Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Mai, Tsuchiya"'
Autor:
Yuto Morishima, Takanori Hata, Sho Nakajima, Kazumasa Shindo, Mai Tsuchiya, Tsubasa Watanabe, Ippei Tahara, Tetsuo Kondo, Akio Kimura, Takayoshi Shimohata, Yuji Ueno
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
A 54-year-old Japanese man presented with headache and fever the day after SARS-CoV-2 vaccination. He became deeply unconscious within a week. Brain MRI showed periventricular linear enhancements and a few spotty lesions in the cerebral white matter.
Externí odkaz:
https://doaj.org/article/16571e58bcc84894877012d342beec9e
Autor:
Kazumasa Shindo, Yuto Morishima, Yumi Suwa, Toko Fukao, Takafumi Kurita, Akane Satake, Mai Tsuchiya, Yuta Ichinose, Takanori Hata, Kishin Koh, Takamura Nagasaka, Yoshihisa Takiyama
Publikováno v:
The Journal of Clinical Hypertension, Vol 23, Iss 1, Pp 175-178 (2021)
Abstract This study evaluated yearly changes in systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rates (HR) for patients with Parkinson's disease (PD). Data were collected for the last 10 years from medical records of 28 PD pa
Externí odkaz:
https://doaj.org/article/f6a9c89fcbb24158bb8a1d771260a69f
Autor:
Takanori Hata, Takamura Nagasaka, Kishin Koh, Mai Tsuchiya, Yuta Ichinose, Haitian Nan, Kazumasa Shindo, Yoshihisa Takiyama
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Non-dystrophic myotonias (NDMs) are skeletal muscle disorders involving myotonia distinct from myotonic dystrophy. It has been reported that the muscle pathology is usually normal or comprises mild myopathic changes in NDMs. We de
Externí odkaz:
https://doaj.org/article/bddeb86745e6419ea9205b1f861fbb32
Autor:
Kazumasa Shindo, Mai Tsuchiya, Takanori Hata, Yuta Ichinose, Kishin Koh, Jun Sone, Takamura Nagasaka, Gen Sobue, Yoshihisa Takiyama
Publikováno v:
Epilepsy and Behavior Case Reports, Vol 11, Iss , Pp 103-106 (2019)
We report a case of neuronal intranuclear inclusion disease (NIID) confirmed by detection of intranuclear inclusions in a skin biopsy specimen. Brain magnetic resonance imaging showed mild cerebral atrophy and linear hyperintensities at the corticome
Externí odkaz:
https://doaj.org/article/e9a5d3c59d68434fbaa02c915b3bf077
Autor:
Yuto Morishima, Yuji Ueno, Akane Satake, Toko Fukao, Mai Tsuchiya, Takanori Hata, Tatsuyuki Ogawa, Naoki Oishi, Sho Nakajima, Shuji Hirata, Kazumasa Shindo, Yoshihisa Takiyama
Publikováno v:
Neurological Sciences.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d3f9f539033141c73d0eb5f70ebe530
https://doi.org/10.1007/s10072-023-06701-3
https://doi.org/10.1007/s10072-023-06701-3
Publikováno v:
Rinsho shinkeigaku = Clinical neurology.
A 55-year-old man presented a slowly progressive sensory disorder, predominantly in both lower limbs, and gait disturbance. Neurological examinations revealed abnormal sensation and spasticity in both lower limbs, and a wide-based gait. Although exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f59cc9414cf1039024d48b313890992
https://pubmed.ncbi.nlm.nih.gov/36567103
https://pubmed.ncbi.nlm.nih.gov/36567103
Autor:
Kazuho Nishimura, Takuya Kumazawa, Takao Kuroda, Naohiro Katagiri, Mai Tsuchiya, Natsuka Goto, Ryohei Furumai, Akiko Murayama, Junn Yanagisawa, Keiji Kimura
Publikováno v:
Cell Reports, Vol 10, Iss 8, Pp 1310-1323 (2015)
The 5S ribonucleoprotein particle (RNP) complex, consisting of RPL11, RPL5, and 5S rRNA, is implicated in p53 regulation under ribotoxic stress. Here, we show that the 5S RNP contributes to p53 activation and promotes cellular senescence in response
Externí odkaz:
https://doaj.org/article/069e6be3279643a59b0f5e89ca0da1da
Autor:
Mai Tsuchiya, Tohko Sato, Yoshihisa Takiyama, Kishin Koh, Kazumasa Shindo, Takafumi Kurita, Takanori Hata, Takahiro Natori, Takamura Nagasaka, Akane Satake
Publikováno v:
Journal of Clinical Neuroscience. 87:80-83
Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder characterized by slowly progressive cerebellar ataxia. Previously, autonomic symptoms or dysfunction have not been reported. To evaluate subclinical auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe31fa8a983dccb369dca0893ea02d9
https://doi.org/10.1016/j.jocn.2021.02.005
https://doi.org/10.1016/j.jocn.2021.02.005
Autor:
Hiroyuki Ishiura, Makio Takahashi, Shoji Tsuji, Mai Tsuchiya, Takeshi Nakamura, Kohei Suzuyama, Hideo Hara, Haruo Shimazaki, Yoshihisa Takiyama, Kishin Koh
Publikováno v:
Journal of Human Genetics. 67:119-121
Hereditary spastic paraplegias (HSPs) comprise a group of neurodegenerative disorders characterized by weakness and leg spasticity. LYST is responsible for Chediak-Higashi syndrome (CHS), which exhibits partial oculocutaneous albinism, primary immuno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc6fa4aee5dc1b435e99dc64d14a6125
https://doi.org/10.1038/s10038-021-00977-z
https://doi.org/10.1038/s10038-021-00977-z
Autor:
Yoshihisa Takiyama, Takahiro Natori, Mai Tsuchiya, Hiroyuki Kinouchi, Ryusuke Takaki, Mitsuto Hanihara
Publikováno v:
Rinsho Shinkeigaku. 61:733-738
We report here a rare case of adult-onset multiloculated hydrocephalus (MLH) after Cryptococcal meningitis. A 63-year-old man had Cryptococcal ventriculitis in 2011, and he recovered with treatment of antimycotic drugs. However, he was admitted again
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77c7d894f0da35507519349d9001a47
https://doi.org/10.5692/clinicalneurol.cn-001611
https://doi.org/10.5692/clinicalneurol.cn-001611