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Current Neurology and Neuroscience Reports|November 27, 2019
Update on KMT2B-Related DystoniaMichael Zech, Daniel D Lam, Juliane WinkelmannNature 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 ZechAnnals 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.Advances in Pharmacology (San Diego, Calif.)|June 24, 2019
Role of MEIS1 in restless legs syndrome: From GWAS to functional studies in miceAaro V Salminen, Daniel D Lam, Juliane WinkelmannDer 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.Cold Spring Harbor Molecular Case Studies|September 29, 2018
A unique de novo gain-of-function variant in CAMK4 associated with intellectual disability and hyperkinetic movement disorderMichael Zech, Daniel D Lam, Sandrina Weber, et al.Journal of Sleep Research|May 19, 2021
Investigation of dopaminergic signalling in Meis homeobox 1 (Meis1) deficient mice as an animal model of restless legs syndromeLucile Cathiard, Valerie Fraulob, Daniel D Lam, 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.Pageof 35