Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases

Genetic prion diseases are a rare and diverse group of fatal neurodegenerative disorders caused by pathogenic sequence variations in the prion protein gene, PRNP. Data on CSF biomarkers in patients with genetic prion diseases are limited and conflicting results have been reported for unclear reasons...

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Detalles Bibliográficos
Autores principales: Schmitz, Matthias, Villar-Piqué, Anna, Hermann, Peter, Escaramís, Geòrgia, Calero, Miguel, Chen, Cao, Kruse, Niels, Cramm, Maria, Golanska, Ewa, Sikorska, Beata, Liberski, Pawel P, Pocchiari, Maurizio, Lange, Peter, Stehmann, Christiane, Sarros, Shannon, Martí, Eulàlia, Baldeiras, Inês, Santana, Isabel, Žáková, Dana, Mitrová, Eva, Dong, Xiao-Ping, Collins, Steven, Poleggi, Anna, Ladogana, Anna, Mollenhauer, Brit, Kovacs, Gabor G, Geschwind, Michael D, Sánchez-Valle, Raquel, Zerr, Inga, Llorens, Franc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014756/
https://www.ncbi.nlm.nih.gov/pubmed/35288744
http://dx.doi.org/10.1093/brain/awab350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014756/
https://www.ncbi.nlm.nih.gov/pubmed/35288744
http://dx.doi.org/10.1093/brain/awab350

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