Kido Jun

キドジュン | Kido Jun

Affiliation and department：

Research field (1)： Fetal medicine/Pediatrics

Research keywords (2)： Pediatrics , Inherited metabolic disease

Research theme for competitive and other funds (6)：

2023 - 2026 iPS細胞を用いたメラノーマに対する新規がん免疫療法の開発
2023 - 2026 血漿Lyso-Gb3と血管内皮細胞解析を駆使した新しいファブリー病診断システムの構築
2020 - 2023 Development of novel pathological analysis and medicine in neuropathic Gaucher disease.
2017 - 2020 Development of novel medicine using iPS cells derived from Gaucher disease type II patients
2015 - 2018 Prediction of DiabetesMellitus by using with iPS cell technology

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Papers (79)：

Jun Kido, Georgios Makris, Saikat Santra, Johannes Häberle. Clinical landscape of citrin deficiency: A global perspective on a multifaceted condition. J Inherit Metab Dis . 2024
Mika Ogata, Takanobu Yoshida, Jun Kido, Natsuko Nishi, Sachiko Shimomura, Nami Hirai, Masaaki Yanai, Tomoyuki Mizukami, Kimitoshi Nakamura. Safety of Oral Food Challenge for Individuals with Low Egg White and Ovomucoid-Specific IgE Antibodies. International Archives of Allergy and Immunology. 2023. 185. 1. 33-42
Jun Kido, Johannes Häberle, Toju Tanaka, Masayoshi Nagao, Yoichi Wada, Chikahiko Numakura, Ryosuke Bo, Hiromi Nyuzuki, Sumito Dateki, Shinsuke Maruyama, et al. Improved sensitivity and specificity for citrin deficiency using selected amino acids and acylcarnitines in the newborn screening. Journal of Inherited Metabolic Disease. 2023
Yusuke Noda, Jun Kido, Yohei Misumi, Keishin Sugawara, Sachiko Ohori, Atsushi Fujita, Naomichi Matsumoto, Mitsuharu Ueda, Kimitoshi Nakamura. Heterozygous c.175C>T variant in PURA gene causes severe developmental delay. Clinical case reports. 2023. 11. 9. e7779
Yusuke Hattori, Takaaki Sawada, Jun Kido, Keishin Sugawara, Shinichiro Yoshida, Shirou Matsumoto, Takahito Inoue, Shinichi Hirose, Kimitoshi Nakamura. Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in Japan. Molecular Genetics and Metabolism Reports. 2023. 37. 101003-101003

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MISC (45)：

澤田貴彰, 城戸淳, 菅原敬信, 吉田真一郎, 松本志郎, 中村公俊. 九州におけるゴーシェ病の新生児スクリーニングの現状. 日本先天代謝異常学会雑誌. 2022. 38
城戸淳, 中村公俊, 三隅洋平, 植田光晴. 熊本大学病院IRUDの取り組みについて-小児科から-. 日本小児科学会雑誌. 2022. 126. 9
城戸淳. 【治療可能な先天代謝異常症を診断しよう!】診断のポイント尿素サイクル異常症. 小児科診療. 2021. 84. 12. 1761-1768
Takaaki Sawada, Jun Kido, Keishin Sugawara, Kimitoshi Nakamura. High-risk screening for fabry disease: A nationwide study in Japan and literature review. Diagnostics. 2021. 11. 10
松本志郎, 坂本理恵子, 城戸淳, 澤田貴彰, 服部祐介, 木下裕哉, 三渕浩, 遠藤文夫, 中村公俊, 中村公俊. Growth and nutrition status in children with organic acidemia. 日本マススクリーニング学会誌. 2021. 31. 2. 181-181

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Books (1)：

Education (1)：

Professional career (1)：

Work history (8)：

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Awards (4)：

2024/04 - 日本小児科学会日本小児科学会学術研究者賞
2023/04 - SOCIETY FOR THE STUDY OF INBORN ERRORS OF METABOLISM ARCHIBALD GARROD AWARD
2016/11 - 九州小児科学会九州小児科学会優秀演題賞
2016/10 - 日本先天代謝異常学会日本先天代謝異常学会奨励賞

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