Kaneko S - Search Results

1

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: kaneko s. Epilepsy Res. 2000 Oct;41(3):191-204. doi: 10.1016/s0920-1211(00)00141-8. Epilepsy Res. 2000. PMID: 10962210 Review.

2

Molecular genetics of human familial epilepsy syndromes.

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

3

Age-dependent modulation of hippocampal excitability by KCNQ-channels.

Okada M, Zhu G, Hirose S, Ito KI, Murakami T, Wakui M, Kaneko S. Okada M, et al. Among authors: kaneko s. Epilepsy Res. 2003 Feb;53(1-2):81-94. doi: 10.1016/s0920-1211(02)00249-8. Epilepsy Res. 2003. PMID: 12576170

4

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: kaneko s. Brain Dev. 2003 Aug;25(5):304-12. doi: 10.1016/s0387-7604(03)00026-3. Brain Dev. 2003. PMID: 12850508 Review.

5

Genetics of idiopathic epilepsies.

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

6

Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC).

Sugiura Y, Nakatsu F, Hiroyasu K, Ishii A, Hirose S, Okada M, Jibiki I, Ohno H, Kaneko S, Ugawa Y. Sugiura Y, et al. Among authors: kaneko s. Epilepsy Res. 2009 Mar;84(1):82-5. doi: 10.1016/j.eplepsyres.2008.12.003. Epub 2009 Jan 23. Epilepsy Res. 2009. PMID: 19167866

7

KCNQ2 abnormality in BECTS: benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2.

Ishii A, Miyajima T, Kurahashi H, Wang JW, Yasumoto S, Kaneko S, Hirose S. Ishii A, et al. Among authors: kaneko s. Epilepsy Res. 2012 Nov;102(1-2):122-5. doi: 10.1016/j.eplepsyres.2012.07.011. Epub 2012 Aug 10. Epilepsy Res. 2012. PMID: 22884718

8

A novel prophylactic effect of furosemide treatment on autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE).

Yamada J, Zhu G, Okada M, Hirose S, Yoshida S, Shiba Y, Migita K, Mori F, Sugawara T, Chen L, Liu F, Yoshida S, Ueno S, Kaneko S. Yamada J, et al. Among authors: kaneko s. Epilepsy Res. 2013 Nov;107(1-2):127-37. doi: 10.1016/j.eplepsyres.2013.08.018. Epub 2013 Sep 3. Epilepsy Res. 2013. PMID: 24045013

9

Association of nonsense mutation in GABRG2 with abnormal trafficking of GABAA receptors in severe epilepsy.

Ishii A, Kanaumi T, Sohda M, Misumi Y, Zhang B, Kakinuma N, Haga Y, Watanabe K, Takeda S, Okada M, Ueno S, Kaneko S, Takashima S, Hirose S. Ishii A, et al. Among authors: kaneko s. Epilepsy Res. 2014 Mar;108(3):420-32. doi: 10.1016/j.eplepsyres.2013.12.005. Epub 2014 Jan 3. Epilepsy Res. 2014. PMID: 24480790

10

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: kaneko s. Epilepsy Res. 2002 Feb;48(3):181-6. doi: 10.1016/s0920-1211(01)00336-9. Epilepsy Res. 2002. PMID: 11904236

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