Human prion diseases in the United States.
<h4>Background</h4>Prion diseases are a family of rare, progressive, neurodegenerative disorders that affect humans and animals. The most common form of human prion disease, Creutzfeldt-Jakob disease (CJD), occurs worldwide. Variant CJD (vCJD), a recently emerged human prion disease, is...
Guardado en:
Autores principales: | Robert C Holman, Ermias D Belay, Krista Y Christensen, Ryan A Maddox, Arialdi M Minino, Arianne M Folkema, Dana L Haberling, Teresa A Hammett, Kenneth D Kochanek, James J Sejvar, Lawrence B Schonberger |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2010
|
Materias: | |
Acceso en línea: | https://doaj.org/article/480beb80972e4d89bb002f1131dbca25 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.
por: Silvio Notari, et al.
Publicado: (2010) -
Early preclinical detection of prions in the skin of prion-infected animals
por: Zerui Wang, et al.
Publicado: (2019) -
The importance of prions.
por: Glenn C Telling
Publicado: (2013) -
Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals
por: Zerui Wang, et al.
Publicado: (2019) -
Virus Infection, Genetic Mutations, and Prion Infection in Prion Protein Conversion
por: Hideyuki Hara, et al.
Publicado: (2021)