Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ban-yu Saitoh"'
Autor:
Ban-yu Saitoh, Takahisa Tateishi, Motoi Yoshimura, Satoshi O. Suzuki, Noriko Isobe, Toru Iwaki, Jun-ichi Kira
Publikováno v:
Internal Medicine. 61:2941-2945
A 59-year-old woman with a diabetes history experienced mild neck pain. A neurological examination revealed only mild neck stiffness. Magnetic resonance imaging showed extensive T2-weighted high-intensity lesions with patchy gadolinium enhancement ma
Autor:
Yuko Nakamuta, Ban yu Saitoh, Norio Yamamoto, Daan van Kruining, Kyoko Iinuma, Hiroo Yamaguchi, Jun Ichi Kira, Koichiro Matsumoto, Ryo Yamasaki, Eizo Tanaka
Publikováno v:
Brain Behavior and Immunity, 95, 362-380. Elsevier Science
Microglia play key roles in synaptic pruning, which primarily occurs from the postnatal period to adolescence. Synaptic pruning is essential for normal brain development and its impairment is implicated in neuropsychiatric developmental diseases such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad1e495320cafcdfa538911c95b2358f
https://cris.maastrichtuniversity.nl/en/publications/26dea6de-1a45-4c47-b44c-f0bf39172a22
https://cris.maastrichtuniversity.nl/en/publications/26dea6de-1a45-4c47-b44c-f0bf39172a22
Autor:
Kunihiro Yoshida, Yoshihiro Mitsunaga, Takuya Matsushita, Jun Ichi Kira, Yasuhiro Maeda, Ban yu Saitoh, Akio Hiwatashi, Ryo Yamasaki, Shintaro Hayashi, Noriko Isobe, Shu-ichi Ikeda
Publikováno v:
Multiple Sclerosis and Related Disorders. 31:22-31
Background Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) is a rare autosomal-dominant white matter disease, typically characterized by juvenile cognitive decline and frontoparietal white matter lesions. A portion of HDLS patient
Autor:
Kyoko Iinuma, Yoshinori Hayashi, Takuya Matsushita, Jun Ichi Kira, Yusaku Nakabeppu, Daisuke Tsuchimoto, Hiroshi Nakanishi, Ryo Yamasaki, Ban yu Saitoh, Takayuki Fujii, Mizuho A. Kido, Shinichi Aishima
Publikováno v:
Annals of Neurology. 84:208-224
OBJECTIVE To identify novel autoantibodies for neuropathic pain (NeP). METHODS We screened autoantibodies that selectively bind to mouse unmyelinated C-fiber type dorsal root ganglion (DRG) neurons using tissue-based indirect immunofluorescence assay
Autor:
Osamu Watanabe, Taira Uehara, Hikaru Doi, Hiroyuki Murai, Jun Ichi Kira, Ryo Yamasaki, Shintaro Hayashi, Katsuya Ogata, Ban yu Saitoh
Publikováno v:
Journal of the Neurological Sciences. 364:133-135
Autor:
Takayuki, Fujii, Ryo, Yamasaki, Kyoko, Iinuma, Daisuke, Tsuchimoto, Yoshinori, Hayashi, Ban-Yu, Saitoh, Takuya, Matsushita, Mizuho A, Kido, Shinichi, Aishima, Hiroshi, Nakanishi, Yusaku, Nakabeppu, Jun-Ichi, Kira
Publikováno v:
Annals of neurology. 84(2)
To identify novel autoantibodies for neuropathic pain (NeP).We screened autoantibodies that selectively bind to mouse unmyelinated C-fiber type dorsal root ganglion (DRG) neurons using tissue-based indirect immunofluorescence assays (IFA) with sera f
Autor:
Yukihiko Washimi, Kazuhiro Fukushima, Ken Ichi Hoshi, Nobuo Araki, Ikuru Yazawa, Michiaki Kinoshita, Shu-ichi Ikeda, Yasufumi Kondo, Ban-yu Saitoh, Jun Ichi Kira, Kunihiro Yoshida, Keisuke Ishizawa
Publikováno v:
INTERNAL MEDICINE. 53(1):21-27
Objective Hereditary diffuse leukoencephalopathy with neuroaxonal spheroids (HDLS) is an adult-onset white matter disease that presents clinically with cognitive, mental and motor dysfunction. Several autopsy reports have indicated that the corpus ca
Autor:
Kunihiro Yoshida, Shintaro Hayashi, Shu-ichi Ikeda, Ban-yu Saitoh, Jun Ichi Kira, Toru Iwaki, Satoshi O. Suzuki, Takashi Kamada, Ryo Yamasaki, Shinya Sato, Hiroyuki Murai
Publikováno v:
Clinical and Experimental Neuroimmunology. 4:76-81
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) is a rare autosomal dominant disease characterized by cerebral white matter degeneration with axonal spheroids. The disease is caused by mutations in the protein tyrosine kinase doma
Autor:
Kunihiro Yoshida, Ryo Yamasaki, Hiroyuki Murai, Ban yu Saitoh, Toru Iwaki, Yasumasa Ohyagi, Jun Ichi Kira, Satoshi Yoshimura, Takahisa Tateishi, Shintaro Hayashi
Publikováno v:
Multiple Sclerosis Journal. 19:1367-1370
We report a sporadic case of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) confirmed by biopsy and colony-stimulating factor 1 receptor ( CSF1R) sequencing. A 28-year-old woman developed progressive spastic gait and dysarthria.
Autor:
Ban-yu Saitoh
Publikováno v:
Rinsho Shinkeigaku. 54:1162-1164
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) is an autosomal dominant inherited leukoencephalopathy characterized by numerous cerebral neuroaxonal spheroids. To date, detection of colony stimulating factor 1 receptor (CSF-1R) g