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Page 1
SGTA associates with intracellular aggregates in neurodegenerative diseases.
Kubota S, Doi H, Koyano S, Tanaka K, Komiya H, Katsumoto A, Ikeda S, Hashiguchi S, Nakamura H, Fukai R, Takahashi K, Kunii M, Tada M, Takeuchi H, Tanaka F. Kubota S, et al. Among authors: komiya h. Mol Brain. 2021 Mar 23;14(1):59. doi: 10.1186/s13041-021-00770-1. Mol Brain. 2021. PMID: 33757575 Free PMC article.
Inhibition of Crmp1 Phosphorylation at Ser522 Ameliorates Motor Function and Neuronal Pathology in Amyotrophic Lateral Sclerosis Model Mice.
Asano T, Nakamura H, Kawamoto Y, Tada M, Kimura Y, Takano H, Yao R, Saito H, Ikeda T, Komiya H, Kubota S, Hashiguchi S, Takahashi K, Kunii M, Tanaka K, Goshima Y, Nakamura F, Takeuchi H, Doi H, Tanaka F. Asano T, et al. Among authors: komiya h. eNeuro. 2022 May 23;9(3):ENEURO.0133-22.2022. doi: 10.1523/ENEURO.0133-22.2022. Print 2022 May-Jun. eNeuro. 2022. PMID: 35523582 Free PMC article.
Anti-inflammatory effects of siponimod on astrocytes.
Ogasawara A, Takeuchi H, Komiya H, Ogawa Y, Nishimura K, Kubota S, Hashiguchi S, Takahashi K, Kunii M, Tanaka K, Tada M, Doi H, Tanaka F. Ogasawara A, et al. Among authors: komiya h. Neurosci Res. 2022 Nov;184:38-46. doi: 10.1016/j.neures.2022.08.003. Epub 2022 Aug 5. Neurosci Res. 2022. PMID: 35940437
Adult-onset vocal cord paralysis in slow-channel congenital myasthenic syndrome.
Nakamura H, Komiya H, Uematsu E, Nakae Y, Tanaka K, Kunii M, Tada M, Joki H, Koyano S, Matsumoto N, Doi H, Takeuchi H, Tanaka F. Nakamura H, et al. Among authors: komiya h. Neurol Clin Pract. 2019 Oct;9(5):e45-e47. doi: 10.1212/CPJ.0000000000000599. Neurol Clin Pract. 2019. PMID: 31750034 Free PMC article. No abstract available.
"COVID arm" detected by MR neurography.
Komiya H, Harada K, Morishita R, Hashiguchi S, Tada M, Tanaka K, Doi H, Takeuchi H, Tanaka F. Komiya H, et al. eNeurologicalSci. 2021 Dec;25:100377. doi: 10.1016/j.ensci.2021.100377. Epub 2021 Nov 3. eNeurologicalSci. 2021. PMID: 34746453 Free PMC article. 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. 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.
161 results