Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Masaki, Kamada"'
Autor:
Tadayuki Takata, Yohei Kokudo, Asahiro Morishita, Kodai Kume, Tatsuo Yachida, Masaki Kamada, Hideki Kobara, Kazushi Deguchi, Tetsuo Touge, Hisashi Masugata, Tsutomu Masaki
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 944-946 (2021)
Abstract Eradication therapy of Helicobacter pylori may be safe if hemin has been intravenously administered in advance, even in patients with a history of recurrent acute porphyria attack.
Externí odkaz:
https://doaj.org/article/87274423f74c419f9e79b6731e74366c
Autor:
Takashi Kurashige, Masahito Kuramochi, Ryosuke Ohsawa, Yui Yamashita, Go Shioi, Hiroyuki Morino, Masaki Kamada, Takashi Ayaki, Hidefumi Ito, Yusuke Sotomaru, Hirofumi Maruyama, Hideshi Kawakami
Publikováno v:
Neurobiology of Disease, Vol 148, Iss , Pp 105215- (2021)
We previously showed that optineurin (OPTN) mutations lead to the development of amyotrophic lateral sclerosis. The association between OPTN mutations and the pathogenesis of amyotrophic lateral sclerosis remains unclear. To investigate the mechanism
Externí odkaz:
https://doaj.org/article/190dffdfc2224b6d86b31a6626a887da
Autor:
Keiji Wakamatsu, Yoichi Chiba, Ryuta Murakami, Yumi Miyai, Koichi Matsumoto, Masaki Kamada, Wakako Nonaka, Naoya Uemura, Ken Yanase, Masaki Ueno
Publikováno v:
Metabolites, Vol 12, Iss 4, p 343 (2022)
Despite recent advances in diagnostic procedures for neurological disorders, it is still difficult to definitively diagnose some neurodegenerative diseases without neuropathological examination of autopsied brain tissue. As pathological processes in
Externí odkaz:
https://doaj.org/article/960fe33bbcd948918c113518f5eca021
Autor:
Tsuyoshi Torii, Hirofumi Maruyama, Ryosuke Ohsawa, Yuhei Kanaya, Yuishin Izumi, Hiroyuki Morino, Kodai Kume, Masaki Kamada, Hideshi Kawakami, Takashi Kurashige
Publikováno v:
Journal of Human Genetics. 66:957-964
Parkinson’s disease (PD) is caused by a combination of genetic and environmental factors. Notably, genetic risk factors vary according to ethnicity and geographical regions, and few studies have analyzed the frequency of PD causative genes in Japan
Autor:
Hiroyuki Naito, Tetsuya Takahashi, Masaki Kamada, Hiroyuki Morino, Hiroyo Yoshino, Nobutaka Hattori, Hirofumi Maruyama, Hideshi Kawakami, Masayasu Matsumoto
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177955 (2017)
Spinocerebellar ataxia type 10 (SCA10) is an autosomal-dominant cerebellar ataxia that is variably accompanied by epilepsy and other neurological disorders. It is caused by an expansion of the ATTCT pentanucleotide repeat in intron 9 of the ATXN10 ge
Externí odkaz:
https://doaj.org/article/72492aeaf3ef42068ebd29ff9abb38d6
Autor:
Wakako Nonaka, Tadayuki Takata, Hisakazu Iwama, Satoshi Komatsubara, Hideki Kobara, Masaki Kamada, Kazushi Deguchi, Tetsuo Touge, Osamu Miyamoto, Takehiro Nakamura, Toshifumi Itano, Tsutomu Masaki
Publikováno v:
Molecular Medicine Reports
Progressive supranuclear palsy (PSP) is a neurodegenerative tauopathy described as a syndrome of postural instability, supranuclear vertical gaze palsy, dysarthria, dystonic rigidity of the neck and trunk, dementia, and pseudobulbar palsy. The clinic
Autor:
Tadayuki Takata, Hideshi Kawakami, Kodai Kume, Yoshimitsu Shimatani, Masaki Kamada, Yuishin Izumi
Publikováno v:
Journal of the neurological sciences. 430
Autor:
Tsutomu Masaki, Masaki Kamada, Kazushi Deguchi, Hisashi Masugata, Hideki Kobara, Asahiro Morishita, Kodai Kume, Tetsuo Touge, Tadayuki Takata, Yohei Kokudo, Tatsuo Yachida
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 944-946 (2021)
Clinical Case Reports
Clinical Case Reports
Eradication therapy of Helicobacter pylori may be safe if hemin has been intravenously administered in advance, even in patients with a history of recurrent acute porphyria attack.
Publikováno v:
Key Engineering Materials. 827:184-189
Carbon nanotube (CNT) is excellent in mechanical and thermal characteristics, and are expected to be used in various fields such as nanoelectronic devices and reinforcing nanofillers for composites. It is expected that mechanical properties can be im
Autor:
Masaki Kamada, Takashi Ayaki, Hiroyuki Morino, Ryosuke Ohsawa, Yui Yamashita, Go Shioi, Yusuke Sotomaru, Hirofumi Maruyama, Masahito Kuramochi, Hideshi Kawakami, Takashi Kurashige, Hidefumi Ito
Publikováno v:
Neurobiology of Disease, Vol 148, Iss, Pp 105215-(2021)
We previously showed that optineurin (OPTN) mutations lead to the development of amyotrophic lateral sclerosis. The association between OPTN mutations and the pathogenesis of amyotrophic lateral sclerosis remains unclear. To investigate the mechanism