Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies.

Acta neuropathologica - 1 Oct 2003

Miserez André R, Clavaguera Florence, Monsch Andreas U, Probst Alphonse, Tolnay Markus

Abstract excerpt

Argyrophilic grain disease (AgD) is a four-repeat tauopathy that is almost exclusively restricted to allocortical areas. Progressive supranuclear palsy and corticobasal degeneration also show predominant deposition of four-repeat tau filaments, and are associated with the tau H1 haplotype. We investigated a possible association between AgD and the tau H1 haplotype. In AgD, no difference between the prevalence of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Haplotypes
Share to Aged, 80 and over
Share to Molecular Biology

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Repetitive Sequences, Nucleic Acid

Share to Sequence Deletion

Share to Supranuclear Palsy, Progressive

Share to tau Proteins

Share to Tauopathies

Source

Identifiers

PMID: 14513264
DOI: 10.1007/s00401-003-0742-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies.PMID 14513264Read ↗

Argyrophilic Grain Pathology in Frontotemporal Lobar Degeneration: Demographic, Clinical, Neuropathological, and Genetic Features.Semantic proximity Read ↗

Argyrophilic grain disease.Semantic proximity Read ↗

Diffuse form of argyrophilic grain disease: a new variant of four-repeat tauopathy different from limbic argyrophilic grain disease.Semantic proximity Read ↗

Argyrophilic grain disease is associated with apolipoprotein E epsilon 2 allele.Semantic proximity Read ↗

Argyrophilic grain pathology as a natural model of tau propagation.Semantic proximity Read ↗

MAPT S305I mutation: implications for argyrophilic grain disease.Semantic proximity Read ↗

Increased frequency of argyrophilic grain disease in Alzheimer disease with 4R tau-specific immunohistochemistry.Semantic proximity Read ↗

Genetic association of argyrophilic grain disease with polymorphisms in alpha-2 macroglobulin and low-density lipoprotein receptor-related protein genes.Semantic proximity Read ↗

H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers.Semantic proximity Read ↗

MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features.Semantic proximity Read ↗

[Argyrophilic grain disease (AgD), a frequent and largely underestimated cause of dementia in old patients].Semantic proximity Read ↗

Neuropathological characterization of two siblings carrying the MAPT S305S mutation demonstrates features resembling argyrophilic grain disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.