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Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging.
Kikumoto M, Nezu T, Shiga Y, Motoda A, Toko M, Kurashige T, Ueno H, Takahashi T, Morino H, Sone J, Iwasaki Y, Sobue G, Maruyama H. Kikumoto M, et al. Among authors: motoda a. Neurol Genet. 2021 Jun 9;7(4):e601. doi: 10.1212/NXG.0000000000000601. eCollection 2021 Aug. Neurol Genet. 2021. PMID: 34131587 Free PMC article. No abstract available.
An autopsied case of ADSSL1 myopathy.
Motoda A, Takahashi T, Watanabe C, Tachiyama Y, Ochi K, Saito Y, Iida A, Nishino I, Maruyama H. Motoda A, et al. Neuromuscul Disord. 2021 Nov;31(11):1220-1225. doi: 10.1016/j.nmd.2021.07.011. Epub 2021 Jul 20. Neuromuscul Disord. 2021. PMID: 34635388
Reversible Brain Atrophy in Cryptogenic New-onset Refractory Status Epilepticus.
Watanabe T, Nakamori M, Ishikawa K, Motoda A, Neshige S, Yamamoto S, Katahira K, Higaki T, Ueno H, Iizuka T, Maruyama H. Watanabe T, et al. Among authors: motoda a. Intern Med. 2023 Jun 15;62(12):1835-1842. doi: 10.2169/internalmedicine.0465-22. Epub 2022 Nov 9. Intern Med. 2023. PMID: 36351577 Free PMC article.
19 results