Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Atsuko Motoda"'
Autor:
Hidetada Yamada, Yu Yamazaki, Yoshiko Takebayashi, Kyosuke Yazawa, Miwako Sasanishi, Atsuko Motoda, Masahiro Nakamori, Hiroyuki Morino, Tetsuya Takahashi, Hirofumi Maruyama
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Heated tobacco products (HTPs) have emerged as novel alternatives to conventional cigarettes (CCs), marketed by the tobacco industry as having a reduced potential for harm. Nevertheless, a significant dearth of information remains regarding
Externí odkaz:
https://doaj.org/article/1b4ea40d4a684312affbdb5d53955478
Autor:
Atsuko Motoda, Tomoyasu Matsubara, Zen‐ichi Tanei, Yasuhiro Sakashita, Mikihiro Yamazaki, Ito Kawakami, Renpei Sengoku, Tomio Arai, Hirofumi Maruyama, Yuko Saito, Shigeo Murayama
Publikováno v:
Neuropathology. 43:129-134
Autor:
Norihiko Kawaguchi, Atsuko Motoda, Tatsuhiro Terada, Naotaka Usui, Kiyohito Terada, Tomoyasu Matsubara, Katsuya Sato, Tetsuyuki Kitamoto, Shigeo Murayama, Tomokazu Obi
Publikováno v:
Epileptic Disorders.
Autor:
Mutsuko Araki, Takeo Shishido, Takashi Kurashige, Atsuko Motoda, Hideshi Kawakami, Tetsuya Takahashi, Hirofumi Maruyama, Kenichi Ishikawa, Hiroyuki Morino, Masayasu Matsumoto, Yoshito Nagano
Publikováno v:
Differentiation. 123:1-8
Mutations in optineurin (OPTN) have been identified in a small proportion of sporadic and familial amyotrophic lateral sclerosis (ALS) cases. Recent evidences suggest that OPTN would be involved in not only the pathophysiological mechanisms of motor
Autor:
Yoshihiko Saito, Chigusa Watanabe, Atsuko Motoda, Ichizo Nishino, Kazuhide Ochi, Tetsuya Takahashi, Hirofumi Maruyama, Yoshiro Tachiyama, Aritoshi Iida
Publikováno v:
Neuromuscular Disorders. 31:1220-1225
ADSSL1 myopathy is an inherited myopathy with limb weakness, respiratory muscle paralysis, dysphagia, and myocardial symptoms. We present an autopsy case of a 66-year-old male carrying compound heterozygous variants c.781G>A (p.D261N) and c.919delA (
Autor:
Tomoaki Watanabe, Masahiro Nakamori, Kenichi Ishikawa, Atsuko Motoda, Shuichiro Neshige, Shotaro Yamamoto, Kento Katahira, Toru Higaki, Hiroki Ueno, Takahiro Iizuka, Hirofumi Maruyama
Publikováno v:
Internal medicine (Tokyo, Japan).
Cryptogenic new-onset refractory status epilepticus (C-NORSE) is a neurologic emergency condition characterized by refractory status epilepticus (RSE) of unknown cause. Brain atrophy in a setting of C-NORSE is usually irreversible. A 33-year-old woma
Autor:
Hidetada Yamada, Shuichiro Neshige, Megumi Nonaka, Yoshiko Takebayashi, Haruka Ishibashi, Atsuko Motoda, Shiro Aoki, Yu Yamazaki, Hirofumi Maruyama
Publikováno v:
Epilepsy & Behavior. 142:109211
Autor:
Tomoaki Watanabe, Masahiro Nakamori, Kenichi Ishikawa, Atsuko Motoda, Shuichiro Neshige, Shotaro Yamamoto, Kento Katahira, Toru Higaki, Hiroki Ueno, Takahiro Iizuka, Hirofumi Maruyama
Publikováno v:
Internal Medicine; 2023, Vol. 62 Issue 12, p1835-1842, 8p
Autor:
Yasuhiro Sakashita, Masako Ikemura, Ito Kawakami, Renpei Sengoku, Mikihiro Yamazaki, Tomio Arai, Shinya Tanaka, Yuko Saito, Shinji Ito, Atsuko Motoda, Tomoyasu Matsubara, Zen-ichi Tanei, Shigeo Murayama
Publikováno v:
Acta Neuropathologica
Lewy body disease (LBD) is a spectrum of progressive neurodegenerative disorders characterized by the wide distribution of Lewy bodies and neurites in the central and peripheral nervous system (CNS, PNS). Clinical diagnoses include Parkinson’s dise
Autor:
Renpei Sengoku, Tomio Arai, Zen-ichi Tanei, Yuko Saito, Ito Kawakami, Yasuhiro Sakashita, Mikihiro Yamazaki, Atsuko Motoda, Shigeo Murayama, Masahito Yamada, Tomoyasu Matsubara, Tadayuki Takata
Publikováno v:
Neuropathology : official journal of the Japanese Society of NeuropathologyREFERENCES. 41(6)
Accumulation of phosphorylated α-synuclein in the central and peripheral nervous systems is a histological hallmark of Lewy body disease (LBD), including Parkinson's disease (PD), dementia with Lewy bodies (DLB), and LB-related pure autonomic failur