Ikeda Y - Search Results

1

Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.

Abe K, Ikeda Y, Kurata T, Ohta Y, Manabe Y, Okamoto M, Takamatsu K, Ohta T, Takao Y, Shiro Y, Shoji M, Kamiya T, Kobayashi H, Koizumi A. Abe K, et al. Among authors: ikeda y. Eur J Neurol. 2012 Aug;19(8):1070-8. doi: 10.1111/j.1468-1331.2012.03669.x. Epub 2012 Feb 21. Eur J Neurol. 2012. PMID: 22353375

2

Characteristic RNA foci of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan).

Liu W, Ikeda Y, Hishikawa N, Yamashita T, Deguchi K, Abe K. Liu W, et al. Among authors: ikeda y. Eur J Neurol. 2014 Nov;21(11):1377-86. doi: 10.1111/ene.12491. Epub 2014 Jul 2. Eur J Neurol. 2014. PMID: 24985895

3

Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan.

Ikeda Y, Shizuka M, Watanabe M, Okamoto K, Shoji M. Ikeda Y, et al. Neurology. 2000 Feb 22;54(4):950-5. doi: 10.1212/wnl.54.4.950. Neurology. 2000. PMID: 10690991

4

Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI.

Ikeda Y, Shizuka-Ikeda M, Watanabe M, Schmitt M, Okamoto K, Shoji M. Ikeda Y, et al. J Neurol Sci. 2000 Dec 15;182(1):76-9. doi: 10.1016/s0022-510x(00)00446-9. J Neurol Sci. 2000. PMID: 11102643

5

A novel familial prion disease causing pan-autonomic-sensory neuropathy and cognitive impairment.

Matsuzono K, Ikeda Y, Liu W, Kurata T, Deguchi S, Deguchi K, Abe K. Matsuzono K, et al. Among authors: ikeda y. Eur J Neurol. 2013 May;20(5):e67-9. doi: 10.1111/ene.12089. Eur J Neurol. 2013. PMID: 23577609 Free article. No abstract available.

6

A new simple score (ABS) for assessing behavioral and psychological symptoms of dementia.

Abe K, Yamashita T, Hishikawa N, Ohta Y, Deguchi K, Sato K, Matsuzono K, Nakano Y, Ikeda Y, Wakutani Y, Takao Y. Abe K, et al. Among authors: ikeda y. J Neurol Sci. 2015 Mar 15;350(1-2):14-7. doi: 10.1016/j.jns.2015.01.029. Epub 2015 Jan 29. J Neurol Sci. 2015. PMID: 25662676 Free article.

7

A novel missense point mutation (S134N) of the Cu/Zn superoxide dismutase gene in a patient with familial motor neuron disease.

Watanabe M, Aoki M, Abe K, Shoji M, Iizuka T, Ikeda Y, Hirai S, Kurokawa K, Kato T, Sasaki H, Itoyama Y. Watanabe M, et al. Among authors: ikeda y. Hum Mutat. 1997;9(1):69-71. doi: 10.1002/(SICI)1098-1004(1997)9:1<69::AID-HUMU14>3.0.CO;2-N. Hum Mutat. 1997. PMID: 8990014 No abstract available.

8

Progressive neurovascular disturbances in the cerebral cortex of Alzheimer's disease-model mice: protection by atorvastatin and pitavastatin.

Kurata T, Miyazaki K, Kozuki M, Morimoto N, Ohta Y, Ikeda Y, Abe K. Kurata T, et al. Among authors: ikeda y. Neuroscience. 2011 Dec 1;197:358-68. doi: 10.1016/j.neuroscience.2011.09.030. Epub 2011 Sep 19. Neuroscience. 2011. PMID: 21955601

9

[Mutation analysis of the CACNL1A3 gene in Japanese hypokalemic periodic paralysis families].

Ikeda Y, Watanabe M, Shoji M. Ikeda Y, et al. Nihon Rinsho. 1997 Dec;55(12):3247-52. Nihon Rinsho. 1997. PMID: 9436445 Review. Japanese.

10

Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controls.

Shizuka M, Watanabe M, Ikeda Y, Mizushima K, Okamoto K, Shoji M. Shizuka M, et al. Among authors: ikeda y. J Neurol Sci. 1998 Nov 26;161(1):85-7. doi: 10.1016/s0022-510x(98)00270-6. J Neurol Sci. 1998. PMID: 9879686

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