Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Toshihiro Hokonohara"'
Autor:
Takeshi Matsuoka, Akira Kondo, Satoshi O. Suzuki, Kensuke Sasaki, Toru Iwaki, Akiko Iwaki, Hiroyuki Honda, Toshihiro Hokonohara, Naoki Fujii
Publikováno v:
Neuropathology. 31:71-76
Basophilic inclusions (BIs), which are characterized by their staining properties of being weakly argyrophilic, reactive with Nissl staining, and immunohistochemically negative for tau and transactive response (TAR) DNA-binding protein 43 (TDP-43), h
Autor:
Nobuyuki Nukina, Yuko Nagara, H. Tashiro, Yasumasa Ohyagi, Shiro Miura, Hirokazu Furuya, Akiko Iwaki, Toshihiro Hokonohara, Jun Ichi Kira, Takahisa Tateishi, Yasuyuki Fukumaki, Ryo Yamasaki, Hitoshi Kikuchi, Toru Iwaki
Publikováno v:
Acta Neuropathologica. 119:355-364
Mutations in the fused in sarcoma gene (FUS) were recently found in patients with familial amyotrophic lateral sclerosis (ALS). The present study aimed to clarify unique features of familial ALS caused by FUS mutation in the Japanese population. We c
Publikováno v:
Nosotchu. 29:514-519
高齢者で多くみられる大脳白質病変は虚血性変化と考えられているが, 白質病変が高度であれば脳梗塞発症の危険が高いことが指摘されている. 今回, 高度の大脳白質病変を背景に発症し
Autor:
Hitoshi Warita, Masashi Aoki, Masaaki Kato, Tetsuya Akiyama, Toshihiro Hokonohara, Naoko Shimakura, Yasuto Itoyama, Hideki Mizuno, Akiko Iwaki, Shinji Togashi, Naoki Suzuki, Hirokazu Furuya, Hidehiko Konno
Publikováno v:
Journal of Human Genetics. 55:252-254
Mutations in the fused in sarcoma (FUS, also known as translated in liposarcoma) gene have been recently discovered to be associated with familial amyotrophic lateral sclerosis (FALS) in African, European and American populations. In a Japanese famil
Autor:
Hidehiko Konno, Tetsuya Akiyama, Naoko Shimakura, Yasuto Itoyama, Hideki Mizuno, Toshihiro Hokonohara, Akiko Iwaki, Shinji Togashi, Hirokazu Furuya, Naoki Suzuki, Masashi Aoki, Hitoshi Warita, Masaaki Kato
Publikováno v:
Journal of Human Genetics. 60:653-654
Autor:
Takeshi, Matsuoka, Naoki, Fujii, Akira, Kondo, Akiko, Iwaki, Toshihiro, Hokonohara, Hiroyuki, Honda, Kensuke, Sasaki, Satoshi O, Suzuki, Toru, Iwaki
Publikováno v:
Neuropathology : official journal of the Japanese Society of Neuropathology. 31(1)
Basophilic inclusions (BIs), which are characterized by their staining properties of being weakly argyrophilic, reactive with Nissl staining, and immunohistochemically negative for tau and transactive response (TAR) DNA-binding protein 43 (TDP-43), h
Autor:
Hiroshi Shigeto, Yasumasa Ohyagi, Michiya Uehara, Yuji Kawano, Jun Ichi Kira, Toshihiro Hokonohara
Publikováno v:
Journal of the Neurological Sciences. 275:157-158
We report the first non-Caucasian case of facial onset sensory and motor neuronopathy (FOSMN) syndrome partially responding to various immunotherapies. A 55-year-old man had first felt paresthesia on his right cheek at age 45. This gradually extended