Dalila De Vita
Caserta, Italy
Last Updated: 09/26/2026
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Found 11 publications
Optimized nuclei isolation and snRNA-seq reveal oligodendrocyte pathway dysregulation in MOGHE brain tissue from pediatric patients.
Journal: Scientific reports
Published: February 02, 2026
Usability and user experience of tablet-based teleneuropsychology platform for the diagnosis of mild cognitive impairment: the Italian experience.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 04, 2025
Accelerating digital innovation in clinical neuropsychology: simulation approach to support medical device certification.
Journal: Frontiers in digital health
Published: June 13, 2025
Correction to: A digital teleneuropsychology platform for the diagnosis of mild cognitive impairment: from concept to certification as a medical device.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 01, 2024
A digital teleneuropsychology platform for the diagnosis of mild cognitive impairment: from concept to certification as a medical device.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 12, 2024
Memory biases in Alzheimer's disease and mild cognitive impairment. A systematic review and metanalysis.
Journal: Neuroscience and biobehavioral reviews
Published: September 20, 2022
Time of isolation, education and gender influence the psychological outcome during COVID-19 lockdown in caregivers of patients with dementia.
Journal: European geriatric medicine
Published: June 23, 2020
Non-invasive brain stimulation in generalized anxiety disorder: A systematic review.
Journal: Progress in neuro-psychopharmacology & biological psychiatry
Published: December 03, 2018
Familial dominant epilepsy and mild pachygyria associated with a constitutional LIS1 mutation.
Journal: American journal of medical genetics. Part A
Published: May 22, 2018
Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations.
Journal: Neurology. Genetics
Published: June 17, 2017
Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.
Journal: Human mutation
Published: July 28, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026