Cargando…

Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD

BACKGROUND: The 14-3-3 test appears to be a valuable aid for the clinical diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) in selected populations. However, its usefulness in routine practice has been challenged. In this study, the influence of the clinical context on the performance of the 14...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cuadrado-Corrales, Natividad, Jiménez-Huete, Adolfo, Albo, Carmen, Hortigüela, Rafael, Vega, Luz, Cerrato, Laura, Sierra-Moros, Maríajosé, Rábano, Alberto, de Pedro-Cuesta, Jesús, Calero, Miguel
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2006
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570138/ https://www.ncbi.nlm.nih.gov/pubmed/16872484 http://dx.doi.org/10.1186/1471-2377-6-25

Ejemplares similares

EEG Observations in Probable Sporadic CJD
por: Mundlamurri, Ravindranadh Chowdary, et al.
Publicado: (2020)

Application of quantitative DTI metrics in sporadic CJD()
por: Caverzasi, E., et al.
Publicado: (2014)

RT-QuIC: a new test for sporadic CJD
por: Green, Alison J E
Publicado: (2019)

Brain microglia were activated in sporadic CJD but almost unchanged in fatal familial insomnia and G114V genetic CJD
por: Shi, Qi, et al.
Publicado: (2013)

Re-Assessment of PrP(Sc) Distribution in Sporadic and Variant CJD
por: Rubenstein, Richard, et al.
Publicado: (2013)

Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD
por: Orrú, Christina D., et al.
Publicado: (2020)

CJD mimics and chameleons
por: Mead, Simon, et al.
Publicado: (2017)

Ocular Tonometry and Sporadic Creutzfeldt - Jakob Disease (sCJD): A Confirmatory Case-Control Study
por: Davanipour, Zoreh, et al.
Publicado: (2014)

Tissue classification for the epidemiological assessment of surgical transmission of sporadic Creutzfeldt-Jakob disease. A proposal on hypothetical risk levels
por: Rábano, Alberto, et al.
Publicado: (2005)

Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patients
por: Douet, Jean-Yves, et al.
Publicado: (2021)

Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJD
por: Fagge, Timothy J, et al.
Publicado: (2007)

PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD)
por: Takao, Masaki, et al.
Publicado: (2018)

Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C “Strain”
por: Gelpi, Ellen, et al.
Publicado: (2021)

vCJD risk in the Republic of Ireland
por: Harney, Michael S, et al.
Publicado: (2003)

Familial CJD- A Brief Commentary
por: Chandra, Satish, et al.
Publicado: (2019)

Towards an Age-Dependent Transmission Model of Acquired and Sporadic Creutzfeldt-Jakob Disease
por: de Pedro-Cuesta, Jesús, et al.
Publicado: (2014)

Nosocomial transmission of sporadic Creutzfeldt–Jakob disease: results from a risk-based assessment of surgical interventions
por: de Pedro-Cuesta, Jesús, et al.
Publicado: (2010)

The Various Faces of Creutzfeldt-Jakob Disease (CJD); a Case of CJD Presenting as Psychosis in a Middle-Aged Woman
por: Sodiya, Olusegun, et al.
Publicado: (2022)

A Common BACE1 Polymorphism Is a Risk Factor for Sporadic Creutzfeldt-Jakob Disease
por: Calero, Olga, et al.
Publicado: (2012)

An enigmatic case of cortical anopsia: Antemortem diagnosis of a 14-3-3 negative Heidenhain-variant MM1-sCJD
por: Obergassel, Julius, et al.
Publicado: (2019)

Variant CJD: 18 years of research and surveillance
por: Diack, Abigail B, et al.
Publicado: (2014)

Progress in CSF biomarker discovery in sCJD
por: Llorens, Franc, et al.
Publicado: (2016)

Genetic Cross-Interaction between APOE and PRNP in Sporadic Alzheimer's and Creutzfeldt-Jakob Diseases
por: Calero, Olga, et al.
Publicado: (2011)

The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD)
por: Yun, Jisuk, et al.
Publicado: (2011)

Comprehensive clinical, radiological, pathological and biochemical analysis required to differentiate VV1 sporadic Creutzfeldt-Jakob disease from suspected variant CJD
por: Holper, Sarah, et al.
Publicado: (2022)

Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt–Jakob Disease (CJD)
por: Won, Sae-Young, et al.
Publicado: (2023)

Epidemiological evidence of higher susceptibility to vCJD in the young
por: Boëlle, Pierre-Yves, et al.
Publicado: (2004)

Updated projections of future vCJD deaths in the UK
por: Ghani, Azra C, et al.
Publicado: (2003)

Preclinical Detection of Variant CJD and BSE Prions in Blood
por: Lacroux, Caroline, et al.
Publicado: (2014)

Public health risks from subclinical variant CJD
por: Diack, Abigail B., et al.
Publicado: (2017)

Transmissible amyloid protein: evidence from iatrogenic CJD
por: Hu, Mo, et al.
Publicado: (2018)

Variant CJD: Reflections a Quarter of a Century on
por: Ritchie, Diane L., et al.
Publicado: (2021)

Assessing initial MRI reports for suspected CJD patients
por: Jesuthasan, Aaron, et al.
Publicado: (2022)

A case-control study of sporadic Creutzfeldt-Jakob disease in Switzerland: analysis of potential risk factors with regard to an increased CJD incidence in the years 2001–2004
por: Ruegger, Jessica, et al.
Publicado: (2009)

Novel mutation of the PRNP gene of a clinical CJD case
por: Kotta, Konstantia, et al.
Publicado: (2006)

Brain-derived proteins in the CSF, do they correlate with brain pathology in CJD?
por: Boesenberg-Grosse, Constanze, et al.
Publicado: (2006)

The management of potential exposures to Cretuzfeld-Jakob Disease (CJD) via endoscopy
por: Iten, A, et al.
Publicado: (2011)

Mad Cows and CJD: A Physicist's View of Prion Brain Diseases
por: Morrison, Douglas Robert Ogston
Publicado: (1997)

Imaging and CSF analyses effectively distinguish CJD from its mimics
por: Rudge, Peter, et al.
Publicado: (2018)

CSF nonphosphorylated Tau as a biomarker for the discrimination of AD from CJD
por: Ermann, Natalia, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_aibicid4c369bd6tt4stt3ejo3