Detalhe da pesquisa
1.
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases.
Brain
; 145(2): 700-712, 2022 04 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35288744
2.
Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases.
Alzheimers Dement
; 13(6): 710-719, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27870938
3.
Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years.
Brain
; 135(Pt 10): 3051-61, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23012332
4.
Geographic accumulation of Creutzfeldt-Jakob disease in Slovakia--environmental metal imbalance as a possible cofactor.
Cent Eur J Public Health
; 19(3): 158-64, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22026293
5.
Genetic Risk Factors of Creutzfeldt-Jakob Disease in the Population of Newborns in Slovakia.
Pathogens
; 10(4)2021 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33917419
6.
Ubiquitin as potential cerebrospinal fluid marker of Creutzfeldt-Jakob disease.
Proteomics
; 10(1): 81-9, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19882659
7.
Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease.
Eur J Neurosci
; 31(11): 2024-31, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20529115
8.
Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.
Alzheimer Dis Assoc Disord
; 24(1): 104-7, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-19571726
9.
A pilot study of a genetic CJD risk factor (E200K) in the general Slovak population.
Eur J Epidemiol
; 29(8): 595-7, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25064618
10.
Genetic Creutzfeldt-Jakob disease affected monozygotic twins: Analysis of survival time, age at death and possible exogenous risk factors.
J Clin Neurosci
; 66: 191-195, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31097381
11.
Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases.
Mol Neurobiol
; 56(4): 2811-2821, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30062673
12.
Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis.
J Neurol
; 254(7): 901-6, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17385081
13.
[Human prion diseases: the Hungarian experience]. / Emberi prionbetegségek: magyarországi tapasztalatok.
Ideggyogy Sz
; 60(11-12): 447-52, 2007 Nov 30.
Artigo
em Húngaro
| MEDLINE | ID: mdl-18200749
14.
Cerebrospinal Fluid Biomarkers in the Diagnosis of Creutzfeldt-Jakob Disease in Slovak Patients: over 10-Year Period Review.
Mol Neurobiol
; 54(8): 5919-5927, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27665282
15.
Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002.
BMC Public Health
; 6: 278, 2006 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-17096829
16.
Stability and Reproducibility Underscore Utility of RT-QuIC for Diagnosis of Creutzfeldt-Jakob Disease.
Mol Neurobiol
; 53(3): 1896-1904, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25823511
17.
Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic.
Mol Neurobiol
; 53(4): 2189-99, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25947081
18.
The Priority position paper: Protecting Europe's food chain from prions.
Prion
; 10(3): 165-81, 2016 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27220820
19.
Characteristic CSF prion seeding efficiency in humans with prion diseases.
Mol Neurobiol
; 51(1): 396-405, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24809690
20.
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Neurobiol Aging
; 35(5): 1177-88, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24360565