Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Hirokazu, Furuya"'
Autor:
Yoshihiro Chadani, Tetsuo Kashibayashi, Takahiro Yamamoto, Atsushi Tsuda, Ryoko Fujito, Masanori Akamatsu, Naoto Kamimura, Ryuichi Takahashi, Takuji Yamagami, Hirokazu Furuya, Tetsuya Ueba, Motoaki Saito, Keiji Inoue, Hiroaki Kazui
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Apathy is frequently observed in idiopathic normal pressure hydrocephalus (iNPH) and worsens cognitive impairment and gait disturbance. In this study, we evaluated the regions associated with apathy in iNPH using statistical imaging analysis
Externí odkaz:
https://doaj.org/article/1a3ce94eed9e44ac99cc7d8c7174bc3a
Autor:
Taku Miyagawa, Susumu Tanaka, Mihoko Shimada, Noriaki Sakai, Kotomi Tanida, Nozomu Kotorii, Tatayu Kotorii, Yu Ariyoshi, Yuji Hashizume, Kimihiro Ogi, Hiroshi Hiejima, Takashi Kanbayashi, Aya Imanishi, Azusa Ikegami, Yuichi Kamei, Akiko Hida, Yamato Wada, Masayuki Miyamoto, Masanori Takami, Hideaki Kondo, Yoshiyuki Tamura, Yukari Taniyama, Naoto Omata, Tomoyuki Mizuno, Shunpei Moriya, Hirokazu Furuya, Mitsuhiro Kato, Kayoko Kato, Jun Ishigooka, Kazuhito Tsuruta, Shigeru Chiba, Naoto Yamada, Masako Okawa, Koichi Hirata, Kenji Kuroda, Kazuhiko Kume, Naohisa Uchimura, Masaaki Kitada, Tohru Kodama, Yuichi Inoue, Seiji Nishino, Kazuo Mishima, Katsushi Tokunaga, Makoto Honda
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-9 (2022)
Abstract Idiopathic hypersomnia (IH) is a rare, heterogeneous sleep disorder characterized by excessive daytime sleepiness. In contrast to narcolepsy type 1, which is a well-defined type of central disorders of hypersomnolence, the etiology of IH is
Externí odkaz:
https://doaj.org/article/d07ab5f0adcd4703970a8ce887df5b95
Autor:
George Umemoto, Shinsuke Fujioka, Hajime Arahata, Nobutaka Sakae, Naokazu Sasagasako, Mine Toda, Hirokazu Furuya, Yoshio Tsuboi
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background Swallowing dysfunction is related to major cause of adverse events and an indicator of shorter survival among patients with neuromuscular disorders (NMD). It is critical to assess the swallowing function during disease progression
Externí odkaz:
https://doaj.org/article/9d07dc087c5a4a7c93fc48d8888c1dc6
Autor:
Haruki Odaka, Tadahiro Numakawa, Minami Soga, Jun Kido, Shiro Matsumoto, Ryutaro Kajihara, Toshika Okumiya, Naoki Tani, Yuki Tanoue, Takaichi Fukuda, Hirokazu Furuya, Takafumi Inoue, Takumi Era
Publikováno v:
Neurobiology of Disease, Vol 152, Iss , Pp 105279- (2021)
Sialidosis is a neuropathic lysosomal storage disease caused by a deficiency in the NEU1 gene-encoding lysosomal neuraminidase and characterized by abnormal accumulation of undigested sialyl-oligoconjugates in systemic organs including brain. Althoug
Externí odkaz:
https://doaj.org/article/d2ee334841064119b1d66c5b560c755b
Autor:
Masashi Fukuoka, Masaki Takahashi, Hiromi Fujita, Tomoko Chiyo, H. Akiko Popiel, Shoko Watanabe, Hirokazu Furuya, Miho Murata, Keiji Wada, Takashi Okada, Yoshitaka Nagai, Hirohiko Hohjoh
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 11, Iss C, Pp 79-90 (2018)
Huntington’s disease (HD) is an intractable neurodegenerative disorder caused by mutant Huntingtin (HTT) proteins that adversely affect various biomolecules and genes. MicroRNAs (miRNAs), which are functional small non-coding RNAs, are also affecte
Externí odkaz:
https://doaj.org/article/223f3142b53e4d84b5a0fd79dddaa324
Autor:
George Umemoto, Yoshio Tsuboi, Hirokazu Furuya, Takayasu Mishima, Shinsuke Fujioka, Naoki Fujii, Hajime Arahata, Miwa Sugahara, Mitsuaki Sakai
Publikováno v:
Case Reports in Neurology, Vol 9, Iss 2, Pp 161-167 (2017)
Background: To investigate the impact of dysphagia in Perry syndrome (PS), an autosomal dominant parkinsonism caused by mutation of DCTN1, which is associated with hypoventilation, depression, and weight loss. Case Presentation: We used tongue pressu
Externí odkaz:
https://doaj.org/article/c89d4104d4e44de08c5caab8474ffee3
Publikováno v:
Rigakuryoho Kagaku. 37:9-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee3d4ab3528aaaf11cece781da726e88
https://doi.org/10.1589/rika.37.9
https://doi.org/10.1589/rika.37.9
Autor:
Yoshihiro Chadani, Tetsuo Kashibayashi, Takahiro Yamamoto, Atsushi Tsuda, Ryoko Fujito, Masanori Akamatsu, Naoto Kamimura, Ryuichi Takahashi, Takuji Yamagami, Hirokazu Furuya, Tetsuya Ueba, Motoaki Saito, Keiji Inoue, Hiroaki Kazui
BackgroundIdiopathic normal pressure hydrocephalus (iNPH) is a slowly progressive syndrome caused by the excessive accumulation of cerebrospinal fluid and is typically characterized by the triad of cognitive, gait, and urinary disturbances and ventri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9dd5e37cd9f53bedb36c9685194e9df
https://doi.org/10.21203/rs.3.rs-1833943/v1
https://doi.org/10.21203/rs.3.rs-1833943/v1
Autor:
Hideomi Hamasaki, Hirokazu Furuya, Naokazu Sasagasako, Satoshi O. Suzuki, Nobutaka Sakae, Toru Iwaki, Hiroyuki Honda, Shinichiro Mori
Publikováno v:
Neuropathology. 41:146-151
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disease, characterized by the progressive ossification of skeletal muscles, fascia, tendons, and ligaments. In most cases, the great toes of patients show symmetrical congenital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::284ab15da8f33c5294fea1742fe80ba4
https://doi.org/10.1111/neup.12715
https://doi.org/10.1111/neup.12715
Autor:
Nahoko Kaniwa, Mayumi Ueta, Ryosuke Nakamura, Yoshimi Okamoto-Uchida, Emiko Sugiyama, Keiko Maekawa, Yukitoshi Takahashi, Hirokazu Furuya, Akiko Yagami, Setsuko Matsukura, Zenro Ikezawa, Kayoko Matsunaga, Chie Sotozono, Michiko Aihara, Shigeru Kinoshita, Yoshiro Saito
Publikováno v:
Allergology International, Vol 64, Iss 4, Pp 379-381 (2015)
Externí odkaz:
https://doaj.org/article/925000f2f2c340f08f594969caf4dd44