An NGS-based genotyping in LQTS; minor genes are no longer minor
Ohno, Seiko, Ozawa, Junichi, Fukuyama, Megumi, Makiyama, Takeru, Horie, Minoru
Published in Journal of human genetics (01.12.2020)
Published in Journal of human genetics (01.12.2020)
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Journal Article
Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome
Yoshinaga, Masao, Ninomiya, Yumiko, Tanaka, Yuji, Fukuyama, Megumi, Kato, Koichi, Ohno, Seiko, Horie, Minoru, Ogata, Hiromitsu
Published in Circulation Journal (25.06.2024)
Published in Circulation Journal (25.06.2024)
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Journal Article
Impact of statin therapy on late target lesion revascularization after everolimus-eluting stent implantation according to pre-interventional vessel remodeling and vessel size of treated lesion
Asada, Kohei, Takeda, Teruki, Higo, Yosuke, Sawayama, Yuichi, Yagi, Noriaki, Fukuyama, Megumi, Yamaji, Masayuki, Sakai, Hiroshi, Mabuchi, Hiroshi, Yamamoto, Takashi, Nakagawa, Yoshihisa
Published in Heart and vessels (01.11.2022)
Published in Heart and vessels (01.11.2022)
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Journal Article
Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population
Sawayama, Yuichi, Yamamoto, Takashi, Tomita, Yukinori, Asada, Kohei, Yagi, Noriaki, Fukuyama, Megumi, Miyamoto, Akashi, Sakai, Hiroshi, Ozawa, Tomoya, Isono, Tetsuichiro, Hira, Daiki, Terada, Tomohiro, Horie, Minoru, Nakagawa, Yoshihisa
Published in Circulation Journal (25.08.2020)
Published in Circulation Journal (25.08.2020)
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Journal Article
High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8
Fukuyama, Megumi, Ohno, Seiko, Ozawa, Junichi, Kato, Koichi, Makiyama, Takeru, Nakagawa, Yoshihisa, Horie, Minoru
Published in Circulation Journal (25.03.2020)
Published in Circulation Journal (25.03.2020)
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Journal Article
Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1
Shimamoto, Keiko, Ohno, Seiko, Kato, Koichi, Takayama, Koichiro, Sonoda, Keiko, Fukuyama, Megumi, Makiyama, Takeru, Okamura, Satomi, Asakura, Koko, Imanishi, Noriaki, Kato, Yoshiaki, Sakaguchi, Heima, Kamakura, Tsukasa, Wada, Mitsuru, Yamagata, Kenichiro, Ishibashi, Kohei, Inoue, Yuko, Miyamoto, Koji, Nagase, Satoshi, Kusano, Kengo, Horie, Minoru, Aiba, Takeshi
Published in Heart (British Cardiac Society) (01.06.2022)
Published in Heart (British Cardiac Society) (01.06.2022)
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Journal Article
Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome
Hirose, Sayako, Murayama, Takashi, Tetsuo, Naoyuki, Hoshiai, Minako, Kise, Hiroaki, Yoshinaga, Masao, Aoki, Hisaaki, Fukuyama, Megumi, Wuriyanghai, Yimin, Wada, Yuko, Kato, Koichi, Makiyama, Takeru, Kimura, Takeshi, Sakurai, Takashi, Horie, Minoru, Kurebayashi, Nagomi, Ohno, Seiko
Published in Europace (London, England) (02.03.2022)
Published in Europace (London, England) (02.03.2022)
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Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
Ozawa, Junichi, Ohno, Seiko, Melgari, Dario, Wang, Qi, Fukuyama, Megumi, Toyoda, Futoshi, Makiyama, Takeru, Yoshinaga, Masao, Suzuki, Hiroshi, Saitoh, Akihiko, Ai, Tomohiko, Horie, Minoru
Published in Scientific reports (08.11.2022)
Published in Scientific reports (08.11.2022)
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Journal Article
School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome
Fukuyama, Megumi, Horie, Minoru, Aoki, Hisaaki, Ozawa, Junichi, Kato, Koichi, Sawayama, Yuichi, Tanaka-Mizuno, Sachiko, Makiyama, Takeru, Yoshinaga, Masao, Nakagawa, Yoshihisa, Ohno, Seiko
Published in Europace (London, England) (13.10.2022)
Published in Europace (London, England) (13.10.2022)
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Journal Article
Calmodulinopathy in Japanese Children ― Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy
