Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Yoshinobu Oyazato"'
Autor:
Kento Souma, Junya Fujimura, Atushi Nishiyama, Yoshinobu Oyazato, Shuya Kaneko, Masaki Shimizu, Takeshi Morisawa
Publikováno v:
International Journal of Rheumatic Diseases. 26:551-553
Publikováno v:
Journal of the Japan Epilepsy Society. 38:28-35
Autor:
Masahiro Nishiyama, Tsukasa Tanaka, Azusa Maruyama, Kazumi Tomioka, Taku Nakagawa, Kazumoto Iijima, Yoshinobu Oyazato, Hiroshi Yamaguchi, Daisaku Toyoshima, Noriyuki Nishimura, Yusuke Ishida, Kaori Sasaki, Kandai Nozu, Ichiro Nakashima, Yuichi Takami, Hiroaki Nagase, Kyoko Fujita
Publikováno v:
Brain and Development. 41:531-537
The detailed clinical time course in acute disseminated encephalomyelitis (ADEM) from initial symptoms, through exacerbation, to remission has not been widely reported. Hence, this study aimed to investigate the clinical time course of pediatric ADEM
Autor:
Pierluigi Martelli, Tom J. de Koning, Takema Kato, Irene Liparulo, Mariko Taniguchi-Ikeda, Tatsushi Toda, Hisayoshi Nakamura, Wilfred F. A. den Dunnen, Giovanna Cenacchi, Sanjiban Chakrabarty, Yu Sheng Yeh, Sushil Kumar Mishra, Rita Casadio, Akira Ohtake, Ichizo Nishino, Roberto De Giorgio, Paolo Picco, Pasquale Striano, Chiara Fiorillo, Isabella Ceccherini, Tsuyoshi Goto, Elisa Boschetti, Makiko Tsutsumi, Eleonora Aronica, Georgios Kellaris, Mariel Alders, Gabor E. Linthorst, Jantima Tanboon, Angela Rita Sementa, Floor A. M. Duijkers, Yu Ichi Goto, Hiroki Kurahashi, Masakazu Mimaki, Gerard Dijkstra, Dik C. van Gent, Mariasavina Severino, Yoshinobu Oyazato, Christian Bergamini, Ikuya Nonaka, Yoshiki Yamaguchi, Ivana Matera, Giuseppe Raiola, Karin Van Spaendonck, Nicholas Katsanis, Luca Masin, Shumpei Uchino, Kenjiro Kosaki, Sara Signa, Anja Raams, Federica Isidori, Elena Bonora, Serena Arrigo, Kandai Nozu, Marc Engelen, Farid Ullah, Ichiro Morioka, Chiara Diquigiovanni, Marco Seri, Valerio Carelli, Francesca Bianco, Mariapia Giuditta Cratere, Nicola Rizzardi, Romana Fato, Alessandra Maresca, Alyson W. MacInnes, Valentina Papa, Kazumoto Iijima
Publikováno v:
Brain : a Journal of Neurology, 144(5), 1451-1466. Oxford University Press
Brain, 144(5), 1451-1466. Oxford University Press
Brain, 144(5), 1451-1466. Oxford University Press
Abnormal gut motility is a feature of several mitochondrial encephalomyopathies, and mutations in genes such as TYMP and POLG, have been linked to these rare diseases. The human genome encodes three DNA ligases, of which only one, ligase III (LIG3),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e470f830e056717e954489f79a11efb4
http://hdl.handle.net/11567/1065221
http://hdl.handle.net/11567/1065221
Autor:
Yoshinobu Oyazato, Shingo Ishimori, Atsushi Nishiyama, Tomoshi Nakajiri, Shizuka Nagase, Masahiko Yonetani, Sora Okita, Atsuko Kanagawa
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 63(7)
Background Continuous negative extra-thoracic pressure (CNEP) can prevent children with apnea developing severe respiratory infection with endotracheal intubation. Little is known about children with mild acute respiratory disease, especially with a
Autor:
Yoshinobu Oyazato, Sora Okita, Ichiro Kamioka, Masahiko Yonetani, Shingo Ishimori, Atsushi Nishiyama, Junya Fujimura
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 30:35-40
Autor:
Azusa Maruyama, Kimihiko Kaneko, Satoshi Takada, Kyoko Fujita, Yoshinobu Oyazato, Kazuhiro Shiraishi, Daisaku Toyoshima, Hiroaki Nagase, Masaaki Matsumoto, Ichiro Nakashima, Masahiro Nishiyama, Toshiyuki Takahashi, Kazumi Tomioka, Keisuke Saeki, Hiroyuki Awano, Tsukasa Tanaka, Kazumoto Iijima
Publikováno v:
Braindevelopment. 39(9)
Background: The clinical features of patients with very early-onset acquired demyelinating syndrome (ADS) with the anti-myelin oligodendrocyte glycoprotein (MOG) antibody are unknown. We investigated the clinical characteristics and described detaile
Autor:
Ayumi Matsumoto, Sumimasa Yamashita, Kenji Sugai, Kazuyuki Nakamura, Kayoko Saito, Mari Maeno, Taku Nakagawa, Kiyomi Nishiyama, Hiroshi Arai, Yoshinobu Oyazato, Ryosuke Kusano, Kaoru Imai, Naomichi Matsumoto, Takanori Yamagata, Shelly K. Weiss, Tami Uster, Hirofumi Kodera, Hirofumi Kashii, Kiyoshi Hayasaka, Noriko Miyake, Mitsuhiro Kato, Hirotomo Saitsu, Yoshinori Tsurusaki, Mitsuko Nakashima, Takanari FujII, David Chitayat, Masaya Kubota
Publikováno v:
Epilepsia. 54:1282-1287
Summary Purpose KCNQ2 mutations have been found in patients with benign familial neonatal seizures, myokymia, or early onset epileptic encephalopathy (EOEE). In this study, we aimed to delineate the clinical spectrum of EOEE associated with KCNQ2 mut
Autor:
Azusa Maruyama, Masafumi Matsuo, Takeo Mure, Hiroaki Nagase, Taku Nakagawa, Yuichi Takami, Yo Okizuka, Masao Adachi, Yoshinobu Oyazato, Satoshi Takada
Publikováno v:
Pediatrics International. 54:892-898
Background This study was conducted with a particular focus on preterm infants with West syndrome (WS) to evaluate differences in the first responses to oral medication based on etiology. Methods Medical records of 53 patients with WS, treated at fiv
Autor:
Ichiro Kamioka, Noriko Ohnishi, Masao Adachi, Aika Watanabe, Hiroaki Taniguchi, Takashi Shiihara, Atsushi Nishiyama, Mitsuro Kobayashi, Yoshinobu Oyazato, Susumu Kusunoki
Publikováno v:
Brain and Development. 34:329-332
We describe a boy with Fisher syndrome. He presented the typical symptoms of Fisher syndrome, including external ophthalmoplegia, abnormality of convergence, and areflexia, after an episode of Campylobacter enterocolitis. Atypically, however, anti-GA