Maryla Rakowicz

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6

Peter Bauer, Dagmar Timmann, Till-Karsten Hauser, 2010, NeuroImage.

Corrigendum to “Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6” [NeuroImage 49 (2010) 158–168]

Peter Bauer, Dagmar Timmann, Till-Karsten Hauser, 2010, NeuroImage.

Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients

Paola Giunti, Bart P C van de Warrenburg, Sylvia Boesch, 2006, Movement disorders : official journal of the Movement Disorder Society.

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.

Self‐rated health status in spinocerebellar ataxia—Results from a European multicenter study

Paola Giunti, Dagmar Timmann, Sylvia Boesch, 2010, Movement disorders : official journal of the Movement Disorder Society.

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

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