Art

J-GLOBAL ID：201702235234600470   Reference number：17A1616184

プリオン病の新規増幅検出法の開発と診断への応用

Author (1)： SHIN RYUICHIRO (宮崎大 医 感染症学 微生物学分野)
Material： 宮崎県医師会医学会誌  (Journal of the Miyazaki Medical Association)
Volume： 41  Issue： 2  Page： 65-70  Publication year： Sep. 29, 2017 
JST Material Number： Y0767A  ISSN： 0389-8288  Document type： Article
Article type： 文献レビュー  Country of issue： Japan (JPN)  Language： JAPANESE (JA)

Thesaurus term： *prion disease ,...
Semi thesaurus term： *Prion Diseases ,...

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JST classification (1)： Diagnostics of infectious diseases,parasitic diseases.  (GD01020S)

Reference (24)：

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• Ohkubo T, Sakasegawa Y, Asada T, et al. Absence of association between codon 129/219 polymorphisms of the prion protein. Ann Neurol 2003 ; 54 (4) : 553-4.
• 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 : 224-33.
• Hsich G, Kenney K, Gibbs CJ, et al. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 1996 ; 335 : 924-30.
• Brandel JP, Delasnerie-Laupretre N, Laplanche JL, et al. Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates. Neurology 2000 ; 54 : 1095-9.

Terms in the title (6)： プリオン病 ,  増幅 ,  検出法 ,  開発 ,  診断 ,  応用