M. Städtler

Observing Huntington’s Disease: the European Huntington’s Disease Network’s REGISTRY

Alexander Münchau, Caroline Hallam, Andrea Ciarmiello, 2011, PLoS currents.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Voxel-based morphometry indicates relative preservation of the limbic prefrontal cortex in early Huntington disease

J. Kassubek, C. Zimmer, A. Weindl, 2007, Journal of Neural Transmission.

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

J. Schiefer, R. Barker, R. Reilmann, 2011, PLoS currents.

Striatal gray matter loss in Huntington's disease is leftward biased

Mark Mühlau, Christian Gaser, Jan Kassubek, 2007, Movement disorders : official journal of the Movement Disorder Society.