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Inga Zerr

Showing results (81-90 of 358) with videos related to

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Cell and Tissue Research|December 19, 2022
Role of different recombinant PrP substrates in the diagnostic accuracy of the CSF RT-QuIC assay in Creutzfeldt-Jakob diseaseSusana Margarida Da Silva Correia, Matthias Schmitz, Andre Fischer, et al.
Translational Neurodegeneration|May 8, 2022
A new paradigm for diagnosis of neurodegenerative diseases: peripheral exosomes of brain originNeelam Younas, Leticia Camila Fernandez Flores, Franziska Hopfner, et al.
Acta Neurologica Belgica|December 7, 2011
Sporadic CJD in a patient with relaplsing-remitting multiple sclerosis on an immunomodulatory treatmentTereza Gabelić, Mario Habek, Inga Zerr, et al.
Journal of Neuropathology and Experimental Neurology|July 18, 2013
Filtration of protein aggregates increases the accuracy for diagnosing prion diseases in brain biopsiesWiebke M Wemheuer, Arne Wrede, Joanna Gawinecka, et al.
Journal of Neurology|February 27, 2014
Diagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference CenterAndré Karch, Lena Maria Raddatz, Claudia Ponto, et al.
Molecular Neurobiology|January 7, 2014
Anchorless 23-230 PrPC interactomics for elucidation of PrPC protective roleSaima Zafar, Abdul R Asif, Sanja Ramljak, et al.
Gerontology|February 16, 2005
Creutzfeldt-Jakob disease and homocysteine levels in plasma and cerebrospinal fluidStefan Bleich, Markus Otto, Inga Zerr, et al.
Neuroscience Letters|November 3, 2004
Plasminogen activities and concentrations in patients with sporadic Creutzfeldt-Jakob diseaseInga Zerr, Monika Bodemer, Ulrich Kaboth, et al.
Prion|January 24, 2009
Anti-LRP/LR antibody W3 hampers peripheral PrPSc propagation in scrapie infected miceChantal Zuber, Gerda Mitteregger, Claudia Pace, et al.
Neuro-Degenerative Diseases|January 4, 2012
Desmoplakin as a potential candidate for cerebrospinal fluid marker to rule out 14-3-3 false positive rates in sporadic Creutzfeldt-Jakob disease differential diagnosisJoanna Gawinecka, Barbara Ciesielczyk, Pascual Sanchez-Juan, et al.
Pageof 36

Showing results (81-90 of 358) with videos related to

Sort By:
Pageof 36
Cell and Tissue Research|December 19, 2022
Role of different recombinant PrP substrates in the diagnostic accuracy of the CSF RT-QuIC assay in Creutzfeldt-Jakob diseaseSusana Margarida Da Silva Correia, Matthias Schmitz, Andre Fischer, et al.
Translational Neurodegeneration|May 8, 2022
A new paradigm for diagnosis of neurodegenerative diseases: peripheral exosomes of brain originNeelam Younas, Leticia Camila Fernandez Flores, Franziska Hopfner, et al.
Acta Neurologica Belgica|December 7, 2011
Sporadic CJD in a patient with relaplsing-remitting multiple sclerosis on an immunomodulatory treatmentTereza Gabelić, Mario Habek, Inga Zerr, et al.
Journal of Neuropathology and Experimental Neurology|July 18, 2013
Filtration of protein aggregates increases the accuracy for diagnosing prion diseases in brain biopsiesWiebke M Wemheuer, Arne Wrede, Joanna Gawinecka, et al.
Journal of Neurology|February 27, 2014
Diagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference CenterAndré Karch, Lena Maria Raddatz, Claudia Ponto, et al.
Molecular Neurobiology|January 7, 2014
Anchorless 23-230 PrPC interactomics for elucidation of PrPC protective roleSaima Zafar, Abdul R Asif, Sanja Ramljak, et al.
Gerontology|February 16, 2005
Creutzfeldt-Jakob disease and homocysteine levels in plasma and cerebrospinal fluidStefan Bleich, Markus Otto, Inga Zerr, et al.
Neuroscience Letters|November 3, 2004
Plasminogen activities and concentrations in patients with sporadic Creutzfeldt-Jakob diseaseInga Zerr, Monika Bodemer, Ulrich Kaboth, et al.
Prion|January 24, 2009
Anti-LRP/LR antibody W3 hampers peripheral PrPSc propagation in scrapie infected miceChantal Zuber, Gerda Mitteregger, Claudia Pace, et al.
Neuro-Degenerative Diseases|January 4, 2012
Desmoplakin as a potential candidate for cerebrospinal fluid marker to rule out 14-3-3 false positive rates in sporadic Creutzfeldt-Jakob disease differential diagnosisJoanna Gawinecka, Barbara Ciesielczyk, Pascual Sanchez-Juan, et al.
Pageof 36