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Article

Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease.

Neurology - 12 Oct 1999

Rosenmann H, Kahana E, Korczyn A D, Kahana I, Chapman J, Gabizon R

Abstract excerpt

Creutzfeldt-Jakob disease (CJD) linked to the E200K mutation of the prion protein (PrP) gene presents within a wide range of phenotypic heterogeneity, including the age at disease onset. We report an earlier disease onset for mutation carriers of the offspring generation when compared with that o...

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Identifiers

PMID: 10522892
DOI: 10.1212/wnl.53.6.1328

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10522892-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease.PMID 10522892Read ↗

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Ascertainment bias causes false signal of anticipation in genetic prion disease.Semantic proximity Read ↗

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Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.Semantic proximity Read ↗

Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.Semantic proximity Read ↗

Genetic Creutzfeldt-Jakob disease linked to the E200K mutation: a large cohort study.Semantic proximity Read ↗

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The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): A prospective longitudinal study protocolSemantic proximity Read ↗

Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene.Semantic proximity Read ↗

[Clinical features of familial Creutzfeldt-Jakob disease and the E200K mutation in Spain].Semantic proximity Read ↗

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