Umberto Sabatini
Catanzaro, Italy
Last Updated: 09/26/2026
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Found 74 publications
Quantitative Assessment of Visible Nigrosome-1 in Patients with Parkinson's Disease.
Journal: Movement disorders clinical practice
Published: December 20, 2025
Substantia Nigra as Brainstem Signature in Pediatric-Onset Huntington's Disease: The RAREST-JHD Study.
Journal: Movement disorders clinical practice
Published: May 15, 2025
MRI evidence of cerebellar vermian hypoplasia in a patient with cervical dystonia.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: November 29, 2024
Challenges in diagnosing vascular parkinsonism: the pitfalls of an old tale.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 02, 2024
Pediatric Huntington Disease Brains Have Distinct Morphologic and Metabolic Traits: the RAREST-JHD Study.
Journal: Movement disorders clinical practice
Published: April 21, 2024
Peculiar CADASIL phenotype in monozygotic twins carrying a novel NOTCH3 pathogenetic variant.
Journal: European review for medical and pharmacological sciences
Published: March 04, 2024
Cervical dystonia in a patient with cervical hydromyelic cavity.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 12, 2023
Hypofractionated Stereotactic Re-irradiation and Anti-PDL1 Durvalumab Combination in Recurrent Glioblastoma: STERIMGLI Phase I Results.
Journal: The oncologist
Published: December 15, 2022
Mid-term follow-up chest CT findings in recovered COVID-19 patients with residual symptoms.
Journal: The British journal of radiology
Published: November 25, 2022
A mid-term follow-up with a lung ultrasonographic score correlates with the severity of COVID-19 acute phase.
Journal: Internal and emergency medicine
Published: July 27, 2022
Early liver steatosis in children with pediatric Huntington disease and highly expanded CAG mutations.
Journal: Parkinsonism & related disorders
Published: June 29, 2022
Last Updated: 09/26/2026