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Nature Reviews. Neurology|January 3, 2024
Next-generation sequencing and bioinformatics in rare movement disordersMichael Zech, Juliane WinkelmannParkinsonism & Related Disorders|September 10, 2022
Genetic intersection between dystonia and neurodevelopmental disorders: Insights from genomic sequencingIvana Dzinovic, Juliane Winkelmann, Michael ZechCurrent Neurology and Neuroscience Reports|November 27, 2019
Update on KMT2B-Related DystoniaMichael Zech, Daniel D Lam, Juliane WinkelmannAnnals of Clinical and Translational Neurology|March 10, 2022
Progressive choreodystonia in X-linked hyper-IgM immunodeficiency: a rare but recurrent presentationMatej Škorvánek, Robert Jech, Juliane Winkelmann, et al.Der Nervenarzt|January 16, 2019
[Exome diagnostics in neurology]Michael Zech, Matias Wagner, Barbara Schormair, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2015
The clinical phenotype of early-onset isolated dystonia caused by recessive COL6A3 mutations (DYT27)Angela Jochim, Michael Zech, Gina Gora-Stahlberg, et al.Movement Disorders Clinical Practice|October 27, 2018
Ataxia Telangiectasia Gene Mutation in Isolated Segmental Dystonia Without Ataxia and TelangiectasiaJán Necpál, Michael Zech, Matej Škorvánek, et al.Brain : a Journal of Neurology|April 19, 2021
HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystoniaEdoardo Monfrini, Michael Zech, Dora Steel, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|September 30, 2024
Tremor-Dominant Movement Disorder in ANKRD11- Associated KBG SyndromeAntonia M Stehr, Thomas Koeglsperger, Maureen Jacob, et al.Neurogenetics|March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variantIvana Dzinovic, Tereza Serranová, Clement Prouteau, et al.Pageof 33