Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Yoshimichi Miyazaki"'
Autor:
Waka Sakai, Naoko Matsui, Mitsuyo Ishida, Takahiro Furukawa, Yoshimichi Miyazaki, Koji Fujita, Ryosuke Miyamoto, Nobuaki Yamamoto, Wataru Sako, Kenta Sato, Kazuya Kondo, Yoshihiko Nishida, Takao Mitsui, Yuishin Izumi, Ryuji Kaji
Publikováno v:
eNeurologicalSci, Vol 2, Iss C, Pp 17-20 (2016)
Objective: The continuous increase in the number of patients presenting with late-onset myasthenia gravis (LOMG) underscores the need for a better understanding of the clinical course and the establishment of an optimal therapeutic strategy. We aimed
Externí odkaz:
https://doaj.org/article/e5ca09d9a4ea43fe9277010f1022eb6f
Autor:
Yu Hiramatsu, Yuji Okamoto, Akiko Yoshimura, Jun-Hui Yuan, Masahiro Ando, Yujiro Higuchi, Akihiro Hashiguchi, Eiji Matsuura, Fumihito Nozaki, Tomohiro Kumada, Kei Murayama, Mikiya Suzuki, Yuki Yamamoto, Naoko Matsui, Yoshimichi Miyazaki, Masamitsu Yamaguchi, Youji Suzuki, Jun Mitsui, Hiroyuki Ishiura, Masaki Tanaka, Shinichi Morishita, Ichizo Nishino, Shoji Tsuji, Hiroshi Takashima
Publikováno v:
Journal of Neurology. 269:4129-4140
Mitochondrial disorders are a group of clinically and genetically heterogeneous multisystem disorders and peripheral neuropathy is frequently described in the context of mutations in mitochondrial-related nuclear genes. This study aimed to identify t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f893b211b0287b22986e09af4ce16b
https://doi.org/10.1007/s00415-022-11026-w
https://doi.org/10.1007/s00415-022-11026-w
Publikováno v:
Rinsho Shinkeigaku. 62:363-368
We have reported a case of a 44-year-old woman with anti-signal recognition particle (SRP) antibody-positive immune-mediated necrotizing myopathy triggered by human parvovirus B19 (PVB19) infection. She was admitted to the hospital because of lower l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1da84888d226909af7168dd1dfae6cd
https://doi.org/10.5692/clinicalneurol.cn-001684
https://doi.org/10.5692/clinicalneurol.cn-001684
Autor:
Yoshimichi Miyazaki
Publikováno v:
Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 54:75-80
INTRODUCTION Familial amyloid polyneuropathy (FAP) is a rare hereditary disorder caused by mutations in the transthyretin (TTR) gene. Tafamidis is a TTR stabilizer able to prevent TTR tetramer dissociation, and several studies have demonstrated its s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a895a4614dcabc1591bc00f9edc409e1
https://doi.org/10.3143/geriatrics.54.75
https://doi.org/10.3143/geriatrics.54.75
Autor:
Nagahisa Murakami, Ryuji Kaji, Masafumi Harada, Wataru Sako, Yuishin Izumi, Yoshimichi Miyazaki, Takashi Abe
Publikováno v:
Journal of the Neurological Sciences. 368:104-108
There are many tools for differentiating between multiple system atrophy with predominant parkinsonian features (MSA-P) and Parkinson's disease (PD). These include middle cerebellar peduncle (MCP) width, apparent diffusion coefficient (ADC) value of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d3a0eca83afcb7e1bd757ec11326a35
https://doi.org/10.1016/j.jns.2016.06.061
https://doi.org/10.1016/j.jns.2016.06.061
Autor:
Mitsuyo Ishida, Yuishin Izumi, Ryuji Kaji, Kenta Sato, Kazuya Kondo, Nobuaki Yamamoto, Takahiro Furukawa, Waka Sakai, Yoshimichi Miyazaki, Takao Mitsui, Ryosuke Miyamoto, Yoshihiko Nishida, Naoko Matsui, Wataru Sako, Koji Fujita
Publikováno v:
eNeurologicalSci, Vol 2, Iss C, Pp 17-20 (2016)
eNeurologicalSci
eNeurologicalSci
Objective The continuous increase in the number of patients presenting with late-onset myasthenia gravis (LOMG) underscores the need for a better understanding of the clinical course and the establishment of an optimal therapeutic strategy. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83eceb98626c952557f3498d48f07fc1
https://doi.org/10.1016/j.ensci.2016.02.004
https://doi.org/10.1016/j.ensci.2016.02.004
Autor:
Ryuji Kaji, Shigeaki Suzuki, Yoshihiko Nishida, Yoshimichi Miyazaki, Ichizo Nishino, Naoko Matsui, Yuya Yamashita, Hiroki Yamazaki, Yuishin Izumi, Ai Tsukamoto, Hiroyuki Nodera
Publikováno v:
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine. 105(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4a4802c9ff63d0ce0cfb1320d1fd43d
https://pubmed.ncbi.nlm.nih.gov/30168990
https://pubmed.ncbi.nlm.nih.gov/30168990
Autor:
Masayasu Matsumoto, Hirofumi Maruyama, Naohisa Hosomi, Yuishin Izumi, Yoshimichi Miyazaki, Tomokazu Nishikawa, Tetsuya Takahashi, Masahiro Nakamori
Publikováno v:
Neuropathology and Applied Neurobiology. 42(7):639-653
Aims Neurofibrillary tangles (NFTs), a cardinal pathological feature of neurodegenerative disorders, such as Alzheimer's disease (AD) are primarily composed of hyper-phosphorylated tau protein. Recently, several other molecules, including flotillin-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29ea2dffde8f7a803c0b2c717cac0275
http://repo.lib.tokushima-u.ac.jp/115647
http://repo.lib.tokushima-u.ac.jp/115647
Autor:
Yuki Yamamoto, Naoko Matsui, Yuishin Izumi, Yu Hiramatsu, Yoshimichi Miyazaki, Hiroyuki Nodera, Hiroshi Takashima, Ryuji Kaji
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 57(2)
A 45-year-old man presented to us due to slowly progressive muscle weakness and sensory disturbances in his lower limbs since his 40's. He reported multiple episodes of exercise-induced severe muscle fatigue and brown urine in his childhood, which di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226efcbdaf6b5ff9e2919a3d572536ce
https://pubmed.ncbi.nlm.nih.gov/28132977
https://pubmed.ncbi.nlm.nih.gov/28132977
Autor:
Hideshi Kawakami, Ryosuke Miyamoto, Shinya Matsuura, Ryuji Kaji, Nagahisa Murakami, Yoshimichi Miyazaki, Kei Fukada, Hiroyuki Morino, Hirofumi Maruyama, Yuishin Izumi, Akio Yoshizawa
Publikováno v:
Journal of the Neurological Sciences. 337:219-223
Progressive myoclonic ataxia (PMA) is a clinical syndrome defined as progressive ataxia and myoclonus and infrequent seizures in the absence of progressive dementia. Due to the extremely heterogeneous nature of PMA, a large proportion of PMA cases re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48c24772df638019d88800bbe5e7fb97
https://doi.org/10.1016/j.jns.2013.11.032
https://doi.org/10.1016/j.jns.2013.11.032