Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tohko Sato"'
Autor:
Kazumasa Shindo, Tohko Sato, Hiroaki Murata, Yuta Ichinose, Takanori Hata, Yoshihisa Takiyama
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background Spinocerebellar ataxia type 31 (SCA 31) is a slowly progressive neurodegenerative disorder characterized by pure cerebellar ataxia. Unlike other CAG repeat diseases, sleep-related problems have not been reported in patients with S
Externí odkaz:
https://doaj.org/article/d910d56666b74e43ab109a91218427a2
Autor:
Mai Tsuchiya, Tohko Sato, Yoshihisa Takiyama, Kishin Koh, Kazumasa Shindo, Takafumi Kurita, Takanori Hata, Takahiro Natori, Takamura Nagasaka, Akane Satake
Publikováno v:
Journal of Clinical Neuroscience. 87:80-83
Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder characterized by slowly progressive cerebellar ataxia. Previously, autonomic symptoms or dysfunction have not been reported. To evaluate subclinical auto
Autor:
Shindo, Kazumasa1 kshindo@yamanashi.ac.jp, Sato, Tohko1 tsato@yamanashi.ac.jp, Murata, Hiroaki1 hmurata@yamanashi.ac.jp, Ichinose, Yuta1 yuta@yamanashi.ac.jp, Hata, Takanori1 thata@yamanashi.ac.jp, Takiyama, Yoshihisa1 ytakiyama@yamanashi.ac.jp
Publikováno v:
BMC Neurology. 1/11/2019, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p. 3 Diagrams.