Zobrazeno 1 - 5
of 5
pro vyhledávání: '"cerebrospinal fluid [Prions]"'
Publikováno v:
Amsterdam [u.a.] : Elsevier, Handbook of Clinical Neurology 146, 115-124 (2018). doi:10.1016/B978-0-12-804279-3.00008-3
Cerebrospinal Fluid in Neurologic Disorders / Zerr, Inga ; : Elsevier, 2018, ; ISSN: 00729752 ; ISBN: 9780128042793 ; doi:10.1016/B978-0-12-804279-3.00008-3
Cerebrospinal Fluid in Neurologic Disorders / Zerr, Inga ; : Elsevier, 2018, ; ISSN: 00729752 ; ISBN: 9780128042793 ; doi:10.1016/B978-0-12-804279-3.00008-3
Cerebrospinal fluid (CSF) contains a dynamic and complex mixture of proteins, which reflects physiologic or pathologic states of the central nervous system. Changes in CSF proteome have been described in various neurodegenerative disorders. Earliest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbc4f86b069fe0925e180dbcb842d476
Autor:
Inga Zerr, Peter Hermann, Katharina Stoeck, Tatjana Poliakova, Saima Zafar, Matthias Schmitz, Franc Llorens, Elisabeth Ebert, Pantelis Oikonomou, Christian Schmidt
Publikováno v:
Neurobiology of aging 36(9), 2597-2606 (2015). doi:10.1016/j.neurobiolaging.2015.05.013
Understanding inflammatory mechanisms in vascular dementia (VD) is pivotal for achieving better insights into changes in brain metabolism. We performed cytokine profiling and measured levels of the cellular prion protein (PrP(C)) in serum and cerebro
Autor:
Ângela Correia, Juan José Badiola, Rosa Bolea, Inga Zerr, Peter Lange, Franc Llorens, Ingolf Lachmann, Matthias Schmitz, Tomás Barrio, Katrin Thüne, Anna Villar-Piqué
Publikováno v:
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2018, 55 (11), pp.8586-8591. ⟨10.1007/s12035-018-1014-z⟩
Molecular neurobiology 55(11), 8586-8591 (2018). doi:10.1007/s12035-018-1014-z
Molecular Neurobiology, Humana Press, 2018, 55 (11), pp.8586-8591. ⟨10.1007/s12035-018-1014-z⟩
Molecular neurobiology 55(11), 8586-8591 (2018). doi:10.1007/s12035-018-1014-z
The analysis of the cerebrospinal fluid (CSF) biomarkers in patients with suspected prion diseases became a useful tool in diagnostic routine. Prion diseases can only be identified at clinical stages when the disease already spread throughout the bra
Autor:
Isidre Ferrer, Belén Ansoleaga, José Antonio del Río, Ellen Gelpi, Irene López-González, Saima Zafar, Jordi Yagüe, Margarita Carmona, Carlos Nos, Inga Zerr, Franc Llorens, Paula Garcia-Esparcia, R. Blanco, Oriol Grau-Rivera
Publikováno v:
Prion 7(5), 383-393 (2013). doi:10.4161/pri.26416
Creutzfeldt-Jakob disease (CJD) is a heterogenic neurodegenerative disorder associated with abnormal post-translational processing of cellular prion protein (PrP(c)). CJD displays distinctive clinical and pathological features which correlate with th
Autor:
Saima Zafar, Franziska Kuhn, Maria Cramm, André Karch, Daniela Varges, Alex Raeber, Inga Zerr, Matthias Schmitz, Eva Mitrova, Bjoern Schroeder
Publikováno v:
Molecular Neurobiology
Molecular neurobiology 51(1), 396-405 (2014). doi:10.1007/s12035-014-8709-6
Molecular neurobiology 51(1), 396-405 (2014). doi:10.1007/s12035-014-8709-6
The development of in vitro amplification systems allows detecting femtomolar amounts of prion protein scrapie (PrPSc) in human cerebrospinal fluid (CSF). We performed a CSF study to determine the effects of prion disease type, codon 129 genotype, Pr