Sara Grisanti
Modena, Italy
Last Updated: 09/26/2026
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Found 18 publications
Retinal structural changes in Parkinson's disease: differences in pRNFL thickness between GBA1-associated and idiopathic cases.
Journal: Parkinsonism & related disorders
Published: August 30, 2025
Artificial Intelligence Predicts GBA1 Mutated Status in Parkinson's Disease Patients.
Journal: Movement disorders clinical practice
Published: May 07, 2025
18F-FDG PET findings in Parkinson's disease associated to RAB32 S71R variant.
Journal: Parkinsonism & related disorders
Published: September 27, 2024
Pathophysiology of COVID-19-Related Extrapyramidal Disorders.
Journal: Advances in experimental medicine and biology
Published: September 16, 2024
Obsessive-compulsive disorder as a first manifestation of Ataxia with Oculomotor Apraxia type 2 due to a novel mutation of SETX gene.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: June 10, 2024
A Case of 18p Chromosomal Deletion Encompassing GNAL in a Patient With Dystonia-Parkinsonism.
Journal: Journal of movement disorders
Published: October 29, 2023
Vestibular Hypofunction in ARSACS Syndrome: A Possible Pitfall in the Differential Diagnosis of Recessive Cerebellar and Afferent Ataxias.
Journal: Neurology. Clinical practice
Published: July 24, 2023
Levodopa responsive asymmetric parkinsonism as clinical presentation of progranulin gene mutation.
Journal: Journal of the neurological sciences
Published: June 21, 2023
Recent Advances in the Treatment of Genetic Forms of Parkinson's Disease: Hype or Hope?
Journal: Cells
Published: January 29, 2023
Deconstructing speech alterations in episodic ataxia type 2: Perceptual-acoustic analysis in a case due to CACNA1A gene mutation.
Journal: Parkinsonism & related disorders
Published: December 21, 2022
Last Updated: 09/26/2026