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Adrian Danek

Showing results (71-80 of 264) with videos related to

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Fortschritte Der Neurologie-Psychiatrie|March 1, 2021
[Cognition in Down's Syndrome: Development across the Life Span and Neuropsychological Assessment in Adults]Sandra V Loosli, Luisa Schmidt, Georg Nübling, et al.
Journal of Neurology|June 4, 2020
Seizures in Alzheimer's disease are highly recurrent and associated with a poor disease courseJonathan Vöglein, Ingrid Ricard, Soheyl Noachtar, et al.
Frontiers in Molecular Neuroscience|May 2, 2022
A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in <i>STUB1</i> and Exacerbated by <i>TBP</i> Repeat ExpansionsMarlen Colleen Reis, Julia Patrun, Nibal Ackl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 15, 2010
Characteristic head drops and axial extension in advanced chorea-acanthocytosisSusanne A Schneider, Anthony E Lang, Elena Moro, et al.
Seizure|January 22, 2011
Bilateral temporal lobe epilepsy confirmed with intracranial EEG in chorea-acanthocytosisBenedikt Bader, Christian Vollmar, Nibal Ackl, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 12, 2026
Proceedings of the 12<sup>th</sup> International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related DisordersFabrizio Vacca, Binnaz Yalcin, Lars Kaestner, et al.
Journal of the Neurological Sciences|March 12, 2005
Neuroacanthocytosis: new developments in a neglected group of dementing disordersAdrian Danek, Hans H Jung, Mariarosa A B Melone, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|November 10, 2012
The anatomy of fronto-occipital connections from early blunt dissections to contemporary tractographyStephanie J Forkel, Michel Thiebaut de Schotten, Jamie M Kawadler, et al.
Movement Disorders Clinical Practice|February 13, 2019
FDG-PET in a Case of Very Late-onset Huntington's DiseaseKatharina Feil, Matthias Brendel, Mira Hensler, et al.
Journal of Movement Disorders|January 7, 2024
Basal Ganglia Syndrome in a Male With an XK Gene Variant but Without XK Disease (McLeod Syndrome)Jeryl Ritzi T Yu, Ruth H Walker, Adrian Danek, et al.
Pageof 27

Showing results (71-80 of 264) with videos related to

Sort By:
Pageof 27
Fortschritte Der Neurologie-Psychiatrie|March 1, 2021
[Cognition in Down's Syndrome: Development across the Life Span and Neuropsychological Assessment in Adults]Sandra V Loosli, Luisa Schmidt, Georg Nübling, et al.
Journal of Neurology|June 4, 2020
Seizures in Alzheimer's disease are highly recurrent and associated with a poor disease courseJonathan Vöglein, Ingrid Ricard, Soheyl Noachtar, et al.
Frontiers in Molecular Neuroscience|May 2, 2022
A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in <i>STUB1</i> and Exacerbated by <i>TBP</i> Repeat ExpansionsMarlen Colleen Reis, Julia Patrun, Nibal Ackl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 15, 2010
Characteristic head drops and axial extension in advanced chorea-acanthocytosisSusanne A Schneider, Anthony E Lang, Elena Moro, et al.
Seizure|January 22, 2011
Bilateral temporal lobe epilepsy confirmed with intracranial EEG in chorea-acanthocytosisBenedikt Bader, Christian Vollmar, Nibal Ackl, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 12, 2026
Proceedings of the 12<sup>th</sup> International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related DisordersFabrizio Vacca, Binnaz Yalcin, Lars Kaestner, et al.
Journal of the Neurological Sciences|March 12, 2005
Neuroacanthocytosis: new developments in a neglected group of dementing disordersAdrian Danek, Hans H Jung, Mariarosa A B Melone, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|November 10, 2012
The anatomy of fronto-occipital connections from early blunt dissections to contemporary tractographyStephanie J Forkel, Michel Thiebaut de Schotten, Jamie M Kawadler, et al.
Movement Disorders Clinical Practice|February 13, 2019
FDG-PET in a Case of Very Late-onset Huntington's DiseaseKatharina Feil, Matthias Brendel, Mira Hensler, et al.
Journal of Movement Disorders|January 7, 2024
Basal Ganglia Syndrome in a Male With an XK Gene Variant but Without XK Disease (McLeod Syndrome)Jeryl Ritzi T Yu, Ruth H Walker, Adrian Danek, et al.
Pageof 27