Ohtani H - Search Results

1

Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.

Ogiwara I, Miyamoto H, Tatsukawa T, Yamagata T, Nakayama T, Atapour N, Miura E, Mazaki E, Ernst SJ, Cao D, Ohtani H, Itohara S, Yanagawa Y, Montal M, Yuzaki M, Inoue Y, Hensch TK, Noebels JL, Yamakawa K. Ogiwara I, et al. Among authors: ohtani h. Commun Biol. 2018;1:96. doi: 10.1038/s42003-018-0099-2. Epub 2018 Jul 19. Commun Biol. 2018. PMID: 30175250 Free PMC article.

2

Stiripentol open study in Japanese patients with Dravet syndrome.

Inoue Y, Ohtsuka Y, Oguni H, Tohyama J, Baba H, Fukushima K, Ohtani H, Takahashi Y, Ikeda S. Inoue Y, et al. Among authors: ohtani h. Epilepsia. 2009 Nov;50(11):2362-8. doi: 10.1111/j.1528-1167.2009.02179.x. Epub 2009 Jun 22. Epilepsia. 2009. PMID: 19552653 Free article.

3

Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome.

Nakayama T, Ogiwara I, Ito K, Kaneda M, Mazaki E, Osaka H, Ohtani H, Inoue Y, Fujiwara T, Uematsu M, Haginoya K, Tsuchiya S, Yamakawa K. Nakayama T, et al. Among authors: ohtani h. Hum Mutat. 2010 Jul;31(7):820-9. doi: 10.1002/humu.21275. Hum Mutat. 2010. PMID: 20506560

4

Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome.

Cao D, Ohtani H, Ogiwara I, Ohtani S, Takahashi Y, Yamakawa K, Inoue Y. Cao D, et al. Among authors: ohtani s, ohtani h. Epilepsia. 2012 Jul;53(7):1140-5. doi: 10.1111/j.1528-1167.2012.03497.x. Epub 2012 May 11. Epilepsia. 2012. PMID: 22578034 Free article.

5

A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.

Ogiwara I, Nakayama T, Yamagata T, Ohtani H, Mazaki E, Tsuchiya S, Inoue Y, Yamakawa K. Ogiwara I, et al. Among authors: ohtani h. Epilepsia. 2012 Dec;53(12):e200-3. doi: 10.1111/epi.12040. Epub 2012 Nov 13. Epilepsia. 2012. PMID: 23148524 Free article.

6

Cutaneous adverse drug reaction in patients with epilepsy after acute encephalitis.

Mogami Y, Takahashi Y, Takayama R, Ohtani H, Ikeda H, Imai K, Shigematu H, Inoue Y. Mogami Y, et al. Among authors: ohtani h. Brain Dev. 2012 Jun;34(6):496-503. doi: 10.1016/j.braindev.2011.09.003. Epub 2011 Oct 11. Brain Dev. 2012. PMID: 21996031

7

[Sleepiness:a frequent adverse reaction of antiepileptic drugs in patients with epilepsy after encephalitis/encephalopathy].

Mogami Y, Takahashi Y, Fukuyama T, Takayama R, Ohtani H, Ikeda H, Imai K, Shigematsu H, Inoue Y. Mogami Y, et al. Among authors: ohtani h. No To Hattatsu. 2012 Nov;44(6):472-6. No To Hattatsu. 2012. PMID: 23240529 Japanese.

8

Individualized phenytoin therapy for Japanese pediatric patients with epilepsy based on CYP2C9 and CYP2C19 genotypes.

Yamamoto Y, Takahashi Y, Imai K, Miyakawa K, Ikeda H, Ueda Y, Yamaguchi T, Nasu H, Ohtani H, Shigematsu H, Kagawa Y, Inoue Y. Yamamoto Y, et al. Among authors: ohtani h. Ther Drug Monit. 2015 Apr;37(2):229-35. doi: 10.1097/FTD.0000000000000128. Ther Drug Monit. 2015. PMID: 25162219

9

Three patients manifesting early infantile epileptic spasms associated with 2q24.3 microduplications.

Yoshitomi S, Takahashi Y, Ishizuka M, Yamaguchi T, Watanabe A, Nasu H, Ueda Y, Ohtani H, Ikeda H, Imai K, Shigematsu H, Inoue Y, Tanahashi Y, Aiba K, Ohta H, Shimada S, Yamamoto T. Yoshitomi S, et al. Among authors: ohtani h. Brain Dev. 2015 Oct;37(9):874-9. doi: 10.1016/j.braindev.2015.03.001. Epub 2015 Apr 3. Brain Dev. 2015. PMID: 25843248

10

CDKL5 deficiency causes epileptic seizures independent of cellular mosaicism.

Takahashi S, Takeguchi R, Tanaka R, Fukuoka M, Koike T, Ohtani H, Inoue K, Fukuda M, Kurahashi H, Nakamura K, Tominaga K, Matsubayashi T, Itoh M, Tanaka T. Takahashi S, et al. Among authors: ohtani h. J Neurol Sci. 2022 Dec 15;443:120498. doi: 10.1016/j.jns.2022.120498. Epub 2022 Nov 16. J Neurol Sci. 2022. PMID: 36417806

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