TAKEUCHI Yoshihiro

J-GLOBAL         Last updated: May 31, 2018 at 16:16
 
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Name
TAKEUCHI Yoshihiro
Affiliation
Shiga University of Medical Science
Section
Undergraduate School of Medicine, Faculty of Medicine, Shiga University of Medical Science Undergraduate School of Medicine Faculty of Medicine
Job title
Professor

Research Areas

 
 

Academic & Professional Experience

 
1980
 - 
1984
Kyoto Prefectural University of Medicine,
 
 
   
 
Postgraduate
 
1989
 - 
1990
Exchange Scietist between Royal Society and
 
 
   
 
Japan Society for the Promotion of Science
 

Education

 
 
 - 
1984
Graduate School, Division of Medicine, Kyoto Prefectural University of Medicine
 
 
 - 
1977
Medical Science, Faculty of Medicine, Tokyo Medical and Dental University
 

Published Papers

 
Lange KW, Hauser J, Lange KM, Makulska-Gertruda E, Nakamura Y, Reissmann A, Sakaue Y, Takano T, Takeuchi Y
Current psychiatry reports   19(2) 8   Feb 2017   [Refereed]
Maruo Y, Nagasaki K, Matsui K, Mimura Y, Mori A, Fukami M, Takeuchi Y
European journal of endocrinology   174(4) 453-463   Apr 2016   [Refereed]
[A case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode/Leigh overlap syndrome].
Matsui J, Takano T, Ryujin F, Anzai Y, Yoshioka S, Takeuchi Y, Goto Y
No to hattatsu. Brain and development   46(5) 363-366   Sep 2014   [Refereed]
Sawai T, Itoh Y, Ozaki H, Isoda N, Okamoto K, Kashima Y, Kawaoka Y, Takeuchi Y, Kida H, Ogasawara K
Immunology   124(2) 155-165   Jun 2008   [Refereed]
Nishimuraa A, Takano T, Mizuguchia T, Saitsua H, Takeuchi Y, Matsumotoa N
Clin Genet   74 288-290   2008
Takano T, Hayashi A, Sokoda T, Sawai C, Sakaue Y, Takeuchi Y
Pediatric neurology   37(6) 417-420   Dec 2007   [Refereed]
Taga T, Sakaue Y, Anzai Y, Takeuchi Y, Ohta S
Pediatr Blood Cancer   48 477-478   2007
Taga T, Sakaue Y, Anzai Y, Takeuchi Y, Ohta S
Pediatr Blood Cancer   48 477-478   2007
Akahori S, Takano T, Fujito H, Takeuchi Y
Pediatric Neurology   37 417-420   2007
Watanabe N, Nakagawa M, Hanato T, Takeuchi Y, Hara M, Yoshida T, Imanaka-Yoshida K
The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology   288A(7) 714-722   Jul 2006   [Refereed]

Misc

 
Akitaka Nomura, Yoshihiro Maruo, Takashi Taga, Yoshihiro Takeuchi
Pediatric Research   80 252-257   Aug 2016
© 2016 International Pediatric Research Foundation, Inc.Background: Chemotherapy for malignant neoplasms sometimes induces unconjugated hyperbilirubinemia, resulting in the early cessation of treatment. We evaluated the role of variations in the b...
Noriko Nishikura, Noriko Nishikura, Tomoyuki Takano, Fukiko Ryujin, Seiichiro Yoshioka, Yoshihiro Maruo, Yoshihiro Takeuchi, Yoshihiro Takeuchi, Kentaro Tamura, Takafumi Sakakibara, Masayuki Ito
Pediatrics International   58 496-500   Jun 2016
© 2016 Japan Pediatric Society.Dysembryoplastic neuroepithelial tumors (DNT) are benign hamartomatous tumors characterized by intractable epilepsy and common localization in the supratentorial cortex, but thalamic involvement in DNT is extremely r...
Yoshihiro Maruo, Sayuri Nakahara, Takahide Yanagi, Akitaka Nomura, Yu Mimura, Katsuyuki Matsui, Hiroshi Sato, Yoshihiro Takeuchi
Journal of Gastroenterology and Hepatology (Australia)   31 403-408   Feb 2016
© 2016 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd.Background and Aims: Hereditary unconjugated hyperbilirubinemias, Crigler-Najjar syndrome type I, Crigler-Najjar syndrome type II (CN-2), and Gilbert sy...
Yoshihiro Maruo, Asami Mori, Yoriko Morioka, Chihiro Sawai, Yu Mimura, Katsuyuki Matui, Yoshihiro Takeuchi
BMC Endocrine Disorders   16    Jan 2016
© 2016 Maruo et al.Background: Resistance to thyroid hormone beta (RTHβ) is a rare and usually dominantly inherited syndrome caused by mutations of the thyroid hormone receptor β gene (THRB). In severe cases, it is rarely challenging to control ma...
Toshiyuki Yamamoto, Seiichiro Yoshioka, Yoshinori Tsurusaki, Shimada Shino, Shimada Shino, Keiko Shimojima, Yosuke Shigematsu, Yoshihiro Takeuchi, Naomichi Matsumoto
Brain and Development   38 142-144   Jan 2016
© 2015 The Japanese Society of Child Neurology.l-2-Hydroxyglutaric aciduria ( l-2-HGA) is a rare inborn error of metabolism. Mainly, patients with this disorder exhibit neurological symptoms and characteristic neuroradiological findings, such as s...

Research Grants & Projects

 
Neurochemical study on monoamine metabolism in spinal muscular atrophy
0085 (Japanese Only)
Project Year: 1992   
Neurochemical study on intractable epilepsy-with special reference to the TRH therapy
0085 (Japanese Only)
Project Year: 1991   
Neuropathological Study on the Significance of Serotonin Neuron System in Brain Plasticity
0085 (Japanese Only)
Project Year: 1989