Significats de human prion en anglès

Amyloid-like fibrils have been associated with the pathogenesis of human prion diseases.

Kuru in the 21st century: an acquired human prion disease with very long incubation periods.

Main outcomes and measures: The main outcome was incidence of human prion disease cases, including identification of variant Creutzfeldt-Jakob disease.

Diffusion Weighted Imaging is extremely important for the diagnosis of probable sporadic Jakob-Creutzfeldt disease, the most common human prion disease.

These data also lead to the hypothesis that similar subclinical disease states may be common for other animal and human prion diseases.

Unlike most human prion diseases, the loss of motor function had been accompanied by cognitive decline, and the post-mortems showed a distinctive neuropathology.

The identification of a novel human prion strain improves our understanding of the pathogenesis of the disease and of possible mechanisms of prion transmission.

Reduction of native prion protein (PrP) levels in the brain is an attractive strategy for the treatment or prevention of human prion disease.

Exposure: Human prion disease diagnosis.