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

[Performance of carriers and non-carriers of the E280A mutation for familial Alzheimer's disease in a naming test].

Revista de neurologia - 1 Jan 2000

Tirado V, Muñoz C, Aguirre C, Pineda D A, Lopera F

Abstract excerpt

INTRODUCTION: Early preclinical diagnosis is the greatest challenge faced by researchers into dementia. Cognitive, neuroanatomical, neurophysiological and genetic markers have been reported. One of the preclinical cognitive markers is anomia and it is often assessed using visual naming tests. AIM...

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 Heterozygote
Share to Membrane Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Neuropsychological Tests

Share to Presenilin-1

Source

Identifiers

PMID: 15340889

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15340889-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Performance of carriers and non-carriers of the E280A mutation for familial Alzheimer's disease in a naming test].PMID 15340889Read ↗

[Analysis of intrusive errors in a memory test as possible pre-clinical marker of familial Alzheimer disease, in E280A presenilin-1 mutation carrier].Semantic proximity Read ↗

Rethinking anomia across the frontotemporal dementia spectrum: marker of language dysfunction or global cognitive decline?Semantic proximity Read ↗

Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations.Semantic proximity Read ↗

Dysexecutive syndrome in amnesic mild cognitive impairment: a multicenter study.Semantic proximity Read ↗

Language deficits across PET-based Braak stages of tau accumulation in Alzheimer’s diseaseSemantic proximity Read ↗

Comparing different approaches for operationalizing subjective cognitive decline: impact on syndromic and biomarker profilesSemantic proximity Read ↗

Distinct Subgroups of Amnestic Mild Cognitive Impairment as Identified by Soft Independent Modeling of Class AnalogySemantic proximity Read ↗

A comparison of unawareness in frontotemporal dementia and Alzheimer's diseaseSemantic proximity Read ↗

Trajectory of Unawareness of Memory Decline in Individuals With Autosomal Dominant Alzheimer Disease.Semantic proximity Read ↗

Memory for Semantically Related Objects Differentiates Cognitively Unimpaired Autosomal Dominant Mutation Carriers from Non-Carrier Family Members.Semantic proximity Read ↗

Neuropsychological study of familial Alzheimer's disease caused by mutation E280A in the presenilin 1 gene.Semantic proximity Read ↗

“A mosquito bites and a butterfly flies": a specific response type of frontal patients in a similarity taskSemantic proximity Read ↗

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