Okazaki T - Search Results

1

Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis.

Okazaki T, Saito Y, Ueda R, Awashima T, Nishimura Y, Yuasa I, Shinohara Y, Adachi K, Sasaki M, Nanba E, Maegaki Y. Okazaki T, et al. Brain Dev. 2017 Jan;39(1):67-71. doi: 10.1016/j.braindev.2016.07.004. Epub 2016 Jul 30. Brain Dev. 2017. PMID: 27485793

2

Late-onset epilepsy in children with acute febrile encephalopathy with prolonged convulsions: A clinical and encephalographic study.

Saito T, Saito Y, Sugai K, Nakagawa E, Komaki H, Okazaki T, Ishido Y, Kaneko Y, Kaido T, Takahashi A, Ohtsuki T, Sakuma H, Sasaki M. Saito T, et al. Among authors: okazaki t. Brain Dev. 2013 Jun;35(6):531-9. doi: 10.1016/j.braindev.2012.08.007. Epub 2012 Sep 13. Brain Dev. 2013. PMID: 22982002

3

Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgery.

Endo Y, Saito Y, Otsuki T, Takahashi A, Nakata Y, Okada K, Hirozane M, Kaido T, Kaneko Y, Takada E, Okazaki T, Enokizno T, Saito T, Komaki H, Nakagawa E, Sugai K, Sasaki M. Endo Y, et al. Among authors: okazaki t. Brain Dev. 2014 Jan;36(1):74-9. doi: 10.1016/j.braindev.2013.01.002. Epub 2013 Feb 8. Brain Dev. 2014. PMID: 24370003

4

Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata.

Okazaki T, Saito Y, Ueda R, Sugihara S, Tamasaki A, Nishimura Y, Ohno K, Togawa M, Ohno T, Horie A, Honda M, Takenaka A, Nagashima H, Maegaki Y. Okazaki T, et al. Pediatr Neurol. 2016 Mar;56:80-85.e2. doi: 10.1016/j.pediatrneurol.2015.11.011. Epub 2015 Dec 13. Pediatr Neurol. 2016. PMID: 26777981

5

Successful treatment of migrating partial seizures in Wolf-Hirschhorn syndrome with bromide.

Itakura A, Saito Y, Nishimura Y, Okazaki T, Ohno K, Sejima H, Yamamoto T, Maegaki Y. Itakura A, et al. Among authors: okazaki t. Brain Dev. 2016 Aug;38(7):658-62. doi: 10.1016/j.braindev.2016.01.001. Epub 2016 Jan 18. Brain Dev. 2016. PMID: 26797656

6

Characterization of SPATA5-related encephalopathy in early childhood.

Kurata H, Terashima H, Nakashima M, Okazaki T, Matsumura W, Ohno K, Saito Y, Maegaki Y, Kubota M, Nanba E, Saitsu H, Matsumoto N, Kato M. Kurata H, et al. Among authors: okazaki t. Clin Genet. 2016 Nov;90(5):437-444. doi: 10.1111/cge.12813. Epub 2016 Jul 4. Clin Genet. 2016. PMID: 27246907

7

Clinical Diagnosis of Mendelian Disorders Using a Comprehensive Gene-Targeted Panel Test for Next-Generation Sequencing.

Okazaki T, Murata M, Kai M, Adachi K, Nakagawa N, Kasagi N, Matsumura W, Maegaki Y, Nanba E. Okazaki T, et al. Yonago Acta Med. 2016 Jun 29;59(2):118-25. eCollection 2016 Jun. Yonago Acta Med. 2016. PMID: 27493482 Free PMC article.

8

Surface electromyogram and muscle ultrasonography for detection of muscle fasciculations in pediatric peripheral neuropathy.

Oguri M, Saito Y, Okazaki T, Matsumura W, Ohno K, Togawa M, Fukuda C, Saito Y, Nishino I, Maegaki Y. Oguri M, et al. Among authors: okazaki t. Brain Dev. 2017 Aug;39(7):617-620. doi: 10.1016/j.braindev.2017.02.006. Epub 2017 Mar 16. Brain Dev. 2017. PMID: 28318780

9

Pharmacoresistant epileptic eyelid twitching in a child with a mutation in SYNGAP1.

Okazaki T, Saito Y, Hiraiwa R, Saitoh S, Kai M, Adachi K, Nishimura Y, Nanba E, Maegaki Y. Okazaki T, et al. Epileptic Disord. 2017 Sep 1;19(3):339-344. doi: 10.1684/epd.2017.0922. Epileptic Disord. 2017. PMID: 28721930

10

Neurodevelopmental disorders in children with macrocephaly: A prevalence study and PTEN gene analysis.

Kurata H, Shirai K, Saito Y, Okazaki T, Ohno K, Oguri M, Adachi K, Nanba E, Maegaki Y. Kurata H, et al. Among authors: okazaki t. Brain Dev. 2018 Jan;40(1):36-41. doi: 10.1016/j.braindev.2017.07.005. Epub 2017 Jul 31. Brain Dev. 2018. PMID: 28774669

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