IR
Ivana Ricca
Fondazione Stella Maris
Research areas: Neuroscience · Cellular and Molecular Neuroscience · Hereditary Neurological Disorders · Genetic Neurodegenerative Diseases · Genomics and Rare Diseases
0000-0001-8939-1447
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Publications (60)
- Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies Save
- An Investigation of Corticospinal Tract Microstructural Integrity in ARSACS Using a Profilometry MRI Analysis: Results From the PROSPAX Study Save
- Feasibility of a smartphone application for remote use in spastic ataxias: an 8-week long-term PROSPAX study Save
- HPDL Biallelic Variants in Cerebral Palsy and Childhood-Onset Hereditary Spastic Paraplegia: Human and Zebrafish Insights Save
- Miglustat does not impact clinical progression in patients with spastic paraplegia type 11 Save
- Multicenter, Phase 3 Randomized Trial of Stereotactic Radiation vs. Hippocampal Avoidance Whole Brain Radiation in Patients with 5-20 Brain Metastases: Recurrence, Salvage Therapy, and Mortality Endpoints Save
- Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses Save
- Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses (vol 272, 94, 2025) Save
- Spastic Ataxia Composite (SPAXCOM): A Scale to Evaluate the Progression of Subjects with Spasticity and Ataxia Save
- Towards patient-relevant, trial-ready digital motor outcomes for SPG7: a cross-sectional prospective multi-center study (PROSPAX) Save
- Correction to: Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort (Journal of Neurology, (2024), 271, 8, (5478-5488), 10.1007/s00415-024-12506-x) Save
- Decreasing ganglioside synthesis delays motor and cognitive symptom onset in <italic>Spg11 </italic>knockout mice Save
- Decreasing ganglioside synthesis delays motor and cognitive symptom onset in Spg11 knockout mice Save
- Genomic and biological panoramas of non-muscle actinopathies Save
- MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study Save
- Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7: A Multicenter PROSPAX Study Save
- Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort Save
- A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A Save
- Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature Save
- POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients Save