Research keywords (5):
genetic cardiology
, cardiovascular function
, congenital heart disease
, Mitochondrial disease
, Pediatric Cardiomyopathy
Research theme for competitive and other funds (6):
2023 - 2026 小児の心筋症におけるミトコンドリア障害と心筋エネルギー代謝に関する研究
2023 - 2026 ミトコンドリア遺伝子治療を実現するゲノム編集技術の創出
2022 - 2025 Elucidating the pathogenesis of childhood-onset pulmonary hypertension through multifaceted pathological investigation based on deep learning
Shohei Honda, Issei Kawakita, Kazuyoshi Okumura, Momoko Ara, Ryoichi Goto, Atsuhito Takeda, Tsuyoshi Shimamura, Insu Kawahara, Akinobu Taketomi. Unusual rapid development of portopulmonary hypertension after shunt closure for congenital portosystemic shunt. Journal of paediatrics and child health. 2024
Gaku Izumi, Satoru Shida, Norio Kobayashi, Hirokuni Yamazawa, Atsuhito Takeda. Initial Holter Electrocardiogram Index to Predict the Burden of Subsequent Persistent Premature Ventricular Complex in Childhood. Circulation journal : official journal of the Japanese Circulation Society. 2024
Ayako Chida-Nagai, Hiroki Sato, Hirokuni Yamazawa, Atsuhito Takeda, Naohiro Yonemoto, Yoshio Tahara, Takanori Lkeda. Impact of the COVID-19 pandemic on pediatric out-of-hospital cardiac arrest outcomes in Japan. Scientific reports. 2024. 14. 1. 11246-11246
Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, et al. Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association. 2024. e032872
Cardiac mitochondrial ultrastructure and respiratory chain enzymatic activities in patients with pediatric hypertrophic cardiomyopathy
(49th Annual Meeting of the Association for European Paediatric and Congenital Cardiology (AEPC) 2015)