Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Hisamasa, Imai"'
Autor:
Akira Uehara, Hiroaki Kawamoto, Hisamasa Imai, Makoto Shirai, Masatomi Sone, Sachiko Noda, Shigeto Sato, Nobutaka Hattori, Yoshiyuki Sankai
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Cybernic treatment involves the generation of an interactive bio-feedback loop between an individual’s nervous system and the worn cyborg Hybrid Assistive Limb (HAL); this treatment has been applied for several intractable neuromuscular di
Externí odkaz:
https://doaj.org/article/3e649abc60854bdab4509da06dcc118d
Autor:
Hikari Nunomura, Taketoshi Kasahara, Taku Hatano, Hitoshi Shimada, Yuhei Takado, Hironobu Endo, Ayako Inoshita, Atsuko Inomata, Toshihisa Murofushi, Shihoko Misawa, Yutaka Machida, Hisamasa Imai
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
We report a 63-year-old female patient with progressive supranuclear palsy (PSP). She presented predominant postural instability and “saccadic ping-pong gaze” (SPPG). She had unprovoked falls recurrently within a year from the onset of gait distu
Externí odkaz:
https://doaj.org/article/776ad5586a56409ca3751183f739c88b
Autor:
Akira Uehara, Hiroaki Kawamoto, Hisamasa Imai, Makoto Shirai, Masatomi Sone, Sachiko Noda, Shigeto Sato, Nobutaka Hattori, Yoshiyuki Sankai
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/b547e14e6484494f9461ce1b70e0db43
Autor:
Kazuyuki Noda, Yuanzhe Li, Takanobu Takei, Hiroyo Yoshino, Hisamasa Imai, Ryoichi Kurisaki, T. Yamashita, Masahiko Tomiyama, Takao Hashimoto, Shigeru Matsuzaki, Fumikazu Kojima, Yoshio Tsuboi, Fusako Yokochi, Naohisa Ueda, Kenya Nishioka, Manabu Funayama, Katsuo Kimura, Kenichi Kashihara, Yuichiro, Morikazu Shibasaki, Shinji Ohara, Shinsuke Fujioka, Nobuya Fujita, Nobuhiro Dougu, Tomoyo Shimada, Hitoshi Yamada, Fumiaki Tanaka, Chizu Wada, Kensuke Daida, Yujiro Higuchi, Yuji Nakatsuji, Yoshinori Hirata, Takenori Uozumi, Nobutaka Hattori, Kazuma Sugie, Nobuyuki Eura, Yasushi Shimo, Chieko Suzuki, Ryoichi Okiyama
Publikováno v:
Neurobiology of aging. 97
This study aimed to evaluate genotype-phenotype correlations of Parkinson’s disease (PD) patients with phospholipase A2 group V (PLA2G6) variants. We analyzed the DNA of 798 patients with PD, including 78 PD patients reported previously, and 336 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb552caaca90ccb62eaa46fbfaeea6b7
https://pubmed.ncbi.nlm.nih.gov/32771225
https://pubmed.ncbi.nlm.nih.gov/32771225
Autor:
Hisamasa Imai, Shigeto Sato, Nobutaka Hattori, Yoshiyuki Sankai, Hiroaki Kawamoto, Masatomi Sone, Makoto Shirai, Sachiko Noda, Akira Uehara
Publikováno v:
SII
Freezing of gait (FOG) is one of the typical locomotion disorders associated with Parkinsonism, and is described as the inability to move the feet despite an attempt to walk. The fear of falling over and other symptoms of FOG can be distressing to pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::becd6493672ea538ffa780b18e3b8847
https://doi.org/10.1109/sii46433.2020.9025882
https://doi.org/10.1109/sii46433.2020.9025882
Publikováno v:
Juntendo Medical Journal. 62:240-247
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cab7899605034db6ec2f8638c1499fd2
https://doi.org/10.14789/jmj.62.240
https://doi.org/10.14789/jmj.62.240
Autor:
Kei-Ichi Ishikawa, Hisamasa Imai, Kotaro Ogaki, Yumiko Motoi, T. Kobayashi, Shigeki Kuzuhara, Masahiko Kishi, Takashi Nonaka, Masato Hasegawa, Keiichi Shioya, Nobutaka Hattori, Hiroyuki Tomiyama, Masashi Takanashi, Yuanzhe Li, Tetsuro Tsukamoto, Masayuki Yokochi, Ryogen Sasaki, Manabu Funayama, Hiroyo Yoshino, Yasumasa Kokubo
Publikováno v:
Parkinsonism & Related Disorders. 19:15-20
Background Mutations in the microtubule associated protein tau ( MAPT ) and progranulin ( PGRN ) have been identified in several neurodegenerative disorders, such as frontotemporal lobar degeneration (FTLD), progressive supranuclear palsy (PSP), and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9807b5a5f3516392a832b52a38a6f5
https://doi.org/10.1016/j.parkreldis.2012.06.019
https://doi.org/10.1016/j.parkreldis.2012.06.019
Autor:
Tomokazu Obi, Kenya Nishioka, Kiichi Ishiwata, Yoshikuni Mizuno, Owen A. Ross, Masashi Takanashi, Yuichi Inoue, Jennifer M. Kachergus, Matthew J. Farrer, Satoshi Kono, Mayumi Kitagawa, Nobutaka Hattori, Hisamasa Imai, Koichi Mizoguchi, Kenji Ishii
Publikováno v:
Movement Disorders. 24:1811-1819
SNCA duplication is a recognized cause of familial Parkinson's disease (PD). We aimed to explore the genetic and clinical variability in the disease manifestation. Molecular characterization was performed using real-time PCR, SNP arrays, and haplotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60b87fab6297fa82c25a3e714da83704
https://doi.org/10.1002/mds.22682
https://doi.org/10.1002/mds.22682
Autor:
Hiroyo Yoshino, Miho Murata, Andrew B. Singleton, Shin Hayashi, Kenichi Sato, Koichi Mizoguchi, Matthew J. Farrer, Tatsushi Toda, Hiroyuki Tomiyama, Nobutaka Hattori, Issei Imoto, Ryu Kuroda, Kenya Nishioka, Johji Inazawa, Yoshikuni Mizuno, Toshiaki Kitami, Hisamasa Imai
Publikováno v:
Annals of Neurology. 59:298-309
Objective Recently, genomic multiplications of α-synuclein gene (SNCA) have been reported to cause hereditary early-onset parkinsonism. The objective of this study was to assess the frequency of SNCA multiplications among autosomal dominant heredita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085c673beb03141572fa60990418e385
https://doi.org/10.1002/ana.20753
https://doi.org/10.1002/ana.20753