Tau pathology in Creutzfeldt-Jakob disease revisited

Author:

Kovacs Gabor G.1,Rahimi Jasmin1,Ströbel Thomas1,Lutz Mirjam I.1,Regelsberger Günther1,Streichenberger Nathalie23,Perret-Liaudet Armand24,Höftberger Romana1,Liberski Pawel P.5,Budka Herbert16,Sikorska Beata5

Affiliation:

1. Institute of Neurology, Medical University of Vienna, and Austrian Reference Center for Human Prion Diseases; Vienna Austria

2. Prion Disease Laboratory, Pathology and Biochemistry; Groupement Hospitalier Est, Hospices Civils de Lyon/Claude Bernard University; Lyon France

3. Institut NeuroMyogène CNRS UMR 5310 - INSERM U1217; Lyon France

4. Centre de Recherche en Neurosciences de Lyon (Laboratoire BioRaN); Université Claude Bernard Lyon 1 - CNRS UMR5292 - INSERM U1028; Lyon France

5. Department of Molecular Pathology and Neuropathology; Medical University of Lodz; Lodz Poland

6. Institute of Neuropathology, University Hospital Zurich; Zurich Switzerland

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Reference72 articles.

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2. Familial early-onset dementia with complex neuropathologic phenotype and genomic background;Alexander;Neurobiol Aging,2016

3. CSF phosphorylated tau protein and mild cognitive impairment: a prospective study;Arai;Exp Neurol,2000

4. Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease;Berghoff;Neuropathology,2015

5. Neuropathological staging of Alzheimer-related changes;Braak;Acta Neuropathol,1991

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