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Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.
Nat Genet. 2004 Mar;36(3):225-7. doi: 10.1038/ng1303. Epub 2004 Feb 8.
Nat Genet. 2004.
PMID: 14770181
Free article.
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. Among authors: shizuka ikeda m.
J Neurol Sci. 2000 Dec 15;182(1):76-9. doi: 10.1016/s0022-510x(00)00446-9.
J Neurol Sci. 2000.
PMID: 11102643
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Presynaptic inhibition of cerebellar GABAergic transmission by glutamate decarboxylase autoantibodies in progressive cerebellar ataxia.
Takenoshita H, Shizuka-Ikeda M, Mitoma H, Song S, Harigaya Y, Igeta Y, Yaguchi M, Ishida K, Shoji M, Tanaka M, Mizusawa H, Okamoto K.
Takenoshita H, et al. Among authors: shizuka ikeda m.
J Neurol Neurosurg Psychiatry. 2001 Mar;70(3):386-9. doi: 10.1136/jnnp.70.3.386.
J Neurol Neurosurg Psychiatry. 2001.
PMID: 11181864
Free PMC article.
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Generation of amyloid beta protein from a presenilin-1 and betaAPP complex.
Shizuka-Ikeda M, Matsubara E, Ikeda M, Kanai M, Tomidokoro Y, Ikeda Y, Watanabe M, Kawarabayashi T, Harigaya Y, Okamoto K, Maruyama K, Castaño EM, St George-Hyslop P, Shoji M.
Shizuka-Ikeda M, et al.
Biochem Biophys Res Commun. 2002 Mar 29;292(2):571-8. doi: 10.1006/bbrc.2002.6681.
Biochem Biophys Res Commun. 2002.
PMID: 11906199
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Dual impairment of GABAA- and GABAB-receptor-mediated synaptic responses by autoantibodies to glutamic acid decarboxylase.
Mitoma H, Ishida K, Shizuka-Ikeda M, Mizusawa H.
Mitoma H, et al. Among authors: shizuka ikeda m.
J Neurol Sci. 2003 Apr 15;208(1-2):51-6. doi: 10.1016/s0022-510x(02)00423-9.
J Neurol Sci. 2003.
PMID: 12639725
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Soluble Abeta homeostasis in AD and DS: impairment of anti-amyloidogenic protection by lipoproteins.
Matsubara E, Sekijima Y, Tokuda T, Urakami K, Amari M, Shizuka-Ikeda M, Tomidokoro Y, Ikeda M, Kawarabayashi T, Harigaya Y, Ikeda S, Murakami T, Abe K, Otomo E, Hirai S, Frangione B, Ghiso J, Shoji M.
Matsubara E, et al. Among authors: shizuka ikeda m.
Neurobiol Aging. 2004 Aug;25(7):833-41. doi: 10.1016/j.neurobiolaging.2003.10.004.
Neurobiol Aging. 2004.
PMID: 15212837
Clinical Trial.
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Genetic analysis of the cystatin C gene in familial and sporadic ALS patients.
Watanabe M, Jackson M, Ikeda M, Mizushima K, Amari M, Takatama M, Hirai S, Ikeda Y, Shizuka-Ikeda M, Okamoto K.
Watanabe M, et al. Among authors: shizuka ikeda m.
Brain Res. 2006 Feb 16;1073-1074:20-4. doi: 10.1016/j.brainres.2005.12.046. Epub 2006 Jan 26.
Brain Res. 2006.
PMID: 16443201
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Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype.
Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown RH Jr, Saito H, Itoyama Y.
Takahashi T, et al. Among authors: shizuka ikeda m.
Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12.
Neurology. 2003.
PMID: 12796534
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