Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mikiko Motoki"'
Autor:
Yoshitsugu Nakamura, Mikiko Motoki, Takahiko Hirose, Takafumi Hosokawa, Shimon Ishida, Shigeki Arawaka
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background Fulminant Guillain-Barré syndrome (GBS) is characterized clinically by rapid progression of severe symptoms, such as the absence of brainstem reflexes, complete tetraplegia and respiratory arrest. The clinical course of fulminant
Externí odkaz:
https://doaj.org/article/642c157d30264b09a5e048d6df4edf61
Autor:
Takahiko Hirose, Shigeki Arawaka, Shimon Ishida, Takafumi Hosokawa, Yoshitsugu Nakamura, Mikiko Motoki
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-4 (2019)
BMC Neurology
BMC Neurology
Background Fulminant Guillain-Barré syndrome (GBS) is characterized clinically by rapid progression of severe symptoms, such as the absence of brainstem reflexes, complete tetraplegia and respiratory arrest. The clinical course of fulminant GBS rema
Autor:
Takahiko Hirose, Eri Sano, Hiroki Tani, Kensuke Kakiuchi, Shigeki Arawaka, Shin Ota, Akihiro Tsukahara, Taro Shigekiyo, Hideto Nakajima, Fumiharu Kimura, Yoshitsugu Nakamura, Simon Ishida, Mikiko Motoki, Kiichi Unoda
Publikováno v:
Muscle & Nerve. 58:770-776
Introduction We evaluated post-noninvasive ventilation survival and factors for the transition to tracheostomy in amyotrophic lateral sclerosis (ALS). Methods We analyzed 197 patients using a prospectively collected database with 114 patients since 2
Autor:
Kensuke Kakiuchi, Yukiyo Yoshimoto, Shin Ota, Mikiko Motoki, Hideto Nakajima, Haruko Kitaoka, Fumiharu Kimura, Hiroki Tani, Shigeki Arawaka, Yoshinari Okumura
Publikováno v:
Nosotchu. 40:382-387
Autor:
Yoshitsugu Nakamura, Taro Shigekiyo, Masakazu Sugino, Shigeki Arawaka, Mikiko Motoki, Yuki Miyano, Ryoko Murakami, Hidenori Sato
Publikováno v:
Clinical Neurology and Neurosurgery. 208:106864
Myasthenia gravis (MG) is an autoimmune disease characterized by impaired neurotransmission at the neuromuscular junction. MG is generally non-inherited but is rarely inherited. Here, we report two patients with MG in the same pedigree: a 62-year-old
Publikováno v:
Neurology. 91:884-886
Neuronal intranuclear inclusion disease (NIID) is a slowly progressive neurodegenerative disorder characterized by eosinophilic hyaline inclusions in neuronal and somatic cells on histopathologic examination.1,2 NIID occurs in both sporadic and hered
Autor:
Hideto Nakajima, Mikiko Motoki
Publikováno v:
Neurology. 93(9)
We thank Lopez-Blanco et al. for the comment on our article.1 Fragile X-associated tremor/ataxia syndrome (FXTAS) is the inherited progressive neurologic disorder showing intention tremor or cerebellar ataxia, and the histopathologic features of FXTA
Autor:
Takahiko, Hirose, Fumiharu, Kimura, Hiroki, Tani, Shin, Ota, Akihiro, Tsukahara, Eri, Sano, Taro, Shigekiyo, Yoshitsugu, Nakamura, Kensuke, Kakiuchi, Mikiko, Motoki, Kiichi, Unoda, Simon, Ishida, Hideto, Nakajima, Shigeki, Arawaka
Publikováno v:
Musclenerve. 58(6)
We evaluated post-noninvasive ventilation survival and factors for the transition to tracheostomy in amyotrophic lateral sclerosis (ALS).We analyzed 197 patients using a prospectively collected database with 114 patients since 2000.Among 114 patients
Autor:
Y. Yoshimoto, Fumiharu Kimura, Akiyoshi Kakita, Mari Tada, Tomoe Sato, Shimon Ishida, Mikiko Motoki, Hideto Nakajima, Shigeki Arawaka
Publikováno v:
Journal of the Neurological Sciences. 381:972
Autor:
Kensuke Kakiuchi, E. Sano, Fumiharu Kimura, Takafumi Hosokawa, Shin Ota, Mikiko Motoki, Hideto Nakajima, Shimon Ishida, Kiichi Unoda, Shigeki Arawaka
Publikováno v:
Journal of the Neurological Sciences. 381:610