Alessandro Capuano
Viterbo, Italy
Last Updated: 09/26/2026
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Found 59 publications
Phenomenology and clinical relevance of minor neurological signs in child neurology and psychiatry.
Journal: Frontiers in neurology
Published: December 05, 2025
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology.
Journal: Parkinsonism & related disorders
Published: April 16, 2024
BCL11B-Related Dystonia: Further Evidence of an Emerging Cause of Childhood-Onset Generalized Dystonia.
Journal: Movement disorders clinical practice
Published: December 19, 2023
Systematic review of drug therapy for chorea in NXK2-1-related disorders: Efficacy and safety evidence from case studies and series.
Journal: European journal of neurology
Published: June 12, 2023
The changing face of reported status dystonicus - A systematic review.
Journal: Parkinsonism & related disorders
Published: March 08, 2023
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments.
Journal: Parkinsonism & related disorders
Published: January 26, 2023
Highlighting the Dystonic Phenotype Related to GNAO1.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 17, 2022
Subacute Sclerosing Panencephalitis in Children: The Archetype of Non-Vaccination.
Journal: Viruses
Published: January 31, 2022
"Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats.
Journal: Journal of personalized medicine
Published: November 22, 2021
A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 18, 2021
Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System.
Journal: Journal of clinical medicine
Published: July 13, 2021
Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile.
Journal: Clinical epigenetics
Published: June 03, 2021
Last Updated: 09/26/2026