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

ANXA11 Mutations in the FTD Spectrum: A Novel Finding in a Patient With Semantic Variant Primary Progressive Aphasia.

European journal of neurology - 1 May 2025

Meng Yaping, Li Wenping, Zhang Yanxin, Li Yaoru, He Yong, Zhang Nan

Abstract excerpt

BACKGROUND: Semantic variant primary progressive aphasia (svPPA) is typically a sporadic disorder, and few cases have been linked to ANXA11 mutations. Comprehensive analyses of genetic mutations in svPPA are limited. Furthermore, the clinical and genetic distinctions between typical svPPA and right temporal variant frontotemporal dementia (rtvFTD) are poorly understood. METHODS: A 68-year-old patient with svPPA...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Annexins
Share to Aphasia, Primary Progressive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Frontotemporal Dementia

Share to APOE gene

Share to GRN gene

Share to MAPT gene

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 40345169
DOI: 10.1111/ene.70187
PMCID: PMC12062875

Genes

ANXA11
APOE
C9ORF72
GRN
MAPT

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

ANXA11 Mutations in the FTD Spectrum: A Novel Finding in a Patient With Semantic Variant Primary Progressive Aphasia.PMID 40345169Read ↗

ANXA11 mutations are associated with amyotrophic lateral sclerosis–frontotemporal dementiaSemantic proximity Read ↗

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

An atypical ALS with PSP-like symptoms caused by ANXA11 p.D40G mutation: A case report and literature reviewSemantic proximity Read ↗

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementiaSemantic proximity Read ↗

Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Classification of primary progressive aphasia: challenges and complexitiesSemantic proximity Read ↗

Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia.Semantic proximity Read ↗

Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population.Semantic proximity Read ↗

GRN mutation spectrum and genotype-phenotype correlation in Chinese dementia patients: data from PUMCH dementia cohort.Semantic proximity Read ↗

Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of Apulia.Semantic proximity Read ↗

Primary progressive aphasia: six questions in search of an answer.Semantic proximity Read ↗

Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population.Semantic proximity Read ↗

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