Eva Mitrova
Bratislava, BL, Slovakia
Last Updated: 09/26/2026
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Found 17 publications
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases.
Journal: Brain : a journal of neurology
Published: March 26, 2021
Genetic Risk Factors of Creutzfeldt-Jakob Disease in the Population of Newborns in Slovakia.
Journal: Pathogens (Basel, Switzerland)
Published: March 04, 2021
Genetic Creutzfeldt-Jakob disease affected monozygotic twins: Analysis of survival time, age at death and possible exogenous risk factors.
Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: November 08, 2018
Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases.
Journal: Molecular neurobiology
Published: May 28, 2018
Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: June 21, 2016
The Priority position paper: Protecting Europe's food chain from prions.
Journal: Prion
Published: May 26, 2016
Cerebrospinal Fluid Biomarkers in the Diagnosis of Creutzfeldt-Jakob Disease in Slovak Patients: over 10-Year Period Review.
Journal: Molecular neurobiology
Published: May 19, 2016
Stability and Reproducibility Underscore Utility of RT-QuIC for Diagnosis of Creutzfeldt-Jakob Disease.
Journal: Molecular neurobiology
Published: December 04, 2014
Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic.
Journal: Molecular neurobiology
Published: November 12, 2014
A pilot study of a genetic CJD risk factor (E200K) in the general Slovak population.
Journal: European journal of epidemiology
Published: April 01, 2014
Characteristic CSF prion seeding efficiency in humans with prion diseases.
Journal: Molecular neurobiology
Published: February 17, 2014
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.
Journal: Neurobiology of aging
Published: July 23, 2013
Last Updated: 09/26/2026