Associated Papers
Enhanced Sensitivity of a Modified Quaking-Induced Conversion Diagnostic Test for the Broad Detection of Sporadic and Inherited Prion Diseases: A Retrospective Study.
Myskiw J et al.
Annals of Neurology, 2026
Therapeutic Trial of anle138b in Mouse Models of Genetic Prion Disease.
Vallabh SM et al.
Journal of Virology, 2023
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Baiardi S et al.
Acta Neuropathologica, 2021
Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases.
Llorens F et al.
Neuropathology and Applied Neurobiology, 2020
Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases.
Villar-Piqué A et al.
Molecular Neurobiology, 2019
Two distinct prions in fatal familial insomnia and its sporadic form.
Takeuchi A et al.
Brain Communications, 2019
Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.
Abu-Rumeileh S et al.
Annals of Neurology, 2018
An antibody to the aggregated synthetic prion protein peptide (PrP106-126) selectively recognizes disease-associated prion protein (PrP) from human brain specimens.
Jones M et al.
Brain Pathology (zurich, Switzerland), 2009
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