Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Mitsuru KAWAI"'
Autor:
Jun-ichi Satoh, Megumi Nakanishi, Fumiko Koike, Sachiko Miyake, Toshiyuki Yamamoto, Mitsuru Kawai, Seiji Kikuchi, Kyouichi Nomura, Kazumasa Yokoyama, Kohei Ota, Takashi Kanda, Toshiyuki Fukazawa, Takashi Yamamura
Publikováno v:
Neurobiology of Disease, Vol 18, Iss 3, Pp 537-550 (2005)
To clarify the molecular mechanisms underlying multiple sclerosis (MS)-promoting autoimmune process, we have investigated a comprehensive gene expression profile of T cell and non-T cell fractions of peripheral blood mononuclear cells (PBMC) isolated
Externí odkaz:
https://doaj.org/article/ecb90de43329462396ff7693a138ac5b
Autor:
Naomasa Miyata, Mitsuru Kawai, Kenichi Kaida, Ichizo Nishino, Takuhisa Tamura, Kana Yatabe, Yutaka Honma, Katsuhisa Ogata, Ikuya Nonaka, Mikiya Suzuki, K. Momma, Masato Kadoya
Publikováno v:
Neuromuscular Disorders. 27:477-480
Limb girdle muscular dystrophy type 2L (LGMD2L) is an adult-onset slowly progressive muscular dystrophy associated with anoctamin 5 (ANO5) gene mutation, mainly reported from Northern and Central Europe. We report the case of a Japanese male patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe92e70e10fd73d5bf7b46be1764bbe
https://doi.org/10.1016/j.nmd.2017.01.012
https://doi.org/10.1016/j.nmd.2017.01.012
Autor:
Eriko Koshimizu, Satomi Mitsuhashi, Masaaki Shiina, Ikuya Nonaka, Satoshi Kuru, Takeshi Mizuguchi, Mikiya Suzuki, Hirotomo Saitsu, Naomichi Matsumoto, Noriko Miyake, Yukiko K. Hayashi, Ichizo Nishino, Satoko Miyatake, Yuzo Tanaka, Yoshinori Tsurusaki, Mitsuko Nakashima, Atsuko Nishikawa, Jeffrey A. Towbin, Mitsuru Kawai, Enkhsaikhan Purevjav, Kazuhiro Ogata, Kana Yatabe, Katsuhisa Ogata
Publikováno v:
The American Journal of Human Genetics. 100:169-178
Nemaline myopathy (NM) is a common form of congenital nondystrophic skeletal muscle disease characterized by muscular weakness of proximal dominance, hypotonia, and respiratory insufficiency but typically not cardiac dysfunction. Wide variation in se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daaf3705934b2771a09649e931763406
https://doi.org/10.1016/j.ajhg.2016.11.017
https://doi.org/10.1016/j.ajhg.2016.11.017
Publikováno v:
Rinsho Shinkeigaku. 55:637-645
It has been suggested that many physicians feel it is difficult to manage patients with Duchenne muscular dystrophy (DMD) and that support from experts is required. Therefore, to assess the effects of Japanese practical guidelines for DMD, we distrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757a9839977b39674867d5b2668b525c
https://doi.org/10.5692/clinicalneurol.cn-000736
https://doi.org/10.5692/clinicalneurol.cn-000736
Publikováno v:
Home Health Care Management & Practice. 27:83-90
We conducted a cross-sectional mail-in survey of families with neuromuscular disorders (ND) or malignant tumors (MT) to compare their preferences for type of future communications in home medical care settings and their previous experience or lack of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e4f29ea4e778d5c39bca9230485bd5
https://doi.org/10.1177/1084822314549994
https://doi.org/10.1177/1084822314549994
Publikováno v:
Neurology and Clinical Neuroscience. 1:214-220
Aim Home medical care is currently a topic of discussion in Japan. It is reported that the key to the success of home medical care is communication. The aim of the present study was to elucidate the characteristics of communication during home medica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49190b9569ff553061eda2e58d8e50d5
https://doi.org/10.1111/ncn3.61
https://doi.org/10.1111/ncn3.61
Autor:
Mitsuru Kawai, Takahiro Nakayam, Masaaki Konagaya, Nobuhiko Tanaka, Satoshi Kuru, Motoko Sakai
Publikováno v:
Neurology and Clinical Neuroscience. 1:63-68
Aim Establishing the natural course of muscular impairment in Duchenne muscular dystrophy (DMD) is essential for defining the effect of treatments in clinical trials. We retrospectively investigated the change of thigh muscle volume in DMD using new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a9702d6c5238b089903a5884dd6f489
https://doi.org/10.1002/ncn3.21
https://doi.org/10.1002/ncn3.21
Autor:
Mitsuru Kawai, Lars-Goran Carlsson, Teresita Aquino, Stefan Ivanov, Tito Atienza, Takahide Kudo, Marcelo Fernandez, Watchara Boonsawat, Jan Ekelund
Publikováno v:
Respirology. 18:354-363
Background and objective To evaluate the efficacy and tolerability of budesonide/formoterol as maintenance and reliever therapy versus budesonide/formoterol maintenance plus terbutaline in adults with persistent asthma not adequately controlled with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c1f567d8e61b8281bd81ccd8ec8eb1
https://doi.org/10.1111/resp.12009
https://doi.org/10.1111/resp.12009
Autor:
Naomichi Matsumoto, Katsuhisa Ogata, Hirotomo Saitsu, Hiroshi Doi, Mitsuru Kawai, Noriko Miyake, Satoko Miyatake
Publikováno v:
Internal Medicine. 51:2221-2226
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an inherited neurodegenerative disorder with symptoms of spastic ataxia, neuropathy, pyramidal sign, finger and foot deformities, and hypermyelination of retinal nerve fibers. SACS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::430bf1d5a0fd5f4f065d06ffe92a921f
https://doi.org/10.2169/internalmedicine.51.7374
https://doi.org/10.2169/internalmedicine.51.7374
Publikováno v:
Advanced Materials Research. 222:3-7
A unique single-photon detector is reported, which utilizes scaled-down silicon-on- insulator (SOI) metal-oxide-semiconductor field-effect transistor (MOSFET) with single-electron sensitivity, and features low-voltage operation without carrier multip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f062ead9d2049e323b0684f5d1a2c699
https://doi.org/10.4028/www.scientific.net/amr.222.3
https://doi.org/10.4028/www.scientific.net/amr.222.3