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Jagota, Priya and Ugawa, Yoshikazu and Aldaajani, Zakiyah and Ibrahim, Norlinah Mohamed and Ishiura, Hiroyuki and Nomura, Yoshiko and Tsuji, Shoji and Diesta, Cid and Hattori, Nobutaka and Onodera, Osamu and Bohlega, Saeed and Al-Din, Amir and Lim, Shen-Yang and Lee, Jee-Young and Jeon, Beomseok and Pal, Pramod Kumar and Shang, Huifang and Fujioka, Shinsuke and Kukkle, Prashanth Lingappa and Phokaewvarangkul, Onanong and Lin, Chin-Hsien and Shambetova, Cholpon and Bhidayasiri, Roongroj (2023) Nine hereditary movement disorders first described in Asia: their history and evolution. Journal of Movement Disorders, 16 (3). pp. 231-247. ISSN 2005-940X, DOI https://doi.org/10.14802/jmd.23065.
Ishiura, Hiroyuki and Shibata, Shota and Yoshimura, Jun and Suzuki, Yuta and Qu, Wei and Doi, Koichiro and Almansour, M. Asem and Kikuchi, Junko Kanda and Taira, Makiko and Mitsui, Jun and Takahashi, Yuji and Ichikawa, Yaeko and Mano, Tatsuo and Iwata, Atsushi and Harigaya, Yasuo and Matsukawa, Miho Kawabe and Matsukawa, Takashi and Tanaka, Masaki and Shirota, Yuichiro and Ohtomo, Ryo and Kowa, Hisatomo and Date, Hidetoshi and Mitsue, Aki and Hatsuta, Hiroyuki and Morimoto, Satoru and Murayama, Shigeo and Shiio, Yasushi and Saito, Yuko and Mitsutake, Akihiko and Kawai, Mizuho and Sasaki, Takuya and Sugiyama, Yusuke and Hamada, Masashi and Ohtomo, Gaku and Terao, Yasuo and Nakazato, Yoshihiko and Takeda, Akitoshi and Sakiyama, Yoshio and Umeda-Kameyama, Yumi and Shinmi, Jun and Ogata, Katsuhisa and Kohno, Yutaka and Lim, Shen Yang and Tan, Ai Huey and Shimizu, Jun and Goto, Jun and Nishino, Ichizo and Toda, Tatsushi and Morishita, Shinichi and Tsuji, Shoji (2019) Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease. Nature Genetics, 51 (8). pp. 1222-1232. ISSN 1061-4036, DOI https://doi.org/10.1038/s41588-019-0458-z.
