Details of a Researcher

* Japanese*

Name

TANAKA Ryosuke

School Attended (except graduate school)

• Asahikawa Medical College , Faculty of Medicine

  2006.03 , Graduated

Employment Record in Research

• Duty , Asahikawa Medical University School of Medicine Medical Course Clinical Medicine Pediatrics Asahikawa Medical University School of Medicine Medical Course Clinical Medicine Pediatrics , Assistant Professor , 2021.06 -

• Duty , Asahikawa Medical University School of Medicine Medical Course Clinical Medicine Pediatrics Asahikawa Medical University Hospital Pediatrics , Medical Staff , 2014.10 - 2021.05

• Duty , Asahikawa Medical University School of Medicine Medical Course Clinical Medicine Pediatrics Asahikawa Medical University Hospital Pediatrics , Medical Staff , 2014.04 - 2014.06

• Duty , Asahikawa Medical University School of Medicine Medical Course Clinical Medicine Pediatrics Asahikawa Medical University Hospital Pediatrics , Medical Staff , 2009.04 - 2009.09

Academic Society Joined

• The Japanese Society of Cnild Neurology

• Japan Epilepsy Society

Research Field (grants-in-aid-for-scientific-research classification)

• Pediatrics

Research Achievement (Published Thesis)

• English: Tanaka, R. and Takeguchi, R. and Kuroda, M. and Suzuki, N. and Makita, Y. and Yanagi, K. and Kaname, T. and Takahashi, S., Novel NARS2 variant causing leigh syndrome with normal lactate levels , Human Genome Variation , vol.9 (1) (p.12 - ) , 2022

• English: Takeguchi Ryo, Takahashi Satoru, Akaba Yuichi, Tanaka Ryosuke, Nabatame Shin, Kurosawa Kenji, Matsuishi Toyojiro, Itoh Masayuki, Early diagnosis of MECP2 duplication syndrome: Insights from a nationwide survey in Japan. , J Neurol Sci , vol.422 (p.117321) , 2021

• English: Akaba Yuichi, Takahashi Satoru, Takeguchi Ryo, Tanaka Ryosuke, Nabatame Shin, Saitsu Hirotomo, Matsumoto Naomichi, Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome. , Clin Case Rep , vol.9 (3) (p.1711 - 1715) , 2021

• English: Akaba, Y. and Takeguchi, R. and Tanaka, R. and Takahashi, S., A Complex Phenotype of a Patient with Spastic Paraplegia Type 4 Caused by a Novel Pathogenic Variant in the SPAST Gene , Case Reports in Neurology , vol.13 (3) (p.763 - 771) , 2021

• English: Takahashi Satoru, Tanaka Ryosuke, Takeguchi Ryo, Kuroda Mami, Akaba Yuichi, Ito Yasushi, The role of molecular analysis of SLC2A1 in the diagnostic workup of glucose transporter 1 deficiency syndrome. , J Neurol Sci , vol.416 (p.117041) , 2020

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Updated on 2022/05/19

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