Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt–Jakob disease-Reference-Cited by-同舟云学术

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Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt–Jakob disease

Published:2010-08-09 Issue:11 Volume:90 Page:1637-1644
ISSN:0023-6837
Container-title:Laboratory Investigation
language:en
Short-container-title:Lab Invest

Author:

Satoh Katsuya,Tobiume Minoru,Matsui Yuki,Mutsukura Kazuo,Nishida Noriyuki,Shiga Yusei,Eguhchi Katsumi,Shirabe Susumu,Sata Testutaro

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Link

http://www.nature.com/articles/labinvest200968.pdf

Reference9 articles.

1. Brandel JP, Delasnerie-Laupretre N, Laplanche JL, et al. Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates. Neurology 2000;54:1095–1099.

2. Satoh K, Shirabe S, Tsujino A, et al. Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease. Dement Geriatr Cogn Disord 2007;24:207–212.

3. Satoh K, Shirabe S, Eguchi H, et al. Chronological changes in MRI and CSF biochemical markers in Creutzfeldt-Jakob disease patients. Dement Geriatr Cogn Disord 2007;23:372–381.

4. Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999;46:224–233.

5. Satoh K, Muramoto T, Tanaka T, et al. Association of an 11–12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases. J Gen Virol 2003;84:2885–2893.

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3. Human prion disease;Clinical and Experimental Neuroimmunology;2021-12-13

4. Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic;Diagnostics;2021-10-01

5. MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type;Journal of Neurology, Neurosurgery & Psychiatry;2020-08-24

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