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Philippe Damier

Showing results (91-100 of 107) with videos related to

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Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2021
Fluoxetine for the Symptomatic Treatment of Multiple System Atrophy: The MSA-FLUO TrialOlivier Rascol, Valérie Cochen de Cock, Anne Pavy-Le Traon, et al.
Frontiers in Neurology|August 28, 2020
Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center CohortSuzanne Lesage, Marion Houot, Graziella Mangone, et al.
Human Molecular Genetics|November 19, 2010
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European populationMohamad Saad, Suzanne Lesage, Aude Saint-Pierre, et al.
Parkinsonism & Related Disorders|July 2, 2019
Programming parameters of subthalamic deep brain stimulators in Parkinson's disease from a controlled trialK Knudsen, P Krack, L Tonder, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2022
The Contribution of Subthalamic Nucleus Deep Brain Stimulation to the Improvement in Motor Functions and Quality of LifeInken Tödt, Bassam Al-Fatly, Oliver Granert, et al.
Parkinsonism & Related Disorders|September 18, 2022
Genetic stratification of motor and QoL outcomes in Parkinson's disease in the EARLYSTIM studyDaniel Weiss, Zied Landoulsi, Patrick May, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2011
Singular DYT6 phenotypes in association with new THAP1 frameshift mutationsArnaud Blanchard, Agathe Roubertie, Marion Simonetta-Moreau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic MovementsClément Tarrano, Cécile Galléa, Asya Ekmen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2021
Fluoxetine for the Symptomatic Treatment of Multiple System Atrophy: The MSA-FLUO TrialOlivier Rascol, Valérie Cochen de Cock, Anne Pavy-Le Traon, et al.
Frontiers in Neurology|August 28, 2020
Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center CohortSuzanne Lesage, Marion Houot, Graziella Mangone, et al.
Human Molecular Genetics|November 19, 2010
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European populationMohamad Saad, Suzanne Lesage, Aude Saint-Pierre, et al.
Parkinsonism & Related Disorders|July 2, 2019
Programming parameters of subthalamic deep brain stimulators in Parkinson's disease from a controlled trialK Knudsen, P Krack, L Tonder, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2022
The Contribution of Subthalamic Nucleus Deep Brain Stimulation to the Improvement in Motor Functions and Quality of LifeInken Tödt, Bassam Al-Fatly, Oliver Granert, et al.
Parkinsonism & Related Disorders|September 18, 2022
Genetic stratification of motor and QoL outcomes in Parkinson's disease in the EARLYSTIM studyDaniel Weiss, Zied Landoulsi, Patrick May, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2011
Singular DYT6 phenotypes in association with new THAP1 frameshift mutationsArnaud Blanchard, Agathe Roubertie, Marion Simonetta-Moreau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic MovementsClément Tarrano, Cécile Galléa, Asya Ekmen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.
Pageof 11