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Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping task.
Tokushige SI, Matsuda S, Tada M, Yabe I, Takeda A, Tanaka H, Hatakenaka M, Enomoto H, Kobayashi S, Shimizu K, Shimizu T, Kotsuki N, Inomata-Terada S, Furubayashi T, Ichikawa Y, Hanajima R, Tsuji S, Ugawa Y, Terao Y. Tokushige SI, et al. Among authors: ichikawa y. Clin Neurophysiol. 2024 Feb;158:1-15. doi: 10.1016/j.clinph.2023.11.018. Epub 2023 Dec 1. Clin Neurophysiol. 2024. PMID: 38113692
Is multiple system atrophy with cerebellar ataxia (MSA-C) like spinocerebellar ataxia and multiple system atrophy with parkinsonism (MSA-P) like Parkinson's disease? - A saccade study on pathophysiology.
Terao Y, Fukuda H, Tokushige S, Inomata-Terada S, Yugeta A, Hamada M, Ichikawa Y, Hanajima R, Ugawa Y. Terao Y, et al. Among authors: ichikawa y. Clin Neurophysiol. 2016 Feb;127(2):1491-1502. doi: 10.1016/j.clinph.2015.07.035. Epub 2015 Aug 22. Clin Neurophysiol. 2016. PMID: 26350408
Time Distortion in Parkinsonism.
Terao Y, Honma M, Asahara Y, Tokushige SI, Furubayashi T, Miyazaki T, Inomata-Terada S, Uchibori A, Miyagawa S, Ichikawa Y, Chiba A, Ugawa Y, Suzuki M. Terao Y, et al. Among authors: ichikawa y. Front Neurosci. 2021 Mar 19;15:648814. doi: 10.3389/fnins.2021.648814. eCollection 2021. Front Neurosci. 2021. PMID: 33815049 Free PMC article.
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Ishiura H, Doi K, Mitsui J, Yoshimura J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koike R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S. Ishiura H, et al. Among authors: ichikawa k, ichikawa y. Nat Genet. 2018 Apr;50(4):581-590. doi: 10.1038/s41588-018-0067-2. Epub 2018 Mar 5. Nat Genet. 2018. PMID: 29507423
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. Among authors: ichikawa y. Neurol Genet. 2016 Jan 7;2(1):e48. doi: 10.1212/NXG.0000000000000048. eCollection 2016 Feb. Neurol Genet. 2016. PMID: 27066585 Free PMC article.
1,985 results