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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.
Saccades abnormalities in posterior cortical atrophy - A case report.
Terao Y, Fukuda H, Tokushige SI, Inomata-Terada S, Hamada M, Ugawa Y. Terao Y, et al. Among authors: tokushige si. Clin Neurophysiol. 2017 Feb;128(2):349-350. doi: 10.1016/j.clinph.2016.12.005. Epub 2016 Dec 18. Clin Neurophysiol. 2017. PMID: 28063320 No abstract available.
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.
33 results