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A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline.

作者信息

Zanusso Gianluigi, Ferrari Sergio, Conte Stefania, Mellina Vittorio, Sacchi Vittorio, Rizzuto Nicola, Monaco Salvatore

出版信息

Brain Pathol. 2006 Jul;16(3):237-8. doi: 10.1111/j.1750-3639.2006.00014_2.x.

DOI:10.1111/j.1750-3639.2006.00014_2.x
PMID:16911482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8095750/
Abstract
摘要

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本文引用的文献

1
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.基于300例受试者的分子和表型分析对散发性克雅氏病的分类
Ann Neurol. 1999 Aug;46(2):224-33.
2
Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case.
Neurology. 1998 Jul;51(1):271-4. doi: 10.1212/wnl.51.1.271.
3
Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter.克雅氏病的全脑病变型：脑白质的原发性受累。
J Neurol Neurosurg Psychiatry. 1981 Feb;44(2):103-15. doi: 10.1136/jnnp.44.2.103.
4
Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis.
Ann Neurol. 1984 Sep;16(3):295-304. doi: 10.1002/ana.410160305.
5
On the white matter lesions of the Creutzfeldt-Jakob disease. Can a new subentity be recognized in man?关于克雅氏病的白质病变。在人类中能否识别出一种新的亚实体？
J Neurol Sci. 1984 Feb;63(2):197-206. doi: 10.1016/0022-510x(84)90196-5.
6
Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.克雅氏病：全球发病模式以及家族性和散发性聚集的意义。
Ann Neurol. 1979 Feb;5(2):177-88. doi: 10.1002/ana.410050212.