Výsledky vyhledávání - Takeru Makiyama

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  1. 1
    Clinical Impact of Left Ventricular Outflow Tract Obstruction in Takotsubo Cardiomyopathy

    Clinical Impact of Left Ventricular Outflow Tract Obstruction in Takotsubo Cardiomyopathy Autor Tetsuma Kawaji, Hiroki Shiomi, Takeshi Morimoto, Junichi Tazaki, Masao Imai, Naritatsu Saito, Takeru Makiyama, Satoshi Shizuta, Koh Ono, Takeshi Kimura

    Vydáno 2015
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  2. 2
    Persistently Increased Serum Concentrations of Cardiac Troponin T in Patients With Idiopathic Dilated Cardiomyopathy Are Predictive of Adverse Outcomes

    Persistently Increased Serum Concentrations of Cardiac Troponin T in Patients With Idiopathic Dilated Cardiomyopathy Are Predictive of Adverse Outcomes Autor Yukihito Sato, Tasuku Yamada, Ryoji Taniguchi, Kozo Nagai, Takeru Makiyama, Hideshi Okada, Kazuaki Kataoka, Haruyasu Ito, Akira Matsumori, Shigetake Sasayama, Yoshiki Takatsu

    Vydáno 2001
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  3. 3
    Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5

    Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5 Autor Taisuke Ishikawa, Naohiko Takahashi, Seiko Ohno, Harumizu Sakurada, Kazufumi Nakamura, Young Keun On, Jeong Euy Park, Takeru Makiyama, Minoru Horie, Takuro Arimura, Naomasa Makita, Akinori Kimura

    Vydáno 2012
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  4. 4
    Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

    Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes Autor Megumi Fukuyama, Qi Wang, Koichi Kato, Seiko Ohno, Wei‐Guang Ding, Futoshi Toyoda, Hideki Itoh, Hiromi Kimura, Takeru Makiyama, Makoto Ito, Hiroshi Matsuura, Minoru Horie

    Vydáno 2014
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  5. 5
    Ultrastructural Maturation of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes in a Long-Term Culture

    Ultrastructural Maturation of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes in a Long-Term Culture Autor Tsukasa Kamakura, Takeru Makiyama, Kenichi Sasaki, Yoshinori Yoshida, Yimin Wuriyanghai, Jia‐Rong Chen, Tetsuhisa Hattori, Seiko Ohno, Toru Kita, Minoru Horie, Shinya Yamanaka, Takeshi Kimura

    Vydáno 2013
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  6. 6
    Impact of CYP2C19 Polymorphisms on the Antiplatelet Effect of Clopidogrel in an Actual Clinical Setting in Japan

    Impact of CYP2C19 Polymorphisms on the Antiplatelet Effect of Clopidogrel in an Actual Clinical Setting in Japan Autor Toshikazu Jinnai, Hisanori Horiuchi, Takeru Makiyama, Junichi Tazaki, Tomohisa Tada, Masaharu Akao, Koh Ono, Kozo Hoshino, Yumiko Naruse, Kanako Takahashi, Haruyo Watanabe, Toru Kita, Takeshi Kimura

    Vydáno 2009
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  7. 7
    A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation

    A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation Autor Takeru Makiyama, Masaharu Akao, Satoshi Shizuta, Takahiro Doi, Kei Nishiyama, Yuko Oka, Seiko Ohno, Yukiko Nishio, Keiko Tsuji, Hideki Itoh, Takeshi Kimura, Toru Kita, Minoru Horie

    Vydáno 2008
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  8. 8
    A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents

    A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents Autor Takashi Hattori, Takeru Makiyama, Masaharu Akao, Eiji Ehara, Seiko Ohno, Moritake Iguchi, Yoshihiko Nishio, Kazuki Sasaki, Hideki Itoh, Masataka Yokode, Toshiyuki Kita, Minoru Horie, Takeshi Kimura

    Vydáno 2011
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  9. 9
    High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations

    High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations Autor Takeru Makiyama, Masaharu Akao, Keiko Tsuji, Takahiro Doi, Seiko Ohno, Kotoe Takenaka, Atsushi Kobori, T. Ninomiya, Hidetada Yoshida, Makoto Takano, Naomasa Makita, Fumiko Yanagisawa, Yukei Higashi, Youichi Takeyama, Toru Kita, Minoru Horie

    Vydáno 2005
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  10. 10
    Non-missense variants of<i>KCNH2</i>show better outcomes in type 2 long QT syndrome

    Non-missense variants of<i>KCNH2</i>show better outcomes in type 2 long QT syndrome Autor Takanori Aizawa, Yuko Wada, Kanae Hasegawa, Hai Huang, Tomohiko Imamura, Jingshan Gao, Asami Kashiwa, Hirohiko Kohjitani, Megumi Fukuyama, Koichi Kato, Eri Kato, Takashi Hisamatsu, Seiko Ohno, Takeru Makiyama, Takeshi Kimura, Minoru Horie

    Vydáno 2023
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  11. 11
    D85N, a KCNE1 Polymorphism, Is a Disease-Causing Gene Variant in Long QT Syndrome

    D85N, a KCNE1 Polymorphism, Is a Disease-Causing Gene Variant in Long QT Syndrome Autor Yukiko Nishio, Takeru Makiyama, Hideki Itoh, Tomoko Sakaguchi, Seiko Ohno, Yin-Zhi Gong, Satoshi Yamamoto, Tomoya Ozawa, Wei‐Guang Ding, Futoshi Toyoda, Mihoko Kawamura, Masaharu Akao, Hiroshi Matsuura, Takeshi Kimura, Toru Kita, Minoru Horie

