ISHII Atsushi

J-GLOBAL         Last updated: Nov 28, 2019 at 03:25
 
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Name
ISHII Atsushi
URL
https://www.scn1a.net/
Affiliation
Fukuoka University
Section
Faculty of Medicine, School of Medicine
Research funding number
90568825

Research Areas

 

Education

 
Apr 1995
 - 
Mar 2001
製薬化学科, 薬学部, Kyoto Pharmaceutical University
 
Apr 2001
 - 
Mar 2007
医学科, 医学部, Fukuoka University
 
Apr 2009
 - 
Mar 2013
先端医療科学系専攻, 医学研究科, Fukuoka University
 

Awards & Honors

 
2006
Best Poster Presentation, 11th International Congress of Human Genetics
 
2012
遺伝医学セミナー模擬試験最高得点, 第21回遺伝医学セミナー
 
2013
豊後賞, 第55回日本小児神経学会学術集会
 
2013
最優秀論文賞, 九州小児科医会
 
2014
最優秀論文賞, 日本小児神経学会
 

Published Papers

 
Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy
Wang, Ji‐wen; Kurahashi, Hirokazu; Ishii, Atsushi; Kojima, Toshio; Ohfu, Masaharu; Inoue, Takahito; Ogawa, Atsushi; Yasumoto, Sawa; Oguni, Hirokazu; Kure, Shigeo;
Epilepsia   49(9) 1528-1534   2008   [Refereed]
Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC)
Sugiura, Yoshihiro; Nakatsu, Fubito; Hiroyasu, Kiwamu; Ishii, Atsushi; Hirose, Shinichi; Okada, Motohiro; Jibiki, Itsuki; Ohno, Hiroshi; Kaneko, Sunao; Ugawa, Yoshikazu;
Epilepsy research   84(1) 82-85   2009   [Refereed]
A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
Ishii, Atsushi; Fukuma, Goryu; Uehara, Akira; Miyajima, Tasuku; Makita, Yoshio; Hamachi, Akiyo; Yasukochi, Midori; Inoue, Takahito; Yasumoto, Sawa; Okada, Motohiro;
Brain and Development   31(1) 27-33   2009   [Refereed]
Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures
H Kurahashi, J-w Wang, A Ishii, T Kojima, S Wakai, T Kizawa, Y Fujimoto, K Kikkawa, K Yoshimura, T Inoue, S Yasumoto, A Ogawa, S Kaneko, S Hirose
Neurology   73(15) 1214-1217   Oct 2009   [Refereed]
Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies
Shi, XiuYu; Huang, Ming-Chih; Ishii, Atsushi; Yoshida, Shuichi; Okada, Motohiro; Morita, Kohtaro; Nagafuji, Hiroshi; Yasumoto, Sawa; Kaneko, Sunao; Kojima, Toshio;
Journal of human genetics   55(6) 375   2010   [Refereed]

Books etc

 
Biology of Seizure Susceptibility in Developing Brain
Kurahashi H, Wang J, Ishii A, Fukuma G, Hamachi A, Yonetani M, Ogawa A, Ohfu M, Inoue T, Yasumoto S, Hirose S. (Part:Joint Work, Progress in genetics of severe myoclonic epilepsy in infancy)
2008   
臨床てんかん学
兼本浩祐、丸栄一、小国弘量、池田昭夫、川合謙介
2015   
臨床てんかん学
兼本浩祐、丸栄一、小国弘量、池田昭夫、川合謙介
2015   
Acute Encephalopathy and Encephalitis in Infancy and Its Related Disorders
Yamanouchi H, Moshe LS, Okumura A.
2017   

Conference Activities & Talks

 
Genetic analysesa of genes encoding KCNQ K+ and Na+ channels in patient with benign neonatal convulsions
Hirose, S., Fukuma, G., Ishii, A., Miyajima, T., Okano, S., Makita, Y., Yasukochi, M., Uehara, A., Hamachi, A., Yonetani, M., Kaneko, S., Mitsudome, A.
25th International Epilepsy Congress   Oct 2003   
Genetic analysesa of genes encoding KCNQ K+ and Na+ channels in patient with benign neonatal convulsions
Hirose, S., Fukuma, G., Ishii, A., Miyajima, T., Okano, S., Makita, Y., Yasukochi, M., Uehara, A., Hamachi, A., Yonetani, M., Kaneko, S., Mitsudome, A.
25th International Epilepsy Congress   Oct 2003   
Candidate gene analyses of benign neonatal and infantile convulsion phenotypes
Hirose, S., Fukuma, G., Ishii, A., Miyajima, T., Okano, S., Hamachi, A., Yonetani, M., Kaneko, S., Mitsudome, A.
The 11th Asian Congress of Pediatrics   Nov 2003   
Candidate gene analyses of benign neonatal and infantile convulsion phenotypes
Hirose, S., Fukuma, G., Ishii, A., Miyajima, T., Okano, S., Hamachi, A., Yonetani, M., Kaneko, S., Mitsudome, A.
The 11th Asian Congress of Pediatrics   Nov 2003   
A novel de novo KCNQ2 nutation in sporadic case of benign neonatal convulsion
Ishii, A., Fukuma, G., Uehara, A., Miyajima, T., Makita, Y., Hamachi, A., Yasukochi, M., Inoue, T., Okada, M., Kaneko, S., Mitsudome, A., Hirose, S.
The 11th Asian Congress of Pediatrics   Nov 2003   

Research Grants & Projects

 
てんかん治療振興財団研究助成「小児交互性片麻痺の分子病態とてんかん原生の解明」
Project Year: 2012 - 2014
臨床医学振興財団研究「ICCA(乳児痙攣・舞踏アテトーゼ)症候群の遺伝学病態の解明」
Project Year: 2012 - 2013
貝原守一医学振興財団 研究助成 「小児交互性片麻痺の責任遺伝子探索と分子病態の解明」
Project Year: 2011 - 2013
小児交互性片麻痺の分子病態の解明
Project Year: 2011 - 2013
財団法人臨床研究奨励基金 臨床研究基金 「自閉症スペクトラム障害の遺伝学的解明」
Project Year: 2011 - 2012