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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 24, 2019
PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survivalFederico Verde, Cinzia Tiloca, Claudia Morelli, et al.European Journal of Neurology|January 6, 2022
Upper motor neuron dysfunction is associated with the presence of behavioural impairment in patients with amyotrophic lateral sclerosisAlessio Maranzano, Barbara Poletti, Federica Solca, et al.Journal of the Neurological Sciences|September 6, 2024
Quantification of serum TDP-43 and neurofilament light chain in patients with amyotrophic lateral sclerosis stratified by UNC13A genotypeValeria Casiraghi, Ilaria Milone, Alberto Brusati, et al.Journal of Clinical Neurology (Seoul, Korea)|January 22, 2021
Ocular Involvement Occurs Frequently at All Stages of Amyotrophic Lateral Sclerosis: Preliminary Experience in a Large Italian CohortFederica Cozza, Andrea Lizio, Lucia Catherine Greco, et al.Frontiers in Psychology|April 21, 2018
The Complex Interplay Between Depression/Anxiety and Executive Functioning: Insights From the ECAS in a Large ALS PopulationLaura Carelli, Federica Solca, Andrea Faini, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 13, 2026
Cognitive and behavioral involvement in spinal and bulbar muscular atrophy (SBMA): a systematic reviewGiulia De Luca, Edoardo Nicolò Aiello, Arianna Moreschi, et al.The Lancet Regional Health. Europe|August 26, 2024
Transcranial static magnetic stimulation for amyotrophic lateral sclerosis: a bicentric, randomised, double-blind placebo-controlled phase 2 trialVincenzo Di Lazzaro, Federico Ranieri, Alberto Doretti, et al.Journal of Neurology|January 24, 2023
Brain positron emission tomography (PET) and cognitive abnormalities one year after COVID-19Roberta Ferrucci, Luca Cuffaro, Antonella Capozza, et al.Journal of Clinical Medicine|February 8, 2020
Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: <i>OPTN</i>, <i>VCP</i>, and <i>SQSTM1</i> Variants Account for 3% of Rare Genetic FormsViviana Pensato, Stefania Magri, Eleonora Dalla Bella, et al.Molecular Genetics and Metabolism Reports|August 2, 2017
A novel nonsense <i>ATP7A</i> pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotypeMaria Teresa Bonati, Federico Verde, Uros Hladnik, et al.Pageof 22