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

1,506 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Clinical features in very early-onset demyelinating disease with anti-MOG antibody.
Nishiyama M, Nagase H, Matsumoto M, Tomioka K, Awano H, Tanaka T, Toyoshima D, Fujita K, Maruyama A, Oyazato Y, Saeki K, Shiraishi K, Takada S, Kaneko K, Takahashi T, Nakashima I, Iijima K. Nishiyama M, et al. Among authors: takada s. Brain Dev. 2017 Oct;39(9):756-762. doi: 10.1016/j.braindev.2017.05.004. Epub 2017 May 24. Brain Dev. 2017. PMID: 28551039
Genotype-phenotype correlations in alternating hemiplegia of childhood.
Sasaki M, Ishii A, Saito Y, Morisada N, Iijima K, Takada S, Araki A, Tanabe Y, Arai H, Yamashita S, Ohashi T, Oda Y, Ichiseki H, Hirabayashi S, Yasuhara A, Kawawaki H, Kimura S, Shimono M, Narumiya S, Suzuki M, Yoshida T, Oyazato Y, Tsuneishi S, Ozasa S, Yokochi K, Dejima S, Akiyama T, Kishi N, Kira R, Ikeda T, Oguni H, Zhang B, Tsuji S, Hirose S. Sasaki M, et al. Among authors: takada s. Neurology. 2014 Feb 11;82(6):482-90. doi: 10.1212/WNL.0000000000000102. Epub 2014 Jan 15. Neurology. 2014. PMID: 24431296
Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.
Kato T, Morisada N, Nagase H, Nishiyama M, Toyoshima D, Nakagawa T, Maruyama A, Fu XJ, Nozu K, Wada H, Takada S, Iijima K. Kato T, et al. Among authors: takada s. Brain Dev. 2015 Oct;37(9):911-5. doi: 10.1016/j.braindev.2015.03.002. Epub 2015 Mar 27. Brain Dev. 2015. PMID: 25819767
Rituximab treatment for relapsed opsoclonus-myoclonus syndrome.
Toyoshima D, Morisada N, Takami Y, Kidokoro H, Nishiyama M, Nakagawa T, Ninchoji T, Nozu K, Takeshima Y, Takada S, Nishio H, Iijima K. Toyoshima D, et al. Among authors: takada s. Brain Dev. 2016 Mar;38(3):346-9. doi: 10.1016/j.braindev.2015.09.002. Epub 2015 Sep 12. Brain Dev. 2016. PMID: 26375512
A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency.
Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, Takada S, Tairaku S, Okamoto N, Morioka I, Kurahashi H, Toda T, Kinoshita T, Iijima K. Nakagawa T, et al. Among authors: takada s. Am J Med Genet A. 2016 Jan;170A(1):183-8. doi: 10.1002/ajmg.a.37397. Epub 2015 Sep 30. Am J Med Genet A. 2016. PMID: 26419326
Short and long-term outcomes in children with suspected acute encephalopathy.
Nishiyama M, Nagase H, Tanaka T, Fujita K, Kusumoto M, Kajihara S, Yamaguchi Y, Maruyama A, Takeda H, Uetani Y, Tomioka K, Toyoshima D, Taniguchi-Ikeda M, Morioka I, Takada S, Iijima K. Nishiyama M, et al. Among authors: takada s. Brain Dev. 2016 Sep;38(8):731-7. doi: 10.1016/j.braindev.2016.02.011. Epub 2016 Mar 4. Brain Dev. 2016. PMID: 26952815
Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-Analysis.
Maeyama K, Tomioka K, Nagase H, Yoshioka M, Takagi Y, Kato T, Mizobuchi M, Kitayama S, Takada S, Nagai M, Sakakibara N, Nishiyama M, Taniguchi-Ikeda M, Morioka I, Iijima K, Nishimura N. Maeyama K, et al. Among authors: takada s. J Autism Dev Disord. 2018 May;48(5):1483-1491. doi: 10.1007/s10803-017-3412-x. J Autism Dev Disord. 2018. PMID: 29185167
1,506 results