Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shoko TOKUNAGA"'
Publikováno v:
Oxford Handbook of Child Protection Systems ISBN: 0197503543
This chapter expounds on the challenges of Japan in terms of serving children who cannot live with their biological parents due to maltreatment issues. The Child Welfare Act (1947) determines the roles of local child welfare authorities and their fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ffab3d217821745d26ea6f2edaf1281
https://doi.org/10.1093/oxfordhb/9780197503546.013.35
https://doi.org/10.1093/oxfordhb/9780197503546.013.35
Autor:
Akiko Yoshimura, Kengo Maeda, Akihiro Hashiguchi, Shoko Tokunaga, Hiroshi Takashima, Takashi Suzuki, Yuji Okamoto, Hiroyo Haruki, Tomonori Nakamura
Publikováno v:
neurogenetics. 13:359-365
We identified the main features of Charcot-Marie-Tooth (CMT) disease, type 4F, caused by a periaxin gene (PRX) mutation in Japanese patients. Periaxin is known as one of the key myelination molecules, forming tight junction between myelin loop and ax
Autor:
L. Zhu, Shoko Tokunaga, H. Shen, Yuji Okamoto, Yusuke Sakiyama, Akihiro Hashiguchi, Hiroshi Takashima, Zhe Zhao, J. Hu
Publikováno v:
Neurology. 78:1644-1649
Objective: To identify a new genetic cause of distal hereditary motor neuropathy (dHMN), which is also known as a variant of Charcot-Marie-Tooth disease (CMT), in a Chinese family. Methods: We investigated a Chinese family with dHMN clinically, elect
Autor:
Akihiro Hashiguchi, Kimiharu Uozumi, Tomonori Nakamura, Shinsuke Suzuki, Shoko Tokunaga, Hiroshi Takashima
Publikováno v:
neurogenetics. 13:77-82
Neurotoxicity is a common side effect of vincristine (VCR) treatment. Severe exacerbations of neuropathy have been reported in patients with Charcot-Marie-tooth disease (CMT) 1A with duplication of the peripheral myelin protein 22 (PMP22) gene. Howev
Autor:
Osamu Watanabe, Hiroshi Takashima, Shoko Tokunaga, Itsuro Higuchi, Yusuke Sakiyama, Kimiyoshi Arimura, Yuji Okamoto, Masanori Nakagawa
Publikováno v:
Annals of Neurology. 70:486-492
Objective: To elucidate the relationship between mitochondrial DNA (mtDNA) alterations and a mitochondrial disease with a distinct combination of characteristic symptoms, namely episodic hyper-creatine kinase (CK)-emia and mild myopathy. Methods: We
Autor:
Eiichi Matsuo, Yukihiro Furuno, Akio Komatsu, Suguru Maekawa, Kenichiroh Murata, Taiyou Kikuchi, Seiji SHIODA, Yasumitsu NAKAI, Shuji Yamashita, H. NAGATA, S. TAKEKOSHI, H. HASEGAWA, J. ITOH, Y. YAMAMOTO, K. WATANABE, Shinji FUSHIKI, Chikako KINOSHITA, Akihiro NAGATA, Toshihiro MAEDA, Yoshimitsu TOKUNAGA, Hitoshi MATSUMURA, Kunio KITAHAMA, Akiko SETO-OHSHIMA, Noriko KAWAMURA, Yasunari TSUCHIHASHI, Takahiro MATSUMOTO, Shoji MITSUFUJI, Kazuhiko TOKITA, Kyohei MARUYAMA, Tadashi KODAMA, Shoichi ISEKI, Yoshio MABUCHI, Hiromichi MARUYAMA, Eisuke SAKUMA, Tsuyoshi SOJI, Teruhiko OKADA, Toshihiro KOBAYASHI, Vadium S ZINCHUK, Harumichi SEGUCHI, Tateo DAIMON, Masami OGUNI, Tomoichi SETOGAWA, Reiji SEMBA, Tetsuya NOGUCHI, Katsuaki KATOU, Hironobu SASANO, Akihiko KIKUCHI, Hiroshi NAGURA, S Tsuyama, D-H Yang, J Ohmori, Y-B Ge, F Murata, Toyoshi FUJIMOTO, Tomoko UNE, Mariko SHIOYA, Hiroshi KOGO, Sadaki YOKOTA, Chieko KURONO, Toshimitsu WATABIKI, Manabu YOSHIDA, Yutaka OKII, Sumitaka YOSHIMURA, Takuma TOKIYASU, Atsushi AKANE, Satoko INOUE, Ichiro NAITO, Satimaru SENO, Chiho MAKIDONO, Shoko TOKUNAGA, Shinji IMAI, Norio Kawai, Tetsuo INOKUCHI, Teruyoshi KONDO, Keisuke OHTA, Hiromichi ANNOH, Yoshihiro ISHIBASHI, Masanori Yasuda, Tsuyoshi Okabe, Susumu Takekoshi, Hideaki Hasegawa, Johbu Itoh, Yoshiyuki Osamura, Keiichi Watanabe, Toshihiro TAIUZAWA, Takuma SAITO, Takashi YASHIRO
Publikováno v:
ACTA HISTOCHEMICA ET CYTOCHEMICA. 31:136-142