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Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes

Myoclonus-Ataxia Syndromes: A Diagnostic Approach

The diagnostic value of clinical neurophysiology in hyperkinetic movement disorders: A systematic review

Not every excessive startle is hyperekplexia, the curious case of SOD1

Myoclonus-dystonia: Distinctive motor and non-motor phenotype from other dystonia syndromes

Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task Force

Progressive myoclonus ataxia: Time for a new definition?

The Influence of the Metabolic Syndrome on the Short- and Long-Term Outcome After Carotid Endarterectomy

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