Variant CJD: Reflections a Quarter of a Century on
Twenty-five years has now passed since variant Creutzfeldt-Jakob disease (vCJD) was first described in the United Kingdom (UK). Early epidemiological, neuropathological and biochemical investigations suggested that vCJD represented a new zoonotic form of human prion disease resulting from dietary ex...
Enregistré dans:
Auteurs principaux: | Diane L. Ritchie, Alexander H. Peden, Marcelo A. Barria |
---|---|
Format: | article |
Langue: | EN |
Publié: |
MDPI AG
2021
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/2fc169e9f4ed4a74b10d93de7ee127ec |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Enfermedad por priones, encefalopatía espongiforme humana y enfermedad de Creutzfeldt-Jakob
par: Cartier-Rovirosa,Luis
Publié: (2019) -
Correlation between Bioassay and Protein Misfolding Cyclic Amplification for Variant Creutzfeldt-Jakob Disease Decontamination Studies
par: Maxime Bélondrade, et autres
Publié: (2020) -
Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures
par: Hervé Cassard, et autres
Publié: (2020) -
Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt–Jakob disease
par: Bagyinszky E, et autres
Publié: (2019) -
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients
par: Christina D. Orrù, et autres
Publié: (2018)