Satoh K - Search Results

1

Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients.

Takatsuki H, Fuse T, Nakagaki T, Mori T, Mihara B, Takao M, Iwasaki Y, Yoshida M, Murayama S, Atarashi R, Nishida N, Satoh K. Takatsuki H, et al. Among authors: satoh k. EBioMedicine. 2016 Oct;12:150-155. doi: 10.1016/j.ebiom.2016.08.033. Epub 2016 Aug 24. EBioMedicine. 2016. PMID: 27612591 Free PMC article.

2

[Iatrogenic Creutzfeldt-Jakob disease].

Satoh K, Shirabe S, Katamine S, Muramoto T, Kitamoto T. Satoh K, et al. Nihon Rinsho. 2004 Jan;62 Suppl:248-51. Nihon Rinsho. 2004. PMID: 15011359 Review. Japanese. No abstract available.

3

Toxicity of quinacrine can be reduced by co-administration of P-glycoprotein inhibitor in sporadic Creutzfeldt-Jakob disease.

Satoh K, Shirabe S, Eguchi K, Yamauchi A, Kataoka Y, Niwa M, Nishida N, Katamine S. Satoh K, et al. Cell Mol Neurobiol. 2004 Dec;24(6):873-5. doi: 10.1007/s10571-004-6926-7. Cell Mol Neurobiol. 2004. PMID: 15672687

4

[A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180].

Tanaka T, Kinoshita I, Saitoh Y, Satoh K, Nishiura Y, Shirabe S, Kitamoto T. Tanaka T, et al. Among authors: satoh k. No To Shinkei. 2004 Dec;56(12):1025-8. No To Shinkei. 2004. PMID: 15729879 Review. Japanese.

5

14-3-3 protein, total tau and phosphorylated tau in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease and neurodegenerative disease in Japan.

Satoh K, Shirabe S, Eguchi H, Tsujino A, Eguchi K, Satoh A, Tsujihata M, Niwa M, Katamine S, Kurihara S, Matsuo H. Satoh K, et al. Among authors: satoh a. Cell Mol Neurobiol. 2006 Feb;26(1):45-52. doi: 10.1007/s10571-006-9370-z. Cell Mol Neurobiol. 2006. PMID: 16633900

6

Chronological changes in MRI and CSF biochemical markers in Creutzfeldt-Jakob disease patients.

Satoh K, Shirabe S, Eguchi H, Tsujino A, Motomura M, Satoh A, Tsujihata M, Eguchi K. Satoh K, et al. Among authors: satoh a. Dement Geriatr Cogn Disord. 2007;23(6):372-81. doi: 10.1159/000101339. Epub 2007 Mar 26. Dement Geriatr Cogn Disord. 2007. PMID: 17389797

7

Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease.

Satoh K, Shirabe S, Tsujino A, Eguchi H, Motomura M, Honda H, Tomita I, Satoh A, Tsujihata M, Matsuo H, Nakagawa M, Eguchi K. Satoh K, et al. Among authors: satoh a. Dement Geriatr Cogn Disord. 2007;24(3):207-12. doi: 10.1159/000107082. Epub 2007 Aug 10. Dement Geriatr Cogn Disord. 2007. PMID: 17690553

8

[Clinical typing and diagnosis of sporadic human prion diseases (classic sproadic CJD, MM2-cortical form CJD, MM2-thalamic form CJD)].

Satoh K, Shirabe S, Eguchi K. Satoh K, et al. Nihon Rinsho. 2007 Aug;65(8):1423-32. Nihon Rinsho. 2007. PMID: 17695279 Review. Japanese.

9

Bone marrow stroma cells are susceptible to prion infection.

Takakura Y, Yamaguchi N, Nakagaki T, Satoh K, Kira J, Nishida N. Takakura Y, et al. Among authors: satoh k. Biochem Biophys Res Commun. 2008 Dec 19;377(3):957-61. doi: 10.1016/j.bbrc.2008.10.099. Epub 2008 Oct 29. Biochem Biophys Res Commun. 2008. PMID: 18976632 Free article.

10

Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images.

Mutsukura K, Satoh K, Shirabe S, Tomita I, Fukutome T, Morikawa M, Iseki M, Sasaki K, Shiaga Y, Kitamoto T, Eguchi K. Mutsukura K, et al. Among authors: satoh k. Dement Geriatr Cogn Disord. 2009;28(6):550-7. doi: 10.1159/000254842. Epub 2009 Dec 30. Dement Geriatr Cogn Disord. 2009. PMID: 20051687 Free PMC article.

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