Satoh K - Search Results

1

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.

Hermann P, Appleby B, Brandel JP, Caughey B, Collins S, Geschwind MD, Green A, Haïk S, Kovacs GG, Ladogana A, Llorens F, Mead S, Nishida N, Pal S, Parchi P, Pocchiari M, Satoh K, Zanusso G, Zerr I. Hermann P, et al. Among authors: satoh k. Lancet Neurol. 2021 Mar;20(3):235-246. doi: 10.1016/S1474-4422(20)30477-4. Lancet Neurol. 2021. PMID: 33609480 Free PMC article. Review.

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

Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution.

Shiga Y, Satoh K, Kitamoto T, Kanno S, Nakashima I, Sato S, Fujihara K, Takata H, Nobukuni K, Kuroda S, Takano H, Umeda Y, Konno H, Nagasato K, Satoh A, Matsuda Y, Hidaka M, Takahashi H, Sano Y, Kim K, Konishi T, Doh-ura K, Sato T, Sasaki K, Nakamura Y, Yamada M, Mizusawa H, Itoyama Y. Shiga Y, et al. Among authors: satoh k, satoh a. J Neurol. 2007 Nov;254(11):1509-17. doi: 10.1007/s00415-007-0540-9. Epub 2007 Nov 2. J Neurol. 2007. PMID: 17965961

10

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.

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