Takahashi Y - Search Results

1

Genetic variations of immunoregulatory genes associated with Rasmussen syndrome.

Takahashi Y, Mogami Y, Mine J, Imai K, Koide Y, Matsuda K, Akasaka N, Konishi T, Imamura A, Inoue Y. Takahashi Y, et al. Epilepsy Res. 2013 Dec;107(3):238-43. doi: 10.1016/j.eplepsyres.2013.09.004. Epub 2013 Oct 5. Epilepsy Res. 2013. PMID: 24269013

2

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. Among authors: takahashi y. Brain. 2003 Mar;126(Pt 3):531-46. doi: 10.1093/brain/awg053. Brain. 2003. PMID: 12566275

3

Serial MR imaging and 1H-MR spectroscopy of unidentified bright objects in a case of neurofibromatosis type 1.

Imamura A, Matsuo N, Okuda M, Morita H, Iwata M, Yamazaki Y, Takahashi Y. Imamura A, et al. Among authors: takahashi y. Brain Dev. 2005 Dec;27(8):595-7. doi: 10.1016/j.braindev.2005.02.008. Brain Dev. 2005. PMID: 15878248

4

Autoantibodies and cell-mediated autoimmunity to NMDA-type GluRepsilon2 in patients with Rasmussen's encephalitis and chronic progressive epilepsia partialis continua.

Takahashi Y, Mori H, Mishina M, Watanabe M, Kondo N, Shimomura J, Kubota Y, Matsuda K, Fukushima K, Shiroma N, Akasaka N, Nishida H, Imamura A, Watanabe H, Sugiyama N, Ikezawa M, Fujiwara T. Takahashi Y, et al. Epilepsia. 2005;46 Suppl 5:152-8. doi: 10.1111/j.1528-1167.2005.01024.x. Epilepsia. 2005. PMID: 15987271 Free article.

5

Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population.

Singh S, Suzuki T, Uchiyama A, Kumada S, Moriyama N, Hirose S, Takahashi Y, Sugie H, Mizoguchi K, Inoue Y, Kimura K, Sawaishi Y, Yamakawa K, Ganesh S. Singh S, et al. Among authors: takahashi y. J Hum Genet. 2005;50(7):347-352. doi: 10.1007/s10038-005-0263-7. Epub 2005 Jul 15. J Hum Genet. 2005. PMID: 16021330

6

MR imaging and 1H-MR spectroscopy of a case of van der Knaap disease.

Morita H, Imamura A, Matsuo N, Tatebayashi K, Omoya K, Takahashi Y, Tsujino S. Morita H, et al. Among authors: takahashi y. Brain Dev. 2006 Aug;28(7):466-9. doi: 10.1016/j.braindev.2005.12.006. Epub 2006 Feb 28. Brain Dev. 2006. PMID: 16504440

7

Vaccination and infection as causative factors in Japanese patients with Rasmussen syndrome: molecular mimicry and HLA class I.

Takahashi Y, Matsuda K, Kubota Y, Shimomura J, Yamasaki E, Kudo T, Fukushima K, Osaka H, Akasaka N, Imamura A, Yamada S, Kondo N, Fujiwara T. Takahashi Y, et al. Clin Dev Immunol. 2006 Jun-Dec;13(2-4):381-7. doi: 10.1080/17402520600589522. Clin Dev Immunol. 2006. PMID: 17162382 Free PMC article.

8

[Rasmussen encephalitis and non-herpetic acute limbic encephalitis].

Takahashi Y, Kubota Y, Yamasaki E, Matsuda K. Takahashi Y, et al. Rinsho Shinkeigaku. 2008 Mar;48(3):163-72. doi: 10.5692/clinicalneurol.48.163. Rinsho Shinkeigaku. 2008. PMID: 18409535 Review. Japanese.

9

Electroclinical features of epilepsy in patients with juvenile type dentatorubral-pallidoluysian atrophy.

Egawa K, Takahashi Y, Kubota Y, Kubota H, Inoue Y, Fujiwara T, Onodera O. Egawa K, et al. Among authors: takahashi y. Epilepsia. 2008 Dec;49(12):2041-9. doi: 10.1111/j.1528-1167.2008.01701.x. Epub 2008 Jun 26. Epilepsia. 2008. PMID: 18616556 Free article. Clinical Trial.

10

[Acute limbic encephalitis and NMDA type-glutamate receptor].

Takahashi Y, Yamazaki E, Nishimura S, Tsunogae H, Niwa K, Dalmau J, Imai K, Fujiwara T. Takahashi Y, et al. Rinsho Shinkeigaku. 2008 Nov;48(11):926-9. doi: 10.5692/clinicalneurol.48.926. Rinsho Shinkeigaku. 2008. PMID: 19198120 Japanese.

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