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Publicaties

Genetic myoclonus

Negative Myoclonus: Neurophysiological Study and Clinical Impact in Progressive Myoclonus Ataxia

Early onset ataxia with comorbid myoclonus and epilepsy: A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies

Myoclonus and other jerky movement disorders

Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update

Towards a Machine Learning Based Classification System for Hyperkinetic Movement Disorders: Generating a Neurophysiological Feature Set

Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes

Myoclonus-Ataxia Syndromes: A Diagnostic Approach

Next move in movement disorders (NEMO): Developing a computer-aided classification tool for hyperkinetic movement disorders

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