Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Miwako Fujisawa"'
Autor:
Masaya Honda, Yukio Takeshita, Eri Ishiguchi, Fumitaka Shimizu, Miwako Fujisawa, Takashi Kanda, Toshihiko Maeda, Yasuteru Sano, Michiaki Koga
Publikováno v:
Clinical and Experimental Neuroimmunology. 12:258-267
Autor:
Miwako, Fujisawa, Takashi, Kanda
Publikováno v:
Brain and nerve = Shinkei kenkyu no shinpo. 74(5)
Sarcoidosis is a granulomatous multiorgan disease of unknown etiology that commonly affects the respiratory system, eyes, and skin, and less commonly affects the nervous system. Because of its rarity, a standard treatment for central nervous system (
Publikováno v:
Journal of neurology. 269(9)
Spinal cord sarcoidosis (SCS) is rare, and its diagnosis is challenging. We examined clinical, laboratory, and imaging features in patients with SCS to obtain useful clues for diagnosis and prognosis. Eleven consecutive patients (four males, seven fe
Autor:
Miwako Fujisawa, Yasuteru Sano, Joe Nemoto, Susumu Fujikawa, Yukio Takeshita, Shota Miyake, Kenichi Serizawa, Takashi Kanda, Fumitaka Shimizu, Kinya Matsuo, Richard M. Ransohoff, Haruna Tomizawa-Shinohara
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
article-version (Version of Record) 3
Background and ObjectivesTo evaluate the pathophysiology of neuromyelitis optica spectrum disorder (NMOSD) and the therapeutic mechanism and levels of interleukin-6 (IL-6) blockade (satralizumab), especially with respect to blood-brain barrier (BBB)
Autor:
Yukio Takeshita, Yasuteru Sano, Takashi Kanda, Haruna Tomizawa-Shinohara, Kinya Matsuo, Miwako Fujisawa, Fumitaka Shimizu, Richard M. Ransohoff, Shota Miyake, Susumu Fujikawa, Kenichi Serizawa, Joe Nemoto
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune astrocytopathy caused by antibodies against the aquaporin 4(AQP4) in end-feet of astrocytes. Breakdown of the blood–brain barrier (BBB) allowing ingress of AQP4 antibodies into the cen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9750e0897fa27e2fc9ab595fb1191ec8
https://doi.org/10.1101/2021.01.28.428564
https://doi.org/10.1101/2021.01.28.428564
Publikováno v:
Brain and nerve = Shinkei kenkyu no shinpo. 72(8)
Spinal cord sarcoidosis is rare, but often appears as a diagnostic challenge in myelopathy of unknown origin. Although definite diagnosis requires histological confirmation of non-caseating epithelioid granuloma in the spinal cord, it is hardly obtai
Autor:
Miwako Fujisawa, Yukio Takeshita, Susumu Fujikawa, Kinya Matsuo, Masashi Okamoto, Masaya Tamada, Fumitaka Shimizu, Yasuteru Sano, Michiaki Koga, Takashi Kanda
Publikováno v:
Journal of Neuroimmunology. 362:577783
Brain-derived neurotrophic factor (BDNF) cannot cross the blood-brain barrier (BBB) when administered peripherally, which hinders its therapeutic potential. We utilized an in vitro BBB model-a tri-culture of a human endothelial cell line, a pericyte
Autor:
Yukio Takeshita, Yasuteru Sano, Takashi Kanda, Ryo Ogawa, Kanako Hara, Ichiro Nakashima, Chihiro Kadono, Yoichi Mizukami, Kazuo Fujihara, Kenji Watanabe, Toshiyuki Takahashi, Tatsuro Misu, Toshihiko Maeda, Fumitaka Shimizu, Miwako Fujisawa
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
article-version (Version of Record) 3
Background and ObjectivesTo analyze (1) the effect of immunoglobulin G (IgG) from patients with anti–myelin oligodendrocyte glycoprotein antibody (MOG-Ab)–associated disorder on the blood-brain barrier (BBB) endothelial cells and (2) the positivi
Autor:
Michiaki Koga, J. Ogasawara, Hiroshi Takashima, Miwako Fujisawa, Masatoshi Omoto, Takashi Kanda, Yasuteru Sano
Publikováno v:
Rinsho Shinkeigaku. 57:515-520
We report a 59-year-old Japanese male who developed gradually worsening weakness and numbness of distal four extremities since age 50. His parents were first cousins, and blood and cerebral spinal examinations were unremarkable. Homozygous mutation o
Autor:
Miwako, Fujisawa, Yasuteru, Sano, Masatoshi, Omoto, Jyun-Ichi, Ogasawara, Michiaki, Koga, Hiroshi, Takashima, Takashi, Kanda
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 57(9)
We report a 59-year-old Japanese male who developed gradually worsening weakness and numbness of distal four extremities since age 50. His parents were first cousins, and blood and cerebral spinal examinations were unremarkable. Homozygous mutation o