2020 | Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy | CHIN-HSIEN LIN ; Tsai, Pei-I; Lin, Han-Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng-Ling; Cheng, Jay; Huang, Cheng-Yen; SHIOU-RU TZENG ; Wu, Yen-Sheng; Lai, Hsing-Jung; Tsai, Hsin-Hsi; RUOH-FANG YEN ; NI-CHUNG LEE ; Lo, Wen-Chun; Hung, Yu-Chien; CHIH-CHIANG CHAN ; Ke, Yi-Ci; CHI-CHAO CHAO ; SUNG-TSANG HSIEH ; Farrer, Matthew; RUEY-MEEI WU | Brain : a journal of neurology | 29 | 32 | |
2023 | Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution | Jagota, Priya; Ugawa, Yoshikazu; Aldaajani, Zakiyah; Ibrahim, Norlinah Mohamed; Ishiura, Hiroyuki; Nomura, Yoshiko; Tsuji, Shoji; Diesta, Cid; Hattori, Nobutaka; Onodera, Osamu; Bohlega, Saeed; Al-Din, Amir; Lim, Shen-Yang; Lee, Jee-Young; Jeon, Beomseok; Pal, Pramod Kumar; Shang, Huifang; Fujioka, Shinsuke; Kukkle, Prashanth Lingappa; Phokaewvarangkul, Onanong; CHIN-HSIEN LIN ; Shambetova, Cholpon; Bhidayasiri, Roongroj | Journal of movement disorders | | | |