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CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3

Inborn Errors of Metabolism in Adults: Two Patients with Movement Disorders Caused by Glutaric Aciduria Type 1

The cerebral metabolic topography of spinocerebellar ataxia type 3

Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes

Transdermal iontophoretic delivery of apomorphine in patients improved by surfactant formulation pretreatment

Calf circumference in Duchenne muscular dystrophy: Reply

Quantitative assessment of calf circumference in Duchenne muscular dystrophy patients

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