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

Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion.

Alzheimer's & dementia : the journal of the Alzheimer's Association - 1 Oct 2014

Gómez-Tortosa Estrella, Serrano Soledad, de Toledo María, Pérez-Pérez Julián, Sainz M José

Abstract excerpt

BACKGROUND: In recent years, a benign variant of frontotemporal lobar degeneration (FTLD) has been recognized, with a particularly slow progression of cognitive deficits and scarce frontotemporal atrophy or hypoperfusion in neuroimaging studies. Patients with FTLD have been considered "phenocopies," with an underlying nondegenerative neurologic process. RESULTS: We report the first family with three affected...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Brain

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to C9orf72 Protein

Share to Cholestasis

Share to DNA Repeat Expansion

Share to Frontotemporal Lobar Degeneration

Share to Pneumonia

Share to Proteins

Source

Identifiers

PMID: 24439166
DOI: 10.1016/j.jalz.2013.09.013

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion.PMID 24439166Read ↗

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.Semantic proximity Read ↗

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion.Semantic proximity Read ↗

Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.Semantic proximity Read ↗

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.Semantic proximity Read ↗

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.Semantic proximity Read ↗

C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?Semantic proximity Read ↗

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.Semantic proximity Read ↗

Cognitive Profile of C9orf72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Semantic proximity Read ↗

Slowly progressive behavioral frontotemporal dementia with C9orf72 mutation. Case report and review of the literature.Semantic proximity Read ↗

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.Semantic proximity Read ↗

Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report.Semantic proximity Read ↗

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72Semantic proximity Read ↗

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