Rchr
J-GLOBAL ID：201701014959280500
Update date: Oct. 06, 2024
Fukuyama Megumi
Fukuyama Megumi
Research field (1)：
Cardiology
Research theme for competitive and other funds (5)：
- 2022 - 2025 遺伝的背景が不明なカテコラミン誘発多型性心室頻拍患者における遺伝子構造多型の検索
- 2021 - 2024 The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology
- 2019 - 2022 Elucidation of pathology of inherited cardiac disease caused by mutations in ryanodine receptor gene
- 2017 - 2019 Elucidation of mechanism of cardiac calcium channel (CaV1.2) abnormality in long QT syndrome
- 2015 - 2017 Mechanism of Inherited Arrhythmia Syndrome with SCN10A mutation
Papers (40)：
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Asami Kashiwa, Hideki Itoh, Takeru Makiyama, Yuko Wada, Junichi Ozawa, Koichi Kato, Megumi Fukuyama, Tadashi Nakajima, Seiko Ohno, Minoru Horie. Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants. Heart rhythm. 2024. 21. 7. 1113-1120
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Masao Yoshinaga, Yumiko Ninomiya, Yuji Tanaka, Megumi Fukuyama, Koichi Kato, Seiko Ohno, Minoru Horie, Hiromitsu Ogata. Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome. Circulation journal : official journal of the Japanese Circulation Society. 2024. 88. 7. 1176-1184
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Aizawa Takanori, Makiyama Takeru, Huang Hai, Imamura Tomohiko, Fukuyama Megumi, Sonoda Keiko, Kato Koichi, Ohno Seiko, Horie Minoru, Ono Koh. Fatal Arrhythmic Events are Higher in Non-missense than in Missense Variants in SCN5A-positive Brugada Syndrome(タイトル和訳中). 日本循環器学会学術集会抄録集. 2024. 88回. FRS5-3
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Lia Crotti, Carla Spazzolini, Mette Nyegaard, Michael T Overgaard, Maria-Christina Kotta, Federica Dagradi, Luca Sala, Takeshi Aiba, Mark D Ayers, Anwar Baban, et al. Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry. European heart journal. 2023. 44. 35. 3357-3370
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Soji Kohyama, Yuichi Sawayama, Kohei Asada, Yousuke Higo, Kenji Kodama, Noriaki Yagi, Megumi Fukuyama, Atsushi Hayashi, Wataru Shioyama, Hiroshi Sakai, et al. FFR-CT is extremely useful in detecting hemodynamically significant left-main coronary artery stenosis with right coronary artery hypoplasia: A case report. Journal of Cardiology Cases. 2023. 28. 2. 64-67
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MISC (38)：
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谷 陽良, 児玉 健二, 肥後 洋祐, 浅田 紘平, 八木 典章, 福山 恵, 酒井 宏, 中川 義久. 多剤抵抗性の難治性冠攣縮性狭心症にベルイシグアトが奏功した1例. 日本心血管インターベンション治療学会抄録集. 2023. 31回. MP33-5
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Fukuyama Megumi, Horie Minoru, Kato Koichi, Ozawa Tomoya, Fujii Yusuke, Okuyama Yusuke, Makiyama Takeru, Ohno Seiko, Nakagawa Yoshihisa. Calmodulinopathy: A Common Cause of Critical Cardiac Phenotypes in Fetus and Infancy(タイトル和訳中). 日本循環器学会学術集会抄録集. 2023. 87回. PL04-6
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Sawayama Yuichi, Kouyama Soji, Higo Yousuke, Kodama Kenji, Asada Kohei, Yagi Noriaki, Fukuyama Megumi, Hayashi Atsushi, Shioyama Wataru, Sakai Hiroshi, et al. Effect of Sex on CYP2C19 Polymorphism in Patients Receiving Percutaneous Coronary Intervention(タイトル和訳中). 日本循環器学会学術集会抄録集. 2023. 87回. PE52-4
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Shimamoto Keiko, Ohno Seiko, Kato Koichi, Takayama Koichiro, Sonoda Keiko, Fukuyama Megumi, Makiyama Takeru, Okamura Satomi, Asakura Koko, Imanishi Noriaki, et al. RYR2遺伝子変異を有する家族性CPVT患者とde Novo CPVT患者の表現型の違い(Phenotypic Differences between Familial and De Novo CPVT Patient Carrying RYR2 Variants). 日本循環器学会学術集会抄録集. 2022. 86回. OE18-7
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Fukuyama Megumi, Ohno Seiko, Kato Koichi, Ozawa Tomoya, Okuyama Yusuke, Fujii Yusuke, Sawayama Yuichi, Higo Yousuke, Asada Kohei, Yagi Noriaki, et al. 不整脈原性心筋症における遺伝子スクリーニングの貢献(Contribution of Genetic Screening for Arrhythmogenic Cardiomyopathy). 日本循環器学会学術集会抄録集. 2021. 85回. PL07-3
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Professional career (1)：
- - (Shiga University of Medical Science)
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