Toshiyuki Yamamoto

J-GLOBAL         Last updated: Jun 11, 2019 at 15:58
 
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Name
Toshiyuki Yamamoto
Affiliation
Tokyo Women's Medical University
ORCID ID
0000-0002-9484-3505

Research Interests

 
 

Research Areas

 
 

Academic & Professional Experience

 
Apr 2002
 - 
Jan 2003
Visiting fellow, Adelaide University, Centre for Medical Genetics
 

Published Papers

 
Yamamoto T, Imaizumi T, Yamamoto-Shimojima K, Lu Y, Yanagishita T, Shimada S, Chong PF, Kira R, Ueda R, Ishiyama A, Takeshita E, Momosaki K, Ozasa S, Akiyama T, Kobayashi K, Oomatsu H, Kitahara H, Yamaguchi T, Imai K, Kurahashi H, Okumura A, Oguni H, Seto T, Okamoto N
Brain & development      Jun 2019   [Refereed]
Yanagishita T, Yamamoto-Shimojima K, Nakano S, Sasaki T, Shigematsu H, Imai K, Yamamoto T
Brain & development   41(5) 452-455   May 2019   [Refereed]
Okumura A, Shimojima K, Kurahashi H, Numoto S, Shimada S, Ishii A, Ohmori I, Takahashi S, Awaya T, Kubota T, Sakakibara T, Ishihara N, Hattori A, Torisu H, Tohyama J, Inoue T, Haibara A, Nishida T, Yuhara Y, Miya K, Tanaka R, Hirose S, Yamamoto T
Seizure   71 1-5   May 2019   [Refereed]
Yamamoto-Shimojima K, Imaizumi T, Aoki Y, Inoue K, Kaname T, Okuno Y, Muramatsu H, Kato K, Yamamoto T
Journal of human genetics      Apr 2019   [Refereed]
Yamamoto-Shimojima K, Okamoto N, Matsumura W, Okazaki T, Yamamoto T
Brain & development   41(3) 257-262   Mar 2019   [Refereed]

Misc

 
YAMAMOTO Toshiyuki, AKASAKA Yuko, OHTANI Kyoichi, HAYASHI Takashi, KASHIWAGI Shiro, ICHIYAMA Takashi, NISHIKAWA Miki, KATO Mitsuhiro, MAEGAKI Yoshihiro, OKA Akira, OHNO Kousaku
脳と発達 = OFFICIAL JOURNAL OF THE JAPANESE SOCIETY OF CHILD NEUROLOGY   37(1) 15-19   Jan 2005
YAMAMOTO Toshiyuki, AKASAKA Yuko, OHTANI Kyoichi, HAYASHI Takashi, KASHIWAGI Shiro, ICHIYAMA Takashi, NISHIKAWA Miki, KATO Mitsuhiro, MAEGAKI Yoshihiro, OKA Akira, OHNO Kousaku
脳と発達 = OFFICIAL JOURNAL OF THE JAPANESE SOCIETY OF CHILD NEUROLOGY   37(1) 20-25   Jan 2005
TOMINAGA R, NANBA E, INADA A, YAMAMOTO T, TAKESHIMA T, KITAMURA Y, TANIGUCHI M, OHNO K, OSHIMA A, MATSUDA J, SUZUKI Y
日本先天代謝異常学会雑誌   14(2)    Oct 1998

Books etc

 
ベン・ポリス (Part:Single Translation)
三輪書店   Jun 2003   ISBN:4895901947

Research Grants & Projects

 
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(C))
Project Year: 2007 - 2008    Investigator(s): Toshiyuki YAMAMOTO
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(B))
Project Year: 2001 - 2003    Investigator(s): Eiji NANBA
The chemical chaperon therapy for inherited metabolic diseases including GM1-gangliosidois have been developed in the study. GM1-gangliosidosis which caused by deficiency of β-galactosidase in lysosome, is manifested by central nervous involvement...
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(一般研究(B), 基盤研究(B))
Project Year: 1994 - 1996    Investigator(s): Kenzo TAKESHITA
The fragile X syndrome is the most common cause of inherited mental retardation. Recently, a genomic locus was identified and the CGG trinucleotide rerepeat expansion has been found. We reported a rapid screening test by a non-radioisotope PCR tec...