研究者
J-GLOBAL ID:201801007900601568   更新日: 2020年11月25日

李 元哲

Li Yuanzhe
所属機関・部署:
職名: 特任助教
研究分野 (3件): 神経内科学 ,  ゲノム生物学 ,  医化学
研究キーワード (3件): ヒトゲノム ,  神経変性疾患 ,  パーキンソン病
論文 (72件):
  • Kenya Nishioka, Yoshio Hashizume, Masashi Takanashi, Kensuke Daida, Yuanzhe Li, Hiroyo Yoshino, Nicola Tambasco, Paolo Prontera, Yuko Hattori, Akihiro Ueda, et al. Pathological findings in a patient with alpha-synuclein p.A53T and familial Parkinson's disease. Parkinsonism & related disorders. 2020. 81. 183-187
  • Chin-Hsien Lin, Pei-I Tsai, Han-Yi Lin, Nobutaka Hattori, Manabu Funayama, Beomseok Jeon, Kota Sato, Koji Abe, Yohei Mukai, Yuji Takahashi, et al. Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy. Brain : a journal of neurology. 2020
  • Masayoshi Nakano, Yuichi Riku, Kenya Nishioka, Masato Hasegawa, Yukihiko Washimi, Yutaka Arahata, Akinori Takeda, Kentaro Horibe, Akiko Yamaoka, Keisuke Suzuki, et al. Unclassified four-repeat tauopathy associated with familial parkinsonism and progressive respiratory failure. Acta neuropathologica communications. 2020. 8. 1. 148-148
  • Kensuke Daida, Kenya Nishioka, Yuanzhe Li, Hiroyo Yoshino, Tomoyo Shimada, Nobuhiro Dougu, Yuji Nakatsuji, Shinji Ohara, Takao Hashimoto, Ryoichi Okiyama, et al. PLA2G6 variants associated with the number of affected alleles in Parkinson's disease in Japan. Neurobiology of aging. 2020
  • Arisa Hayashida, Yuanzhe Li, Hiroyo Yoshino, Kensuke Daida, Aya Ikeda, Kotaro Ogaki, Atsuhito Fuse, Akio Mori, Masashi Takanashi, Toshiki Nakahara, et al. The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1. Neurobiology of aging. 2020
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MISC (8件):
  • N. Hattori, K. Nishioka, T. Matsushima, Y. Li, H. Yoshino, M. Takanashi, M. Funayama. Clinicogenetic study of CHCHD2 in patients with autosomal dominant familial Parkinson's disease. JOURNAL OF THE NEUROLOGICAL SCIENCES. 2015. 357. E58-E59
  • H. Tomiyama, M. Ando, Y. Li, H. Yoshino, N. Hattori. Mutation analysis for DNAJC6 in patients with early-onset Parkinson's disease. MOVEMENT DISORDERS. 2013. 28. S400-S401
  • 李 元哲, 寧 玉萍, 舩山 学, 吉野 浩代, 佐藤 栄人, 金井 数明, 朝比奈 正人, 服部 孝道, 今道 洋子, 水野 美邦, et al. ATP13A2(PARK9)の新規遺伝子変異の同定. 臨床神経学. 2007. 47. 12. 1152-1152
  • Funayama M, Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, Hattori N. LRRK2 G2385R is susceptible to sporadic Parkinson’s disease in Asian population. Neuroreport. 2007. 18. 273-5
  • Y. Li, R. Kumazawa, H. Tomiyama, Y. Imamichi, M. Funayama, H. Yoshino, K. Sato, H. Takahashi, F. Yoshii, N. Hattori, et al. Clinicogenetic study of PINK1 mutations in Parkinson disease. MOVEMENT DISORDERS. 2006. 21. S414-S414
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学位 (1件):
  • 医学 (順天堂大学)
所属学会 (2件):
日本神経学会 ,  日本人類遺伝学会
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