Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Takanori Hata"'
Autor:
Yuji Ueno, Yuto Morishima, Takanori Hata, Atsuhiko Shindo, Hiroaki Murata, Tatsuya Saito, Yuki Nakamura, Kazumasa Shindo
Publikováno v:
Neurobiology of Disease, Vol 200, Iss , Pp 106639- (2024)
Introduction: Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and lower motor neurons, leading to death resulting mainly from respiratory failure, for which there is currently no curative treatment. Unde
Externí odkaz:
https://doaj.org/article/e41338ef7ee44638b182bffaff238deb
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:
Akane Satake, Takamura Nagasaka, Takafumi Kurita, Hiroaki Murata, Takanori Hata, Hiroyuki Shinmura, Hirochika Matsubara, Kazumasa Shindo, Yoshihisa Takiyama
Publikováno v:
eNeurologicalSci, Vol 27, Iss , Pp 100395- (2022)
We report a 77-year-old woman with a thymoma, anti-LGI1antibody associated encephalitis (LGI1 encephalitis), and MG accompanied by positive anti-acetylcholine receptor antibodies (AchR Ab) and anti-titin antibodies (titin Ab). She was treated with th
Externí odkaz:
https://doaj.org/article/5c3bc55084934a8f8848ad2f1a676f57
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:
Kazumasa Shindo, Tohko Sato, Hiroaki Murata, Yuta Ichinose, Takanori Hata, Yoshihisa Takiyama
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background Spinocerebellar ataxia type 31 (SCA 31) is a slowly progressive neurodegenerative disorder characterized by pure cerebellar ataxia. Unlike other CAG repeat diseases, sleep-related problems have not been reported in patients with S
Externí odkaz:
https://doaj.org/article/d910d56666b74e43ab109a91218427a2
Autor:
Keisuke Shimozono, Haitian Nan, Takanori Hata, Kozo Saito, Yeon-Jeong Kim, Hiroaki Nagatomo, Toshihisa Ohtsuka, Schuichi Koizumi, Yoshihisa Takiyama
Publikováno v:
Journal of Human Genetics. 67:679-686
SPG80 is a neurodegenerative disorder characterized by a pure type of juvenile-onset hereditary spastic paraplegia and is caused by a heterozygous mutation of the UBAP1 (ubiquitin-associated protein 1) gene. UBAP1 is one of the subunits of the endoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::371769b47e712db1bb5438276e6e3f4f
https://doi.org/10.1038/s10038-022-01073-6
https://doi.org/10.1038/s10038-022-01073-6
Autor:
Yuto Morishima, Akane Satake, Takanori Hata, Kishin Koh, Takamura Nagasaka, Toshiyuki Takahashi, Kazumasa Shindo, Yoshihisa Takiyama
Publikováno v:
Clinical and Experimental Neuroimmunology. 13:246-250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a98c7272ccc294e858301faf48b70f98
https://doi.org/10.1111/cen3.12708
https://doi.org/10.1111/cen3.12708
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