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Mutations of the SCN1A gene in acute encephalopathy.
Saitoh M, Shinohara M, Hoshino H, Kubota M, Amemiya K, Takanashi JL, Hwang SK, Hirose S, Mizuguchi M. Saitoh M, et al. Epilepsia. 2012 Mar;53(3):558-64. doi: 10.1111/j.1528-1167.2011.03402.x. Epub 2012 Feb 6. Epilepsia. 2012. PMID: 22309220 Free article.
Clinical and genetic features of acute encephalopathy in children taking theophylline.
Saitoh M, Shinohara M, Ishii A, Ihara Y, Hirose S, Shiomi M, Kawawaki H, Kubota M, Yamagata T, Miyamoto A, Yamanaka G, Amemiya K, Kikuchi K, Kamei A, Akasaka M, Anzai Y, Mizuguchi M. Saitoh M, et al. Brain Dev. 2015 May;37(5):463-70. doi: 10.1016/j.braindev.2014.07.010. Epub 2014 Aug 23. Brain Dev. 2015. PMID: 25156649
A case of recurrent encephalopathy with SCN2A missense mutation.
Fukasawa T, Kubota T, Negoro T, Saitoh M, Mizuguchi M, Ihara Y, Ishii A, Hirose S. Fukasawa T, et al. Among authors: saitoh m. Brain Dev. 2015 Jun;37(6):631-4. doi: 10.1016/j.braindev.2014.10.001. Epub 2014 Oct 27. Brain Dev. 2015. PMID: 25457084
ADORA2A polymorphism predisposes children to encephalopathy with febrile status epilepticus.
Shinohara M, Saitoh M, Nishizawa D, Ikeda K, Hirose S, Takanashi J, Takita J, Kikuchi K, Kubota M, Yamanaka G, Shiihara T, Kumakura A, Kikuchi M, Toyoshima M, Goto T, Yamanouchi H, Mizuguchi M. Shinohara M, et al. Among authors: saitoh m. Neurology. 2013 Apr 23;80(17):1571-6. doi: 10.1212/WNL.0b013e31828f18d8. Epub 2013 Mar 27. Neurology. 2013. PMID: 23535492 Free PMC article.
940 results