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Panencephalopathic Type of Creutzfeldt-Jakob Disease: Primary Involvement of the Cerebral White Matter

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Date 1981 Feb 1
PMID 7012278
Citations 27
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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.

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References
1.
Gibbs Jr C, Gajdusek D, Asher D, Alpers M, Beck E, Daniel P . Creutzfeldt-Jakob disease (spongiform encephalopathy): transmission to the chimpanzee. Science. 1968; 161(3839):388-9. DOI: 10.1126/science.161.3839.388. View

2.
MAY W . Creutzfeldt-Jakob disease. 1. Survey of the literature and clinical diagnosis. Acta Neurol Scand. 1968; 44(1):1-32. DOI: 10.1111/j.1600-0404.1968.tb07440.x. View

3.
Beck E, Daniel P, Matthews W, Stevens D, Alpers M, Asher D . Creutzfeldt-Jakob disease. The neuropathology of a transmission experiment. Brain. 1969; 92(4):699-716. DOI: 10.1093/brain/92.4.699. View

4.
Chou S, Martin J . Kuru-plaques in a case of Creutzfeldt-Jakob disease. Acta Neuropathol. 1971; 17(2):150-5. DOI: 10.1007/BF00687490. View

5.
Kinoshita J, Mizuno R, Yagishita S, Iida M, Matsushita M . [2 autopsy cases of Creutzfeldt-Jakob disease]. Shinkei Kenkyu No Shimpo. 1972; 16(3):452-9. View