Adolf Weindl

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.

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

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

Clinical Aspects of Sensory Motor Integration

A. Struppler, A. Weindl, A. Struppler, 1987, Advances in Applied Neurological Sciences.

Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: A neuropsychological and voxel-based morphometric study

Jan Kassubek, Alexander Peinemann, A. Weindl, 2005, Journal of the Neurological Sciences.

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.

Global cerebral atrophy in early stages of Huntington's disease: quantitative MRI study

Jan Kassubek, Rainer Muche, Daniel Ecker, 2004, Neuroreport.