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Demet Önder

Showing results (1-10 of 9) with videos related to

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Movement Disorders Clinical Practice|September 29, 2023
Comparison of Live and Remote Video Ratings of the Scale for Assessment and Rating of AtaxiaArian Taheri Amin, Jennifer Faber, Demet Önder, et al.
Epilepsy & Behavior : E&B|March 22, 2020
CD19+ B-cells in autoantibody-negative limbic encephalitisNiels Hansen, Demet Önder, Kerstin Schwing, et al.
Journal of Translational Autoimmunity|October 17, 2022
Increased T- and B-cells associated with the phenotype of autoimmune limbic encephalitis with mainly memory dysfunctionNiels Hansen, Guido Widman, Demet Önder, et al.
Epilepsy & Behavior : E&B|December 18, 2019
Low CSF CD4/CD8+ T-cell proportions are associated with blood-CSF barrier dysfunction in limbic encephalitisNiels Hansen, Kerstin Schwing, Demet Önder, et al.
Ebiomedicine|April 24, 2025
The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohortDanique Beijer, David Mengel, Demet Önder, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 14, 2022
Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERD<sub>ND</sub> ): Time to Move Beyond the SkinIsabell Cordts, Demet Önder, Andreas Traschütz, et al.
Ebiomedicine|December 24, 2025
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichmentHannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
Nature Genetics|June 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Movement Disorders Clinical Practice|September 29, 2023
Comparison of Live and Remote Video Ratings of the Scale for Assessment and Rating of AtaxiaArian Taheri Amin, Jennifer Faber, Demet Önder, et al.
Epilepsy & Behavior : E&B|March 22, 2020
CD19+ B-cells in autoantibody-negative limbic encephalitisNiels Hansen, Demet Önder, Kerstin Schwing, et al.
Journal of Translational Autoimmunity|October 17, 2022
Increased T- and B-cells associated with the phenotype of autoimmune limbic encephalitis with mainly memory dysfunctionNiels Hansen, Guido Widman, Demet Önder, et al.
Epilepsy & Behavior : E&B|December 18, 2019
Low CSF CD4/CD8+ T-cell proportions are associated with blood-CSF barrier dysfunction in limbic encephalitisNiels Hansen, Kerstin Schwing, Demet Önder, et al.
Ebiomedicine|April 24, 2025
The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohortDanique Beijer, David Mengel, Demet Önder, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 14, 2022
Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERD<sub>ND</sub> ): Time to Move Beyond the SkinIsabell Cordts, Demet Önder, Andreas Traschütz, et al.
Ebiomedicine|December 24, 2025
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichmentHannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
Nature Genetics|June 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Pageof 1