TY  - GEN
AU  - Llorens, Franc
AU  - Villar-Piqué, Anna
AU  - Hermann, Peter
AU  - Schmitz, Matthias
AU  - Calero, Olga
AU  - Stehmann, Christiane
AU  - Sarros, Shannon
AU  - Moda, Fabio
AU  - Ferrer, Isidre
AU  - Poleggi, Anna
AU  - Pocchiari, Maurizio
AU  - Catania, Marcella
AU  - Klotz, Sigrid
AU  - O'Regan, Carl
AU  - Brett, Francesca
AU  - Heffernan, Josephine
AU  - Ladogana, Anna
AU  - Collins, Steven J
AU  - Calero, Miguel
AU  - Kovacs, Gabor G
AU  - Zerr, Inga
PY  - 2020
DO  - 10.3390/biom10020290
UR  - http://hdl.handle.net/20.500.12105/9107
AB  - 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...
LA  - eng
PB  - Multidisciplinary Digital Publishing Institute (MDPI)
KW  - Iatrogenic Creutzfeldt-Jakob disease
KW  - RT-QuIC
KW  - Biomarker
KW  - Cerebrospinal fluid
KW  - Corneal transplant
KW  - Dura matter graft
KW  - Electroencephalogram
KW  - Growth hormone
KW  - Magnetic resonance imaging
TI  - Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease
TY  - research article
ER  -