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

Precocious loss of physiological sleep in a case of Creutzfeldt Jakob disease: a serial polygraphic study.

Sleep - 1 Dec 1995

Terzano M G, Parrino L, Pietrini V, Mancia D, Spaggiari M C, Rossi G, Tagliavini F

Abstract excerpt

Creutzfeldt-Jakob disease (CJD) is a prion-related subacute encephalopathy producing widespread neuronal degeneration and spongiform pathological changes, especially in the neocortex. Progressive dementia, motor signs and electroencephalographic (EEG) alterations characterize the full stage of the disease. A series of eight 24-hour polygraphic recordings were carried out in the last 3 months of life of a...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Brain
Share to Creutzfeldt-Jakob Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Primers

Share to Electroencephalography

Share to Gene Amplification

Share to Genotype

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 8746391

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

Precocious loss of physiological sleep in a case of Creutzfeldt Jakob disease: a serial polygraphic study.PMID 8746391Read ↗

Early pathology in sleep studies of patients with familial Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Periodic sharp wave complexes identify a distinctive phenotype in Creutzfeldt-Jacob disease.Semantic proximity Read ↗

A sleep that never comes: Prions and their role in fatal familial insomnia - a literature review.Semantic proximity Read ↗

Characterization of sleep disorders in patients with E200K familial Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Longitudinal analysis of the electroencephalogram and sleep phenotype in the R6/2 mouse model of Huntington's disease.Semantic proximity Read ↗

Sleep and Sleep Regulation in Normal and Prion Protein-Deficient MiceSemantic proximity Read ↗

Bilateral tonic-clonic seizure and focal cortical hyperexcitability in familial Creutzfeldt-Jakob disease with E200K mutation of the prion protein.Semantic proximity Read ↗

Sleep alterations in a mouse model of Spinocerebellar ataxia type 3Semantic proximity Read ↗

Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype.Semantic proximity Read ↗

β Oscillation during Slow Wave Sleep and Rapid Eye Movement Sleep in the Electroencephalogram of a Transgenic Mouse Model of Huntington’s DiseaseSemantic proximity Read ↗

Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study.Semantic proximity Read ↗

Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.Semantic proximity Read ↗

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