Teije van Prooije

9PUBLICATIONS
43CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Autonomic nervous systemGene mappingGene and molecular therapy
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Publications (9)

|Apr 09, 2026
Early and Progressive Spinal Cord Atrophy in Spinocerebellar Ataxia Type 1.

Colette J M Reniers, Teije H van Prooije, Kirsten C J Kapteijns

|May 07, 2025
Longitudinal Assessment Reveals Stage-Dependent Utility of Digital Motor Markers in SCA1.

Ilse H J Willemse, Teije van Prooije, Kirsten C J Kapteijns

|Feb 20, 2025
Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohort.

Moritz Berger, Hector Garcia-Moreno, Monica Ferreira

|Aug 03, 2024
Multimodal, Longitudinal Profiling of SCA1 Identifies Predictors of Disease Severity and Progression.

Teije H van Prooije, Kirsten C J Kapteijns, Jack J A van Asten

|Jul 08, 2024
A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.

Teije H van Prooije, Maartje Pennings, Lucille Dorresteijn

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