Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

181 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
PLPBP mutations cause variable phenotypes of developmental and epileptic encephalopathy.
Shiraku H, Nakashima M, Takeshita S, Khoo CS, Haniffa M, Ch'ng GS, Takada K, Nakajima K, Ohta M, Okanishi T, Kanai S, Fujimoto A, Saitsu H, Matsumoto N, Kato M. Shiraku H, et al. Among authors: okanishi t. Epilepsia Open. 2018 Nov 1;3(4):495-502. doi: 10.1002/epi4.12272. eCollection 2018 Dec. Epilepsia Open. 2018. PMID: 30525118 Free PMC article.
CDKL5 alterations lead to early epileptic encephalopathy in both genders.
Liang JS, Shimojima K, Takayama R, Natsume J, Shichiji M, Hirasawa K, Imai K, Okanishi T, Mizuno S, Okumura A, Sugawara M, Ito T, Ikeda H, Takahashi Y, Oguni H, Imai K, Osawa M, Yamamoto T. Liang JS, et al. Among authors: okanishi t. Epilepsia. 2011 Oct;52(10):1835-42. doi: 10.1111/j.1528-1167.2011.03174.x. Epub 2011 Jul 19. Epilepsia. 2011. PMID: 21770923 Free article.
Acute encephalopathy in children with Dravet syndrome.
Okumura A, Uematsu M, Imataka G, Tanaka M, Okanishi T, Kubota T, Sudo A, Tohyama J, Tsuji M, Ohmori I, Naiki M, Hiraiwa-Sofue A, Sato H, Saitoh S, Shimizu T. Okumura A, et al. Among authors: okanishi t. Epilepsia. 2012 Jan;53(1):79-86. doi: 10.1111/j.1528-1167.2011.03311.x. Epub 2011 Nov 16. Epilepsia. 2012. PMID: 22092154 Free article.
Successful hemispherotomy for a patient with intractable epilepsy secondary to bilateral congenital brain malformation with lateralized pyramidal tract of diffusion tensor image tractography.
Nagai Y, Fujimoto A, Okanishi T, Motoi H, Kanai S, Yokota T, Enoki H, Nishimura M, Yamamoto T. Nagai Y, et al. Among authors: okanishi t. Epilepsy Behav Case Rep. 2016 Feb 11;6:30-2. doi: 10.1016/j.ebcr.2016.01.005. eCollection 2016. Epilepsy Behav Case Rep. 2016. PMID: 27453818 Free PMC 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. Among authors: okanishi t. 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: okanishi t. 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
181 results