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

Clinical and radiological features of posterior cortical atrophy (PCA) in a GRN mutation carrier: a case report.

European journal of neurology - 1 Jan 2021

Giunta M, Libri I, Premi E, Brattini C, Paghera B, Archetti S, Gasparotti R, Padovani A, Borroni B, Benussi A

Abstract excerpt

BACKGROUND AND PURPOSE: Posterior cortical atrophy (PCA) is a rare neurodegenerative syndrome, defined by a distinctive clinical-radiological profile, with Alzheimer's disease (AD) pathology accounting for the majority of cases. The aim of this report was to present the case of a patient with impairment of visual and constructional abilities as initial manifestations. METHOD: The patient underwent a...

Read the complete abstract on PubMed

Topics

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

Share to Alzheimer Disease
Share to Atrophy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cerebral Cortex

Share to Mutation

Share to Occipital Lobe

Share to Progranulins

Source

Identifiers

PMID: 33030763
DOI: 10.1111/ene.14574

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and radiological features of posterior cortical atrophy (PCA) in a GRN mutation carrier: a case report.PMID 33030763Read ↗

Posterior cortical atrophy as an extreme phenotype of GRN mutations.Semantic proximity Read ↗

Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy.Semantic proximity Read ↗

Posterior cortical atrophy as a primary clinical phenotype of corticobasal syndrome with a progranulin gene rs5848 TT genotype.Semantic proximity Read ↗

Towards an earlier diagnosis of Alzheimer's disease presenting with visuospatial disorders (posterior cortical atrophy).Semantic proximity Read ↗

Data-driven detection of latent atrophy factors related to phenotypical variants of posterior cortical atrophySemantic proximity Read ↗

Latent atrophy factors related to phenotypical variants of posterior cortical atrophy.Semantic proximity Read ↗

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.Semantic proximity Read ↗

Language Profile of Posterior Cortical Atrophy: A Comparative Study with Alzheimer’s Disease VariantsSemantic proximity Read ↗

Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: broadening the clinical and neuropsychological phenotype.Semantic proximity Read ↗

Basal ganglia calcifications (Fahr’s syndrome): related conditions and clinical featuresSemantic proximity Read ↗

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.Semantic proximity Read ↗

Cognitive deficits in familial Alzheimer's disease associated with M239V mutation of presenilin 2.Semantic proximity Read ↗

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