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Dravet syndrome: a genetic epileptic disorder.
Akiyama M, Kobayashi K, Ohtsuka Y. Akiyama M, et al. Among authors: ohtsuka y. Acta Med Okayama. 2012;66(5):369-76. doi: 10.18926/AMO/48961. Acta Med Okayama. 2012. PMID: 23093055 Free article. Review.
A long-term follow-up study of Dravet syndrome up to adulthood.
Akiyama M, Kobayashi K, Yoshinaga H, Ohtsuka Y. Akiyama M, et al. Among authors: ohtsuka y. Epilepsia. 2010 Jun;51(6):1043-52. doi: 10.1111/j.1528-1167.2009.02466.x. Epub 2009 Dec 22. Epilepsia. 2010. PMID: 20041943 Free article.
CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.
Ohmori I, Ouchida M, Kobayashi K, Jitsumori Y, Mori A, Michiue H, Nishiki T, Ohtsuka Y, Matsui H. Ohmori I, et al. Among authors: ohtsuka y. Neurobiol Dis. 2013 Feb;50:209-17. doi: 10.1016/j.nbd.2012.10.016. Epub 2012 Oct 25. Neurobiol Dis. 2013. PMID: 23103419
Rasmussen encephalitis associated with SCN 1 A mutation.
Ohmori I, Ouchida M, Kobayashi K, Jitsumori Y, Inoue T, Shimizu K, Matsui H, Ohtsuka Y, Maegaki Y. Ohmori I, et al. Among authors: ohtsuka y. Epilepsia. 2008 Mar;49(3):521-6. doi: 10.1111/j.1528-1167.2007.01411.x. Epub 2007 Nov 21. Epilepsia. 2008. PMID: 18031552 Free article.
755 results