Hasil Pencarian - Naomasa Makita, MD, PhD

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  1. 1
    Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias

    Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias oleh Yukiomi Tsuji, MD, PhD, Taisuke Ishikawa, DVM, PhD, Naomasa Makita, MD, PhD

    Diterbitkan 2014-08-01
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  2. 2
    Inherited bradyarrhythmia: A diverse genetic background

    Inherited bradyarrhythmia: A diverse genetic background oleh Taisuke Ishikawa, DVM, PhD, Yukiomi Tsuji, MD, PhD, Naomasa Makita, MD, PhD

    Diterbitkan 2016-10-01
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  3. 3
    A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest

    A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest oleh Kazuhiro Takahashi, MD, PhD, Taisuke Ishikawa, DVM, PhD, Naomasa Makita, MD, PhD, Kiyotaka Takefuta, MD, Taisuke Nabeshima, MD, Mami Nakayashiro, MD

    Diterbitkan 2017-01-01
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  4. 4
    Progressive atrial myocardial fibrosis in a 4-year-old girl with atrial standstill associated with an SCN5A gene mutation

    Progressive atrial myocardial fibrosis in a 4-year-old girl with atrial standstill associated with an SCN5A gene mutation oleh Yoshiaki Kato, MD, PhD, Yoshihiro Nozaki, MD, PhD, Miho Takahashi-Igari, MD, Masato Sugano, MD, Naomasa Makita, MD, PhD, Hitoshi Horigome, MD, PhD

    Diterbitkan 2022-09-01
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  5. 5
    Normal dose of pilsicainide showed marked negative inotropic effects in a patient who had no underlying heart disease

    Normal dose of pilsicainide showed marked negative inotropic effects in a patient who had no underlying heart disease oleh Masayoshi Yoshida, MD, Shin-ichi Ando, MD, PhD, Akiko Chishaki, MD, PhD, Naomasa Makita, MD, PhD, Yoshiyuki Hasegawa, MD, PhD, Sumito Narita, MD, Hidetoshi Momii, MD, PhD, Toshiaki Kadokami, MD, PhD

    Diterbitkan 2014-02-01
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  6. 6
    A rare KCNE1 polymorphism, D85N, as a genetic modifier of long QT syndrome

    A rare KCNE1 polymorphism, D85N, as a genetic modifier of long QT syndrome oleh Kanae Hasegawa, MD, Seiko Ohno, MD, PhD, Hideki Itoh, MD, PhD, Takeru Makiyama, MD, PhD, Takeshi Aiba, MD, PhD, Yasutaka Nakano, MD, PhD, Wataru Shimizu, MD, PhD, Hiroshi Matsuura, MD, PhD, Naomasa Makita, MD, PhD, Minoru Horie, MD, PhD

    Diterbitkan 2014-06-01
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  7. 7
    Variable phenotype expression with a frameshift mutation of the cardiac sodium channel gene SCN5A

    Variable phenotype expression with a frameshift mutation of the cardiac sodium channel gene SCN5A oleh Hiroshi Kawakami, MD, Takeshi Aiba, MD, PhD, Tadakatsu Yamada, MD, PhD, Hideki Okayama, MD, PhD, Yukio Kazatani, MD, PhD, Kyoko Konishi, MD, PhD, Ikutaro Nakajima, MD, Koji Miyamoto, MD, Yuko Yamada, MD, Hideo Okamura, MD, Takashi Noda, MD, PhD, Kazuhiro Satomi, MD, PhD, Shiro Kamakura, MD, PhD, Naomasa Makita, MD, PhD, Wataru Shimizu, MD, PhD

    Diterbitkan 2013-10-01
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