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Journal of Neurology|April 3, 2013
Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein geneDaniela Varges, Walter J Schulz-Schaeffer, Wiebke M Wemheuer, et al.
Nature Protocols|October 14, 2016
The real-time quaking-induced conversion assay for detection of human prion disease and study of other protein misfolding diseasesMatthias Schmitz, Maria Cramm, Franc Llorens, et al.
Human Molecular Genetics|April 9, 2016
Identification of new molecular alterations in fatal familial insomniaFranc Llorens, Katrin Thüne, Matthias Schmitz, et al.
Molecular Neurobiology|March 22, 2017
Validation of α-Synuclein as a CSF Biomarker for Sporadic Creutzfeldt-Jakob DiseaseFranc Llorens, Niels Kruse, André Karch, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 22, 2016
Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseasesFranc Llorens, Niels Kruse, Matthias Schmitz, et al.
Acta Neuropathologica Communications|April 29, 2017
Altered Ca<sup>2+</sup> homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob diseaseFranc Llorens, Katrin Thüne, Beata Sikorska, et al.
Annals of Neurology|February 27, 2019
Seeding variability of different alpha synuclein strains in synucleinopathiesNiccolò Candelise, Matthias Schmitz, Franc Llorens, et al.
Annals of Neurology|May 1, 2016
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international studyLynne I McGuire, Anna Poleggi, Ilaria Poggiolini, et al.
Brain : a Journal of Neurology|March 15, 2022
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseasesMatthias Schmitz, Anna Villar-Piqué, Peter Hermann, et al.
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