Search Results - "Golanska, Ewa"
-
1
Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic
Published in Molecular neurobiology (01-05-2016)“…At present, the testing of 14-3-3 protein in cerebrospinal fluid (CSF) is a standard biomarker test in suspected sporadic Creutzfeldt-Jakob disease (sCJD)…”
Get full text
Journal Article -
2
Cerebrospinal Fluid Biomarker-Based Diagnosis of Sporadic Creutzfeldt-Jakob Disease: A Validation Study for Previously Established Cutoffs
Published in Dementia and geriatric cognitive disorders (01-01-2017)“…Several biomarkers have been proposed to discriminate sporadic Creutzfeldt-Jakob disease (sCJD) from other dementias and control cases. However, their clinical…”
Get more information
Journal Article -
3
Screening for THAP1 Mutations in Polish Patients with Dystonia Shows Known and Novel Substitutions
Published in PloS one (18-06-2015)“…The aim of this study was to assess the presence of DYT6 mutations in Polish patients with isolated dystonia and to characterize their phenotype. We sequenced…”
Get full text
Journal Article -
4
Arrested neural and advanced mesenchymal differentiation of glioblastoma cells-comparative study with neural progenitors
Published in BMC cancer (14-02-2009)“…Although features of variable differentiation in glioblastoma cell cultures have been reported, a comparative analysis of differentiation properties of normal…”
Get full text
Journal Article -
5
High variability of clinical symptoms in a Polish family with a novel THAP1 mutation
Published in International journal of neuroscience (03-10-2015)“…Background. Mutations in the THAP1 gene are associated with a broad spectrum of dystonia including focal and generalized forms. Missense, nonsense and…”
Get full text
Journal Article -
6
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases
Published in Brain (London, England : 1878) (18-04-2022)“…Genetic prion diseases are a rare and diverse group of fatal neurodegenerative disorders caused by pathogenic sequence variations in the prion protein gene,…”
Get full text
Journal Article -
7
Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases
Published in Alzheimer's & dementia (01-06-2018)“…Neurofilament light (NFL) levels in the cerebrospinal fluid are increased in several neurodegenerative dementias. However, their diagnostic accuracy in the…”
Get full text
Journal Article -
8
Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases
Published in Alzheimer's & dementia (01-06-2017)“…Abstract Introduction Accurate diagnosis of prion diseases and discrimination from alternative dementias gain importance in the clinical routine, but partial…”
Get full text
Journal Article -
9
Validation of α-Synuclein as a CSF Biomarker for Sporadic Creutzfeldt-Jakob Disease
Published in Molecular neurobiology (01-03-2018)“…The analysis of cerebrospinal fluid (CSF) biomarkers gains importance in the differential diagnosis of prion diseases. However, no single diagnostic tool or…”
Get full text
Journal Article -
10
PRND 3′UTR polymorphism may be associated with behavioral disturbances in Alzheimer disease
Published in Prion (01-01-2012)“…The etiology of behavioral and psychological symptoms of dementia (BPSD) is complex, including putative biological, psychological, social and environmental…”
Get full text
Journal Article -
11
Mitochondrial DNA differentiates Alzheimer's disease from Creutzfeldt-Jakob disease
Published in Alzheimer's & dementia (01-05-2016)“…Low content of cell-free mitochondrial DNA (mtDNA) in cerebrospinal fluid (CSF) is a biomarker of early stage Alzheimer's disease (AD), but whether mtDNA is…”
Get full text
Journal Article -
12
Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease
Published in Journal of clinical neuroscience (01-02-2019)“…•Cerebrospinal fluid Neurofilament Light is increased in sCJD.•CSF Neurofilament in sCJD was associated neither to age nor to sex.•CSF Neurofilament in sCJD…”
Get full text
Journal Article -
13
Mitochondrial DNA differentiates Alzheimer from Creutzfeldt-Jakob disease
Published in Alzheimer's & dementia (2016)“…Abstract Introduction Low content of cell-free mitochondrial DNA (mtDNA) in cerebrospinal fluid (CSF) is a biomarker of early stage Alzheimer's disease (AD),…”
Get full text
Journal Article -
14
Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease
Published in Journal of clinical neuroscience (01-02-2019)“…Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of human prion disease. It is invariably fatal and displays a short clinical disease stage…”
Get full text
Journal Article -
15
Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases
Published in Alzheimer's & dementia (01-06-2018)“…Introduction: neurofilament light (NFL) levels in the cerebrospinal fluid are increased in several neurodegenerative dementias. However, their diagnostic…”
Get full text
Journal Article -
16
Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases
Published in Alzheimer's & dementia (01-06-2018)“…Introduction: neurofilament light (NFL) levels in the cerebrospinal fluid are increased in several neurodegenerative dementias. However, their diagnostic…”
Get full text
Journal Article -
17
Selection of reference genes for gene expression studies in astrocytomas
Published in Analytical biochemistry (2011)“…This study was aimed to test a panel of six housekeeping genes ( GAPDH, HPRT1, POLR2A, RPLP0, ACTB, and H3F) so as to identify and validate the most suitable…”
Get full text
Journal Article -
18
APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians
Published in Experimental gerontology (01-04-2013)“…APBB2 gene encodes for β-amyloid precursor protein-binding family B member 2, (APBB2, FE65-like, FE65L1), an adaptor protein binding to the cytoplasmatic…”
Get full text
Journal Article -
19
Cerebrospinal fluid markers of prion diseases
Published in Neurologia i neurochirurgia polska (01-09-2008)“…There are no non-invasive tests allowing for definite premortem diagnosis of Creutzfeldt-Jakob disease (CJD). The paper presents the current knowledge about…”
Get more information
Journal Article -
20
Białko 14-3-3 w diagnostyce sporadycznej choroby Creutzfeldta-Jakoba
Published in Aktualności neurologiczne (01-04-2011)“…Choroba Creutzfeldta-Jakoba (CJD) należy do grupy chorób wywoływanych przez priony, w których do ustalenia definitywnego rozpoznania konieczne jest badanie…”
Get full text
Journal Article