Nicoline Voet

9PUBLICATIONS
51CO-AUTHORS
BiomechanicsMicroelectromechanical systems (MEMS)Pacific Peoples and disabilityMedical genetics (excl. cancer genetics)Gene and molecular therapy
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Publications (9)

|Jul 02, 2026
Physical exercise in facioscapulohumeral muscular dystrophy: state of the art and future challenges beyond common misconceptions.

|Apr 08, 2026
Multidimensional Measurements of Dysarthria in Myotonic Dystrophy Type 1.

Sanne van Hellemond, Nicole Voet, Rosemarie Kroon

|Nov 11, 2024
Experiences of living with GSD5 (McArdle) disease: challenges and strategies. A qualitative study in the Netherlands.

Ronne van Haaren-Pater, Walaa Karazi, Daphne Maas

|Nov 07, 2024
A 5-year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials.

Joost Kools, Sanne Vincenten, Baziel G M van Engelen

|Mar 15, 2023
Smartphone and Wearable Sensors for the Estimation of Facioscapulohumeral Muscular Dystrophy Disease Severity: Cross-sectional Study.

Ahnjili Zhuparris, Ghobad Maleki, Ingrid Koopmans

|Mar 10, 2023
Best practice recommendations for speech-language pathology in children with neuromuscular disorders: A Delphi-based consensus study.

Mieke Kooi-van Es, Corrie E Erasmus, Nicoline B M Voet

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Frequent Collaborators

2 joint publications

Robert J Doll

2 joint publications

Emilie van Brummelen

2 joint publications

Ingrid Koopmans

2 joint publications

Joris H De Maeyer