Claudia Ravelli

Paris, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 19 publications

Highlighting the value of polymyography in childhood onset movement disorders.

Highlighting the value of polymyography in childhood onset movement disorders.

Journal: Frontiers in neurology

Published: December 19, 2025

Bilateral Globus Pallidus Deep Brain Stimulation Improves Motor Function in ADCY5-Related Disorder.

Bilateral Globus Pallidus Deep Brain Stimulation Improves Motor Function in ADCY5-Related Disorder.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 18, 2025

International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.

International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 03, 2025

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

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

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: July 28, 2025

Deep brain stimulation in patients with mixed movement disorders linked to ADCY5.

Deep brain stimulation in patients with mixed movement disorders linked to ADCY5.

Journal: Revue neurologique

Published: July 02, 2025

Atypical ADCY5-related movement disorders: Highlighting adolescent/adult-onset cervical dystonia.

Atypical ADCY5-related movement disorders: Highlighting adolescent/adult-onset cervical dystonia.

Journal: Parkinsonism & related disorders

Published: November 09, 2024

STARDEV Study: Neurodevelopmental Trajectory and Long-Term Outcomes of Patients with Startle Disease/Hyperekplexia.

STARDEV Study: Neurodevelopmental Trajectory and Long-Term Outcomes of Patients with Startle Disease/Hyperekplexia.

Journal: Movement disorders clinical practice

Published: October 18, 2024

Case Series of Anesthetic Management of Gene Therapy in Children With Aromatic L-Amino Acid Decarboxylase Deficiency.

Case Series of Anesthetic Management of Gene Therapy in Children With Aromatic L-Amino Acid Decarboxylase Deficiency.

Journal: Paediatric anaesthesia

Published: September 30, 2024

Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies.

Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies.

Journal: Frontiers in neurology

Published: March 19, 2024

CHD8-related disorders redefined: an expanding spectrum of dystonic phenotypes.

CHD8-related disorders redefined: an expanding spectrum of dystonic phenotypes.

Journal: Journal of neurology

Published: January 08, 2024

Choice of compound, dosage, and management of side effects for long-term corticosteroid treatment in Duchenne muscular dystrophy: Guidelines from the Neuromuscular Commission of the French Society of Pediatric Neurology.

Choice of compound, dosage, and management of side effects for long-term corticosteroid treatment in Duchenne muscular dystrophy: Guidelines from the Neuromuscular Commission of the French Society of Pediatric Neurology.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: December 20, 2023

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.

Journal: Annals of neurology

Published: November 16, 2023

Showing 1-12 of 19

Last Updated: 09/26/2026