Tau pathology in Creutzfeldt-Jakob disease revisited

Dura mater is a potential source of Aβ seeds

(2016) Gabor G. Kovacs et al.   ACTA NEUROPATHOLOGICA

Familial early-onset dementia with complex neuropathologic phenotype and genomic background

(2016) John Alexander et al.   NEUROBIOLOGY OF AGING

PART, a distinct tauopathy, different from classical sporadic Alzheimer disease

(2015) Kurt A. Jellinger et al.   ACTA NEUROPATHOLOGICA

Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

(2015) Gabor G. Kovacs et al.   ACTA NEUROPATHOLOGICA

Prion Disease Induces Alzheimer Disease—Like Neuropathologic Changes

(2015) Thomas Tousseyn et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Familial Behavioral Variant Frontotemporal Dementia Associated With Astrocyte-Predominant Tauopathy

(2015) Isidre Ferrer et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Clinicopathological Correlations and Concomitant Pathologies in Rapidly Progressive Dementia: A Brain Bank Series

(2015) Oriol Grau-Rivera et al.   Neurodegenerative Diseases

Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease

(2015) Anna S. Berghoff et al.   NEUROPATHOLOGY

Invited review: Neuropathology of tauopathies: principles and practice

(2015) G. G. Kovacs   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Primary age-related tauopathy (PART): a common pathology associated with human aging

(2014) John F. Crary et al.   ACTA NEUROPATHOLOGICA

Patterns of Hippocampal Tau Pathology Differentiate Neurodegenerative Dementias

(2014) Ivan Milenkovic et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene

(2014) Junji Komatsu et al.   Prion

Non-Alzheimer neurodegenerative pathologies and their combinations are more frequent than commonly believed in the elderly brain: a community-based autopsy series

(2013) Gabor G. Kovacs et al.   ACTA NEUROPATHOLOGICA

Glial and Neuronal Tau Pathology in Tauopathies

(2013) Isidre Ferrer et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

TARDBPmutation p.Ile383Val associated with semantic dementia and complex proteinopathy

(2013) E. Gelpi et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Characterization of Novel CSF Tau and ptau Biomarkers for Alzheimer’s Disease

(2013) Jere E. Meredith Jr. et al.   PLoS One

Rare V203I mutation in thePRNPgene of a Chinese patient with Creutzfeldt–Jakob disease

(2013) Qi Shi et al.   Prion

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

(2012) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

Intraneuronal Immunoreactivity for the Prion Protein Distinguishes a Subset of E200K Genetic From Sporadic Creutzfeldt-Jakob Disease

(2012) Gabor G. Kovacs et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

A peculiar constellation of tau pathology defines a subset of dementia in the elderly

(2011) Gabor G. Kovacs et al.   ACTA NEUROPATHOLOGICA

Current concepts of neuropathological diagnostics in practice: neurodegenerative diseases

(2011) G.G. Kovacs et al.   CLINICAL NEUROPATHOLOGY

Gene Knockout of tau Expression Does Not Contribute to the Pathogenesis of Prion Disease

(2011) Victoria A. Lawson et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Tau, prions and Aβ: the triad of neurodegeneration

(2010) Lilla Reiniger et al.   ACTA NEUROPATHOLOGICA

Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy

(2010) Gabor G. Kovacs et al.   ACTA NEUROPATHOLOGICA

Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein

(2010) Wen-Quan Zou et al.   ANNALS OF NEUROLOGY

Changes of tau profiles in brains of the hamsters infected with scrapie strains 263 K or 139 A possibly associated with the alteration of phosphate kinases

(2010) Gui-Rong Wang et al.   BMC INFECTIOUS DISEASES

Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment

(2010) B-H. Jeong et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits

(2010) C. Jansen et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Molecular Pathology of Human Prion Diseases

(2009) Gabor Kovacs et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Concomitant progressive supranuclear palsy and multiple system atrophy: More than a simple twist of fate?

(2009) Laura Silveira-Moriyama et al.   NEUROSCIENCE LETTERS

Cerebral amyloid angiopathy and its relationship to Alzheimer’s disease

(2008) Dietmar Rudolf Thal et al.   ACTA NEUROPATHOLOGICA

A novel human disease with abnormal prion protein sensitive to protease

(2008) Pierluigi Gambetti et al.   ANNALS OF NEUROLOGY

Mixed Brain Pathologies in Dementia: The BrainNet Europe Consortium Experience

(2008) Gabor G. Kovacs et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases

(2008) A. M. Isaacs et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease

(2008) B. Sikorska et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Tauopathy in human and experimental variant Creutzfeldt-Jakob disease

(2007) G. Giaccone et al.   NEUROBIOLOGY OF AGING