Advanced in Hereditary Ataxia

Perrine Charles

Paris, FR 
Advanced in Hereditary Ataxia
Paris, FR 
OverviewLocationsClinical Research

Overview

Perrine Charles practices in Paris, France. Dr. Charles is rated as an Advanced expert by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Acute Cerebellar Ataxia, Spinocerebellar Ataxia, Drug Induced Dyskinesia, Spinocerebellar Ataxia Type 5, and Deep Brain Stimulation.

Her clinical research consists of co-authoring 123 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 9 articles and participated in 1 clinical trial in the study of Hereditary Ataxia.

Gender
Female

Locations

Paris, France
Other Locations
103 Gd Rue De La Croix Rousse, Lyon, 69004, France
Bron, France
Nantes, France
Montpellier, France
Equipe 01 Neuropsychologie Interventionnelle, Paris Et Université Paris Est, Creteil, France

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

2 Clinical Trials

Patient Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS)
Patient Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS)
Enrollment Status: Completed
Publish Date: October 03, 2025
Clinical, Molecular and by Neuroimaging Characterization of Monogenic Forms of Parkinsonism Syndromes: Mutations of the LRRK2 Gene.
Clinical, Molecular and by Neuroimaging Characterization of Monogenic Forms of Parkinsonism Syndromes: Mutations of the LRRK2 Gene.
Enrollment Status: Completed
Publish Date: January 23, 2025
View 1 Less Clinical Trial

123 Total Publications

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Journal: medRxiv : the preprint server for health sciences
Published: September 15, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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