Search Results - "Golanska, Ewa"

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    Cerebrospinal Fluid Biomarker-Based Diagnosis of Sporadic Creutzfeldt-Jakob Disease: A Validation Study for Previously Established Cutoffs by Llorens, Franc, Karch, André, Golanska, Ewa, Schmitz, Matthias, Lange, Peter, Sikorska, Beata, Liberski, Pawel P, Zerr, Inga

    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…”
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    Journal Article
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    Screening for THAP1 Mutations in Polish Patients with Dystonia Shows Known and Novel Substitutions by Golanska, Ewa, Gajos, Agata, Sieruta, Monika, Szybka, Malgorzata, Rudzinska, Monika, Ochudlo, Stanislaw, Kmiec, Tomasz, Liberski, Pawel P, Bogucki, Andrzej

    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…”
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    High variability of clinical symptoms in a Polish family with a novel THAP1 mutation by Gajos, Agata, Golańska, Ewa, Sieruta, Monika, Szybka, Małgorzata, Liberski, Paweł P., Bogucki, Andrzej

    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…”
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    Validation of α-Synuclein as a CSF Biomarker for Sporadic Creutzfeldt-Jakob Disease by Llorens, Franc, Kruse, Niels, Karch, André, Schmitz, Matthias, Zafar, Saima, Gotzmann, Nadine, Sun, Ting, Köchy, Silja, Knipper, Tobias, Cramm, Maria, Golanska, Ewa, Sikorska, Beata, Liberski, Pawel P., Sánchez-Valle, Raquel, Fischer, Andre, Mollenhauer, Brit, Zerr, Inga

    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…”
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    PRND 3′UTR polymorphism may be associated with behavioral disturbances 
in Alzheimer disease by Flirski, Marcin, Sieruta, Monika, Golanska, Ewa, Kłoszewska, Iwona, Liberski, Paweł P., Sobow, Tomasz M.

    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…”
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    Mitochondrial DNA differentiates Alzheimer's disease from Creutzfeldt-Jakob disease by Podlesniy, Petar, Llorens, Franc, Golanska, Ewa, Sikorska, Beata, Liberski, Pawel, Zerr, Inga, Trullas, Ramon

    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…”
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    Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease by Kanata, Eirini, Golanska, Ewa, Villar-Piqué, Anna, Karsanidou, Aikaterini, Dafou, Dimitra, Xanthopoulos, Konstantinos, Schmitz, Matthias, Ferrer, Isidro, Karch, André, Sikorska, Beata, Liberski, Pawel P., Sklaviadis, Theodoros, Zerr, Inga, Llorens, Franc

    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…”
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    Mitochondrial DNA differentiates Alzheimer from Creutzfeldt-Jakob disease by Podlesniy, Petar, Llorens, Franc, Golanska, Ewa, Sikorska, Beata, Liberski, Pawel, Zerr, Inga, Trullas, Ramon

    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),…”
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    Selection of reference genes for gene expression studies in astrocytomas by Gresner, Sylwia M., Golanska, Ewa, Kulczycka-Wojdala, Dominika, Jaskolski, Dariusz J., Papierz, Wielislaw, Liberski, Pawel P.

    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…”
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    APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians by Golanska, Ewa, Sieruta, Monika, Gresner, Sylwia M., Pfeffer, Anna, Chodakowska-Zebrowska, Malgorzata, Sobow, Tomasz M., Klich, Izabela, Mossakowska, Malgorzata, Szybinska, Aleksandra, Barcikowska, Maria, Liberski, Pawel P.

    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…”
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    Cerebrospinal fluid markers of prion diseases by Golańska, Ewa, Gresner, Sylwia, Sieruta, Monika, Liberski, Paweł

    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…”
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    Białko 14-3-3 w diagnostyce sporadycznej choroby Creutzfeldta-Jakoba by Ewa Golańska, Paweł P. Liberski

    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…”
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