Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

doi:10.1080/13554794.2012.732087

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

Community

Back to search

Article

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

Neurocase - 1 Jan 2014

Sitek Emilia J, Narozanska Ewa, Barczak Anna, Jasinska-Myga Barbara, Harciarek Michał, Chodakowska-Zebrowska Małgorzata, Kubiak Małgorzata, Wieczorek Dariusz, Konieczna Seweryna, Rademakers Rosa, Baker Matt, Berdynski Mariusz, Brockhuis Bogna, Barcikowska Maria, Zekanowski Cezary, Heilman Kenneth M, Wszolek Zbigniew K, Slawek Jarosław

Abstract excerpt

OBJECTIVES: Patients with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) may be agraphic. The study aimed at characterizing agraphia in individuals with a P301L MAPT mutation. METHODS: Two pairs of siblings with FTDP-17 were longitudinally examined for agraphia in relation to language and cognitive deficits. RESULTS: All patients presented with dysexecutive agraphia. In addition, in...

Read the complete abstract on PubMed

Topics

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

Share to Brain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 17

Share to Disease Progression

Share to Frontotemporal Dementia

Share to Longitudinal Studies

Share to Mutation

Share to Parkinsonian Disorders

Share to tau Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 23121543
DOI: 10.1080/13554794.2012.732087
PMCID: PMC3710298

Genes

MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?PMID 23121543Read ↗

Apraxia phenotypes and frontotemporal lobar degeneration.Semantic proximity Read ↗

Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphia.Semantic proximity Read ↗

Progranulin-associated primary progressive aphasia: a distinct phenotype?Semantic proximity Read ↗

Dysgraphic features in motor neuron disease: a reviewSemantic proximity Read ↗

Testing motor grounding and somatotopic effects for literal and figurative action-language in Motor Neuron Diseases: a multiple-case analysisSemantic proximity Read ↗

Discordant performance on the 'Reading the Mind in the Eyes' Test, based on disease onset in amyotrophic lateral sclerosis.Semantic proximity Read ↗

Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy.Semantic proximity Read ↗

Familial primary progressive aphasia.Semantic proximity Read ↗

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