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Characteristics of epilepsy occurring in the first four months.
Fukasawa T, Suzuki M, Kato T, Hayakawa F, Miura K, Kidokoro H, Kubota T, Okumura A, Maruyama K, Hishikawa Y, Itomi K, Negoro T, Watanabe K, Natsume J. Fukasawa T, et al. Among authors: miura k. Brain Dev. 2014 Oct;36(9):752-7. doi: 10.1016/j.braindev.2013.10.011. Epub 2013 Nov 15. Brain Dev. 2014. PMID: 24246311
Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.
Shimada S, Shimojima K, Okamoto N, Sangu N, Hirasawa K, Matsuo M, Ikeuchi M, Shimakawa S, Shimizu K, Mizuno S, Kubota M, Adachi M, Saito Y, Tomiwa K, Haginoya K, Numabe H, Kako Y, Hayashi A, Sakamoto H, Hiraki Y, Minami K, Takemoto K, Watanabe K, Miura K, Chiyonobu T, Kumada T, Imai K, Maegaki Y, Nagata S, Kosaki K, Izumi T, Nagai T, Yamamoto T. Shimada S, et al. Among authors: miura k. Brain Dev. 2015 May;37(5):515-26. doi: 10.1016/j.braindev.2014.08.002. Epub 2014 Aug 27. Brain Dev. 2015. PMID: 25172301
The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N. Yamada Y, et al. Among authors: miura k. Am J Med Genet A. 2014 Aug;164A(8):1899-908. doi: 10.1002/ajmg.a.36551. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715670
Shuffling babies and autism spectrum disorder.
Okai Y, Nakata T, Miura K, Ohno A, Wakako R, Takahashi O, Maki Y, Tanaka M, Sakaguchi Y, Ito Y, Yamamoto H, Kidokoro H, Takahashi Y, Natsume J. Okai Y, et al. Among authors: miura k. Brain Dev. 2021 Feb;43(2):181-185. doi: 10.1016/j.braindev.2020.08.007. Epub 2020 Aug 30. Brain Dev. 2021. PMID: 32878720
4,749 results