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Three-Year Follow-Up of High-Dose Ubiquinol Supplementation in a Case of Familial Multiple System Atrophy with Compound Heterozygous COQ2 Mutations.
Mitsui J, Koguchi K, Momose T, Takahashi M, Matsukawa T, Yasuda T, Tokushige SI, Ishiura H, Goto J, Nakazaki S, Kondo T, Ito H, Yamamoto Y, Tsuji S. Mitsui J, et al. Among authors: tokushige si. Cerebellum. 2017 Jun;16(3):664-672. doi: 10.1007/s12311-017-0846-9. Cerebellum. 2017. PMID: 28150130 Free PMC article.
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum.
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. Mano KK, et al. Neurol Genet. 2016 Jan 7;2(1):e48. doi: 10.1212/NXG.0000000000000048. eCollection 2016 Feb. Neurol Genet. 2016. PMID: 27066585 Free PMC article.
Effect of subthalamic nucleus deep brain stimulation on visual scanning.
Tokushige SI, Matsuda SI, Oyama G, Shimo Y, Umemura A, Sasaki T, Inomata-Terada S, Yugeta A, Hamada M, Ugawa Y, Tsuji S, Hattori N, Terao Y. Tokushige SI, et al. Clin Neurophysiol. 2018 Nov;129(11):2421-2432. doi: 10.1016/j.clinph.2018.08.003. Epub 2018 Aug 30. Clin Neurophysiol. 2018. PMID: 30292079
Premature saccades: A detailed physiological analysis.
Tokushige SI, Matsuda S, Inomata-Terada S, Hamada M, Ugawa Y, Tsuji S, Terao Y. Tokushige SI, et al. Clin Neurophysiol. 2021 Jan;132(1):63-76. doi: 10.1016/j.clinph.2020.09.026. Epub 2020 Oct 22. Clin Neurophysiol. 2021. PMID: 33254099
33 results