Neuropathologic Overlap of Progressive Supranuclear Palsy, Pickʼs Disease and Corticobasal Degeneration
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Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filamentsComparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's diseaseREVIEW: tau protein pathology in Alzheimer's disease and related disorders.Differential diagnosis of parkinsonism.Stains for the differential diagnosis of degenerative dementias.Chronic traumatic encephalopathy - neuropathology in athletes and war veterans.Are pathological lesions in neurodegenerative disorders the cause or the effect of the degeneration?Clinical manifestations of Parkinson's disease and parkinsonism.Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndromeMAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies.Deep clinical and neuropathological phenotyping of Pick disease.Phenotypic variation of autosomal-dominant corticobasal degeneration.Therapy and clinical trials in frontotemporal dementia: past, present, and future.Visual signs and symptoms of progressive supranuclear palsy.Extrapyramidal syndromes in frontotemporal degeneration.Tau accumulation in the retina promotes early neuronal dysfunction and precedes brain pathology in a mouse model of Alzheimer's disease.An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.Missense point mutations of tau to segregate with FTDP-17 exhibit site-specific effects on microtubule structure in COS cells: a novel action of R406W mutation.Argyrophilic grain disease is a sporadic 4-repeat tauopathy.Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.Substantia nigra in progressive supranuclear palsy, corticobasal degeneration, and parkinsonism-dementia complex of Guam: specific pathological features.Microglial activation parallels system degeneration in progressive supranuclear palsy and corticobasal degeneration.Oligodendroglial tau filament formation in transgenic mice expressing G272V tau.Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy.Degeneration of Pick bodies visualized by methenamine-silver staining and immunohistochemistry.The formation of straight and twisted filaments from short tau peptides.Protein astrogliopathies in human neurodegenerative diseases and aging.Motor neuron disease-inclusion dementia presenting as cortical-basal ganglionic degeneration.Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.Progressive supranuclear palsy: neuronal and glial cytoskeletal pathology in the higher order processing autonomic nuclei of the lower brainstem.Distribution and dynamic process of neuronal cytoplasmic inclusion (NCI) in MSA: correlation of the density of NCI and the degree of involvement of the pontine nuclei.Cortical synapse loss in progressive supranuclear palsy.Complex tauopathies versus tangle predominant dementia.Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia.Late-onset frontotemporal dementia associated with progressive supranuclear palsy/argyrophilic grain disease/Alzheimer's disease pathology.Different distribution of phosphorylated tau protein isoforms in Alzheimer's and Pick's diseases.Phosphorylation of specific sets of tau isoforms reflects different neurofibrillary degeneration processes.Progressive Supranuclear Palsy and Corticobasal Degeneration
P2860
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P2860
Neuropathologic Overlap of Progressive Supranuclear Palsy, Pickʼs Disease and Corticobasal Degeneration
description
im Jahr 1996 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 1996
@uk
name
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@en
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@nl
type
label
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@en
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@nl
prefLabel
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@en
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@nl
P2093
P1476
Neuropathologic Overlap of Pro ...... and Corticobasal Degeneration
@en
P2093
Dennis W. Dickson
Linda A. Mattiace
Mel B. Feany
P356
10.1097/00005072-199601000-00006
P577
1996-01-01T00:00:00Z