Profile

• Degree

  2005.3 PhD in Medical Science(Tokushima University)

• Current research field (keyword)

  小児神経学　発達障害

• Current fields of research and their synopses

  発達障害児の行動面・適応面に関する研究

• Major subjects overseen

  (大学院) 発達障害児への理解と対応
  (大学院) 発達障害児生理・発達学研究
  (大学院) 発達障害児支援医学演習
  (学部) 子どもの保健Ⅰ
  (学部) 肢体不自由者の心理・生理・病理
  (学部) 重複・ＬＤ等の特性
  (学部) 病弱者の心理・生理・病理 

• Affiliated academic societies

  日本小児科学会、日本小児神経学会、日本てんかん学会、日本小児科医会、日本小児精神神経学会、日本小児心身医学会、全国大学保健管理協会、国立大学保健管理施設協議会

• Major activities in academic societies and society

  <学会活動>
  ・日本小児神経学会評議員
  ・日本小児神経学会　社会活動・広報委員会　
  ・日本小児神経学会中国四国地方会幹事
  ・四国小児神経症例検討会幹事
  ・徳島県小児保健協会理事
  ・国立大学保健管理施設協議会　[大学における健康診断・健康関連情報の標準化と利活用に関わる
  　調査研究委員会」委員
  ・全国大学保健管理協会中国四国地方部会幹事
  
  <認定医・専門医・指導医>
  ・認定小児科指導医 (日本小児科学会)
  ・小児神経専門医 (日本小児神経学会)
  ・てんかん専門医指導医 (日本てんかん学会)
  ・子どもの心相談医 (日本小児科医会)
  ・子どものこころ専門医 (子どものこころ専門医機構)
  ・日本医師会認定産業医 (日本医師会)

• Major research achievement

  J Autism Dev Disord., Growth of head circumference in autistic infants during the first year of life., Joint authorship, 2008
  Brain Dev, Serial brain imaging analysis of stroke-like episodes in MELAS., Joint authorship, 2008
  Pediatr Int, Pathophysiology of the transient temporal lobe lesion in a patient with Menkes disease , Joint authorship, 2008
  Brain Dev, Neuroimaging of stroke-like episodes in MELAS. , Joint authorship, 2011
  Brain Dev., Transient left temporal lobe lesion in Menkes disease may influence the generation of tonic spasms. , Joint authorship, 2011
  Brain Dev., A proton magnetic resonance spectroscopic study in autism spectrum disorders: Amygdala and orbito-frontal cortex. , Joint authorship, 2013
  Brain Dev., Effective treatment of a 13-year-old boy with steroid-dependent ocular myasthenia gravis using tacrolimus., Joint authorship, 2013
  J Child Neurol., Age-related changes in a patient with Pelizaeus-Merzbacher disease determined by repeated 1H-magnetic resonance spectroscopy., Joint authorship, 2014
  Pediatr Int., Case of early childhood-onset narcolepsy with cataplexy: comparison with a monozygotic co-twin., Joint authorship, 2014
  Journal of Medical Investigation, Neuroimaging in autism spectrum disorders: 1H-MRS and NIRS study., Joint authorship, 2015
  Human　Genome　Variation, Detection of 1p36 deletion syndrome by clinical exome-first diagnostic approach., Joint authorship, 2016
  Journal of Medical Investigation, Default mode network abnormalities in children with autistic spectrum disorder detected by resting-state functional magnetic resonance imaging., Joint authorship, 2016
  PLoS One, Assessment of Anterior Cingulate Cortex (ACC) and Left Cerebellar Metabolism in Asperger's Syndrome with Proton Magnetic Resonance Spectroscopy (MRS)., Joint authorship, 2017
  Journal of Child Neurology, A proton magnetic resonance spectroscopic study in autism spectrum disorder using a 3-tesla clinical magnetic resonance imaging (MRI) system: The anterior cingulate cortex and the left cerebellum., Joint authorship, 2017
  Am J Med Genet A., A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation, Joint authorship, 2018
  

• Research activities over the past five years

  Journal of Medical Investigation, Neuroimaging in autism spectrum disorders: 1H-MRS and NIRS study., Joint authorship, 2015
  Human　Genome　Variation, Detection of 1p36 deletion syndrome by clinical exome-first diagnostic approach., Joint authorship, 2016
  Journal of Medical Investigation, Default mode network abnormalities in children with autistic spectrum disorder detected by resting-state functional magnetic resonance imaging., Joint authorship, 2016
  PLoS One, Assessment of Anterior Cingulate Cortex (ACC) and Left Cerebellar Metabolism in Asperger's Syndrome with Proton Magnetic Resonance Spectroscopy (MRS)., Joint authorship, 2017
  Journal of Child Neurology, A proton magnetic resonance spectroscopic study in autism spectrum disorder using a 3-tesla clinical magnetic resonance imaging (MRI) system: The anterior cingulate cortex and the left cerebellum., Joint authorship, 2017
  Am J Med Genet A., A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation, Joint authorship, 2018