Publikationen

Sauter S, Miterski B, Klimpe S, Bönsch D, Schöls L, Visbeck A, Papke T, Hopf HC, Engel W, Deufel T, Epplen JT, Neesen J. Mutation Analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spapstic paraplegia. Human Mutation 2002;20:127-132


Schulte T, Miterski B, Börnke C, Przuntek H, Epplen JT, Schöls L. Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia. Neurology 2003;60:1529-1532


Schüle R, Holland-Letz T, Klimpe S, Kassubek J, Otto S, Schöls L. Development and validation of a rating scale for hereditary spastic paraplegia. Akt Neurol 2005;32:S227