Demet Onder
Bonn, NW, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichment.
Journal: EBioMedicine
Published: June 30, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: June 24, 2025
Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohort.
Journal: medRxiv : the preprint server for health sciences
Published: February 20, 2025
Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohort.
Journal: The Lancet regional health. Europe
Published: February 01, 2025
Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3.
Journal: Journal of neurology
Published: September 05, 2024
The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohort.
Journal: EBioMedicine
Published: August 20, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: July 19, 2023
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3.
Journal: Annals of neurology
Published: April 16, 2023
Comparison of Live and Remote Video Ratings of the Scale for Assessment and Rating of Ataxia.
Journal: Movement disorders clinical practice
Published: March 22, 2023
Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 12, 2022
Increased T- and B-cells associated with the phenotype of autoimmune limbic encephalitis with mainly memory dysfunction.
Journal: Journal of translational autoimmunity
Published: August 20, 2022
Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND ): Time to Move Beyond the Skin.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 05, 2022
Last Updated: 09/26/2026