Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease
Silvio Notari(Azienda Sanitaria Unità Locale di Reggio Emilia), Piero Parchi(Istituto delle Scienze Neurologiche di Bologna), Maura Cescatti(Istituto delle Scienze Neurologiche di Bologna), Pierluigi Gambetti(Case Western Reserve University), Bernardino Ghetti(Indiana University School of Medicine), Rosaria Strammiello(Istituto delle Scienze Neurologiche di Bologna), Jan Langeveld(Wageningen University & Research), Sabina Capellari(Istituto delle Scienze Neurologiche di Bologna), Hans A. Kretzschmar(Ludwig-Maximilians-Universität München), Wen‐Quan Zou(Jiangxi Provincial Academy of Medical Sciences), Jacques Grassi(Universidade Federal do Espírito Santo), Armin Giese(Institut für Leichte Elektrische Antriebe und Generatoren (Germany))
Cited by 85
Related Papers
Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease
|New England Journal of Medicine|2012|3.8k
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
|Movement Disorders|2017|2.3k
Cryo-EM structures of tau filaments from Alzheimer’s disease
|Nature|2017|2.1k
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
|Proceedings of the National Academy of Sciences|1998|1.5k
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
|Annals of Neurology|1999|1.4k