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Michael Zech

Showing results (21-30 of 195) with videos related to

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Orphanet Journal of Rare Diseases|February 17, 2022
Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clueElisabetta Indelicato, Michael Zech, Matthias Amprosi, et al.
Parkinsonism & Related Disorders|May 10, 2023
A de novo GRIA3 variant with complex hyperkinetic movement disorder in a girl with developmental delay and self-limited epilepsyJán Necpál, Juliane Winkelmann, Michael Zech, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2015
Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystoniaMichael Zech, Florian Castrop, Bernhard Haslinger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 23, 2022
GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia PhenotypeMartin Krenn, Rudolf Sommer, Thomas Sycha, et al.
Annals 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.
European Journal of Medical Genetics|June 15, 2023
De novo retinoic acid receptor beta (RARB) variant associated with microphthalmia and dystoniaGesa Trieschmann, Christian Wilhelm, Steffen Berweck, et al.
Acta Neurologica Belgica|October 22, 2024
Paradoxical caffeine-responsive paroxysmal nonkinesigenic dyskinesiasJán Necpál, Susanne A Schneider, Michael Zech, et al.
Neuropediatrics|November 14, 2025
Novel Pathogenic GCH1 Variant in Familial DOPA-Responsive DystoniaJohanna Engel, Ivana Dzinovic, Michael Zech, et al.
Annual Review of Pathology|September 22, 2023
Genetics and Pathogenesis of DystoniaMirja Thomsen, Lara M Lange, Michael Zech, et al.
Annals of Neurology|December 11, 2020
Reply to "Truncating VPS16 Mutations are Rare in Early-Onset Dystonia"Michael Zech, Dora Steel, Manju A Kurian, et al.
Pageof 20

Showing results (21-30 of 195) with videos related to

Sort By:
Pageof 20
Orphanet Journal of Rare Diseases|February 17, 2022
Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clueElisabetta Indelicato, Michael Zech, Matthias Amprosi, et al.
Parkinsonism & Related Disorders|May 10, 2023
A de novo GRIA3 variant with complex hyperkinetic movement disorder in a girl with developmental delay and self-limited epilepsyJán Necpál, Juliane Winkelmann, Michael Zech, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2015
Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystoniaMichael Zech, Florian Castrop, Bernhard Haslinger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 23, 2022
GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia PhenotypeMartin Krenn, Rudolf Sommer, Thomas Sycha, et al.
Annals 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.
European Journal of Medical Genetics|June 15, 2023
De novo retinoic acid receptor beta (RARB) variant associated with microphthalmia and dystoniaGesa Trieschmann, Christian Wilhelm, Steffen Berweck, et al.
Acta Neurologica Belgica|October 22, 2024
Paradoxical caffeine-responsive paroxysmal nonkinesigenic dyskinesiasJán Necpál, Susanne A Schneider, Michael Zech, et al.
Neuropediatrics|November 14, 2025
Novel Pathogenic GCH1 Variant in Familial DOPA-Responsive DystoniaJohanna Engel, Ivana Dzinovic, Michael Zech, et al.
Annual Review of Pathology|September 22, 2023
Genetics and Pathogenesis of DystoniaMirja Thomsen, Lara M Lange, Michael Zech, et al.
Annals of Neurology|December 11, 2020
Reply to "Truncating VPS16 Mutations are Rare in Early-Onset Dystonia"Michael Zech, Dora Steel, Manju A Kurian, et al.
Pageof 20