Suppr超能文献

克雅氏病的全脑病变型:脑白质的原发性受累。

Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter.

作者信息

Mizutani T, Okumura A, Oda M, Shiraki H

出版信息

J Neurol Neurosurg Psychiatry. 1981 Feb;44(2):103-15. doi: 10.1136/jnnp.44.2.103.

Abstract

Eight necropsy cases of a "panencephalopathic" type of Creutzfeldt-Jakob disease (CJD) in the Japanese are reported. The reasons why this type should be discussed separately from other types of CJD are that there is primary involvement of the cerebral white matter as well as the cerebral cortex, and that the white matter lesion of one Japanese human brain with CJD similar to the present group has been successfully transmitted to experimental animals.

摘要

本文报告了8例日本“全脑病变型”克雅氏病(CJD)的尸检病例。之所以要将此类型与其他类型的CJD分开讨论,原因在于脑白质以及大脑皮层均有原发性病变,并且1例与本研究组类似的患CJD的日本人脑白质病变已成功传播给实验动物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a7/490840/189d9372ea32/jnnpsyc00058-0016-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验