A test for Creutzfeldt-Jakob disease using nasal brushings
BACKGROUND: Definite diagnosis of sporadic Creutzfeldt-Jakob disease in living patients remains a challenge. A test that detects the specific marker for Creutzfeldt-Jakob disease, the prion protein (PrP(CJD)), by means of real-time quaking-induced ...
Fiorini M +21 more
core +1 more source
É apresentado caso sugestivo de doença de Creutzfeldt-Jakob em adulto jovem. O estudo anátomo-patológico revelou alteração difusa no córtice cerebral, núcleos da base e medula, constituídas por degeneração neuronal, gliose, espongiose e infiltração ...
Osvaldo J. M. Nascimento +1 more
doaj
Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease.
Currently, definite peripheral markers for the in vivo diagnosis of sporadic Creutzfeldt-Jakob disease (CJD) are not available. Here, we report the presence of pathological prion protein in the olfactory mucosa of a case with sporadic Creutzfeldt-Jakob ...
Colucci M. +6 more
core +1 more source
Barriers to Creutzfeldt-Jakob Disease Autopsies, California
Creutzfeldt-Jakob disease (CJD) surveillance relies on autopsy and neuropathologic evaluation. The 1990–2000 CJD autopsy rate in California was 21%. Most neurologists were comfortable diagnosing CJD (83%), but few pathologists felt comfortable diagnosing
Janice K. Louie +6 more
core +1 more source
Report of the Working Group `Overall Blood Supply Strategy with Regard to Variant Creutzfeldt-Jakob Disease (vCJD)' [PDF]
von Koenig, Carl-Heinz Wirsing +19 more
core +1 more source
CDC and Florida Department of Health investigate a likely case of new variant Creutzfeldt Jakob disease in a U.K. citizen residing in the U.S [PDF]
Thursday, April 18, 2002, 19:12 EST (7:12 PM EST)CDCHAN-00085-2002-04-18-UPD-NThe Florida Department of Health and the CDC are investigating a likely case of new variant Creutzfeldt Jakob disease (vCJD) in a 22-year-old citizen of the United Kingdom ...
core
Genome-wide association study of behavioural and psychiatric features in human prion disease.
Prion diseases are rare neurodegenerative conditions causing highly variable clinical syndromes, which often include prominent neuropsychiatric symptoms.
Carswell, C +9 more
core
A case of CreutzfeldtâJakob disease presenting with bilingual Gerstmann syndrome
openaire +1 more source
Prion disease in human - Creutzfeldt-Jakob disease
Charles University in Prague, Faculty of Pharmacy in Hradec Králové Department of Biological and Medical Sciences Candidate: Bc. Veronika Sedláková Leader: PharmDr. Jana Rathouská, Ph.D. Consultant: Ing. Magdalena Smětáková Title of diploma thesis: Human
Sedláková, Veronika
core
An EEG-Based Edge-AI Framework for Alzheimer's and Creutzfeldt-Jakob Disease Classification. [PDF]
Suffian M +5 more
europepmc +1 more source

