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

Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7.

Journal of neurology, neurosurgery, and psychiatry - 1 Jun 2000

d'Aignaux J H, Laplanche J L, Delasnerie-Lauprêtre N, Brandel J P, Peoc'h K, Salomon D, Hauw J J, Alpérovitch A

Abstract excerpt

This study examined trends in mortality from sporadic Creutzfeldt-Jakob disease in France for 1992-7 by age, genotype at the codon 129 of the prion protein gene, and geographical area. Case ascertainment was based on notifications by neurologists, neuropathologists, and laboratories; 324 deaths from definite or probable Creutzfeldt-Jakob disease were registered during the study period. The yearly number of deaths...

Read the complete abstract on PubMed

Topics

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

Share to Cause of Death
Share to Codon

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Creutzfeldt-Jakob Syndrome

Share to France

Share to Incidence

Share to Methionine

Share to Prions

Share to Valine

Source

Open in PubMed Open full text

Identifiers

PMID: 10811709
DOI: 10.1136/jnnp.68.6.787
PMCID: PMC1736947

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

Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7.PMID 10811709Read ↗

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

Creutzfeldt-Jakob disease in Slovenia from 1985 to 2003.Semantic proximity Read ↗

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.Semantic proximity Read ↗

Strain-specific clustering of sporadic Creutzfeldt-Jakob disease in France (1992-2016)Semantic proximity Read ↗

Creutzfeldt-Jakob disease in Hungary.Semantic proximity Read ↗

Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance.Semantic proximity Read ↗

Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium.Semantic proximity Read ↗

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

Creutzfeldt-Jakob disease and related diseases in France from 1998 to 2000.Semantic proximity Read ↗

A systematic review of sporadic Creutzfeldt-Jakob disease clusters: do clinical, epidemiologic, and genetic features reflect infectious clustering mechanisms?Semantic proximity Read ↗

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

[Human prion diseases: the Hungarian experience].Semantic proximity Read ↗

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