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

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.

European journal of neurology - 1 Sept 2002

Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues J-F, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-Lauprêtre N, Mary J Y, Laplanche J-L

Abstract excerpt

We report the molecular and phenotypic analysis of a French cluster of three cases of Creutzfeldt-Jakob disease (CJD), two of them occurring in 1998 in the same village and the other in 1995 in a neighboring village. Analyses of the occurrence of these events in a close area with less than 3000 inhabitants over the 1992-1999 notification period confirmed that they are rare. This could be explained either by a...

Read the complete abstract on PubMed

Topics

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

Share to Brain
Share to Cluster Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Creutzfeldt-Jakob Syndrome

Share to France

Share to Genetic Testing

Share to Methionine

Share to PrPSc Proteins

Source

Identifiers

PMID: 12220376
DOI: 10.1046/j.1468-1331.2002.00456.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.PMID 12220376Read ↗

Genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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

Molecular classification of sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

A novel phenotype of sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.Semantic proximity Read ↗

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.Semantic proximity Read ↗

Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.Semantic proximity Read ↗

Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.Semantic proximity Read ↗

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.Semantic proximity Read ↗

Prion disease genetics.Semantic proximity Read ↗

Sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.Semantic proximity Read ↗

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