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34 results

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Page 1
Clinical characteristics of SARS-CoV-2-associated encephalopathy in children: Nationwide epidemiological study.
Kasai M, Sakuma H, Abe Y, Kuki I, Maegaki Y, Murayama K, Murofushi Y, Nagase H, Nishiyama M, Okumura A, Sakai Y, Tada H, Mizuguchi M, Takanashi JI; Japanese Pediatric Neuro-COVID-19 Study Group. Kasai M, et al. J Neurol Sci. 2024 Feb 15;457:122867. doi: 10.1016/j.jns.2024.122867. Epub 2024 Jan 3. J Neurol Sci. 2024. PMID: 38199023 Free article.
Wolf-Hirschhorn (4p-) syndrome with West syndrome.
Motoi H, Okanishi T, Kanai S, Yokota T, Yamazoe T, Nishimura M, Fujimoto A, Yamamoto T, Enoki H. Motoi H, et al. Epilepsy Behav Case Rep. 2016 Jul 15;6:39-41. doi: 10.1016/j.ebcr.2016.07.001. eCollection 2016. Epilepsy Behav Case Rep. 2016. PMID: 27504263 Free PMC article.
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
Mizuguchi T, Nakashima M, Kato M, Yamada K, Okanishi T, Ekhilevitch N, Mandel H, Eran A, Toyono M, Sawaishi Y, Motoi H, Shiina M, Ogata K, Miyatake S, Miyake N, Saitsu H, Matsumoto N. Mizuguchi T, et al. Among authors: motoi h. J Hum Genet. 2017 Apr;62(5):525-529. doi: 10.1038/jhg.2016.163. Epub 2017 Jan 12. J Hum Genet. 2017. PMID: 28077841
De novo GABRA1 mutations in Ohtahara and West syndromes.
Kodera H, Ohba C, Kato M, Maeda T, Araki K, Tajima D, Matsuo M, Hino-Fukuyo N, Kohashi K, Ishiyama A, Takeshita S, Motoi H, Kitamura T, Kikuchi A, Tsurusaki Y, Nakashima M, Miyake N, Sasaki M, Kure S, Haginoya K, Saitsu H, Matsumoto N. Kodera H, et al. Among authors: motoi h. Epilepsia. 2016 Apr;57(4):566-73. doi: 10.1111/epi.13344. Epub 2016 Feb 25. Epilepsia. 2016. PMID: 26918889 Free article.
Erratum: PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
Mizuguchi T, Nakashima M, Kato M, Yamada K, Okanishi T, Ekhilevitch N, Mandel H, Eran A, Toyono M, Sawaishi Y, Motoi H, Shiina M, Ogata K, Miyatake S, Miyake N, Saitsu H, Matsumoto N. Mizuguchi T, et al. Among authors: motoi h. J Hum Genet. 2017 Apr;62(5):587. doi: 10.1038/jhg.2017.13. Epub 2017 Feb 16. J Hum Genet. 2017. PMID: 28202951 No abstract available.
34 results