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Page 1
Neural mechanisms of foreign accent syndrome: Lesion and network analysis.
Higashiyama Y, Hamada T, Saito A, Morihara K, Okamoto M, Kimura K, Joki H, Kishida H, Doi H, Ueda N, Takeuchi H, Tanaka F. Higashiyama Y, et al. Neuroimage Clin. 2021;31:102760. doi: 10.1016/j.nicl.2021.102760. Epub 2021 Jul 8. Neuroimage Clin. 2021. PMID: 34274725 Free PMC article.
A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy.
Higashiyama Y, Doi H, Wakabayashi M, Tsurusaki Y, Miyake N, Saitsu H, Ohba C, Fukai R, Miyatake S, Joki H, Koyano S, Suzuki Y, Tanaka F, Kuroiwa Y, Matsumoto N. Higashiyama Y, et al. Mov Disord. 2013 Apr;28(4):552-3. doi: 10.1002/mds.25296. Epub 2013 Jan 16. Mov Disord. 2013. PMID: 23325613 No abstract available.
A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.
Kunii M, Doi H, Higashiyama Y, Kugimoto C, Ueda N, Hirata J, Tomita-Katsumoto A, Kashikura-Kojima M, Kubota S, Taniguchi M, Murayama K, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N, Tanaka F. Kunii M, et al. Among authors: higashiyama y. J Hum Genet. 2015 Apr;60(4):187-91. doi: 10.1038/jhg.2015.7. Epub 2015 Feb 5. J Hum Genet. 2015. PMID: 25652355 Review.
The Neural Basis of Typewriting: A Functional MRI Study.
Higashiyama Y, Takeda K, Someya Y, Kuroiwa Y, Tanaka F. Higashiyama Y, et al. PLoS One. 2015 Jul 28;10(7):e0134131. doi: 10.1371/journal.pone.0134131. eCollection 2015. PLoS One. 2015. PMID: 26218431 Free PMC article.
Cerebrospinal fluid level of Nogo receptor 1 antagonist lateral olfactory tract usher substance (LOTUS) correlates inversely with the extent of neuroinflammation.
Takahashi K, Takeuchi H, Kurihara Y, Doi H, Kunii M, Tanaka K, Nakamura H, Fukai R, Tomita-Katsumoto A, Tada M, Higashiyama Y, Joki H, Koyano S, Takei K, Tanaka F. Takahashi K, et al. Among authors: higashiyama y. J Neuroinflammation. 2018 Feb 17;15(1):46. doi: 10.1186/s12974-018-1084-x. J Neuroinflammation. 2018. PMID: 29454354 Free PMC article.
Novel VRK1 Mutations in a Patient with Childhood-onset Motor Neuron Disease.
Yamaura G, Higashiyama Y, Kusama K, Kunii M, Tanaka K, Koyano S, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Iwahashi Y, Joki H, Matsumoto N, Doi H, Tanaka F. Yamaura G, et al. Among authors: higashiyama y. Intern Med. 2019 Sep 15;58(18):2715-2719. doi: 10.2169/internalmedicine.2126-18. Epub 2019 Jun 7. Intern Med. 2019. PMID: 31178479 Free PMC article.
146 results