Shibata T - Search Results

1

A Japanese case of β-ureidopropionase deficiency with dysmorphic features.

Akiyama T, Shibata T, Yoshinaga H, Kuhara T, Nakajima Y, Kato T, Maeda Y, Ohse M, Oka M, Kageyama M, Kobayashi K. Akiyama T, et al. Among authors: shibata t. Brain Dev. 2017 Jan;39(1):58-61. doi: 10.1016/j.braindev.2016.08.001. Epub 2016 Aug 21. Brain Dev. 2017. PMID: 27553092

2

Efficacy of topiramate for intractable childhood generalized epilepsy with epileptic spasms: with special reference to electroencephalographic changes.

Endoh F, Kobayashi K, Hayashi Y, Shibata T, Yoshinaga H, Ohtsuka Y. Endoh F, et al. Among authors: shibata t. Seizure. 2012 Sep;21(7):522-8. doi: 10.1016/j.seizure.2012.05.009. Epub 2012 Jun 13. Seizure. 2012. PMID: 22698380 Free article.

3

[Peculiar involuntary movements in premature babies with specific cerebellar injuries].

Yoshinaga H, Kobayashi K, Endoh F, Ishizaki Y, Shibata T, Ohtsuka Y. Yoshinaga H, et al. Among authors: shibata t. No To Hattatsu. 2012 May;44(3):239-43. No To Hattatsu. 2012. PMID: 22712228 Japanese.

4

Clinical implications of preceding positive spikes in patients with benign partial epilepsy and febrile seizures.

Yoshinaga H, Kobayashi K, Akiyama T, Shibata T, Endoh F, Ohtsuka Y. Yoshinaga H, et al. Among authors: shibata t. Brain Dev. 2013 Apr;35(4):299-306. doi: 10.1016/j.braindev.2012.06.006. Epub 2012 Jul 15. Brain Dev. 2013. PMID: 22800933

5

Manifestation of both emetic seizures and sylvian seizures in the same patients with benign partial epilepsy.

Yoshinaga H, Kobayashi K, Shibata T, Inoue T, Oka M, Akiyama T. Yoshinaga H, et al. Among authors: shibata t. Brain Dev. 2015 Jan;37(1):13-7. doi: 10.1016/j.braindev.2014.01.013. Epub 2014 Feb 26. Brain Dev. 2015. PMID: 24582114

6

[West syndrome associated with epileptic negative myoclonus].

Shibata T, Yoshinaga H, Oka M, Kobayashi K. Shibata T, et al. No To Hattatsu. 2014 Sep;46(5):354-8. No To Hattatsu. 2014. PMID: 25403066 Japanese.

7

Phenotypic variability in childhood of skeletal muscle sodium channelopathies.

Yoshinaga H, Sakoda S, Shibata T, Akiyama T, Oka M, Yuan JH, Takashima H, Takahashi MP, Kitamura T, Murakami N, Kobayashi K. Yoshinaga H, et al. Among authors: shibata t. Pediatr Neurol. 2015 May;52(5):504-8. doi: 10.1016/j.pediatrneurol.2015.01.014. Epub 2015 Jan 29. Pediatr Neurol. 2015. PMID: 25724373

8

SSADH deficiency possibly associated with enzyme activity-reducing SNPs.

Akiyama T, Osaka H, Shimbo H, Kuhara T, Shibata T, Kobayashi K, Kurosawa K, Yoshinaga H. Akiyama T, et al. Among authors: shibata t. Brain Dev. 2016 Oct;38(9):871-4. doi: 10.1016/j.braindev.2016.03.008. Epub 2016 Apr 4. Brain Dev. 2016. PMID: 27056292

9

Novel PLA2G6 mutations associated with an exonic deletion due to non-allelic homologous recombination in a patient with infantile neuroaxonal dystrophy.

Yamamoto T, Shimojima K, Shibata T, Akiyama M, Oka M, Akiyama T, Yoshinaga H, Kobayashi K. Yamamoto T, et al. Among authors: shibata t. Hum Genome Var. 2015 Nov 19;2:15048. doi: 10.1038/hgv.2015.48. eCollection 2015. Hum Genome Var. 2015. PMID: 27081553 Free PMC article.

10

Idiopathic focal epilepsies: the "lost tribe".

Pal DK, Ferrie C, Addis L, Akiyama T, Capovilla G, Caraballo R, de Saint-Martin A, Fejerman N, Guerrini R, Hamandi K, Helbig I, Ioannides AA, Kobayashi K, Lal D, Lesca G, Muhle H, Neubauer BA, Pisano T, Rudolf G, Seegmuller C, Shibata T, Smith A, Striano P, Strug LJ, Szepetowski P, Valeta T, Yoshinaga H, Koutroumanidis M. Pal DK, et al. Among authors: shibata t. Epileptic Disord. 2016 Sep 1;18(3):252-88. doi: 10.1684/epd.2016.0839. Epileptic Disord. 2016. PMID: 27435520 Review. English.

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