Last Updated: 09/26/2026
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Found 19 publications
Functional and structural neuroplasticity of somatosensory system in hemiplegic cerebral palsy.
Journal: Brain communications
Published: August 22, 2025
Genetic Panel Reveals Coexisting Neuromuscular Disorders in Patients With Duchenne Muscular Dystrophy.
Journal: Journal of child neurology
Published: October 21, 2024
Spatiotemporal dynamics of cortical somatosensory network in typically developing children.
Journal: Cerebral cortex (New York, N.Y. : 1991)
Published: May 21, 2023
Long-Term Follow-Up of Pediatric Patients with Dyskinetic Cerebral Palsy and Deep Brain Stimulation.
Long-Term Follow-Up of Pediatric Patients with Dyskinetic Cerebral Palsy and Deep Brain Stimulation.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 24, 2023
Myalgic Becker Muscular Dystrophy Due to an Exon 15 Point Mutation: Case Series and Literature Review.
Journal: Journal of clinical neuromuscular disease
Published: November 21, 2022
Highlighting the Dystonic Phenotype Related to GNAO1.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 17, 2022
Quality of Life After Deep Brain Stimulation of Pediatric Patients with Dyskinetic Cerebral Palsy: A Prospective, Single-Arm, Multicenter Study with a Subsequent Randomized Double-Blind Crossover (STIM-CP).
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 10, 2021
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial.
Journal: Journal of neuromuscular diseases
Published: June 14, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss.
Journal: American journal of human genetics
Published: May 28, 2021
Aberrant somatosensory phase synchronization in children with hemiplegic cerebral palsy.
Journal: Neuroscience letters
Published: May 11, 2021
De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment.
Journal: American journal of human genetics
Published: July 01, 2020
Management of movement disorders in children - Authors' reply.
Journal: The Lancet. Neurology
Published: October 03, 2016
Last Updated: 09/26/2026