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Inga Zerr

Showing results (41-50 of 358) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|June 11, 2018
Amplification and Detection of Minuscule Amounts of Misfolded Prion Protein by Using the Real-Time Quaking-Induced ConversionMatthias Schmitz, Niccolò Candelise, Franc Llorens, et al.
CNS Spectrums|April 24, 2010
Pulvinar sign in Wernicke's encephalopathyChristian Schmidt, Steffen Plickert, David Summers, et al.
Folia Neuropathologica|August 15, 2006
Clinical findings and diagnostic tests in Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob diseaseAnna Krasnianski, Bettina Meissner, Uta Heinemann, et al.
Handbook of Clinical Neurology|November 8, 2017
Cerebrospinal fluid in Creutzfeldt-Jakob diseaseInga Zerr, Saima Zafar, Matthias Schmitz, et al.
The Lancet. Neurology|January 24, 2026
Advances in biomarkers for diagnosis and prognosis of prion diseasesInga Zerr, Peter Hermann, Tze How Mok, et al.
Plos One|July 11, 2013
Prion peptide uptake in microglial cells--the effect of naturally occurring autoantibodies against prion proteinYvonne Roettger, Inga Zerr, Richard Dodel, et al.
Dementia and Geriatric Cognitive Disorders|March 15, 2012
Alzheimer's disease: genetic polymorphisms and rate of declineChristian Schmidt, Martin Wolff, Nicolas von Ahsen, et al.
Biomolecules|January 23, 2024
Current Technologies Unraveling the Significance of Post-Translational Modifications (PTMs) as Crucial Players in NeurodegenerationSaima Zafar, Shehzadi Irum Fatima, Matthias Schmitz, et al.
The Journal of Clinical Psychiatry|May 5, 2015
Psychiatric symptoms in patients with sporadic Creutzfeldt-Jakob disease in GermanyAnna Krasnianski, Geeske T Bohling, Markus Harden, et al.
Prion|December 18, 2014
Behavioral abnormalities in prion protein knockout mice and the potential relevance of PrP(C) for the cytoskeletonMatthias Schmitz, Saima Zafar, Christopher J Silva, et al.
Pageof 36

Showing results (41-50 of 358) with videos related to

Sort By:
Pageof 36
Methods in Molecular Biology (Clifton, N.J.)|June 11, 2018
Amplification and Detection of Minuscule Amounts of Misfolded Prion Protein by Using the Real-Time Quaking-Induced ConversionMatthias Schmitz, Niccolò Candelise, Franc Llorens, et al.
CNS Spectrums|April 24, 2010
Pulvinar sign in Wernicke's encephalopathyChristian Schmidt, Steffen Plickert, David Summers, et al.
Folia Neuropathologica|August 15, 2006
Clinical findings and diagnostic tests in Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob diseaseAnna Krasnianski, Bettina Meissner, Uta Heinemann, et al.
Handbook of Clinical Neurology|November 8, 2017
Cerebrospinal fluid in Creutzfeldt-Jakob diseaseInga Zerr, Saima Zafar, Matthias Schmitz, et al.
The Lancet. Neurology|January 24, 2026
Advances in biomarkers for diagnosis and prognosis of prion diseasesInga Zerr, Peter Hermann, Tze How Mok, et al.
Plos One|July 11, 2013
Prion peptide uptake in microglial cells--the effect of naturally occurring autoantibodies against prion proteinYvonne Roettger, Inga Zerr, Richard Dodel, et al.
Dementia and Geriatric Cognitive Disorders|March 15, 2012
Alzheimer's disease: genetic polymorphisms and rate of declineChristian Schmidt, Martin Wolff, Nicolas von Ahsen, et al.
Biomolecules|January 23, 2024
Current Technologies Unraveling the Significance of Post-Translational Modifications (PTMs) as Crucial Players in NeurodegenerationSaima Zafar, Shehzadi Irum Fatima, Matthias Schmitz, et al.
The Journal of Clinical Psychiatry|May 5, 2015
Psychiatric symptoms in patients with sporadic Creutzfeldt-Jakob disease in GermanyAnna Krasnianski, Geeske T Bohling, Markus Harden, et al.
Prion|December 18, 2014
Behavioral abnormalities in prion protein knockout mice and the potential relevance of PrP(C) for the cytoskeletonMatthias Schmitz, Saima Zafar, Christopher J Silva, et al.
Pageof 36