Rchr
J-GLOBAL ID：202001000088140741
Update date: Jan. 02, 2025
Kakumoto Toshiyuki
カクモト トシユキ | Kakumoto Toshiyuki
Affiliation and department：
Research field (3)：
Genetics
, Neurology
, Cell biology
Research theme for competitive and other funds (4)：
- 2023 - 2027 Research on neurodegenerative disorders
- 2023 - 2026 Investigation of small nuclei by brain-dedicated PET
- 2022 - 2025 Searching for biomarkers to discriminate the disease forms of adrenoleukodystrophy and to determine the indications for treatment
- 2010 - 2012 シグナル伝達の光制御法の開発と神経への応用
Papers (17)：
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Toshiyuki Kakumoto, Kenta Orimo, Takashi Matsukawa, Jun Mitsui, Tomohiko Ishihara, Osamu Onodera, Yuta Suzuki, Shinichi Morishita, Ayaka Chikada, Kenta Orimo, et al. Frequency of FGF14 intronic GAA repeat expansion in patients with multiple system atrophy and undiagnosed ataxia in the Japanese population. European Journal of Human Genetics. 2024
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So Okubo, Toshiyuki Kakumoto, Masahiko Tsujita, Kyosuke Muramatsu, Sho Fujiwara, Masashi Hamada, Wataru Satake, Tatsushi Toda. Extremely Longitudinally Extensive Transverse Myelitis in a Patient With Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease. Cureus. 2024. 16. 5. e59938
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Egashira S, Akatsuki Kubota, Kakumoto T, Kawasaki R, Kotani R, Sakuishi K, Iwata A, Bae SK, Akamatsu N, Hasegawa K, et al. Long-term survival from progressive multifocal leukoencephalopathy in living-donor liver transplant recipient with preformed donor-specific antibody. Journal of neurovirology. 2023. 29. 5. 519-523
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Kenta Orimo, Toshiyuki Kakumoto, Ryo Hara, Ryoji Goto, Hiroyuki Ishiura, Jun Mitsui, Chiharu Yoshida, Yoshikazu Uesaka, Yuta Suzuki, Shinichi Morishita, et al. A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant. Journal of the Neurological Sciences. 2023. 120732-120732
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Toshiyuki Kakumoto, Takashi Matsukawa, Hiroyuki Ishiura, Harushi Mori, Shoji Tsuji, Tatsushi Toda. Neurofilament light chain levels in cerebrospinal fluid as a sensitive biomarker for cerebral adrenoleukodystrophy. Annals of clinical and translational neurology. 2023
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MISC (54)：
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青木 修一郎, 中村 奈津子, 角元 利行, 成瀬 紘也, 濱田 雅, 戸田 達史. Neurogenic muscle weakness,ataxia,retinitis pigmentosaの1例. 眼科臨床紀要. 2024. 17. 8. 633-633
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辻田 真比古, 村松 恭祐, 大久保 颯, 角元 利行, 濱田 雅, 佐竹 渉, 戸田 達史. 脊髄に極長大病変を呈した抗MOG抗体関連疾患の29歳男性. 臨床神経学. 2024. 64. 6. 442-442
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勝瀬 一登, 久保田 暁, 柿沼 一雄, 太田 祥子, 菅野 重範, 角元 利行, 代田 悠一郎, 濱田 雅, 戸田 達史, 鈴木 匡子. 運動感覚障害を伴わず,純粋失書・タイピング障害のみを示した左内包後脚梗塞の症例. 高次脳機能研究. 2024. 44. 1. 69-69
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横山 敬士, 井川 彩土, 角元 利行, 石浦 浩之, 濱田 雅, 青木 修一郎, 佐竹 渉, 戸田 達史. 網膜色素変性症と軽度の小脳失調及び脳波異常を認めNeurogenic muscle weakness,ataxia,and retinitis pigmentosa(NARP)と診断した25歳女性例. 臨床神経学. 2023. 63. 11. 774-774
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小玉 聡, 代田 悠一郎, 濱田 雅, 前田 明子, 角元 利行, 國井 尚人, 嶋田 勢二郎, 池村 雅子, 張 琢成, 河合 美津保, et al. 歩行誘発発作を示す焦点てんかんに対し補足運動野切除が有効であった一例. 臨床神経生理学. 2023. 51. 5. 597-597
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Lectures and oral presentations (3)：
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Frequency of FGF14 Intronic GAA Repeat Expansion in Patients with Multiple System Atrophy and Undiagnosed Ataxia in the Japanese Population
(ASHG 2024 Annual Meeting 2024)
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Neurofilament light chain levels in cerebrospinal fluid is useful for evaluating the disease activities of cerebral adrenoleukodystrophy
(ASHG 2023 Annual Meeting 2023)
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A novel missense mutation in valosin-containing protein gene identified in a Japanese family with a pure form of hereditary spastic paraplegia
(World Congress of Neurology 2017)
Work history (1)：
- 2025/01 - 現在 The University of Tokyo Faculty of Medicine University Hospital
Association Membership(s) (1)：
American Society for Human Genetics
