Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease

Human prion diseases are classified into sporadic, genetic, and acquired forms. Within this last group, iatrogenic Creutzfeldt–Jakob disease (iCJD) is caused by human-to-human transmission through surgical and medical procedures. After reaching an incidence peak in the 1990s, it is believed that the...

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Detalles Bibliográficos
Autores principales: Llorens, Franc, Villar-Piqué, Anna, Hermann, Peter, Schmitz, Matthias, Calero, Olga, Stehmann, Christiane, Sarros, Shannon, Moda, Fabio, Ferrer, Isidre, Poleggi, Anna, Pocchiari, Maurizio, Catania, Marcella, Klotz, Sigrid, O’Regan, Carl, Brett, Francesca, Heffernan, Josephine, Ladogana, Anna, Collins, Steven J., Calero, Miguel, Kovacs, Gabor G., Zerr, Inga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072321/
https://www.ncbi.nlm.nih.gov/pubmed/32059611
http://dx.doi.org/10.3390/biom10020290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072321/
https://www.ncbi.nlm.nih.gov/pubmed/32059611
http://dx.doi.org/10.3390/biom10020290

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