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Eva C Schulte

Showing results (11-20 of 92) with videos related to

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Der Nervenarzt|May 29, 2026
[Associations Between Genetic Causes of Psychiatric Disorders and Rare Monogenic Epilepsies]Caroline Baumgartner, Tobias Baumgartner, Alexandra Philipsen, et al.
Annals of Neurology|June 3, 2010
Acyclovir resistance in herpes simplex encephalitisEva C Schulte, Andreas Sauerbrei, Dieter Hoffmann, et al.
Journal of Neuroinflammation|January 31, 2019
Cerebrovascular manifestations of herpes simplex virus infection of the central nervous system: a systematic reviewLarissa Hauer, Slaven Pikija, Eva C Schulte, et al.
Frontiers in Neuroscience|February 28, 2022
Editorial: Cross-disorder Genetics in NeuropsychiatryEvelien Van Assche, Eva C Schulte, Ole A Andreassen, et al.
Plos One|April 27, 2010
Characterization of age-dependent and progressive cortical neuronal degeneration in presenilin conditional mutant miceMary Wines-Samuelson, Eva C Schulte, Miriam J Smith, et al.
Human Genome Variation|April 16, 2016
Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's diseaseEva C Schulte, Alexander Kurz, Panagiotis Alexopoulos, et al.
Der Nervenarzt|June 23, 2025
[Genetically informed treatment in psychiatry: new dynamics through APOE and antibody treatment of Alzheimer's disease]Daniel J Müller, Christine M Freitag, Urs Heilbronner, et al.
European Journal of Neurology|January 11, 2021
Cerebral venous thrombosis and severe acute respiratory syndrome coronavirus-2 infection: A systematic review and meta-analysisTommaso Baldini, Gian Maria Asioli, Michele Romoli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2013
Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulationEva C Schulte, Malte C Claussen, Angela Jochim, et al.
Neurogenetics|June 19, 2012
Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's diseaseEva C Schulte, Brit Mollenhauer, Alexander Zimprich, et al.
Pageof 10

Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
Der Nervenarzt|May 29, 2026
[Associations Between Genetic Causes of Psychiatric Disorders and Rare Monogenic Epilepsies]Caroline Baumgartner, Tobias Baumgartner, Alexandra Philipsen, et al.
Annals of Neurology|June 3, 2010
Acyclovir resistance in herpes simplex encephalitisEva C Schulte, Andreas Sauerbrei, Dieter Hoffmann, et al.
Journal of Neuroinflammation|January 31, 2019
Cerebrovascular manifestations of herpes simplex virus infection of the central nervous system: a systematic reviewLarissa Hauer, Slaven Pikija, Eva C Schulte, et al.
Frontiers in Neuroscience|February 28, 2022
Editorial: Cross-disorder Genetics in NeuropsychiatryEvelien Van Assche, Eva C Schulte, Ole A Andreassen, et al.
Plos One|April 27, 2010
Characterization of age-dependent and progressive cortical neuronal degeneration in presenilin conditional mutant miceMary Wines-Samuelson, Eva C Schulte, Miriam J Smith, et al.
Human Genome Variation|April 16, 2016
Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's diseaseEva C Schulte, Alexander Kurz, Panagiotis Alexopoulos, et al.
Der Nervenarzt|June 23, 2025
[Genetically informed treatment in psychiatry: new dynamics through APOE and antibody treatment of Alzheimer's disease]Daniel J Müller, Christine M Freitag, Urs Heilbronner, et al.
European Journal of Neurology|January 11, 2021
Cerebral venous thrombosis and severe acute respiratory syndrome coronavirus-2 infection: A systematic review and meta-analysisTommaso Baldini, Gian Maria Asioli, Michele Romoli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2013
Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulationEva C Schulte, Malte C Claussen, Angela Jochim, et al.
Neurogenetics|June 19, 2012
Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's diseaseEva C Schulte, Brit Mollenhauer, Alexander Zimprich, et al.
Pageof 10