Argyrophilic grain disease is a sporadic 4-repeat tauopathy. - Wikidata - awgldk - TriplyDB

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

http://www.wikidata.org/entity/Q39527344

about

Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease Functional MAPT haplotypes: bridging the gap between genotype and neuropathology Neuropathology of non-Alzheimer degenerative disorders Characteristics of Tau and Its Ligands in PET Imaging Brain collection, standardized neuropathologic assessment, and comorbidity in Alzheimer's Disease Neuroimaging Initiative 2 participants Concomitant pathologies among a spectrum of parkinsonian disorders Argyrophilic grain disease Neurofibrillary tangle-predominant dementia: comparison with classical Alzheimer disease Clinicopathological outcomes of prospectively followed normal elderly brain bank volunteers.Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration Complex proteinopathy with accumulations of prion protein, hyperphosphorylated tau, α-synuclein and ubiquitin in experimental bovine spongiform encephalopathy of monkeys.Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly.Modeling the association between 43 different clinical and pathological variables and the severity of cognitive impairment in a large autopsy cohort of elderly persons.Specific profile of tau isoforms in argyrophylic grain disease.Linkage disequilibrium and association of MAPT H1 in Parkinson disease Autopsy consent, brain collection, and standardized neuropathologic assessment of ADNI participants: the essential role of the neuropathology core.The neuropathology, pathophysiology and genetics of multiple system atrophy.Clinicopathological correlates in frontotemporal dementia.The role of tau (MAPT) in frontotemporal dementia and related tauopathies.Neurofibrillary tangles and the deposition of a beta amyloid peptide with a novel N-terminal epitope in the brains of wild Tsushima leopard cats Primary age-related tauopathy (PART): a common pathology associated with human aging Tau aggregation influences cognition and hippocampal atrophy in the absence of beta-amyloid: a clinico-imaging-pathological study of primary age-related tauopathy (PART).Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant.Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study.Hippocampal sclerosis dementia differs from hippocampal sclerosis in frontal lobe degeneration Biochemical analysis of tau proteins in argyrophilic grain disease, Alzheimer's disease, and Pick's disease : a comparative study Regulation of human MAPT gene expression.TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.Gene-environment interplay in neurogenesis and neurodegeneration.Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies.Required techniques and useful molecular markers in the neuropathologic diagnosis of neurodegenerative diseases.The behavioural/dysexecutive variant of Alzheimer's disease: clinical, neuroimaging and pathological features.Neuropathologically defined subtypes of Alzheimer's disease differ significantly from neurofibrillary tangle-predominant dementia.Silver diagnosis in neuropathology: principles, practice and revised interpretation.Corticobasal degeneration with olivopontocerebellar atrophy and TDP-43 pathology: an unusual clinicopathologic variant of CBD.Progressive supranuclear palsy: pathology and genetics.Frontotemporal lobar degeneration: current concepts in the light of recent advances.Brain homogenates from human tauopathies induce tau inclusions in mouse brain Age and apoE associations with complex pathologic features in Alzheimer's disease.The importance of tau phosphorylation for neurodegenerative diseases

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P2860

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

http://www.wikidata.org/entity/Q39527344

description

2002 nî lūn-bûn

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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2002年论文

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2002年论文

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name

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@en

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@nl

type

label

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@en

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@nl

prefLabel

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@en

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@nl

P1433

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P2860

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P1433

Journal of Neuropathology & Experimental Neurology

P1476

Argyrophilic grain disease is a sporadic 4-repeat tauopathy.

@en

P2093

Dennis W Dickson

http://www.w3.org/2001/XMLSchema#string

Mike Hutton

http://www.w3.org/2001/XMLSchema#string

Naruhiko Sahara

http://www.w3.org/2001/XMLSchema#string

Natalie Cookson

http://www.w3.org/2001/XMLSchema#string

Rohan de Silva

http://www.w3.org/2001/XMLSchema#string

Shu-Hui Yen

http://www.w3.org/2001/XMLSchema#string

Takashi Ishizawa

http://www.w3.org/2001/XMLSchema#string

Takashi Togo

http://www.w3.org/2001/XMLSchema#string

P2860

Early diagnosis of dementia: neuropsychology

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

Neuropathological stageing of Alzheimer-related changes

Dementia with grains (argyrophilic grain disease)

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

Recent advances in the understanding of tau protein and movement disorders.

Argyrophilic grains: characteristic pathology of cerebral cortex in cases of adult onset dementia without Alzheimer changes.

Astrocytic plaques and tufts of abnormal fibers do not coexist in corticobasal degeneration and progressive supranuclear palsy.

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

P304

547-556

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scholarly article

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10.1093/JNEN/61.6.547

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6

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61

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Andrew John Lees

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2002-06-01T00:00:00Z

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P5875

11302458

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P698

12071638

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