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Article

Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.

Neurology - 1 Jun 1992

Chapman J, Brown P, Rabey J M, Goldfarb L G, Inzelberg R, Gibbs C J, Gajdusek D C, Korczyn A D

Abstract excerpt

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 1351274
DOI: 10.1212/wnl.42.6.1249-a

Genes

PRNP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.PMID 1351274Read ↗

Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews.Semantic proximity Read ↗

Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.Semantic proximity Read ↗

Complete Penetrance of Creutzfeldt-Jakob Disease in Libyan Jews Carrying the E200K Mutation in the Prion Protein GeneSemantic proximity Read ↗

Genetics and biochemistry of Creutzfeldt-Jakob disease in Libyan Jews.Semantic proximity Read ↗

Genetic and environmental factors determining the development of Creutzfeldt-Jakob disease in Libyan Jews.Semantic proximity Read ↗

Genetic Creutzfeldt-Jakob disease in Turkish Jews-demographic and clinical features.Semantic proximity Read ↗

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.Semantic proximity Read ↗

A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin.Semantic proximity Read ↗

Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD.Semantic proximity Read ↗

Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease.Semantic proximity Read ↗

The molecular genetics of familial Creutzfeldt-Jakob disease in France.Semantic proximity Read ↗

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