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Dagmar Timmann

Showing results (191-200 of 269) with videos related to

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Journal of Neurology|June 16, 2024
An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX studyAlessandra Scaravilli, Ilaria Gabusi, Gaia Mari, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 1, 2022
Bi-Allelic COQ4 Variants Cause Adult-Onset Ataxia-Spasticity Spectrum DiseaseIsabell Cordts, Luisa Semmler, Jannik Prasuhn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 26, 2025
The cerebellum contributes to prediction error coding in reinforcement learning in humansDana M Huvermann, Adam M Berlijn, Andreas Thieme, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 7, 2024
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX StudyAlessandra Scaravilli, Davide Negroni, Claudio Senatore, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
Comparison of three clinical rating scales in Friedreich ataxia (FRDA)Katrin Bürk, Ulrike Mälzig, Stefanie Wolf, et al.
Brain : a Journal of Neurology|May 21, 2016
Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrumInès Mademan, Florian Harmuth, Ilaria Giordano, et al.
Neuroimage|July 28, 2009
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6Jörg B Schulz, Johannes Borkert, Stefanie Wolf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6Christoph Globas, Sophie Tezenas du Montcel, Laslo Baliko, et al.
Movement Disorders Clinical Practice|October 27, 2018
Standardized Assessment of Hereditary Ataxia Patients in Clinical StudiesBrigitte K Paap, Sandra Roeske, Alexandra Durr, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 3, 2023
Intronic <i>FGF14</i> GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathyDavid Pellerin, Carlo Wilke, Andreas Traschütz, et al.
Pageof 27

Showing results (191-200 of 269) with videos related to

Sort By:
Pageof 27
Journal of Neurology|June 16, 2024
An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX studyAlessandra Scaravilli, Ilaria Gabusi, Gaia Mari, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 1, 2022
Bi-Allelic COQ4 Variants Cause Adult-Onset Ataxia-Spasticity Spectrum DiseaseIsabell Cordts, Luisa Semmler, Jannik Prasuhn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 26, 2025
The cerebellum contributes to prediction error coding in reinforcement learning in humansDana M Huvermann, Adam M Berlijn, Andreas Thieme, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 7, 2024
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX StudyAlessandra Scaravilli, Davide Negroni, Claudio Senatore, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
Comparison of three clinical rating scales in Friedreich ataxia (FRDA)Katrin Bürk, Ulrike Mälzig, Stefanie Wolf, et al.
Brain : a Journal of Neurology|May 21, 2016
Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrumInès Mademan, Florian Harmuth, Ilaria Giordano, et al.
Neuroimage|July 28, 2009
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6Jörg B Schulz, Johannes Borkert, Stefanie Wolf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6Christoph Globas, Sophie Tezenas du Montcel, Laslo Baliko, et al.
Movement Disorders Clinical Practice|October 27, 2018
Standardized Assessment of Hereditary Ataxia Patients in Clinical StudiesBrigitte K Paap, Sandra Roeske, Alexandra Durr, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 3, 2023
Intronic <i>FGF14</i> GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathyDavid Pellerin, Carlo Wilke, Andreas Traschütz, et al.
Pageof 27