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Isolated Unilateral Ptosis due to Paramedian Midbrain Infarction.
Sugawara E, Nakamura H, Endo M, Tanaka F, Takahashi T. Sugawara E, et al. Among authors: takahashi t. J Stroke Cerebrovasc Dis. 2015 May;24(5):e121-3. doi: 10.1016/j.jstrokecerebrovasdis.2015.01.027. Epub 2015 Mar 25. J Stroke Cerebrovasc Dis. 2015. PMID: 25817621
Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy.
Sone J, Kitagawa N, Sugawara E, Iguchi M, Nakamura R, Koike H, Iwasaki Y, Yoshida M, Takahashi T, Chiba S, Katsuno M, Tanaka F, Sobue G. Sone J, et al. Among authors: takahashi t. J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):354-6. doi: 10.1136/jnnp-2013-306084. Epub 2013 Sep 13. J Neurol Neurosurg Psychiatry. 2014. PMID: 24039026 No abstract available.
A Case of McLeod Syndrome with A Novel XK Missense Mutation.
Komiya H, Takasu M, Hashiguchi S, Uematsu E, Fukai R, Tanaka K, Tada M, Joki H, Takahashi T, Koyano S, Doi H, Takeuchi H, Tanaka F. Komiya H, et al. Among authors: takahashi t. Mov Disord Clin Pract. 2018 Apr 6;5(3):333-336. doi: 10.1002/mdc3.12614. eCollection 2018 May-Jun. Mov Disord Clin Pract. 2018. PMID: 30800707 Free PMC article. No abstract available.
GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy.
Okubo M, Doi H, Fukai R, Fujita A, Mitsuhashi S, Hashiguchi S, Kishida H, Ueda N, Morihara K, Ogasawara A, Kawamoto Y, Takahashi T, Takahashi K, Nakamura H, Kunii M, Tada M, Katsumoto A, Fukuda H, Mizuguchi T, Miyatake S, Miyake N, Suzuki J, Ito Y, Sone J, Sobue G, Takeuchi H, Matsumoto N, Tanaka F. Okubo M, et al. Among authors: takahashi k, takahashi t. Ann Neurol. 2019 Dec;86(6):962-968. doi: 10.1002/ana.25586. Epub 2019 Oct 22. Ann Neurol. 2019. PMID: 31433517
Therapeutic efficacy of heparin and direct factor Xa inhibitors in cancer-associated cryptogenic ischemic stroke with venous thromboembolism.
Yamaura G, Ito T, Miyaji Y, Ueda N, Nakae Y, Momoo T, Nakano T, Johmura Y, Higashiyama Y, Joki H, Doi H, Takeuchi H, Takahashi T, Koyano S, Yamaguchi S, Yokoyama M, Tanaka F. Yamaura G, et al. Among authors: takahashi t. Thromb Res. 2021 Oct;206:99-103. doi: 10.1016/j.thromres.2021.08.016. Epub 2021 Aug 23. Thromb Res. 2021. PMID: 34454242
Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndrome.
Miyatake S, Yoshida K, Koshimizu E, Doi H, Yamada M, Miyaji Y, Ueda N, Tsuyuzaki J, Kodaira M, Onoue H, Taguri M, Imamura S, Fukuda H, Hamanaka K, Fujita A, Satoh M, Miyama T, Watanabe N, Kurita Y, Okubo M, Tanaka K, Kishida H, Koyano S, Takahashi T, Ono Y, Higashida K, Yoshikura N, Ogata K, Kato R, Tsuchida N, Uchiyama Y, Miyake N, Shimohata T, Tanaka F, Mizuguchi T, Matsumoto N. Miyatake S, et al. Among authors: takahashi t. Brain. 2022 Apr 29;145(3):1139-1150. doi: 10.1093/brain/awab363. Brain. 2022. PMID: 35355059
Long-read sequencing revealing intragenic deletions in exome-negative spastic paraplegias.
Fukuda H, Mizuguchi T, Doi H, Kameyama S, Kunii M, Joki H, Takahashi T, Komiya H, Sasaki M, Miyaji Y, Ohori S, Koshimizu E, Uchiyama Y, Tsuchida N, Fujita A, Hamanaka K, Misawa K, Miyatake S, Tanaka F, Matsumoto N. Fukuda H, et al. Among authors: takahashi t. J Hum Genet. 2023 Oct;68(10):689-697. doi: 10.1038/s10038-023-01170-0. Epub 2023 Jun 12. J Hum Genet. 2023. PMID: 37308565
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