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

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

Journal of neurology - 1 Oct 2008

Stoeck Katharina, Hess Klaus, Amsler Lorenz, Eckert Tobias, Zimmermann Dieter, Aguzzi Adriano, Glatzel Markus

Abstract excerpt

Incidences of human transmissible spongiform encephalopathies are monitored by national registries in the majority of countries in Western Europe. During the past 13 years incidences for Creutzfeldt-Jakob disease (CJD) in Switzerland fluctuated between 0.4 and 2.63 cases/10(6) inhabitants. We have compared clinicpathological patient profiles including geographic and gender distribution, age at disease onset,...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Age of Onset

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Creutzfeldt-Jakob Syndrome

Share to Incidence

Share to Prion Proteins

Share to Prions

Share to Sex Factors

Share to Switzerland

Source

Identifiers

PMID: 19005626
DOI: 10.1007/s00415-008-0900-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profiles.PMID 19005626Read ↗

Sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

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

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

Sporadic Creutzfeldt-Jakob disease: discrete subtypes or a spectrum of disease?Semantic proximity Read ↗

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

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

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

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

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

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

Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD.Semantic proximity Read ↗

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