Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Takafumi SAKAKIBARA"'
Autor:
Kentaro TAMURA, Ryota SASAKI, Takafumi SAKAKIBARA, Riju DAHAL, Yasuhiro TAKESHIMA, Ryosuke MATSUDA, Shuichi YAMADA, Fumihiko NISHIMURA, Ichiro NAKAGAWA, Young-Soo PARK, Hidehiro HIRABAYASHI, Hiroyuki NAKASE
Publikováno v:
Neurologia Medico-Chirurgica, Vol 63, Iss 7, Pp 273-282 (2023)
A vagus nerve stimulation (VNS) device delivers electrical pulses to the vagus nerve at a rhythm defined by the duty cycle. The standard therapeutic range is advocated for an output current of 1.5-2.25 mA and a duty cycle of 10%. As the optimal setti
Externí odkaz:
https://doaj.org/article/f2d4b9513b2747b699777540e5336a20
Autor:
Yi Shiau Ng, Nichola Z. Lax, Paul Maddison, Charlotte L. Alston, Emma L. Blakely, Philippa D. Hepplewhite, Gillian Riordan, Surita Meldau, Patrick F. Chinnery, Germaine Pierre, Efstathia Chronopoulou, Ailian Du, Imelda Hughes, Andrew A. Morris, Smaragda Kamakari, Georgia Chrousos, Richard J. Rodenburg, Christiaan G.J. Saris, Catherine Feeney, Steven A. Hardy, Takafumi Sakakibara, Akira Sudo, Yasushi Okazaki, Kei Murayama, Helen Mundy, Michael G. Hanna, Akira Ohtake, Andrew M. Schaefer, Mike P. Champion, Doug M. Turnbull, Robert W. Taylor, Robert D.S. Pitceathly, Robert McFarland, Gráinne S. Gorman
Publikováno v:
EBioMedicine, Vol 30, Iss , Pp 86-93 (2018)
Mutations in the m.13094T>C MT-ND5 gene have been previously described in three cases of Leigh Syndrome (LS). In this retrospective, international cohort study we identified 20 clinically affected individuals (13 families) and four asymptomatic carri
Externí odkaz:
https://doaj.org/article/3670bb9d88df4ad19193530872b41183
Publikováno v:
Brain and Development. 44:546-550
Adrenocorticotropic hormone (ACTH) therapy is a first-line treatment for infantile spasms, which may rarely cause intracranial hemorrhage. However, the changes in blood coagulation during ACTH therapy are poorly understood, with little description in
Autor:
Ken Saida, Pin Fee Chong, Asuka Yamaguchi, Naka Saito, Hajime Ikehara, Eriko Koshimizu, Rie Miyata, Akira Ishiko, Kazuyuki Nakamura, Hidenori Ohnishi, Kei Fujioka, Takafumi Sakakibara, Hideo Asada, Kohei Ogawa, Kyoko Kudo, Eri Ohashi, Michiko Kawai, Yuichi Abe, Naomi Tsuchida, Yuri Uchiyama, Kohei Hamanaka, Atsushi Fujita, Takeshi Mizuguchi, Satoko Miyatake, Noriko Miyake, Mitsuhiro Kato, Ryutaro Kira, Naomichi Matsumoto
Publikováno v:
Human Genetics. 141:1771-1784
Pigmentary mosaicism of the Ito type, also known as hypomelanosis of Ito, is a neurocutaneous syndrome considered to be predominantly caused by somatic chromosomal mosaicism. However, a few monogenic causes of pigmentary mosaicism have been recently
Autor:
Masamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, Akihiko Ishiyama, Hirofumi Komaki, Takashi Saito, Eri Takeshita, Yuko Shimizu-Motohashi, Kazuhiro Haginoya, Tomoko Kobayashi, Tomohide Goto, Yu Tsuyusaki, Mizue Iai, Kenji Kurosawa, Hitoshi Osaka, Jun Tohyama, Yu Kobayashi, Nobuhiko Okamoto, Yume Suzuki, Satoko Kumada, Kenji Inoue, Hideaki Mashimo, Atsuko Arisaka, Ichiro Kuki, Harumi Saijo, Kenji Yokochi, Mitsuhiro Kato, Yuji Inaba, Yuko Gomi, Shinji Saitoh, Kentaro Shirai, Masafumi Morimoto, Yuishin Izumi, Yoriko Watanabe, Shin-ichiro Nagamitsu, Yasunari Sakai, Shinobu Fukumura, Kazuhiro Muramatsu, Tomomi Ogata, Keitaro Yamada, Keiko Ishigaki, Kyoko Hirasawa, Konomi Shimoda, Manami Akasaka, Kosuke Kohashi, Takafumi Sakakibara, Masashi Ikuno, Noriko Sugino, Takahiro Yonekawa, Semra Gürsoy, Tayfun Cinleti, Chong Ae Kim, Keng Wee Teik, Chan Mei Yan, Muzhirah Haniffa, Chihiro Ohba, Shuuichi Ito, Hirotomo Saitsu, Ken Saida, Naomi Tsuchida, Yuri Uchiyama, Eriko Koshimizu, Atsushi Fujita, Kohei Hamanaka, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, Noriko Miyake, Naomichi Matsumoto
