Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

896 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Acute encephalopathy with a novel point mutation in the SCN2A gene.
Kobayashi K, Ohzono H, Shinohara M, Saitoh M, Ohmori I, Ohtsuka Y, Mizuguchi M. Kobayashi K, et al. Among authors: saitoh m. Epilepsy Res. 2012 Nov;102(1-2):109-12. doi: 10.1016/j.eplepsyres.2012.04.016. Epub 2012 May 14. Epilepsy Res. 2012. PMID: 22591750
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
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.
896 results