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Genetic abnormalities underlying familial epilepsy syndromes.
Hirose S, Okada M, Yamakawa K, Sugawara T, Fukuma G, Ito M, Kaneko S, Mitsudome A. Hirose S, et al. Brain Dev. 2002 Jun;24(4):211-22. doi: 10.1016/s0387-7604(02)00056-6. Brain Dev. 2002. PMID: 12015163 Review.
Mutation (Ser284Leu) of neuronal nicotinic acetylcholine receptor alpha 4 subunit associated with frontal lobe epilepsy causes faster desensitization of the rat receptor expressed in oocytes.
Matsushima N, Hirose S, Iwata H, Fukuma G, Yonetani M, Nagayama C, Hamanaka W, Matsunaka Y, Ito M, Kaneko S, Mitsudome A, Sugiyama H. Matsushima N, et al. Among authors: hirose s. Epilepsy Res. 2002 Feb;48(3):181-6. doi: 10.1016/s0920-1211(01)00336-9. Epilepsy Res. 2002. PMID: 11904236
Genetics of epilepsy: current status and perspectives.
Kaneko S, Okada M, Iwasa H, Yamakawa K, Hirose S. Kaneko S, et al. Among authors: hirose s. Neurosci Res. 2002 Sep;44(1):11-30. doi: 10.1016/s0168-0102(02)00065-2. Neurosci Res. 2002. PMID: 12204289 Review.
[Autosomal dominant nocturnal frontal lobe epilepsy(ADNFLE)].
Kaneko S, Iwasa H, Okada M, Hirose S. Kaneko S, et al. Among authors: hirose s. Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):315-7. Ryoikibetsu Shokogun Shirizu. 2002. PMID: 12483890 Review. Japanese. No abstract available.
Essential roles of perforin in antigen-specific cytotoxicity mediated by human CD4+ T lymphocytes: analysis using the combination of hereditary perforin-deficient effector cells and Fas-deficient target cells.
Yanai F, Ishii E, Kojima K, Hasegawa A, Azuma T, Hirose S, Suga N, Mitsudome A, Zaitsu M, Ishida Y, Shirakata Y, Sayama K, Hashimoto K, Yasukawa M. Yanai F, et al. Among authors: hirose s. J Immunol. 2003 Feb 15;170(4):2205-13. doi: 10.4049/jimmunol.170.4.2205. J Immunol. 2003. PMID: 12574394
2,091 results