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Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndrome.
Termglinchan T, Hisamatsu S, Ohmori J, Suzumura H, Sumitomo N, Imataka G, Arisaka O, Murakami N, Minami N, Akihiko I, Sasaki M, Goto Y, Noguchi S, Nonaka I, Mitsuhashi S, Nishino I. Termglinchan T, et al. Among authors: sumitomo n. Neurol Genet. 2016 Sep 14;2(5):e95. doi: 10.1212/NXG.0000000000000095. eCollection 2016 Oct. Neurol Genet. 2016. PMID: 27660820 Free PMC article.
Corpus callosotomy in pediatric patients with non-lesional epileptic encephalopathy with electrical status epilepticus during sleep.
Yokosako S, Muraoka N, Watanabe S, Kosugi K, Takayama Y, Iijima K, Kimura Y, Kaneko Y, Sumitomo N, Saito T, Nakagawa E, Iwasaki M. Yokosako S, et al. Among authors: sumitomo n. Epilepsy Behav Rep. 2021 Jun 8;16:100463. doi: 10.1016/j.ebr.2021.100463. eCollection 2021. Epilepsy Behav Rep. 2021. PMID: 34195590 Free PMC article.
Ictal deafness in drug-resistant MRI-negative epilepsy.
Ikegaya N, Nakagawa E, Sugai K, Sasaki M, Saito T, Sumitomo N, Iijima K, Kimura Y, Kaneko Y, Iwasaki M. Ikegaya N, et al. Among authors: sumitomo n. Epileptic Disord. 2019 Apr 1;21(2):215-220. doi: 10.1684/epd.2019.1042. Epileptic Disord. 2019. PMID: 30977730
216 results