Search research articles
Contact Us
Filters
Showing results (141-150 of 196) with videos related to
Page
of 20
Sort By:
Brain : a Journal of Neurology
|
March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystonia
Alessia 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 Modulation
Daniel 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 Ahead
Robert 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 dystonia
Michael 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 Paraplegia
Derek E Neilson, Michael Zech, Robert B Hufnagel, et al.
Plos One
|
January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders
Michael Zech, Georg Nübling, Florian Castrop, et al.
Movement Disorders Clinical Practice
|
January 31, 2024
Dominant VPS16 Pathogenic Variants: Not Only Isolated Dystonia
Edoardo Monfrini, Laura Avanzino, Giovanni Palermo, et al.
Molecular Neurodegeneration
|
September 27, 2025
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological features
Christof 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 features
Christof Brücke, Mohammed Al-Azzani, Nagendran Ramalingam, et al.
Page
of 20
Search research articles
Search
Showing results (141-150 of 196) with videos related to
Sort By:
Page
of 20
Brain : a Journal of Neurology
|
March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystonia
Alessia 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 Modulation
Daniel 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 Ahead
Robert 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 dystonia
Michael 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 Paraplegia
Derek E Neilson, Michael Zech, Robert B Hufnagel, et al.
Plos One
|
January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders
Michael Zech, Georg Nübling, Florian Castrop, et al.
Movement Disorders Clinical Practice
|
January 31, 2024
Dominant VPS16 Pathogenic Variants: Not Only Isolated Dystonia
Edoardo Monfrini, Laura Avanzino, Giovanni Palermo, et al.
Molecular Neurodegeneration
|
September 27, 2025
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological features
Christof 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 features
Christof Brücke, Mohammed Al-Azzani, Nagendran Ramalingam, et al.
Page
of 20