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

A cognitive chameleon: lessons from a novel MAPT mutation case.

Neurocase - 1 Jan 2014

Liang Yuying, Gordon Elizabeth, Rohrer Jonathan, Downey Laura, de Silva Rohan, Jäger Hans Rolf, Nicholas Jennifer, Modat Marc, Cardoso M Jorge, Mahoney Colin, Warren Jason, Rossor Martin, Fox Nick, Caine Diana

Abstract excerpt

We report a case of frontotemporal dementia caused by a novel MAPT mutation (Q351R) with a remarkably long amnestic presentation mimicking familial Alzheimer's disease. Longitudinal clinical, neuropsychological and imaging data provide convergent evidence for predominantly bilateral anterior medi...

Read the complete abstract on PubMed

Topics

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

Share to MAPT gene
Share to Alzheimer Disease
Share to Brain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Disease Progression

Share to Frontotemporal Dementia

Share to Hippocampus

Share to Mutation

Share to tau Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 23998300
DOI: 10.1080/13554794.2013.826697
PMCID: PMC4151790

Genes

MAPT

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23998300-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A cognitive chameleon: lessons from a novel MAPT mutation case.PMID 23998300Read ↗

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

Presymptomatic semantic impairment in a case of fronto-temporal lobar degeneration associated with the +16 mutation in MAPT.Semantic proximity Read ↗

Isolated medial temporal lobe amnesia (MTLA): Predictor of cerebral amyloidosis or marker of phenotype-specific vulnerability?Semantic proximity Read ↗

Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia.Semantic proximity Read ↗

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.Semantic proximity Read ↗

Frontal temporal dementia: dissecting the aetiology and pathogenesis.Semantic proximity Read ↗

MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian family.Semantic proximity Read ↗

Clinical features and biomarkers of semantic variant primary progressive aphasia with MAPT mutation.Semantic proximity Read ↗

Structural Brain Changes in Pre-Clinical FTD MAPT Mutation Carriers.Semantic proximity Read ↗

Clinical characteristics of semantic variant of primary progressive aphasia with TDP-43- and tau-related gene variants.Semantic proximity Read ↗

Semantic dementia associated with mutation V363I in the tau gene.Semantic proximity Read ↗

The MAPP Room Memory Test: Examining Contextual Memory Using a Novel Computerized Test in Cognitively-Unimpaired Individuals with Autosomal Dominant Alzheimer's Disease.Semantic proximity Read ↗

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