Fukuyama, Megumi, Horie, Minoru, Kato, Koichi, Aoki, Hisaaki, Fujita, Shuhei, Yoshida, Yoko, Sakazaki, Hisanori, Toda, Takako, Ueno, Michihiko, Izumi, Gaku, Momoi, Nobuo, Muneuchi, Jun, Makiyama, Takeru, Nakagawa, Yoshihisa, Ohno, Seiko
Published in Circulation Journal (24.11.2023)
Published in Circulation Journal (24.11.2023)
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Journal Article
Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
Ohno, Seiko, Nagaoka, Iori, Fukuyama, Megumi, Kimura, Hiromi, Itoh, Hideki, Makiyama, Takeru, Shimizu, Akihiko, Horie, Minoru
Published in Circulation Journal (23.10.2020)
Published in Circulation Journal (23.10.2020)
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Journal Article
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes
Ichikawa, Mari, Aiba, Takeshi, Ohno, Seiko, Shigemizu, Daichi, Ozawa, Junichi, Sonoda, Keiko, Fukuyama, Megumi, Itoh, Hideki, Miyamoto, Yoshihiro, Tsunoda, Tatsuhiko, Makiyama, Takeru, Tanaka, Toshihiro, Shimizu, Wataru, Horie, Minoru
Published in Circulation Journal (25.11.2016)
Published in Circulation Journal (25.11.2016)
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Journal Article
Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
Ohno, Seiko, Nagaoka, Iori, Fukuyama, Megumi, Kimura, Hiromi, Itoh, Hideki, Makiyama, Takeru, Shimizu, Akihiko, Horie, Minoru
Published in Circulation Journal (2013)
Published in Circulation Journal (2013)
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Journal Article
A Common Mutation of Long QT Syndrome Type 1 in Japan
Itoh, Hideki, Dochi, Kenichi, Shimizu, Wataru, Denjoy, Isabelle, Ohno, Seiko, Aiba, Takeshi, Kimura, Hiromi, Kato, Koichi, Fukuyama, Megumi, Hasagawa, Kanae, Schulze-Bahr, Eric, Guicheney, Pascale, Horie, Minoru
Published in Circulation Journal (2015)
Published in Circulation Journal (2015)
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Journal Article
Nonsense-mediated mRNA decay due to a CACNA1C splicing mutation in a patient with Brugada syndrome
Fukuyama, Megumi, MD, Ohno, Seiko, MD, PhD, Wang, Qi, BSc, Shirayama, Takeshi, MD, PhD, Itoh, Hideki, MD, PhD, Horie, Minoru, MD, PhD
Published in Heart rhythm (01.04.2014)
Published in Heart rhythm (01.04.2014)
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Journal Article
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family
Ichikawa, Mari, Ohno, Seiko, Fujii, Yusuke, Ozawa, Junichi, Sonoda, Keiko, Fukuyama, Megumi, Kato, Koichi, Kimura, Hiromi, Itoh, Hideki, Hayashi, Hideki, Horie, Minoru
Published in Internal Medicine (01.01.2016)
Published in Internal Medicine (01.01.2016)
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Journal Article
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Fukumoto, Daisuke, Ding, Wei-Guang, Wada, Yuko, Fujii, Yusuke, Ichikawa, Mari, Takayama, Koichiro, Fukuyama, Megumi, Kato, Koichi, Itoh, Hideki, Makiyama, Takeru, Omatsu-Kanbe, Mariko, Matsuura, Hiroshi, Horie, Minoru, Ohno, Seiko
Published in Journal of cardiology (01.04.2018)
Published in Journal of cardiology (01.04.2018)
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Journal Article
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes
Fukuyama, Megumi, Wang, Qi, Kato, Koichi, Ohno, Seiko, Ding, Wei-Guang, Toyoda, Futoshi, Itoh, Hideki, Kimura, Hiromi, Makiyama, Takeru, Ito, Makoto, Matsuura, Hiroshi, Horie, Minoru
Published in Europace (London, England) (01.12.2014)
Published in Europace (London, England) (01.12.2014)
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Journal Article
Genetic screening of KCNJ8 in Japanese patients with J-wave syndromes or idiopathic ventricular fibrillation
Wang, Qi, BSc, Ohno, Seiko, MD, PhD, Kato, Koichi, MD, Fukuyama, Megumi, MD, Makiyama, Takeru, MD, PhD, Kimura, Hiromi, MD, PhD, Naiki, Nobu, MD, Kawamura, Mihoko, MD, Hayashi, Hideki, MD, PhD, Horie, Minoru, MD, PhD
Published in Journal of arrhythmia (01.10.2013)
Published in Journal of arrhythmia (01.10.2013)
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