Area of research
Neurology · Cellular and Molecular Neuroscience
Research interest
Research interests include Neurological disorders and treatments, Parkinson's Disease Mechanisms and Treatments, Genetic Neurodegenerative Diseases, and Glycogen Storage Diseases and Myoclonus.
Genotype–phenotype correlation in PRKN-associated Parkinson’s disease
Prognosis of impulse control disorders in Parkinson’s disease: a prospective controlled study
Contribution of the Mitochondrial Complex I Inhibitor Annonacin to the Alpha-synuclein/Tau Co-pathology in Caribbean Atypical Parkinsonism (P2-3.010)
Scoping Review on <scp>ADCY5</scp>‐Related Movement Disorders
Efficacy of Caffeine in <scp>ADCY5</scp>‐Related Dyskinesia: A Retrospective Study
Clinical Features and Evolution of Blepharospasm: A Multicenter International Cohort and Systematic Literature Review
Cerebrospinal fluid biomarkers in SARS-CoV-2 patients with acute neurological syndromes
Histoire reproductive et incidence de la maladie de Parkinson chez les femmes : résultats de la cohorte prospective française E3N
Quality of life in isolated dystonia: non-motor manifestations matter
Oromandibular Dystonia: A Clinical Examination of 2,020 Cases
Treatable Hyperkinetic Movement Disorders Not to Be Missed
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and Recommendations
Characterization of Recessive Parkinson Disease in a Large Multicenter Study
Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort
Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase–Associated Neurodegeneration
Characterization of Tremor in Children Using Accelerometry and The Kinarm. (5158)
Risk of spread in adult-onset isolated focal dystonia: a prospective international cohort study
Functional Motor Symptoms in Parkinson’s Disease and Functional Parkinsonism: A Systematic Review
Invalidation of Parkinson's disease diagnosis after years of follow-up based on clinical, radiological and neurophysiological examination
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1
Health-Related Quality of Life Is Severely Affected in Primary Orthostatic Tremor
<i>DCC</i>mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome
A post hoc study on gene panel analysis for the diagnosis of dystonia
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome
Clinical and demographic characteristics related to onset site and spread of cervical dystonia
<i>ADCY5</i> -related dyskinesia
Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiency
Severe phenotypic spectrum of biallelic mutations in<i>PRRT2</i>gene
29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype