Takahashi S - Search Results

1

Characterization of intragenic tandem duplication in the PAFAH1B1 gene leading to isolated lissencephaly sequence.

Takahashi S, Tanaka R, Okano S, Okayama A, Suzuki N, Azuma H. Takahashi S, et al. Mol Cytogenet. 2015 Oct 31;8:84. doi: 10.1186/s13039-015-0186-8. eCollection 2015. Mol Cytogenet. 2015. PMID: 26523152 Free PMC article.

2

Actigraphic assessment of sleep disorders in children with chronic fatigue syndrome.

Ohinata J, Suzuki N, Araki A, Takahashi S, Fujieda K, Tanaka H. Ohinata J, et al. Among authors: takahashi s. Brain Dev. 2008 May;30(5):329-33. doi: 10.1016/j.braindev.2007.10.004. Epub 2007 Nov 26. Brain Dev. 2008. PMID: 18031961

3

Molecular analysis and anticonvulsant therapy in two patients with glucose transporter 1 deficiency syndrome: a successful use of zonisamide for controlling the seizures.

Takahashi S, Ohinata J, Suzuki N, Amamiya S, Kajihama A, Sugai R, Araki A, Fujieda K, Tanaka H. Takahashi S, et al. Epilepsy Res. 2008 Jul;80(1):18-22. doi: 10.1016/j.eplepsyres.2008.03.010. Epub 2008 May 1. Epilepsy Res. 2008. PMID: 18455367

4

Effect of neonatal hypoxia on the development of intraspinal serotonergic fibers in relation to spinal motoneurons.

Tanaka H, Amamiya S, Takahashi S, Suzuki N, Araki A, Ohinata J, Fujieda K. Tanaka H, et al. Among authors: takahashi s. Brain Dev. 2010 Apr;32(4):268-74. doi: 10.1016/j.braindev.2008.12.009. Epub 2009 Feb 3. Brain Dev. 2010. PMID: 19193506

5

Silent exonic mutation in the acid-alpha-glycosidase gene that causes glycogen storage disease type II by affecting mRNA splicing.

Maimaiti M, Takahashi S, Okajima K, Suzuki N, Ohinata J, Araki A, Tanaka H, Mukai T, Fujieda K. Maimaiti M, et al. Among authors: takahashi s. J Hum Genet. 2009 Aug;54(8):493-6. doi: 10.1038/jhg.2009.66. Epub 2009 Jul 17. J Hum Genet. 2009. PMID: 19609281

6

Improved prefrontal activity in AD/HD children treated with atomoxetine: a NIRS study.

Araki A, Ikegami M, Okayama A, Matsumoto N, Takahashi S, Azuma H, Takahashi M. Araki A, et al. Among authors: takahashi m, takahashi s. Brain Dev. 2015 Jan;37(1):76-87. doi: 10.1016/j.braindev.2014.03.011. Epub 2014 Apr 22. Brain Dev. 2015. PMID: 24767548 Clinical Trial.

7

Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series.

Matsumoto N, Takahashi S, Okayama A, Araki A, Azuma H. Matsumoto N, et al. Among authors: takahashi s. J Med Case Rep. 2014 Jun 1;8:174. doi: 10.1186/1752-1947-8-174. J Med Case Rep. 2014. PMID: 24886244 Free PMC article.

8

Human herpesvirus-6 infection-associated acute encephalopathy without skin rash.

Yamamoto S, Takahashi S, Tanaka R, Okayama A, Araki A, Katano H, Tanaka-Taya K, Azuma H. Yamamoto S, et al. Among authors: takahashi s. Brain Dev. 2015 Sep;37(8):829-32. doi: 10.1016/j.braindev.2014.12.005. Epub 2015 Jan 9. Brain Dev. 2015. PMID: 25582898

9

Electroclinical features of epileptic encephalopathy caused by SCN8A mutation.

Takahashi S, Yamamoto S, Okayama A, Araki A, Saitsu H, Matsumoto N, Azuma H. Takahashi S, et al. Pediatr Int. 2015 Aug;57(4):758-62. doi: 10.1111/ped.12622. Epub 2015 May 6. Pediatr Int. 2015. PMID: 25951352

10

Focal frontal epileptiform discharges in a patient with eyelid myoclonia and absence seizures.

Takahashi S, Yamamoto S, Tanaka R, Okayama A, Araki A, Azuma H. Takahashi S, et al. Epilepsy Behav Case Rep. 2015 Jun 25;4:35-7. doi: 10.1016/j.ebcr.2015.06.006. eCollection 2015. Epilepsy Behav Case Rep. 2015. PMID: 26155465 Free PMC article.

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