Emmanuel Roze

28PUBLICATIONS
206CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Sensory processes, perception and performancePredictive and prognostic markersNeurogenetics
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Publications (28)

|Aug 26, 2026
Paroxysmal Kinesigenic Dyskinesia and Progressive Ataxia-Spasticity Syndrome Caused by a Biallelic Variant in KCNJ10.

|Jul 02, 2026
Gene Therapy for Amino Acid Decarboxylase Deficiency: Clinical and Imaging Outcomes in a French Cohort.

|May 01, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic Movements.

|Apr 29, 2026
Revisiting the Association Between Calcium Channel Blockers and Parkinson's Disease in the E3N Cohort.

|Mar 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.

Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli

|Dec 22, 2025
Transforming Pediatric Movement Disorders Assessment: From Expert Consensus to Collaborative Approaches.

Hortensia Gimeno, Clément Desjardins, Christelle Nilles

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Frequent Collaborators

8 joint publications

Aurélie Méneret

4 joint publications

Marie Vidailhet

4 joint publications

Alexis Elbaz

4 joint publications

Clément Desjardins