Ogiwara I - Search Results

1

CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice.

Yamagata T, Raveau M, Kobayashi K, Miyamoto H, Tatsukawa T, Ogiwara I, Itohara S, Hensch TK, Yamakawa K. Yamagata T, et al. Among authors: ogiwara i. Neurobiol Dis. 2020 Jul;141:104954. doi: 10.1016/j.nbd.2020.104954. Epub 2020 May 21. Neurobiol Dis. 2020. PMID: 32445790 Free article.

2

Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.

Rhodes TH, Vanoye CG, Ohmori I, Ogiwara I, Yamakawa K, George AL Jr. Rhodes TH, et al. Among authors: ogiwara i. J Physiol. 2005 Dec 1;569(Pt 2):433-45. doi: 10.1113/jphysiol.2005.094326. Epub 2005 Oct 6. J Physiol. 2005. PMID: 16210358 Free PMC article.

3

A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy.

Singh B, Ogiwara I, Kaneda M, Tokonami N, Mazaki E, Baba K, Matsuda K, Inoue Y, Yamakawa K. Singh B, et al. Among authors: ogiwara i. Neurobiol Dis. 2006 Nov;24(2):245-53. doi: 10.1016/j.nbd.2006.07.001. Epub 2006 Aug 24. Neurobiol Dis. 2006. PMID: 16934482

4

SCN1A mutation mosaicism in a family with severe myoclonic epilepsy in infancy.

Morimoto M, Mazaki E, Nishimura A, Chiyonobu T, Sawai Y, Murakami A, Nakamura K, Inoue I, Ogiwara I, Sugimoto T, Yamakawa K. Morimoto M, et al. Among authors: ogiwara i. Epilepsia. 2006 Oct;47(10):1732-6. doi: 10.1111/j.1528-1167.2006.00645.x. Epilepsia. 2006. PMID: 17054696 Free article.

5

Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.

Osaka H, Ogiwara I, Mazaki E, Okamura N, Yamashita S, Iai M, Yamada M, Kurosawa K, Iwamoto H, Yasui-Furukori N, Kaneko S, Fujiwara T, Inoue Y, Yamakawa K. Osaka H, et al. Among authors: ogiwara i. Epilepsy Res. 2007 Jun;75(1):46-51. doi: 10.1016/j.eplepsyres.2007.03.018. Epub 2007 May 15. Epilepsy Res. 2007. PMID: 17507202

6

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.

Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, Takeuchi T, Itohara S, Yanagawa Y, Obata K, Furuichi T, Hensch TK, Yamakawa K. Ogiwara I, et al. J Neurosci. 2007 May 30;27(22):5903-14. doi: 10.1523/JNEUROSCI.5270-06.2007. J Neurosci. 2007. PMID: 17537961 Free PMC article.

7

De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies.

Ogiwara I, Ito K, Sawaishi Y, Osaka H, Mazaki E, Inoue I, Montal M, Hashikawa T, Shike T, Fujiwara T, Inoue Y, Kaneda M, Yamakawa K. Ogiwara I, et al. Neurology. 2009 Sep 29;73(13):1046-53. doi: 10.1212/WNL.0b013e3181b9cebc. Neurology. 2009. PMID: 19786696 Free PMC article.

8

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: ogiwara i. Hum Mutat. 2010 Jul;31(7):820-9. doi: 10.1002/humu.21275. Hum Mutat. 2010. PMID: 20506560

9

Acute encephalopathy in a patient with Dravet syndrome.

Tsuji M, Mazaki E, Ogiwara I, Wada T, Iai M, Okumura A, Yamashita S, Yamakawa K, Osaka H. Tsuji M, et al. Among authors: ogiwara i. Neuropediatrics. 2011 Feb;42(2):78-81. doi: 10.1055/s-0031-1279725. Epub 2011 Jun 6. Neuropediatrics. 2011. PMID: 21647847

10

Different degrees of loss of function between GEFS+ and SMEI Nav 1.1 missense mutants at the same residue induced by rescuable folding defects.

Sugiura Y, Ogiwara I, Hoshi A, Yamakawa K, Ugawa Y. Sugiura Y, et al. Among authors: ogiwara i. Epilepsia. 2012 Jun;53(6):e111-4. doi: 10.1111/j.1528-1167.2012.03467.x. Epub 2012 Apr 23. Epilepsia. 2012. PMID: 22525008 Free article.

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