Ivana Ricca
Via Dei Giacinti 2
Pisa, 56128, Italy
Pisa, 56128, Italy
Last Updated: 09/26/2026
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Found 39 publications
Correction: Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses.
Correction: Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses.
Journal: Journal of neurology
Published: October 15, 2025
Miglustat does not impact clinical progression in patients with spastic paraplegia type 11.
Journal: Neurogenetics
Published: August 28, 2025
Feasibility of a smartphone application for remote use in spastic ataxias: an 8-week long-term PROSPAX study.
Journal: Journal of neurology
Published: August 20, 2025
Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies.
Journal: American journal of human genetics
Published: July 17, 2025
HPDL Biallelic Variants in Cerebral Palsy and Childhood-Onset Hereditary Spastic Paraplegia: Human and Zebrafish Insights.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 25, 2025
Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7: A Multicenter PROSPAX Study.
Journal: Neurology
Published: December 02, 2024
Correction to: Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Journal: Journal of neurology
Published: November 05, 2024
Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses.
Journal: Journal of neurology
Published: May 28, 2024
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Journal: Journal of neurology
Published: April 22, 2024
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 13, 2024
Decreasing ganglioside synthesis delays motor and cognitive symptom onset in Spg11 knockout mice.
Journal: Neurobiology of disease
Published: January 30, 2024
A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A.
Journal: Journal of neurology
Published: May 09, 2023
Last Updated: 09/26/2026