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 features of sporadic fatal insomnia.

Reviews in neurological diseases - 1 Jan 2009

Barash Jed A

Abstract excerpt

Recent advances in neuropathology, genotyping, and physiochemical characterization of proteins have allowed for the classification and verification of MM2-thalamic Creutzfeldt-Jakob disease (CJD). CJD is a fatal neurodegenerative illness belonging to the transmissible spongiform encephalopathies, also known as prion diseases. Sporadic CJD is generally classified by the genotype at codon 129 of the prion protein...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Creutzfeldt-Jakob Syndrome
Share to Diagnosis, Differential

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

Share to Disease Progression

Share to Predictive Value of Tests

Share to PrPSc Proteins

Share to Radionuclide Imaging

Share to Thalamus

Source

Identifiers

PMID: 19898273

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

Clinical features of sporadic fatal insomnia.PMID 19898273Read ↗

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

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

A subtype of sporadic prion disease mimicking fatal familial insomnia.Semantic proximity Read ↗

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

Sporadic and familial CJD: classification and characterisation.Semantic proximity Read ↗

Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.Semantic proximity Read ↗

A sleep that never comes: Prions and their role in fatal familial insomnia - a literature review.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 ↗

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

Fatal familial insomniaSemantic proximity Read ↗

Sporadic human prion diseases: molecular insights and diagnosis.Semantic proximity Read ↗

Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.Semantic proximity Read ↗

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