Zobrazeno 1 - 10 of 57 pro vyhledávání: '"Yusei Shiga"'
1
Akademický článek
Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.
Autor: Maya Higuma, Nobuo Sanjo, Katsuya Satoh, Yusei Shiga, Kenji Sakai, Ichiro Nozaki, Tsuyoshi Hamaguchi, Yosikazu Nakamura, Tetsuyuki Kitamoto, Susumu Shirabe, Shigeo Murayama, Masahito Yamada, Jun Tateishi, Hidehiro Mizusawa
Publikováno v: PLoS ONE, Vol 8, Iss 3, p e60003 (2013)
A national system for surveillance of prion diseases (PrDs) was established in Japan in April 1999. Here, we analyzed the relationships among prion protein gene (PRNP) mutations and the clinical features, cerebrospinal fluid (CSF) markers, and pathol
Externí odkaz: https://doaj.org/article/8293e2f339d946c9b321b5f8ff1fac3e
Zobrazit plný text záznamu
2
Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt–Jakob disease
Autor: Minoru Tobiume, Susumu Shirabe, Yusei Shiga, Katsuya Satoh, Kazuo Mutsukura, Katsumi Eguhchi, Noriyuki Nishida, Testutaro Sata, Yuki Matsui
Publikováno v: Laboratory Investigation. 90:1637-1644
Periodic sharp wave complexes observed on an electroencephalographic recording and the presence of a 14-3-3 protein in the cerebrospinal fluid (CSF) are both included in the diagnostic criteria for the Creutzfeldt-Jakob disease (CJD) supplied by the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a23f7a64426348f132d318304b63b1b5
https://doi.org/10.1038/labinvest.2009.68
Zobrazit plný text záznamu
3
Encephalomyelopathy due to vitamin B12 deficiency with seizures as a predominant symptom
Autor: Itaru Kimura, Kinya Hisanaga, Yusei Shiga, Arifumi Matsumoto, Hiroshi Shimizu
Publikováno v: Rinsho Shinkeigaku. 49:179-185
We report a 39-year-old man who developed seizures as a predominant symptom of vitamin B12 deficiency. About a month before admission to our hospital, he experienced flickering vision, and had generalized convulsive seizures about ten times a day. On
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0607a3116bd3c5e0dfe6120a84b8e1ef
https://doi.org/10.5692/clinicalneurol.49.179
Zobrazit plný text záznamu
5
Anti-aquaporin-4 antibody is involved in the pathogenesis of NMO: a study on antibody titre
Autor: Yasuto Itoyama, Ichiro Nakashima, Isabelle Miyazawa, Chihiro Kanaoka, Tatsuro Misu, Masashi Nakamura, Shohei Watanabe, Yusei Shiga, Kazuo Fujihara, Toshiyuki Takahashi, Juichi Fujimori, Shigeru Sato
Publikováno v: Brain. 130:1235-1243
NMO-IgG is a disease-specific autoantibody for neuromyelitis optica (NMO) and its target antigen is aquaporin-4 (AQP4) water channel. Recently, we established a sensitive anti-AQP4 antibody assay using human AQP4-transfected cells, which appeared mor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f9c6329100413da0cbece182ef8c36de
https://doi.org/10.1093/brain/awm062
Zobrazit plný text záznamu
7
Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease
Autor: Koichi Miyazawa, S. Higano, Shunji Mugikura, Satoshi Shibuya, Yusei Shiga, S. Takahashi, Hidehiko Konno, Yasuto Itoyama, Y. Sato, H. Tamura, Katsumi Doh-ura, R. Fukushima, S. Sato
Publikováno v: Neurology. 63:443-449
Objective: To evaluate the usefulness of diffusion-weighted MRI (DWI) for the early diagnosis of Creutzfeldt–Jakob disease (CJD). Methods: Thirty-six consecutive patients (age 56 to 82 years) were enrolled, and 26 were examined by DWI. Nine were de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c274316d6cc4c390b780ff63d5471fab
https://doi.org/10.1212/01.wnl.0000134555.59460.5d
Zobrazit plný text záznamu
8
Familial Inclusion Body Myositis: A Report on Two Japanese Sisters
Autor: Koichi Narikawa, Yuzuru Taguchi, Muneshige Tobita, Takafumi Hasegawa, Atsushi Takeda, Yusei Shiga, Yasuto Itoyama, Maki Tateyama, Ryo Sakuma, Naohiro Saito, Ayumu Ohnuma, Yoshiaki Onodera, Kazuo Fujihara
Publikováno v: Internal Medicine. 42:1035-1038
Familial occurrence of inclusion body myositis is extremely rare, and only a few cases in Western countries have been reported. In these reports, a strong association of this disease with DR3 (DRB1*0301/0302) and the efficacy of immunosuppressants su
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01dcfc9ab5058066d475deac6eb0e87a
https://doi.org/10.2169/internalmedicine.42.1035
Zobrazit plný text záznamu
9
[Untitled]
Autor: Yusei Shiga
Publikováno v: The Japanese Journal of Rehabilitation Medicine. 39:780-784
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::751483d7332a849d036be2463fd4822d
https://doi.org/10.2490/jjrm1963.39.780
Zobrazit plný text záznamu
10
Clinical and physiological significance of abnormally prolonged central motor conduction time in HAM/TSP
Autor: Yasuto Itoyama, Kazuo Fujihara, Ayumu Ohnuma, Hiroshi Shimizu, Yusei Shiga
Publikováno v: Journal of the Neurological Sciences. 185:39-42
We measured the central motor conduction time (CMCT), central sensory conduction time (CSCT), F wave and mean F wave/M wave amplitude ratio in patients with HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) and controls. CMCTs in up
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd7df4b6f1d466e5c4806561a4ffe9c1
https://doi.org/10.1016/s0022-510x(01)00455-5
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje