Zobrazeno 1 - 10 of 51 pro vyhledávání: '"Reiji, Aoki"'
1
Akademický článek
Higher longitudinal brain white matter atrophy rate in aquaporin-4 IgG-positive NMOSD compared with healthy controls
Autor: Hiroki Masuda, Masahiro Mori, Shigeki Hirano, Akiyuki Uzawa, Tomohiko Uchida, Mayumi Muto, Ryohei Ohtani, Reiji Aoki, Yoshiyuki Hirano, Japanese Alzheimer’s Disease Neuroimaging Initiative (J-ADNI), Satoshi Kuwabara
Publikováno v: Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract We aimed to compare longitudinal brain atrophy in patients with neuromyelitis optica spectrum disorder (NMOSD) with healthy controls (HCs). The atrophy rate in patients with anti-aquaporin-4 antibody-positive NMOSD (AQP4 + NMOSD) was compare
Externí odkaz: https://doaj.org/article/d4e69a73ba97431aa09c443cd37a3941
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2
Akademický článek
Elevated serum levels of bone morphogenetic protein-9 are associated with better outcome in AQP4-IgG seropositive NMOSD
Autor: Hiroki Masuda, Masahiro Mori, Akiyuki Uzawa, Tomohiko Uchida, Mayumi Muto, Ryohei Ohtani, Reiji Aoki, Satoshi Kuwabara
Publikováno v: Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Lymphatic drainage in the central nervous system is regulated by meningeal lymphatic vasculature, and recurrent neuroinflammation alters lymphatic vessel remodeling. Patients with aquaporin-4 antibody-positive neuromyelitis optica spectrum d
Externí odkaz: https://doaj.org/article/e5008498960642a48fbdcea2dcd6858b
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3
Delayed Appearance of Brain Magnetic Resonance Imaging Abnormalities in a Patient with Glial Fibrillary Acidic Protein Astrocytopathy
Autor: Michiko, Izumi, Akiyuki, Uzawa, Reiji, Aoki, Masahide, Suzuki, Koki, Yoshizawa, Yutaro, Suzuki, Akio, Kimura, Takayoshi, Shimohata, Satoshi, Kuwabara
Publikováno v: Internal Medicine. 62:465-468
Recent studies have reported that autoantibodies against glial fibrillary acidic protein (GFAP), a major cytoskeletal protein expressed in astrocytes, can lead to GFAP astrocytopathy, an autoimmune central nervous system inflammatory disease. We here
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99d4e6663dd1a9316963ed7e714ed6f5
https://doi.org/10.2169/internalmedicine.9724-22
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5
Silent progression of brain atrophy in aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder
Autor: Akiyuki Uzawa, Shigeki Hirano, Masahiro Mori, Reiji Aoki, Ryohei Ohtani, Satoshi Kuwabara, Mayumi Muto, Hiroki Masuda, Tomohiko Uchida
Publikováno v: Journal of Neurology, Neurosurgery, and Psychiatry
ObjectiveTo investigate longitudinal brain atrophy in patients with neuromyelitis optica spectrum disorder (NMOSD).MethodsWe investigated the longitudinal brain atrophy rate in patients with aquaporin-4 antibody-positive NMOSD (AQP4+NMOSD) and those
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93dc5c6cfc2abdc91f01ee31a0cbdba
https://doi.org/10.1136/jnnp-2021-326386
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6
Akademický článek
The distinct effects of orally administered Lactobacillus rhamnosus GG and Lactococcus lactis subsp. lactis C59 on gene expression in the murine small intestine.
Autor: Chise Suzuki, Ayako Aoki-Yoshida, Reiji Aoki, Keisuke Sasaki, Yoshiharu Takayama, Koko Mizumachi
Publikováno v: PLoS ONE, Vol 12, Iss 12, p e0188985 (2017)
The molecular mechanisms of strain-specific probiotic effects and the impact of the oral administration of probiotic strains on the host's gene expression are not yet well understood. The aim of this study was to investigate the strain-specific effec
Externí odkaz: https://doaj.org/article/60a0dbedbe2644f783735d0e6c807781
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7
Peroxiredoxins are involved in the pathogenesis of multiple sclerosis and neuromyelitis optica spectrum disorder
Autor: Hiroki Masuda, Tomohiko Uchida, Akiyuki Uzawa, Ryohei Ohtani, Reiji Aoki, Masahiro Mori, Satoshi Kuwabara
Publikováno v: Clin Exp Immunol
Summary Peroxiredoxins (PRXs) are intracellular anti-oxidative enzymes but work as inflammatory amplifiers under the extracellular condition. To date, the function of PRXs in the pathogenesis of multiple sclerosis (MS) and neuromyelitis optica spectr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::382961331d078cd03fcfae8a302bd368
https://doi.org/10.1111/cei.13487
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10
Clinical difference after the first optic neuritis between aquaporin-4-IgG-associated and myelin oligodendrocyte glycoprotein-IgG-associated disorders
Autor: Reiji Aoki, Masahiro Mori, Ryohei Ohtani, Hirotaka Yokouchi, Satoshi Kuwabara, Akiyuki Uzawa, Shuichi Yamamoto, Mayumi Muto, Hiroki Masuda, Tomohiko Uchida
Publikováno v: Journal of neurology. 269(4)
To investigate the difference in clinical course after the first optic neuritis (ON) between aquaporin-4 IgG-associated disorder (AQPAD) and myelin oligodendrocyte glycoprotein-IgG-associated disorder (MOGAD) METHODS: In this study, 31 eyes in 24 pat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1343121fc795db7bdfa24dcca8dc1e75
https://pubmed.ncbi.nlm.nih.gov/34455476
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