    Vydáno 2009
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  12. 12
    Long-Term Follow-Up of a Pediatric Cohort With Short QT Syndrome

    Long-Term Follow-Up of a Pediatric Cohort With Short QT Syndrome Autor Juan Villafañe, Joseph Atallah, Michael H. Gollob, Philippe Maury, Christian Wolpert, Roman Gebauer, Hiroshi Watanabe, Minoru Horie, Olli Anttonen, Prince J. Kannankeril, Brett Faulknier, J Bleiz, Takeru Makiyama, Wataru Shimizu, Robert M. Hamilton, Ming‐Lon Young

    Vydáno 2013
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  13. 13
    Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics

    Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics Autor Keisuke Abé, Taku Machida, Naokata Sumitomo, Hirokazu Yamamoto, Kimie Ohkubo, Ichiro Watanabe, Takeru Makiyama, Satoki Fukae, Masaki Kohno, Daniel Toshio Harrell, Taisuke Ishikawa, Yukiomi Tsuji, Akihiko Nogami, Taichi Watabe, Yasushi Oginosawa, Haruhiko Abe, Koji Maemura, Hideki Motomura, Naomasa Makita

    Vydáno 2014
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  14. 14
    Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation

    Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation Autor Yuta Yamamoto, Takeru Makiyama, Takeshi Harita, Kenichi Sasaki, Yimin Wuriyanghai, Mamoru Hayano, Suguru Nishiuchi, Hirohiko Kohjitani, Sayako Hirose, Jia‐Rong Chen, Fumika Yokoi, Taisuke Ishikawa, Seiko Ohno, Kazuhisa Chonabayashi, Hideki Motomura, Yoshinori Yoshida, Minoru Horie, Naomasa Makita, Takeshi Kimura

    Vydáno 2017
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  15. 15
    Genotype-phenotype correlations ofKCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome

    Genotype-phenotype correlations ofKCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome Autor Yoshisumi Haruna, Atsushi Kobori, Takeru Makiyama, Hidetada Yoshida, Masaharu Akao, Takahiro Doi, Keiko Tsuji, Seiko Ono, Yukiko Nishio, Wataru Shimizu, Takehiko Inoue, Tomoaki Murakami, Naoya Tsuboi, Hideo Yamanouchi, Hiroya Ushinohama, Yoshihide Nakamura, Masao Yoshinaga, Hitoshi Horigome, Yoshifusa Aizawa, Toru Kita, Minoru Horie

    Vydáno 2007
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  16. 16
    Phenotype Variability in Patients Carrying <i>KCNJ2</i> Mutations

    Phenotype Variability in Patients Carrying <i>KCNJ2</i> Mutations Autor Hiromi Kimura, Jun Zhou, Mihoko Kawamura, Hideki Itoh, Yuka Mizusawa, Wei‐Guang Ding, Jie Wu, Seiko Ohno, Takeru Makiyama, Akashi Miyamoto, Nobu Naiki, Qi Wang, Yu Xie, Tsugutoshi Suzuki, Shigeru Tateno, Yoshihide Nakamura, Wei‐Jin Zang, Makoto Ito, Hiroshi Matsuura, Minoru Horie

    Vydáno 2012
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  17. 17
    The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

    The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome Autor Naomasa Makita, Elijah R. Behr, Wataru Shimizu, Minoru Horie, Akihiko Sunami, Lia Crotti, Eric Schulze‐Bahr, Shigetomo Fukuhara, Naoki Mochizuki, Takeru Makiyama, Hideki Itoh, Michael Christiansen, Pascal McKeown, Koji Miyamoto, Shiro Kamakura, Hiroyuki Tsutsui, Peter J. Schwartz, Alfred L. George, Dan M. Roden

    Vydáno 2008
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  18. 18
    Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

    Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan Autor Mihoko Kawamura, Seiko Ohno, Nobu Naiki, Iori Nagaoka, Kenichi Dochi, Qi Wang, Kanae Hasegawa, Hiromi Kimura, Akashi Miyamoto, Yuka Mizusawa, Hideki Itoh, Takeru Makiyama, Naokata Sumitomo, Hiroya Ushinohama, Kotaro Oyama, Nobuyuki Murakoshi, Kazutaka Aonuma, Hitoshi Horigome, Takafumi Honda, Masao Yoshinaga, Makoto Ito, Minoru Horie

    Vydáno 2013
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  19. 19
    The genetics underlying acquired long QT syndrome: impact for genetic screening

    The genetics underlying acquired long QT syndrome: impact for genetic screening Autor Hideki Itoh, Lia Crotti, Takeshi Aiba, Carla Spazzolini, Isabelle Denjoy, Véronique Fressart, Kenshi Hayashi, Tadashi Nakajima, Seiko Ohno, Takeru Makiyama, Jie Wu, Kanae Hasegawa, Elisa Mastantuono, Federica Dagradi, Matteo Pedrazzini, Masakazu Yamagishi, Myriam Berthet, Yoshitaka Murakami, Wataru Shimizu, Pascale Guicheney, Peter J. Schwartz, Minoru Horie

    Vydáno 2015
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  20. 20
    Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia

    Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventric... Autor Kenichi Sasaki, Takeru Makiyama, Yoshinori Yoshida, Yimin Wuriyanghai, Tsukasa Kamakura, Suguru Nishiuchi, Mamoru Hayano, Takeshi Harita, Yuta Yamamoto, Hirohiko Kohjitani, Sayako Hirose, Jia‐Rong Chen, Mihoko Kawamura, Seiko Ohno, Hideki Itoh, Ayako Takeuchi, Satoshi Matsuoka, Masaru Miura, Naokata Sumitomo, Minoru Horie, Shinya Yamanaka, Takeshi Kimura

    Vydáno 2016
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