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(12)
Cerebellar hypoplasia and atrophy (CBHA) in children is an extremely heterogeneous group of disorders, but few comprehensive genetic studies have been reported. Comprehensive genetic analysis of CBHA patients may help differentiating atrophy and hypo
Autor:
Toshiyuki Yamamoto, Takuji Nishida, Hiroyuki Torisu, Akihisa Okumura, Akiko Haibara, Yukihiro Yuhara, Naoko Ishihara, Takeshi Inoue, Kazushi Miya, Jun Tohyama, Hirokazu Kurahashi, Shino Shimada, Ayako Hattori, Shinichi Hirose, Takafumi Sakakibara, Keiko Shimojima, Satoru Takahashi, Tetsuo Kubota, Atsushi Ishii, Shingo Numoto, Tomonari Awaya, Ryuta Tanaka, Iori Ohmori
Publikováno v:
Seizure. 71:1-5
Purpose This study was performed to clarify the clinical features of Japanese patients with PRRT2 mutations. Methods The PRRT2 gene was analyzed in 135 patients with benign infantile epilepsy (BIE) or paroxysmal kinesigenic dyskinesia (PKD) using a d
Autor:
Akiko Abe, Satoshi Tsurui, Soichiro Toda, Muneaki Matsuo, Hiroko Iwamatsu, Takuji Nakamura, Ayako Senju, Hidenori Tanaka, Takushi Inoue, Atsushi Kawaguchi, Ryutaro Kira, Tomomi Naitou, Kenji Furuno, Takafumi Sakakibara, Mitsuo Motobayashi, Marina Hashiguchi, Tatsuharu Sato, Naoya Higuchi, Nobuyoshi Sugiyama, Masami Togawa, Ken ichi Torii, Shigeki Ishii, Kazunari Takamura, Yuko Ichimiya, Fumio Ichinose
Publikováno v:
Braindevelopment. 44(1)
Objective To clarify the incidence and risk factors of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) in pediatric patients with febrile status epilepticus (FSE). Methods We retrospectively surveyed patients with FSE (
Autor:
Keigo Saeki, Naoki Miki, Seiji Kinoshita, Toru Hoshida, Takafumi Sakakibara, Toshiaki Doi, Yasuko Furuichi, Kenji Obayashi, Midori Shima, Norio Kurumatani, Satoko Nezu
Publikováno v:
Braindevelopment. 43(1)
Background There is a paucity of studies on self-assessed generic health-related quality of life (HRQOL) in children with epilepsy. The purpose of this study was to investigate generic HRQOL and associated factors among Japanese children with epileps
Autor:
Tsuyoshi Shuto, Madoka Fukaura, Hidetoshi Arima, Takafumi Sakakibara, Katsumi Higaki, Tetsumi Irie, Muneaki Matsuo, Shunsuke Kamei, Toru Takeo, Yoshio Sakiyama, Naoki Ushihama, Naomi Nakagata, Hiroshi Katsuki, Keiichi Motoyama, Hirofumi Kai, Takumi Era, Yoichi Ishituka, Taishi Higashi, Yuki Kurauchi, Yuki Kondo
Publikováno v:
Proceedings for Annual Meeting of The Japanese Pharmacological Society. :PO3-8
Autor:
Tomokatsu Yoshida, Kengo Kora, Tenshin Okubo, Takafumi Sakakibara, Takeo Kato, Shu Hamada, Minako Ide, Tatsuya Kawaguchi, Takayuki Tanaka
Publikováno v:
Epilepsy Research. 170:106519
In infantile Alexander disease (iAxD), one of the serious symptoms is intractable epilepsy, and some reports have suggested that neuroinflammation may be involved in the pathophysiology of the disease. Drug-resistant seizures adversely affect not onl