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Michael Zech

Showing results (141-150 of 196) with videos related to

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Brain : a Journal of Neurology|March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystoniaAlessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 30, 2021
Collagen VI Regulates Motor Circuit Plasticity and Motor Performance by Cannabinoid ModulationDaniel D Lam, Rhîannan H Williams, Ernesto Lujan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 2, 2026
Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers AheadRobert Jech, Petra Havránková, Eugenia Tsoma, et al.
Clinical Genetics|March 20, 2026
Expanding the Phenotypic Spectrum of the Recurrent De Novo FBXO31 p.Asp334Asn Variant: Evidence for a Novel Neurodevelopmental Disorder (Kruer Syndrome)Carolina I Galaz-Montoya, Sara A Lewis, Maureen K Galindo, et al.
Parkinsonism & Related Disorders|July 7, 2020
Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystoniaMichael Zech, Theresa Brunet, Matej Škorvánek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2021
A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic ParaplegiaDerek E Neilson, Michael Zech, Robert B Hufnagel, et al.
Plos One|January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disordersMichael Zech, Georg Nübling, Florian Castrop, et al.
Movement Disorders Clinical Practice|January 31, 2024
Dominant VPS16 Pathogenic Variants: Not Only Isolated DystoniaEdoardo Monfrini, Laura Avanzino, Giovanni Palermo, et al.
Molecular Neurodegeneration|September 27, 2025
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological featuresChristof Brücke, Mohammed Al-Azzani, Nagendran Ramalingam, et al.
Medrxiv : the Preprint Server for Health Sciences|October 14, 2024
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological featuresChristof Brücke, Mohammed Al-Azzani, Nagendran Ramalingam, et al.
Pageof 20

Showing results (141-150 of 196) with videos related to

Sort By:
Pageof 20
Brain : a Journal of Neurology|March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystoniaAlessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 30, 2021
Collagen VI Regulates Motor Circuit Plasticity and Motor Performance by Cannabinoid ModulationDaniel D Lam, Rhîannan H Williams, Ernesto Lujan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 2, 2026
Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers AheadRobert Jech, Petra Havránková, Eugenia Tsoma, et al.
Clinical Genetics|March 20, 2026
Expanding the Phenotypic Spectrum of the Recurrent De Novo FBXO31 p.Asp334Asn Variant: Evidence for a Novel Neurodevelopmental Disorder (Kruer Syndrome)Carolina I Galaz-Montoya, Sara A Lewis, Maureen K Galindo, et al.
Parkinsonism & Related Disorders|July 7, 2020
Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystoniaMichael Zech, Theresa Brunet, Matej Škorvánek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2021
A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic ParaplegiaDerek E Neilson, Michael Zech, Robert B Hufnagel, et al.
Plos One|January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disordersMichael Zech, Georg Nübling, Florian Castrop, et al.
Movement Disorders Clinical Practice|January 31, 2024
Dominant VPS16 Pathogenic Variants: Not Only Isolated DystoniaEdoardo Monfrini, Laura Avanzino, Giovanni Palermo, et al.
Molecular Neurodegeneration|September 27, 2025
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological featuresChristof Brücke, Mohammed Al-Azzani, Nagendran Ramalingam, et al.
Medrxiv : the Preprint Server for Health Sciences|October 14, 2024
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological featuresChristof Brücke, Mohammed Al-Azzani, Nagendran Ramalingam, et al.
Pageof 20