Zobrazeno 1 - 10
of 148
pro vyhledávání: '"Koji Abe"'
Autor:
Toru Yamashita, Koji Abe
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 5, p 2945 (2024)
The brain is susceptible to oxidative stress, which is associated with various neurological diseases. Edaravone (MCI-186, 3-methyl-1 pheny-2-pyrazolin-5-one), a free radical scavenger, has promising effects by quenching hydroxyl radicals (∙OH) and
Externí odkaz:
https://doaj.org/article/c6ed3eed92844d33b867697294bb47d2
Autor:
Toru Yamashita, Yumiko Nakano, Ryo Sasaki, Koh Tadokoro, Yoshio Omote, Taijun Yunoki, Yuko Kawahara, Namiko Matsumoto, Yuki Taira, Chika Matsuoka, Ryuta Morihara, Koji Abe
Publikováno v:
Cell Transplantation, Vol 32 (2023)
Amyotrophic lateral sclerosis (ALS) is characterized by progressive loss of motor neurons. Multilineage-differentiating stress-enduring (Muse) cells are unique endogenous stem cells that show therapeutic effects on motor function in ALS mouse models.
Externí odkaz:
https://doaj.org/article/5ff48f4404954d2cb411e219c297aefc
Autor:
Hongming Sun, Ryuta Morihara, Tian Feng, Zhihong Bian, Haibo Yu, Xiao Hu, Xinran Hu, Yuting Bian, Ryo Sasaki, Yusuke Fukui, Mami Takemoto, Taijun Yunoki, Yumiko Nakano, Koji Abe, Toru Yamashita
Publikováno v:
Cell Transplantation, Vol 32 (2023)
Human cord blood–endothelial progenitor cells (hCB-EPCs) isolated from the human umbilical cord can be used to repair damaged arteries. In this study, we used an animal model with pathological changes that mimics artery wall damage caused by stent
Externí odkaz:
https://doaj.org/article/8cf223bf45c843d3979752c99ed01a22
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 380-383 (2021)
We report a 72-year-old woman with Miller-Fisher syndrome (MFS) with syndrome of inappropriate secretion of antidiuretic hormone (SIADH). She developed diplopia and unsteady gait a week after an upper respiratory infection. Neurologic examination rev
Externí odkaz:
https://doaj.org/article/0712550559724cbcb089d9c36b9e5aac
Publikováno v:
Reproductive Biology and Endocrinology, Vol 19, Iss 1, Pp 1-14 (2021)
Abstract Growing evidence indicates that reduced uterine perfusion pressure (RUPP) triggers the cascade of events leading to preeclampsia. Edaravone is a powerful free radical scavenger used for the treatment of ischemia/reperfusion diseases due to i
Externí odkaz:
https://doaj.org/article/15c397ae738e4634bf4916fc65dade29
Autor:
Shunya Fujiwara, Yasuhiro Manabe, Yumiko Nakano, Yoshio Omote, Taijun Yunoki, Syoichiro Kono, Hisashi Narai, Koji Abe
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 1, Pp 78-83 (2021)
We report 2 cases of probable neuro-Behçet’s disease (NBD) with longitudinally extensive transverse myelitis (LETM). In both cases, the patients presented paraplegia, as well as sensory, bladder, and rectal disturbances. Magnetic resonance imaging
Externí odkaz:
https://doaj.org/article/8252b7c756e84b1bb65c150aaa5d3503
Autor:
Toru Yamashita, Yoshihiro Kushida, Shohei Wakao, Koh Tadokoro, Emi Nomura, Yoshio Omote, Mami Takemoto, Nozomi Hishikawa, Yasuyuki Ohta, Mari Dezawa, Koji Abe
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/0008d16f6e06481e8232886b89a380b8
Autor:
Yuriko Yamamura, Yoshinori Matsumoto, Koh Tadokoro, Yasuyuki Ohta, Kota Sato, Toru Yamashita, Masahiro Yamamura, Ken-Ei Sada, Koji Abe, Jun Wada
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Statin-associated necrotizing myopathy (SANM) is a rare autoimmune disorder caused by administration of statins. SANM is characterized by weakness due to necrosis and regeneration of myofibers. Here we report the first case of SAN
Externí odkaz:
https://doaj.org/article/3f2ac79a96f84a3eb84fdd05324b7bdd
Autor:
Shunya Fujiwara, Yasuhiro Manabe, Ryuta Morihara, Taijun Yunoki, Syoichiro Kono, Hisashi Narai, Koji Abe
Publikováno v:
Case Reports in Neurology, Vol 12, Iss 1, Pp 13-17 (2020)
We report two cases of very-late-onset neuromyelitis optica spectrum disorder (NMOSD) in patients over the age of 80 with transverse myelopathy as the initial manifestation. In both cases, the patients presented with paraplegia and sensory, bladder,
Externí odkaz:
https://doaj.org/article/941d8f2e56f44456984ec5213194ac1c
Publikováno v:
Case Reports in Neurology, Vol 11, Iss 3, Pp 299-303 (2019)
We report a rare case of Campylobacter fetus meningitis and pyogenic spondylodiscitis in a healthy young woman. A 35-year-old woman without significant medical history presented with fever, headache, and low back pain. C. fetus was detected from the
Externí odkaz:
https://doaj.org/article/cbb471df5ca840d39c8b6e06100d7443