2014 - 2016 Establishment of induced pluripotent stem cells from glycogen storage disease type Ib patient and making disease models
2004 - 2005 Develop a new system for inborn errors of purine and pyrimidine metabolism
Papers (85)：
Mika Ishige, Tetsuya Ito, Takashi Hamazaki, Mitsuhiro Kuwahara, Lawrence Lee, Haruo Shintaku. Two-year interim safety and efficacy of pegvaliase in Japanese adults with phenylketonuria. Molecular genetics and metabolism. 2023. 140. 3. 107697-107697
Tokiko Fukuda, Tetsuya Ito, Takashi Hamazaki, Ayano Inui, Mika Ishige, Reiko Kagawa, Norio Sakai, Yoriko Watanabe, Hironori Kobayashi, Yosuke Wasaki, et al. Blood glucose trends in glycogen storage disease type Ia: A cross-sectional study. Journal of inherited metabolic disease. 2023. 46. 4. 618-633
Katsuyuki Yokoi, Yoko Nakajima, Yoshihisa Takahashi, Takashi Hamajima, Go Tajima, Kazuyoshi Saito, Shunsuke Miyai, Hidehito Inagaki, Tetsushi Yoshikawa, Hiroki Kurahashi, et al. Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case report. JIMD reports. 2023. 64. 1. 3-9
Katsuyuki Yokoi, Yoko Nakajima, Yuta Sudo, Tasuku Mariya, Rie Kawamura, Makiko Tsutsumi, Hidehito Inagaki, Tetsushi Yoshikawa, Tetsuya Ito, Hiroki Kurahashi. Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts BCKDHA: A case report. JIMD reports. 2022. 63. 6. 575-580
Yuji Matsumoto, Yohei Ikezumi, Tomomi Kondoh, Katsuyuki Yokoi, Yoko Nakajima, Naonori Kumagai, Takema Kato, Hiroki Kurahashi, Tetsuya Ito. An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 Deletion. The Tohoku journal of experimental medicine. 2022. 258. 3. 183-193
