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Brain : a Journal of Neurology
|
February 27, 2021
Striatal and cerebellar vesicular acetylcholine transporter expression is disrupted in human DYT1 dystonia
Joachim Mazere, Bixente Dilharreguy, Gwenaëlle Catheline, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2009
The p.Asp216His TOR1A allele effect is not found in the French population
Mélissa Yana Frédéric, Fabienne Clot, Arnaud Blanchard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 23, 2018
Deep brain stimulation treated dystonia-trajectory via status dystonicus
Elodie Nerrant, Victoria Gonzalez, Christophe Milesi, et al.
Journal of Clinical Medicine
|
December 11, 2019
Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor Improvement
Annika Danielsson, Miryam Carecchio, Laura Cif, et al.
Frontiers in Human Neuroscience
|
July 17, 2020
Secondary Worsening Following DYT1 Dystonia Deep Brain Stimulation: A Multi-country Cohort
Takashi Tsuboi, Laura Cif, Philippe Coubes, et al.
Frontiers in Neurology
|
June 21, 2024
Dyskinetic crisis in <i>GNAO1</i>-related disorders: clinical perspectives and management strategies
Jana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, et al.
Journal of the Neurological Sciences
|
August 15, 2018
Deep brain stimulation is effective in pediatric patients with GNAO1 associated severe hyperkinesia
Anne Koy, Sebahattin Cirak, Victoria Gonzalez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)
Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
Parkinsonism & Related Disorders
|
April 26, 2020
Increased diagnostic yield in complex dystonia through exome sequencing
Thomas Wirth, Christine Tranchant, Nathalie Drouot, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 27, 2011
Singular DYT6 phenotypes in association with new THAP1 frameshift mutations
Arnaud Blanchard, Agathe Roubertie, Marion Simonetta-Moreau, et al.
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of 8
Search research articles
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Showing results (61-70 of 76) with videos related to
Sort By:
Page
of 8
Brain : a Journal of Neurology
|
February 27, 2021
Striatal and cerebellar vesicular acetylcholine transporter expression is disrupted in human DYT1 dystonia
Joachim Mazere, Bixente Dilharreguy, Gwenaëlle Catheline, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2009
The p.Asp216His TOR1A allele effect is not found in the French population
Mélissa Yana Frédéric, Fabienne Clot, Arnaud Blanchard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 23, 2018
Deep brain stimulation treated dystonia-trajectory via status dystonicus
Elodie Nerrant, Victoria Gonzalez, Christophe Milesi, et al.
Journal of Clinical Medicine
|
December 11, 2019
Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor Improvement
Annika Danielsson, Miryam Carecchio, Laura Cif, et al.
Frontiers in Human Neuroscience
|
July 17, 2020
Secondary Worsening Following DYT1 Dystonia Deep Brain Stimulation: A Multi-country Cohort
Takashi Tsuboi, Laura Cif, Philippe Coubes, et al.
Frontiers in Neurology
|
June 21, 2024
Dyskinetic crisis in <i>GNAO1</i>-related disorders: clinical perspectives and management strategies
Jana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, et al.
Journal of the Neurological Sciences
|
August 15, 2018
Deep brain stimulation is effective in pediatric patients with GNAO1 associated severe hyperkinesia
Anne Koy, Sebahattin Cirak, Victoria Gonzalez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)
Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
Parkinsonism & Related Disorders
|
April 26, 2020
Increased diagnostic yield in complex dystonia through exome sequencing
Thomas Wirth, Christine Tranchant, Nathalie Drouot, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 27, 2011
Singular DYT6 phenotypes in association with new THAP1 frameshift mutations
Arnaud Blanchard, Agathe Roubertie, Marion Simonetta-Moreau, et al.
Page
of 8