
    By:
    • Watanabe, Hiroki;
    • Shiomi, Hiroki;
    • Nakatsuma, Kenji;
    • Morimoto, Takeshi;
    • Taniguchi, Tomohiko;
    • Furukawa, Yutaka;
    • Nakagawa, Yoshihisa;
    • Horie, Minoru;
    • Kimura, Takeshi;
    • Sakata, Ryuzo;
    • Marui, Akira;
    • Matsuda, Mitsuo;
    • Mitsuoka, Hirokazu;
    • Onoe, Masahiko;
    • Yamanaka, Kazuo;
    • Fujiwara, Hisayoshi;
    • Takatsu, Yoshiki;
    • Ohno, Nobuhisa;
    • Nohara, Ryuji;
    • Murakami, Tomoyuki
    Publication type:
    journal article
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    Identification of transmembrane protein 168 mutation in familial Brugada syndrome.

    Published in:
    FASEB Journal, 2020, v. 34, n. 5, p. 6399, doi. 10.1096/fj.201902991R
    By:
    • Shimizu, Akio;
    • Zankov, Dimitar P.;
    • Sato, Akira;
    • Komeno, Masahiro;
    • Toyoda, Futoshi;
    • Yamazaki, Satoru;
    • Makita, Toshinori;
    • Noda, Taichi;
    • Ikawa, Masahito;
    • Asano, Yoshihiro;
    • Miyashita, Yohei;
    • Takashima, Seiji;
    • Morita, Hiroshi;
    • Ishikawa, Taisuke;
    • Makita, Naomasa;
    • Hitosugi, Masahito;
    • Matsuura, Hiroshi;
    • Ohno, Seiko;
    • Horie, Minoru;
    • Ogita, Hisakazu
    Publication type:
    Article
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    Novel KCNQ1 Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents.

    Published in:
    Frontiers in Physiology, 2024, p. 1, doi. 10.3389/fphys.2024.1401822
    By:
    • Tadashi Nakajima;
    • Shuntaro Tamura;
    • Kawabata-Iwakawa, Reika;
    • Hideki Itoh;
    • Hiroshi Hasegawa;
    • Takashi Kobari;
    • Shun Harasawa;
    • Akiko Sekine;
    • Masahiko Nishiyama;
    • Masahiko Kurabayashi;
    • Keiji Imoto;
    • Yoshiaki Kaneko;
    • Yosuke Nakatani;
    • Minoru Horie;
    • Hideki Ishii
    Publication type:
    Article
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