S. Weller

Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patients

J. Gärtner, H. Rosewich, S. Weller, 2008, Journal of Inherited Metabolic Disease.

Genetic and clinical aspects of X‐linked hydrocephalus (L1 disease): Mutations in the L1CAM gene

J. Gärtner, S. Weller, 2001, Human mutation.

Characteristic Clinical Features of Idiopathic Neuralgic Amyotrophy in Childhood

H. Lenard, J. Gärtner, S. Weller, 2001, Neuropediatrics.