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Current Neurology and Neuroscience Reports|January 10, 2026
Dystonia: Insights into Mechanisms and Novel TherapeuticsIvana Dzinovic, Michael Zech
Parkinsonism & Related Disorders|September 10, 2022
Genetic intersection between dystonia and neurodevelopmental disorders: Insights from genomic sequencingIvana Dzinovic, Juliane Winkelmann, Michael Zech
Neuropediatrics|November 14, 2025
Novel Pathogenic GCH1 Variant in Familial DOPA-Responsive DystoniaJohanna Engel, Ivana Dzinovic, Michael Zech, 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.
Molecular Psychiatry|August 20, 2025
De novo protein-coding gene variants in developmental stutteringElse Eising, Ivana Dzinovic, Arianna Vino, et al.
American Journal of Medical Genetics. Part A|April 14, 2026
CACNA1C-Related Channelopathy Presenting With Adult-Onset Combined Dystonia-Parkinsonism: A Novel Neurological PresentationDonatella Ottaviani, Ruggero Bacchin, Arlend Pjeçi, 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.
Parkinsonism & Related Disorders|August 16, 2021
Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case seriesIvana Dzinovic, Matej Škorvánek, Ján Necpál, et al.
Parkinsonism & Related Disorders|July 25, 2022
Genetic overlap between dystonia and other neurologic disorders: A study of 1,100 exomesIvana Dzinovic, Sylvia Boesch, Matej Škorvánek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate SynthasePhilip Harrer, Magdalena Krygier, Martin Krenn, et al.
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