Associated Papers
Overexpression of bank vole PrP(I109) in mice induces a spontaneous atypical prion disease with sex-dependent onset, early NfL elevation, and universal prion strain permissiveness.
Eraña H et al.
Acta Neuropathologica Communications, 2026
Creutzfeldt-Jakob disease: A comprehensive review of current understanding and research.
Noor H et al.
Journal of the Neurological Sciences, 2024
Biomarker changes preceding symptom onset in genetic prion disease.
Vallabh SM et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions.
Aguilar-Calvo P et al.
Acta Neuropathologica, 2020
Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients.
Zerr I et al.
Biomolecules, 2019
Molecular Characterization of the Danish Prion Diseases Cohort With Special Emphasis on Rare and Unique Cases.
Areškevičiūtė A et al.
Journal of Neuropathology and Experimental Neurology, 2019
Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases.
Zerr I et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2018
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