• ＜大学院＞神経内科学

• 神経内科学、臨床ゲノム・遺伝学

• 神経変性疾患、遺伝性神経疾患

【researchmap】
https://researchmap.jp/read0184935

1. Mano KK, Matsukawa T, Mitsui J, Ishiura H, Tokushige S, Takahashi Y, Sato NS, Nakamoto FK, Ichikawa Y, Nagashima Y, Terao Y, Shimizu J, Hamada M, Uesaka Y, Oyama G, Ogawa G, Yoshimura J, Doi K, Morishita S, Tsuji S, Goto J. Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum. Neurol Genet. 2016 Jan 7;2(1):e48. doi: 10.1212/NXG.0000000000000048. eCollection 2016 Feb. PubMed PMID: 27066585; PubMed Central PMCID: PMC4817902.
2. Nishikawa A, Mori-Yoshimura M, Segawa K, Hayashi YK, Takahashi T, Saito Y, Nonaka I, Krahn M, Levy N, Shimizu J, Mitsui J, Kimura E,Goto J, Yonemoto N, Aoki M, Nishino I, Oya Y, Murata M. Respiratory and cardiac function in japanese patients with dysferlinopathy. Muscle Nerve. 2016 Mar;53(3):394-401. doi: 10.1002/mus.24741. Epub 2016 Jan 27. PubMed PMID: 26088049.
3. Williams KL, Topp S, Yang S, Smith B, Fifita JA, Warraich ST, Zhang KY, Farrawell N, Vance C, Hu X, Chesi A, Leblond CS, Lee A, Rayner SL, Sundaramoorthy V, Dobson-Stone C, Molloy MP, van Blitterswijk M, Dickson DW, Petersen RC, Graff-Radford NR, Boeve BF, Murray ME, Pottier C, Don E, Winnick C, McCann EP, Hogan A, Daoud H, Levert A, Dion PA, Mitsui J, Ishiura H, Takahashi Y,Goto J, Kost J, Gellera C, Gkazi AS, Miller J, Stockton J, Brooks WS, Boundy K, Polak M, Muñoz-Blanco JL, Esteban-Pérez J, Rábano A, Hardiman O, Morrison KE, Ticozzi N, Silani V, de Belleroche J, Glass JD, Kwok JB, Guillemin GJ, Chung RS, Tsuji S, Brown RH Jr, García-Redondo A, Rademakers R, Landers JE, Gitler AD, Rouleau GA, Cole NJ, Yerbury JJ, Atkin JD, Shaw CE, Nicholson GA, Blair IP. CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia. Nat Commun. 2016 Apr 15;7:11253. doi: 10.1038/ncomms11253. PubMed PMID: 27080313; PubMed Central PMCID: PMC4835537.
4. Matsukawa T, Koshi KM, Mitsui J, Bannai T, Kawabe M, Ishiura H, Terao Y, Shimizu J, Murayama K, Yoshimura J, Doi K, Morishita S, Tsuji S, Goto J. Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing. J Neurol Sci. 2017 Jan 15;372:6-10. doi: 10.1016/j.jns.2016.11.009. Epub 2016 Nov 9. PubMed PMID: 28017249.
5. Sato NS, Maekawa R, Ishiura H, Mitsui J, Naruse H, Tokushige SI, Sugie K, Tate　G, Shimizu J, Goto J, Tsuji S, Shiio Y. Partial duplication of DHH causes　minifascicular neuropathy: A novel mutation detection of DHH. Ann Clin Transl　Neurol. 2017 May 22;4(6):415-421. doi: 10.1002/acn3.417. eCollection 2017 Jun.　PubMed PMID: 28589169; PubMed Central PMCID: PMC5454394.

• 東京大学卒
• 東京大学大学院博士（医学）

• 前東京大学大学院医学系研究科脳神経医学専攻神経内科学准教授
• 日本神経学会認定指導医・神経内科専門医、日本内科学会認定内科医、日本人類遺伝学会認定指導医・臨床遺伝専門医

• 科学的思考力、医療プロフェッシャナリズム、国際性を身に着け、チーム医療の中核として、患者中心の質の高い医療を実践できる医師になることを目指してほしい。

• 【TEL】03-3451-8121
  【FAX】03-3454-0067
  【E-Mail】goto@iuhw.ac.jp