Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Hirofumi Kusaka"'
Autor:
Masataka Nakamura, Kentaro Nakayama, Aya Murakami, Satoshi Morise, Satoshi Kaneko, Hirofumi Kusaka, Yusuke Yakushiji
Publikováno v:
eNeurologicalSci, Vol 28, Iss , Pp 100413- (2022)
An autopsy case of sporadic amyotrophic lateral sclerosis (ALS) with lower urinary tract (LUT) and bowel dysfunction is reported. The dysfunction occurred simultaneously with motor neuron symptoms in the early stages of the illness. A 75-year-old man
Externí odkaz:
https://doaj.org/article/73ff5df20d1549cd96d8c0e0c45cf3fc
Autor:
Takenobu Kunieda, Kosuke Miyake, Hiroki Sakamoto, Masataka Nakamura, Yusuke Yakushiji, Hirofumi Kusaka
Publikováno v:
Interdisciplinary Neurosurgery, Vol 24, Iss , Pp 101092- (2021)
Objective: Optimal therapy to avoid cerebral hyperperfusion (CHP) after carotid artery stenting (CAS) is yet to be established. The purpose of this study was to determine whether pretreatment with a free radical scavenger, edaravone, could prevent CH
Externí odkaz:
https://doaj.org/article/323efcb6741f4f08ac53eef63d1375ea
Autor:
Naoki Suzuki, Madoka Mori-Yoshimura, Satoshi Yamashita, Satoshi Nakano, Ken-ya Murata, Megumi Mori, Yukie Inamori, Naoko Matsui, En Kimura, Hirofumi Kusaka, Tomoyoshi Kondo, Hidefumi Ito, Itsuro Higuchi, Akihiro Hashiguchi, Hiroyuki Nodera, Ryuji Kaji, Maki Tateyama, Rumiko Izumi, Hiroya Ono, Masaaki Kato, Hitoshi Warita, Toshiaki Takahashi, Ichizo Nishino, Masashi Aoki
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Sporadic inclusion body myositis (sIBM) is the most prevalent muscle disease in elderly people, affecting the daily activities. sIBM is progressive with unknown cause and without effective treatment. In 2015, sIBM was classified a
Externí odkaz:
https://doaj.org/article/d90db870023f4f18ac3c75896e30fe96
Autor:
Kentaro Nakayama, Masataka Nakamura, Akiko Konishi, Satoshi Kaneko, Kazuo Nakamichi, Masayuki Saijo, Yusuke Yakushiji, Hirofumi Kusaka
Publikováno v:
eNeurologicalSci, Vol 21, Iss , Pp 100269- (2020)
Externí odkaz:
https://doaj.org/article/1b54faf800b54116899b16ceac04b175
Autor:
Syugo Ueki, Masataka Nakamura, Risa Sasaki, Yoichiro Okada, Keisuke Yoshikawa, Susumu Kusunoki, Kazuyoshi Ishii, Hirofumi Kusaka, Takayuki Kondo
Publikováno v:
Case Reports in Neurology, Vol 10, Iss 1, Pp 88-94 (2018)
A 71-year-old man with Waldenström macroglobulinemia (WM) presented with a slowly progressive sensory disturbance and mild weakness predominantly affecting the distal portion of the limbs over the course of 6 months. Cervical magnetic resonance imag
Externí odkaz:
https://doaj.org/article/e9410dd5cbac46999fbfe6f76277b73a
Autor:
Naoki Suzuki, Madoka Mori-Yoshimura, Satoshi Yamashita, Satoshi Nakano, Ken-ya Murata, Yukie Inamori, Naoko Matsui, En Kimura, Hirofumi Kusaka, Tomoyoshi Kondo, Itsuro Higuchi, Ryuji Kaji, Maki Tateyama, Rumiko Izumi, Hiroya Ono, Masaaki Kato, Hitoshi Warita, Toshiaki Takahashi, Ichizo Nishino, Masashi Aoki
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-7 (2016)
Abstract Background Sporadic inclusion body myositis (sIBM) is the most prevalent acquired muscle disease in the elderly. sIBM is an intractable and progressive disease of unknown cause and without effective treatment. The etiology of sIBM is still u
Externí odkaz:
https://doaj.org/article/ccf1c87722e743dcae8206450e0f9648
Autor:
Hirofumi Kusaka, Yusuke Yakushiji, Aya Murakami, Masataka Nakamura, Yoshimi Nakamura, Satoshi Kaneko
Publikováno v:
Neuropathology. 41:357-365
We describe an autopsy case of neuronal intermediate filament inclusion disease (NIFID), a subtype of frontotemporal lobar degeneration (FTLD) with the appearance of fused-in-sarcoma (FUS) inclusions (FTLD-FUS). A 57-year-old man developed dysarthria
Autor:
Yuko Kataoka, Yusuke Yakushiji, Jun Takahashi, Hatsue Ishibashi-Ueda, Kazutaka Sonoda, Masatoshi Koga, Hirofumi Kusaka, Kazunori Toyoda
Publikováno v:
Journal of NeuroInterventional Surgery. 14:464-468
BackgroundThe procoagulant state in cancer increases the thrombotic risk, and underlying cancer could affect treatment strategies and outcomes in patients with ischemic stroke. However, the histopathological characteristics of retrieved thrombi in pa
Autor:
Masayuki Shintaku, Daita Kaneda, Takeshi Nakamura, Akiyo Shinde, Hirofumi Kusaka, Tetsuyuki Kitamoto, Atsuko Takeuchi
Publikováno v:
Neuropathology. 41:206-213
Genetic Creutzfeldt-Jakob disease (gCJD) with a methionine to arginine substitution at codon 232 of the prion protein gene (gCJD-M232R) is rare and has only been reported in Japan. We report an autopsy case of gCJD-M232R showing alleles of codon 129
Autor:
Satoshi Kaneko, Hirofumi Kusaka, Masataka Nakamura, Satoshi Morise, Norihiro Takenouchi, Rie Tohge, Mitsuaki Oki, Aya Murakami, Yusuke Yakushiji
Publikováno v:
Neuropharmacology. 198
Glutamate, GABA, acetylcholine, dopamine, and serotonin interact with each other to regulate the flow of neural information in the striatum. Serotonin type 1A receptor (5HT1A) is primarily expressed on glutamatergic nerve terminals, and 5HT1B is expr