Fujiwara T - Search Results

1

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

2

Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.

Sugawara T, Tsurubuchi Y, Fujiwara T, Mazaki-Miyazaki E, Nagata K, Montal M, Inoue Y, Yamakawa K. Sugawara T, et al. Among authors: fujiwara t. Epilepsy Res. 2003 May;54(2-3):201-7. doi: 10.1016/s0920-1211(03)00084-6. Epilepsy Res. 2003. PMID: 12837571

3

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.

Kamiya K, Kaneda M, Sugawara T, Mazaki E, Okamura N, Montal M, Makita N, Tanaka M, Fukushima K, Fujiwara T, Inoue Y, Yamakawa K. Kamiya K, et al. Among authors: fujiwara t. J Neurosci. 2004 Mar 17;24(11):2690-8. doi: 10.1523/JNEUROSCI.3089-03.2004. J Neurosci. 2004. PMID: 15028761 Free PMC article.

4

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: fujiwara t. 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

5

Long-term course of Dravet syndrome: a study from an epilepsy center in Japan.

Takayama R, Fujiwara T, Shigematsu H, Imai K, Takahashi Y, Yamakawa K, Inoue Y. Takayama R, et al. Among authors: fujiwara t. Epilepsia. 2014 Apr;55(4):528-38. doi: 10.1111/epi.12532. Epub 2014 Feb 6. Epilepsia. 2014. PMID: 24502503 Free article.

6

In response to terminology and prognosis of Dravet syndrome.

Takayama R, Fujiwara T, Shigematsu H, Imai K, Takahashi Y, Yamakawa K, Inoue Y. Takayama R, et al. Among authors: fujiwara t. Epilepsia. 2014 Jun;55(6):943. doi: 10.1111/epi.12640. Epilepsia. 2014. PMID: 24924645 Free article. No abstract available.

7

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.

Fujiwara T, Sugawara T, Mazaki-Miyazaki E, Takahashi Y, Fukushima K, Watanabe M, Hara K, Morikawa T, Yagi K, Yamakawa K, Inoue Y. Fujiwara T, et al. Brain. 2003 Mar;126(Pt 3):531-46. doi: 10.1093/brain/awg053. Brain. 2003. PMID: 12566275

8

[Effectiveness of topiramate in eleven patients with Dravet syndrome].

Takahashi H, Takahashi Y, Mine J, Mukaida S, Ikegami M, Ikeda H, Ohtani H, Shimomura J, Kubota Y, Fujiwara T. Takahashi H, et al. Among authors: fujiwara t. No To Hattatsu. 2010 Jul;42(4):273-6. No To Hattatsu. 2010. PMID: 20666132 Japanese.

9

Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome.

Sakauchi M, Oguni H, Kato I, Osawa M, Hirose S, Kaneko S, Takahashi Y, Takayama R, Fujiwara T. Sakauchi M, et al. Among authors: fujiwara t. Epilepsia. 2011 Jun;52(6):1144-9. doi: 10.1111/j.1528-1167.2011.03053.x. Epub 2011 Apr 11. Epilepsia. 2011. PMID: 21480880 Free article.

10

Temporal changes in brain MRI findings in Rasmussen syndrome.

Yamazaki E, Takahashi Y, Akasaka N, Fujiwara T, Inoue Y. Yamazaki E, et al. Among authors: fujiwara t. Epileptic Disord. 2011 Sep;13(3):229-39. doi: 10.1684/epd.2011.0464. Epileptic Disord. 2011. PMID: 21926050 Free article.

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