Mitsudome A - Search Results

1

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: mitsudome a. J Immunol. 2003 Feb 15;170(4):2205-13. doi: 10.4049/jimmunol.170.4.2205. J Immunol. 2003. PMID: 12574394

2

X-linked mental retardation and epilepsy: pathogenetic significance of ARX mutations.

Hirose S, Mitsudome A. Hirose S, et al. Among authors: mitsudome a. Brain Dev. 2003 Apr;25(3):161-5. doi: 10.1016/s0387-7604(02)00169-9. Brain Dev. 2003. PMID: 12689693 Review.

3

Molecular genetics of human familial epilepsy syndromes.

Hirose S, Okada M, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: mitsudome a. Epilepsia. 2002;43 Suppl 9:21-5. doi: 10.1046/j.1528-1157.43.s.9.6.x. Epilepsia. 2002. PMID: 12383275 Free article.

4

A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G-->A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency.

Kanai N, Yanai F, Hirose S, Nibu K, Izuhara K, Tani T, Kubota T, Mitsudome A. Kanai N, et al. Among authors: mitsudome a. Hum Genet. 1999 Jan;104(1):36-42. doi: 10.1007/s004390050907. Hum Genet. 1999. PMID: 10071190

5

Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis.

Hirose S, Okada M, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: mitsudome a. Epilepsy Res. 2000 Oct;41(3):191-204. doi: 10.1016/s0920-1211(00)00141-8. Epilepsy Res. 2000. PMID: 10962210 Review.

6

The genetics of febrile seizures and related epilepsy syndromes.

Hirose S, Mohney RP, Okada M, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: mitsudome a. Brain Dev. 2003 Aug;25(5):304-12. doi: 10.1016/s0387-7604(03)00026-3. Brain Dev. 2003. PMID: 12850508 Review.

7

Genetics of idiopathic epilepsies.

Hirose S, Mitsudome A, Okada M, Kaneko S; Epilepsy Genetic Study Group, Japan. Hirose S, et al. Among authors: mitsudome a. Epilepsia. 2005;46 Suppl 1:38-43. doi: 10.1111/j.0013-9580.2005.461011.x. Epilepsia. 2005. PMID: 15816978 Free article. Review.

8

An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.

Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A. Kanaumi T, et al. Among authors: mitsudome a. Pediatr Neurol. 2006 Mar;34(3):235-8. doi: 10.1016/j.pediatrneurol.2005.08.024. Pediatr Neurol. 2006. PMID: 16504796

9

Developmental changes in the expression of GABAA receptor alpha 1 and gamma 2 subunits in human temporal lobe, hippocampus and basal ganglia: an implication for consideration on age-related epilepsy.

Kanaumi T, Takashima S, Iwasaki H, Mitsudome A, Hirose S. Kanaumi T, et al. Among authors: mitsudome a. Epilepsy Res. 2006 Sep;71(1):47-53. doi: 10.1016/j.eplepsyres.2006.05.019. Epub 2006 Jul 10. Epilepsy Res. 2006. PMID: 16829043

10

[Sympathetic skin response in patients with severe motor and intellectual disabilities].

Ogawa A, Hamamoto K, Hirose S, Fujikawa M, Mitsudome A. Ogawa A, et al. Among authors: mitsudome a. No To Hattatsu. 2007 Sep;39(5):347-50. No To Hattatsu. 2007. PMID: 17879607 Japanese.

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