研究者

J-GLOBAL ID：201801008139203258 更新日: 2022年07月28日

岡明

オカアキラ | Akira Oka

所属機関・部署：
職名：教授
論文 (49件)：

Kubota Y, Arakawa Y, Sekiguchi M, Watanabe K, Hiwatari M, Kishimoto H, Nakazawa A, Yoshida A, Ogawa S, Hanada R, et al. A case of malignant rhabdoid tumor mimicking yolk sac tumor. Pediatric blood & cancer. 2019. 66. 8. e27784
Takanobu Inoue, Hideaki Yagasaki, Junko Nishioka, Akie Nakamura, Keiko Matsubara, Satoshi Narumi, Kazuhiko Nakabayashi, Kazuki Yamazawa, Tomoko Fuke, Akira Oka, et al. Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology. Journal of medical genetics. 2019. 56. 6. 413-418
Satoshi Takenaka, Yukiko Kuroda, Sayaka Ohta, Yoko Mizuno, Mitsuteru Hiwatari, Satoko Miyatake, Naomichi Matsumoto, Akira Oka. A Japanese patient with RAD51-associated Fanconi anemia. American journal of medical genetics. Part A. 2019. 179. 6. 900-902
Aoki Y, Hanai S, Sukigara S, Otsuki T, Saito T, Nakagawa E, Kaido T, Kaneko Y, Takahashi A, Ikegaya N, et al. Altered Expression of Astrocyte-Related Receptors and Channels Correlates With Epileptogenesis in Hippocampal Sclerosis. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 2019. 22. 6. 1093526619855488-539
Yu Nakagama, Kohei Hamanaka, Masakazu Mimaki, Haruo Shintaku, Satoko Miyatake, Naomichi Matsumoto, Koji Hirohata, Ryo Inuzuka, Akira Oka. Leaky splicing variant in sepiapterin reductase deficiency: Are milder cases escaping diagnosis?. Neurology. Genetics. 2019. 5. 2. e319

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