Toshitaka Kawarai

カワライトシタカ | Toshitaka Kawarai

Affiliation and department：

Research field (1)： Neurology

Research keywords (3)： bioinformatics , linkage study , sequence analyses

Research theme for competitive and other funds (4)：

2019 - 2022 Investigation of molecular pathogenesis and therapeutic development for DYT-KMT2B by analysis of animal models
2014 - 2017 Analysis of TFG gene and development of treatment for motor neuron diseases
2012 - 2015 Research on molecular pathogenesis and next-generation therapeutic agent for dystonia-parkinsonism
2011 - 2013 Development of a novel therapeutic approach for ALS using anti-TNF antibody

Papers (145)：

Ma Daisy Tabuena, Ryoma Morigaki, Ryosuke Miyamoto, Hideo Mure, Nobuaki Yamamoto, Kazuhisa Miyake, Taku Matsuda, Yuishin Izumi, Yasushi Takagi, Rollin P Tabuena, et al. Ataxia with vitamin E deficiency in the Philippines : A case report of two siblings. The journal of medical investigation : JMI. 2021. 68. 3.4. 400-403
Ryosuke Miyamoto, Toshitaka Kawarai, Toshiaki Takeuchi, Yuishin Izumi, Satoshi Goto, Ryuji Kaji. Efficacy of Istradefylline for the Treatment of ADCY5-Related Disease. Movement disorders clinical practice. 2020. 7. 7. 852-853
黒田一駿, 瓦井俊孝, 村上永尚, 宮本亮介, 和泉唯信, 梶龍兒. 長期間経過観察しえたchoreaとmyoclonusを含む不随意運動症例. 臨床神経学. 2019. 59. 6. 387-387
Toshitaka Kawarai, Hiroki Yamazaki, Ryosuke Miyamoto, Naoko Takamatsu, Atsuko Mori, Yusuke Osaki, Antonio Orlacchio, Hiroyuki Nodera, Akihiro Hashiguchi, Yujiro Higuchi, et al. PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability. Neuromuscular Disorders. 2019. 29. 6. 422-426
Fumiko Nakazeki, Itaru Tsuge, Takahiro Horie, Keiko Imamura, Kayoko Tsukita, Akitsu Hotta, Osamu Baba, Yasuhide Kuwabara, Tomohiro Nishino, Tetsushi Nakao, et al. is a therapeutic target in SPG4-related hereditary spastic paraplegia human neurons. Clinical Science. 2019. Vol.133. No.4. 583-595

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MISC (13)：

Chizuru Ikeda, Toshitaka Kawarai, Chisa Setoyama, Antonio Orlacchio, Hoseki Imamura. Recurrent de novo missense variant E210K in UBTF causes juvenile dystonia-parkinsonism. Neurological Sciences. 2021. 42. 3. 1217-1219
福本竜也, 宮本亮介, 山崎博輝, 村上永尚, 大崎裕亮, 藤田浩司, 野寺裕之, 瓦井俊孝, 和泉唯信, 梶龍兒. 特異な歩行障害を呈したGerstmann-Straeussler-Scheinker病の31歳男性例. 臨床神経学(Web). 2019. 59. 6
織田雅也, 中野雄太, 伊藤聖, 瓦井俊孝, 村山繁雄, 和泉唯信, 和泉唯信. 上位運動ニューロン徴候を認めない運動ニューロン疾患の剖検例. 臨床神経学(Web). 2015. 55. 4
Yoshimichi Miyazaki, 宮本亮介, 小泉英貴, Toshitaka Kawarai, Ryuji Kaji. 若年発症全身性捻転ジストニアにおけるゾルピデム内服治療の有効性. ジストニアの分子病態解明と新規治療法開発に関する研究班(平成26年度). 2015. 29-30
Toshitaka Kawarai. 新規運動ニューロン病遺伝子TFGの機能解析. ブレインサイエンス・レビュー2015. 2015. 79-90

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Professional career (1)：

Work history (1)：

Association Membership(s) (3)：

The Japanese Society of Neurology , The Japanese Society of Internal Medicine , Societas Neurologica Japonica

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