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Journal of Psychiatric Research
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October 17, 2017
One year double blind study of high vs low frequency subcallosal cingulate stimulation for depression
Renana Eitan, Denys Fontaine, Michel Benoît, et al.
Annals of Neurology
|
January 31, 2025
Spiking Patterns in the Globus Pallidus Highlight Convergent Neural Dynamics across Diverse Genetic Dystonia Syndromes
Ahmet Kaymak, Fabiana Colucci, Mahboubeh Ahmadipour, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 8, 2021
Subcutaneous Levodopa Infusion for Parkinson's Disease: 1-Year Data from the Open-Label BeyoND Study
Werner Poewe, Fabrizio Stocchi, David Arkadir, et al.
Journal of Inherited Metabolic Disease
|
April 4, 2020
The definition of neuronopathic Gaucher disease
Raphael Schiffmann, Jeff Sevigny, Arndt Rolfs, et al.
Neurology. Genetics
|
May 21, 2021
Occurrence of Amyotrophic Lateral Sclerosis in Type 1 Gaucher Disease
Lais M Oliveira, Tara Rastin, Graeme A M Nimmo, et al.
Parkinsonism & Related Disorders
|
July 5, 2025
Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study
Saar Anis, Caroline Weill, Penina Ponger, et al.
Nature Genetics
|
May 27, 2017
Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Esther Meyer, Keren J Carss, Julia Rankin, et al.
Nature Genetics
|
December 20, 2016
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Esther Meyer, Keren J Carss, Julia Rankin, et al.
Plos One
|
October 3, 2023
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.
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Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
Journal of Psychiatric Research
|
October 17, 2017
One year double blind study of high vs low frequency subcallosal cingulate stimulation for depression
Renana Eitan, Denys Fontaine, Michel Benoît, et al.
Annals of Neurology
|
January 31, 2025
Spiking Patterns in the Globus Pallidus Highlight Convergent Neural Dynamics across Diverse Genetic Dystonia Syndromes
Ahmet Kaymak, Fabiana Colucci, Mahboubeh Ahmadipour, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 8, 2021
Subcutaneous Levodopa Infusion for Parkinson's Disease: 1-Year Data from the Open-Label BeyoND Study
Werner Poewe, Fabrizio Stocchi, David Arkadir, et al.
Journal of Inherited Metabolic Disease
|
April 4, 2020
The definition of neuronopathic Gaucher disease
Raphael Schiffmann, Jeff Sevigny, Arndt Rolfs, et al.
Neurology. Genetics
|
May 21, 2021
Occurrence of Amyotrophic Lateral Sclerosis in Type 1 Gaucher Disease
Lais M Oliveira, Tara Rastin, Graeme A M Nimmo, et al.
Parkinsonism & Related Disorders
|
July 5, 2025
Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study
Saar Anis, Caroline Weill, Penina Ponger, et al.
Nature Genetics
|
May 27, 2017
Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Esther Meyer, Keren J Carss, Julia Rankin, et al.
Nature Genetics
|
December 20, 2016
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Esther Meyer, Keren J Carss, Julia Rankin, et al.
Plos One
|
October 3, 2023
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.
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of 10