about
The genetics and neuropathology of frontotemporal lobar degenerationMolecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision MedicineMixed tau and TDP-43 pathology in a patient with unclassifiable primary progressive aphasia.Neuropathologic substrates of Parkinson disease dementia.Identification of the nature of reading frame transitions observed in prokaryotic genomes.Pericellular innervation of neurons expressing abnormally hyperphosphorylated tau in the hippocampal formation of Alzheimer's disease patients.TOC1: a valuable tool in assessing disease progression in the rTg4510 mouse model of tauopathy.Complex proteinopathy with accumulations of prion protein, hyperphosphorylated tau, α-synuclein and ubiquitin in experimental bovine spongiform encephalopathy of monkeys.Specific profile of tau isoforms in argyrophylic grain disease.Primary age-related tauopathy (PART): a common pathology associated with human agingTau, prions and Aβ: the triad of neurodegeneration.Pattern of brain atrophy rates in autopsy-confirmed dementia with Lewy bodies.Typical or atypical progressive supranuclear palsy: a comparative clinicopathologic study of three Chinese cases.Familial behavioral variant frontotemporal dementia associated with astrocyte-predominant tauopathyFrontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.A pilot study of bacterial genes with disrupted ORFs reveals a surprising profusion of protein sequence recoding mediated by ribosomal frameshifting and transcriptional realignment.Tauopathies as clinicopathological entities.Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review.Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy.Argyrophilic grain disease differs from other tauopathies by lacking tau acetylation.Argyrophilic Grain Disease: Demographics, Clinical, and Neuropathological Features From a Large Autopsy StudyAcetylated tau neuropathology in sporadic and hereditary tauopathies.Re-evaluation of clinical dementia diagnoses with pittsburgh compound B positron emission tomography.The role of extracellular Tau in the spreading of neurofibrillary pathology.Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.Clinicopathological correlates of lewy body disease: fundamental issues.Challenges of multimorbidity of the aging brain: a critical update.Invited review: Neuropathology of tauopathies: principles and practice.Tau and neurodegenerative disorders.Probable Alzheimer's disease patients presenting as "focal temporal lobe dysfunction" show a slow rate of cognitive decline.A Simple Model to Study Tau Pathology.Overlapping but distinct TDP-43 and tau pathologic patterns in aged hippocampi.Neuropathologic features of suicide victims who presented with acute poststroke depression: significance of association with neurodegenerative disorders.Multiple comorbid neuropathologies in the setting of Alzheimer's disease neuropathology and implications for drug development.Progression of limb apraxia in corticobasal syndrome: neuropychological and functional neuroimaging report of a case series.Emerging Diagnostic and Therapeutic Strategies for Tauopathies.Argyrophilic grain disease: An underestimated tauopathy.Argyrophilic grain disease: an update about a frequent cause of dementia.Tauopathies: Mechanisms and Therapeutic Strategies.Sisyphus in Neverland.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Argyrophilic grain disease
@ast
Argyrophilic grain disease
@en
Argyrophilic grain disease
@nl
type
label
Argyrophilic grain disease
@ast
Argyrophilic grain disease
@en
Argyrophilic grain disease
@nl
prefLabel
Argyrophilic grain disease
@ast
Argyrophilic grain disease
@en
Argyrophilic grain disease
@nl
P2093
P2860
P356
P1433
P1476
Argyrophilic grain disease
@en
P2093
Fred W van Leeuwen
Gabriel Santpere
Isidro Ferrer
P2860
P304
P356
10.1093/BRAIN/AWM305
P407
P577
2008-06-01T00:00:00Z