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Parkinsonism & 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|January 10, 2026
Dystonia: Insights into Mechanisms and Novel TherapeuticsIvana Dzinovic, Michael ZechNeurogenetics|March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variantIvana Dzinovic, Tereza Serranová, Clement Prouteau, et al.Nature Reviews. Neurology|January 3, 2024
Next-generation sequencing and bioinformatics in rare movement disordersMichael Zech, Juliane WinkelmannNeuropediatrics|November 14, 2025
Novel Pathogenic GCH1 Variant in Familial DOPA-Responsive DystoniaJohanna Engel, Ivana Dzinovic, Michael Zech, et al.Current 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.Annals of Clinical and Translational Neurology|March 6, 2021
Variant recurrence confirms the existence of a FBXO31-related spastic-dystonic cerebral palsy syndromeIvana Dzinovic, Matej Škorvánek, Petra Pavelekova, 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.Pageof 33