Epidemiological and clinical characteristics of patients with late-onset Creutzfeldt-Jakob disease
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DOI: 10.1007/s10072-022-05929-9
Abstract: Creutzfeldt-Jacob disease (CJD) is a fatal neuro-degenerative disease, characterized by rapid and intense deterioration, mainly cognitive, leading to death. The typical onset of the disease is around the age of 67. To characterize the demographic… read more here.
Keywords: late onset; creutzfeldt; onset years; disease ... See more keywords
Creutzfeldt astrocytes may be seen in IDH‐wildtype glioblastoma and retain expression of DNA repair and chromatin binding proteins
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DOI: 10.1111/bpa.12604
Abstract: Astrocytes with multiple micronuclei (“Creutzfeldt cells”) in a brain biopsy are classically associated with demyelinating disease. However, glioblastoma may also have prominent Creutzfeldt astrocytes, along with granular mitoses. Therefore, Creutzfeldt cells may raise the diagnostic… read more here.
Keywords: dna repair; creutzfeldt; dna; expression ... See more keywords