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

Clinical, histopathological and genetic studies in a case of fatal familial insomnia with review of the literature.

International journal of clinical and experimental pathology - 1 Jan 2015

Peng Bin, Zhang Shenqi, Dong Hongjuan, Lu Zuneng

Abstract excerpt

To explore clinical, histopathological and genetic features of a case with fatal familial insomnia (FFI) and review the related literatures. A middle-aged woman who complained of "insomnia for 9 months and psychosis for 3 months" was suspicious of FFI. The clinical features of the patient were analyzed, and the dead patient was examined by autopsy and the brain tissues were obtained for histopathological studies,...

Read the complete abstract on PubMed

Topics

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

Share to Fatal Outcome
Share to PRNP gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gliosis

Share to Mutation

Share to Pedigree

Share to Prion Proteins

Share to Prions

Share to Thalamus

Source

Open in PubMed Open full text

Identifiers

PMID: 26617725
PMCID: PMC4637540

Genes

PRNP

Variants

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 · 12 closest

Clinical, histopathological and genetic studies in a case of fatal familial insomnia with review of the literature.PMID 26617725Read ↗

Clinical, histopathological and genetic studies in a family with fatal familial insomnia.Semantic proximity Read ↗

[Clinical, neuroimaging and genetic features of two Chinese families with fatal familial insomnia].Semantic proximity Read ↗

[Analysis for clinical and genetic characteristics of a sporadic FFI case].Semantic proximity Read ↗

Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations.Semantic proximity Read ↗

Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan.Semantic proximity Read ↗

Sporadic fatal insomnia with clinical, laboratory, and genetic findings.Semantic proximity Read ↗

Fatal familial insomnia and the widening spectrum of prion diseases.Semantic proximity Read ↗

A fatal familial insomnia patient newly diagnosed as having depression: A case report.Semantic proximity Read ↗

Fatal familial insomnia and sporadic fatal insomnia.Semantic proximity Read ↗

Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia.Semantic proximity Read ↗

Fatal familial insomnia: Reporting a case of the rare nightmare.Semantic proximity Read ↗

Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.Semantic proximity Read ↗

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