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Increased levels of soluble LR11 in cerebrospinal fluid of patients with Alzheimer disease.
Ikeuchi T, Hirayama S, Miida T, Fukamachi I, Tokutake T, Ebinuma H, Takubo K, Kaneko H, Kasuga K, Kakita A, Takahashi H, Bujo H, Saito Y, Nishizawa M. Ikeuchi T, et al. Among authors: tokutake t. Dement Geriatr Cogn Disord. 2010;30(1):28-32. doi: 10.1159/000315539. Epub 2010 Jul 30. Dement Geriatr Cogn Disord. 2010. PMID: 20689279
Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients.
Watanabe Y, Hirao Y, Kasuga K, Tokutake T, Semizu Y, Kitamura K, Ikeuchi T, Nakamura K, Yamamoto T. Watanabe Y, et al. Among authors: tokutake t. Dement Geriatr Cogn Dis Extra. 2019 Feb 8;9(1):53-65. doi: 10.1159/000496100. eCollection 2019 Jan-Apr. Dement Geriatr Cogn Dis Extra. 2019. PMID: 31043964 Free PMC article.
Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.
Miura T, Mezaki N, Konno T, Iwasaki A, Hara N, Miura M, Funayama M, Unai Y, Tashiro Y, Okita K, Kihara T, Ito N, Kanatsuka Y, Jones DT, Hara N, Ishiguro T, Tokutake T, Kasuga K, Nozaki H, Dickson DW, Onodera O, Wszolek ZK, Ikeuchi T. Miura T, et al. Among authors: tokutake t. J Neurol. 2018 Oct;265(10):2415-2424. doi: 10.1007/s00415-018-9017-2. Epub 2018 Aug 22. J Neurol. 2018. PMID: 30136118 Free PMC article.
Evidence for a Common Founder and Clinical Characteristics of Japanese Families with the MAPT R406W Mutation.
Ikeuchi T, Imamura T, Kawase Y, Kitade Y, Tsuchiya M, Tokutake T, Kasuga K, Yajima R, Tsukie T, Miyashita A, Sugishita M, Kuwano R, Nishizawa M. Ikeuchi T, et al. Among authors: tokutake t. Dement Geriatr Cogn Dis Extra. 2011 Jan;1(1):267-75. doi: 10.1159/000331243. Epub 2011 Sep 20. Dement Geriatr Cogn Dis Extra. 2011. PMID: 22545037 Free PMC article.
43 results