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

Young-onset CJD: age and disease phenotype in variant and sporadic forms.

Functional neurology - 1 Jan 2000

Corato Manuel, Cereda Cristina, Cova Emanuela, Ferrarese Carlo, Ceroni Mauro

Abstract excerpt

Since 1996, there have been over 140 reports of a Creutzfeldt-Jakob disease variant (vCJD), with a striking prevalence of these cases in the UK. The main peculiarity of vCJD is its onset in young people, but other features also distinguish it from sporadic CJD. Despite epidemiological data suggesting a link with bovine spongiform encephalopathy, the origin of vCJD is not completely understood. We hypothesized...

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 Aging
Share to Creutzfeldt-Jakob Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electroencephalography

Share to Plaque, Amyloid

Share to Prions

Share to Survival

Share to Survival Analysis

Source

Identifiers

PMID: 17367581

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

Young-onset CJD: age and disease phenotype in variant and sporadic forms.PMID 17367581Read ↗

Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance.Semantic proximity Read ↗

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Human prion diseases: Molecular, cellular and population biologySemantic proximity Read ↗

New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests.Semantic proximity Read ↗

Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profiles.Semantic proximity Read ↗

Infectious and Sporadic Prion Diseases.Semantic proximity Read ↗

Variant CJD. 18 years of research and surveillance.Semantic proximity Read ↗

Genome wide association study of clinical duration and age at onset of sporadic CJDSemantic proximity Read ↗

Sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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

Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada.Semantic proximity Read ↗

Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.Semantic proximity Read ↗

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