[The spectrum of prion pathology broadens: fatal familial insomnia].

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

Back to search

Article

[The spectrum of prion pathology broadens: fatal familial insomnia].

Revista de neurologia - 1 Dec 1997

Delgado-Reyes S, Feito-Ibarz N, Ruiz-Aláez A, García de la Rocha M L, Martín-Araguz A, Moreno-Martínez J M

Abstract excerpt

INTRODUCTION: The small group of prion diseases, caused by accumulation in the brain of an abnormal protein characterized by its aggregation and relative resistance to proteases (the PrPSc) in man is comprised of Creutzfeldt-Jacob disease (CJE), the Gerstmann-Straussler-Scheinker syndrome, kuru a...

Topics

Adult
Aged
Circadian Rhythm
Codon
Dysautonomia, Familial
Endopeptidases
Female
Humans
Male
Middle Aged
Phenotype
Point Mutation
Polymorphism, Genetic
PrPC Proteins
Prion Diseases
Sleep Initiation and Maintenance Disorders
Thalamus

Source

Open in PubMed

Identifiers

PMID: 9528048

Genes

PRNP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9528048-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics