Zobrazeno 1 - 10
of 27
pro vyhledávání: '"cerebrospinal fluid [Creutzfeldt-Jakob Syndrome]"'
Autor:
Samir Abu-Rumeileh, Peggy Barschke, Patrick Oeckl, Simone Baiardi, Angela Mammana, Andrea Mastrangelo, Mhd Rami Al Shweiki, Petra Steinacker, Anna Ladogana, Sabina Capellari, Markus Otto, Piero Parchi
Publikováno v:
International journal of molecular sciences 23(4), 2051 (2022). doi:10.3390/ijms23042051
Proenkephalin (PENK) and prodynorphin (PDYN) are endogenous opioid peptides mainly produced in the striatum and, to a lesser extent, in the cerebral cortex. Dysregulated metabolism and altered cerebrospinal fluid (CSF) levels of PENK and PDYN have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0f0f169ec3d2bec56ffd9935f874906
Autor:
David Mengel, Tze How Mok, Akin Nihat, Wen Liu, Robert A. Rissman, Douglas Galasko, Henrik Zetterberg, Simon Mead, John Collinge, Dominic M. Walsh
Publikováno v:
Cells 10(12), 3514 (2021). doi:10.3390/cells10123514 special issue: "Biomarkers of Alzheimer’s Disease: New Insights"
Cells
Cells; Volume 10; Issue 12; Pages: 3514
Cells, Vol 10, Iss 3514, p 3514 (2021)
Cells
Cells; Volume 10; Issue 12; Pages: 3514
Cells, Vol 10, Iss 3514, p 3514 (2021)
This study investigates the diagnostic and prognostic potential of different forms of tau in biofluids from patients with Creutzfeldt-Jakob disease (CJD). Extracellular tau, which is molecularly heterogeneous, was measured using ultra-sensitive custo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a219f92400312281a1ff784ae8f39b17
https://pub.dzne.de/record/163418
https://pub.dzne.de/record/163418
Autor:
Anna Villar-Piqué, Ingolf Lachmann, Stefan Goebel, Katharina Waniek, Inga Zerr, Franc Llorens, Matthias Schmitz, Peter Hermann
Publikováno v:
Journal of neurology 267(2), 543-550 (2019). doi:10.1007/s00415-019-09610-8
Cerebrospinal fluid (CSF) non-phosphorylated tau (non-p-tau) is increased in sporadic Creutzfeldt–Jakob disease (CJD), but its accuracy in the differential diagnosis has not been previously established. Here, we first used a retrospective cohort of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::999dabc7fb21381b148b4afc241b0ea9
Autor:
Dimitra Dafou, Matthias Schmitz, Theodoros Sklaviadis, Inga Zerr, Dietmar Appelhans, Anna Villar-Piqué, Katrin Thüne, Eirini Kanata, Niccolò Candelise, Susana Margarida da Silva Correia, Franc Llorens
Publikováno v:
Molecular neurobiology 57(4), 1863-1874 (2019). doi:10.1007/s12035-019-01837-w
Prion diseases, such as the sporadic Creutzfeldt-Jakob disease (sCJD), are a class of fatal neurodegenerative disorders. Currently, there is no efficient treatment or therapy available. Hence, the search for molecules that may inhibit the conversion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c395b621418f299b2c2ed833e17bf6c2
https://pub.dzne.de/record/145025
https://pub.dzne.de/record/145025
Autor:
Llorens, Franc, Villar-Piqué, Anna, Hermann, Peter, Schmitz, Matthias, Calero, Olga, Stehmann, Christiane, Sarros, Shannon, Moda, Fabio, Ferrer, Isidre, Poleggi, Anna, Pocchiari, Maurizio, Catania, Marcella, Klotz, Sigrid, O'Regan, Carl, Brett, Francesca, Heffernan, Josephine, Ladogana, Anna, Collins, Steven J, Calero, Miguel, Kovacs, Gabor G, Zerr, Inga
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Biomolecules, Vol 10, Iss 2, p 290 (2020)
Biomolecules 10(2), 290 (2020). doi:10.3390/biom10020290
Biomolecules
Volume 10
Issue 2
Repisalud
Instituto de Salud Carlos III (ISCIII)
Universidad de Barcelona
Biomolecules, Vol 10, Iss 2, p 290 (2020)
Biomolecules 10(2), 290 (2020). doi:10.3390/biom10020290
Biomolecules
Volume 10
Issue 2
Repisalud
Instituto de Salud Carlos III (ISCIII)
Human prion diseases are classified into sporadic, genetic, and acquired forms. Within this last group, iatrogenic Creutzfeldt&ndash
Jakob disease (iCJD) is caused by human-to-human transmission through surgical and medical procedures. After rea
Jakob disease (iCJD) is caused by human-to-human transmission through surgical and medical procedures. After rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::881f9e30ba11bb50bfed9b0956c6a5b3
http://hdl.handle.net/2445/173289
http://hdl.handle.net/2445/173289
Autor:
Peter Hermann, Philip Haller, Stefan Goebel, Timothy Bunck, Christian Schmidt, Jens Wiltfang, Inga Zerr
Publikováno v:
Viruses; Volume 14; Issue 2; Pages: 276
Viruses 14(2), 276 (2022). doi:10.3390/v14020276
Viruses 14(2), 276 (2022). doi:10.3390/v14020276
Background: CSF total-tau (t-tau) became a standard cerebrospinal fluid biomarker in Alzheimer’s disease (AD). In parallel, extremely elevated levels were observed in Creutzfeldt-Jakob disease (CJD). Therefore, tau is also considered as an alternat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47346473aae9ca52d3187dd390d5643a
https://doi.org/10.3390/v14020276
https://doi.org/10.3390/v14020276
Autor:
Peter Hermann, Isidro Ferrer Abizanda, Enric Vidal, Kaj Blennow, Henrik Zetterberg, Anna Villar-Piqué, Matthias Schmitz, Daniela Diaz-Lucena, André Karch, Franc Llorens, Inga Zerr
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry 90(8), 846-853 (2019). doi:10.1136/jnnp-2018-320155
IRTA Pubpro. Open Digital Archive
Institut de Recerca i Tecnologia Agroalimentàries (IRTA)
Journal of neurology, neurosurgery, and psychiatry
England
IRTA Pubpro. Open Digital Archive
Institut de Recerca i Tecnologia Agroalimentàries (IRTA)
Journal of neurology, neurosurgery, and psychiatry
England
ObjectiveTo investigate whether cerebrospinal fluid (CSF) neurogranin concentrations are altered in sporadic Creutzfeldt-Jakob disease (CJD), comparatively with Alzheimer’s disease (AD), and associated with neuronal degeneration in brain tissue.Met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fda046573d2ed197bc3c0c8aff6de21
Autor:
Beata Sikorska, Isidro Ferrer, André Karch, Pawel P. Liberski, Konstantinos Xanthopoulos, Dimitra Dafou, Anna Villar-Piqué, Franc Llorens, Matthias Schmitz, Ewa Golanska, Aikaterini Karsanidou, Inga Zerr, Theodoros Sklaviadis, Eirini Kanata
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of clinical neuroscience 60, 124-127 (2019). doi:10.1016/j.jocn.2018.09.031
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of clinical neuroscience 60, 124-127 (2019). doi:10.1016/j.jocn.2018.09.031
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. The key event in sCJD is the propagation of a beta-sheet rich conformer of the physiological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c514d45b8d77e7850cd8bbb145c2fc09
https://pubmed.ncbi.nlm.nih.gov/30309804
https://pubmed.ncbi.nlm.nih.gov/30309804
Autor:
Steinacker, Petra, Verde, Federico, Fliessbach, Klaus, Foerstl, Hans, Giese, Armin, Jahn, Holger, Kassubek, Jan, Kornhuber, Johannes, Landwehrmeyer, G Bernhard, Lauer, Martin, Pinkhardt, Elmar Hans, Prudlo, Johannes, Fang, Lubin, Rosenbohm, Angela, Schneider, Anja, Schroeter, Matthias L, Tumani, Hayrettin, von Arnim, Christine A F, Weishaupt, Jochen, Weydt, Patrick, Ludolph, Albert C, Yilmazer Hanke, Deniz, Otto, Markus, Feneberg, Emily, group, FTLDc study, Ackl, Nibal, Arlt, Sönke, Albrecht, Franziska, Bisenius, Sandrine, Gehlhaar, Svenja, Gleiss, Jakob, Halder, Theresa, Lehmbeck, Jan, Lampe, Leonie, Oeckl, Patrick, Levin, Johannes, Maler, Manuel, Oberhauser, Felix, Oberstein, Timo, Prix, Catharina, Raiser, Theresa, Richter-Schmiedinger, Tanja, Saur, Dorothee, Schachner, Lisa, Schönecker, Sonja, Roeber, Sigrun, Schuemberg, Katharina, Stenglein-Krapf, Gisela, Wlasich, Elisabeth, Anderl-Straub, Sarah, Danek, Adrian, Diehl-Schmid, Janine, Fassbender, Klaus
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry
Journal of neurology, neurosurgery, and psychiatry 89(3), 239-247 (2018). doi:10.1136/jnnp-2017-317138
Journal of neurology, neurosurgery, and psychiatry 89(3), 239-247 (2018). doi:10.1136/jnnp-2017-317138
ObjectivesNeurochemical markers of amyotrophic lateral sclerosis (ALS) that reflect underlying disease mechanisms might help in diagnosis, staging and prediction of outcome. We aimed at determining the origin and differential diagnostic and prognosti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcf6063172be297370e16198878fca46
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