Tau pathology in Creutzfeldt-Jakob disease revisited (Q48640345)

13 February 2018

title

Tau pathology in Creutzfeldt-Jakob disease revisited (English)

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Creutzfeldt-Jakob disease

main subject

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1

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Paweł P. Liberski

9

object named as

Pawel P Liberski

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Beata Sikorska

object named as

Beata Sikorska

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Herbert Budka

object named as

Herbert Budka

10

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author name string

Jasmin Rahimi

2

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13 February 2018

Thomas Ströbel

3

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Mirjam I Lutz

4

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Günther Regelsberger

5

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Nathalie Streichenberger

6

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Armand Perret-Liaudet

7

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Romana Höftberger

8

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publication date

5 July 2016

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13 February 2018

published in

Brain Pathology

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volume

27

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issue

3

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page(s)

332-344

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

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21 January 2018

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Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease

21 January 2018

1 reference

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

21 January 2018

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Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob disease

21 January 2018

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Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia

21 January 2018

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Quantitative neuropathological study of Alzheimer-type pathology in the hippocampus: Comparison of senile dementia of Alzheimer type, senile dementia of Lewy body type, Parkinson's disease and non-demented elderly control patients

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

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

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

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

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Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob disease

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21 January 2018

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Gene knockout of tau expression does not contribute to the pathogenesis of prion disease

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21 January 2018

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Patterns of hippocampal tau pathology differentiate neurodegenerative dementias

21 January 2018

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21 January 2018

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Prion peptide induces neuronal cell death through a pathway involving glycogen synthase kinase 3

21 January 2018

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Alzheimer-type neuropathology in a 28 year old patient with iatrogenic Creutzfeldt-Jakob disease after dural grafting

21 January 2018

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Molecular diagnosis of human prion disease

21 January 2018

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Tau, prions and Aβ: the triad of neurodegeneration

21 January 2018

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No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

21 January 2018

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Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease

21 January 2018

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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

21 January 2018

1 reference

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

21 January 2018

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Two types of sporadic cerebral amyloid angiopathy.

21 January 2018

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Cerebral amyloid angiopathy and its relationship to Alzheimer's disease.

21 January 2018

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Phases of A beta-deposition in the human brain and its relevance for the development of AD.

21 January 2018

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Prion Disease Induces Alzheimer Disease-Like Neuropathologic Changes

21 January 2018

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Coexistence of CJD and Alzheimer's disease: an autopsy case showing typical clinical features of CJD.

21 January 2018

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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

21 January 2018

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Human tau protein forms complex with PrP and some GSS- and fCJD-related PrP mutants possess stronger binding activities with tau in vitro

21 January 2018

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Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles

21 January 2018

1 reference

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/BPA.12411

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13 February 2018

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13 February 2018