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Thomas Wirth

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Professor (full)

University of Strasbourg

France

Research Interests

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Recent Grants

Grant: Open

Evaluation of long-read genome sequencing for dystonia molecular diagnosis: a prospective multicenter study(GenoDYT)

Open Date: 2025-01-01

Close Date: 2029-12-01

Grant: Close

Combined RNA and whole genome sequencing for the genetic diagnosis of early-onset Parkinson's disease (ParkOmics)

Open Date: 2024-06-01

Close Date: 2026-06-01

Grant: Close

Unravelling the missing genetic causes of Parkinson's disease

Open Date: 2024-01-01

Close Date: 2025-12-01

Grant: Close

Assessment of cerebellar ataxia in essential tremor patients treated by Vim deep brain stimulation: a multimodal study

Open Date: 2019-11-01

Close Date: 2020-10-01

Grant: Close

Identification of genes associated with movement disorders through exome sequencing

Open Date: 2017-11-01

Close Date: 2018-10-01

Articles (20)

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Professeur des Universités

Université de Nantes

FRANCE

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Fabrice Berna

Professor (Full Time)

University of Strasbourg

FRANCE

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Ralf-Dieter Hilgers

Professor

RWTH Aachen University

GERMANY

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Tiago A. Mestre

CANADA

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Kevin Bihan

Pharmacien - praticien hospitalier

Assistance Publique - Hôpitaux de Paris

FRANCE

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Wassilios Meissner

University of Bordeaux

FRANCE

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jerome Honnorat

Professeur

Université Claude Bernard Lyon 1

FRANCE

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Universitätsklinikum Essen Institut für Humangenetik

GERMANY

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Jennifer Faber

Head of Ataxia Clinic

University Hospital Bonn

GERMANY

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Thomas Smol

PU-PH

Université de Lille

FRANCE

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jean-christophe corvol

Professor of Neurology

Sorbonne Université Campus Pierre et Marie Curie

FRANCE

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Thomas Wirth

Research Interests

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Recent Grants

Articles (20)

Effect on Dyskinesia of the Early Combination of Amantadine to Levodopa‐Therapy in Parkinson's Disease: A Randomized, Placebo‐Controlled Study (PREMANDYSK)

Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia

Longitudinal progression, metrics, age-dependence, and modifiers of ataxia severity in SCA27B: a multicentre study of 219 patients

Acute Post‐Partum Psychosis and Dystonia Reveals Late‐Onset MPAN

Bispecific antibody therapy in multiple myeloma and risk of progressive multifocal leukoencephalopathy

No role of intronic expansions in HSF1 for essential tremor in Europe.

Building Scalable Recruitment Models for Precision Medicine in Parkinson's Disease: Insights from GBA1 Trials

Expanding the ABCA2-associated neurodevelopmental phenotype

Radiological signature of levodopa responsiveness in Parkinson's disease: A data driven approach in a deep brain stimulation cohort

Does CANVAS mimic MSA-C? A prospective multimodal study

Deep Learning Pose Estimation for Phenotyping of Co‐Occurring Hyperkinetic Movement Disorders

RFC1-related disorders: A case series of 4-aminopyridine and acetyl-DL-leucine treatment

Confirmation of biallelic VPS11 variants as a cause of complex dystonic syndrome

Progress and challenges in sporadic late-onset cerebellar ataxias

Validation of the French Translation of the Movement Disorder Society Non‐Motor Symptoms Scale (MDS‐NMS) in Parkinson's Disease

Training in movement disorders during neurology residency in France: A national survey on educational gaps and future perspectives

Neuropathy in GAA‐FGF14 Late‐Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics

The Spectrum of Neurologic Phenotypes Associated With <i>NUS1</i> Pathogenic Variants: A Comprehensive Case Series

ADCY5-Mosaic Variants: A Diagnosis Not to Be Missed

Long‐Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia

Collaborators (23)

Bigna K. Bölsterli

Emmanuel Roze

Jean Muller

Sebastien Lhomme

Sheng Luo

Michelle Hyczy de Siqueira Tosin

Mickael Aubignat

Giulietta Riboldi

Clément Desjardins

Philippe DAMIER

Fabrice Berna

Ralf-Dieter Hilgers

Tiago A. Mestre

Kevin Bihan

Wassilios Meissner

jerome Honnorat

Elisabeth Bosch

Fabienne Ory Magne

Deepak Gill

Christel Depienne

Jennifer Faber

Thomas Smol

jean-christophe corvol

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