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Handbook of Clinical Neurology|September 25, 2024
Rare forms of hypomyelination and delayed myelinationEleonora Mura, Cecilia Parazzini, Davide TondutiMolecular Genetics and Metabolism|February 22, 2023
Type I Alexander disease: Update and validation of the clinical evolution-based classificationYlenia Vaia, Eleonora Mura, Davide TondutiDisability and Health Journal|December 28, 2020
Impact of COVID-19 lockdown in children with neurological disorders in ItalyStefania Maria Bova, Martina Basso, Marta Francesca Bianchi, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 8, 2026
Complicated Spastic Paraparesis: Study of a Patient With a De Novo Pathogenic Variant in ELOVL1Ylenia Vaia, Eleonora Mura, Fabio Bruschi, et al.Journal of Human Genetics|March 31, 2021
Spinal cord involvement and paroxysmal events in "Infantile Onset Transient Hypomyelination" due to TMEM63A mutationDavide Tonduti, Eleonora Mura, Silvia Masnada, et al.Metabolic Brain Disease|March 15, 2021
Ruxolitinib in Aicardi-Goutières syndromeEleonora Mura, Silvia Masnada, Clara Antonello, et al.International Journal of Cancer|November 10, 2018
Comprehensive analysis of HPV infection, EGFR exon 20 mutations and LINE1 hypomethylation as risk factors for malignant transformation of sinonasal-inverted papilloma to squamous cell carcinomaNora Sahnane, Giorgia Ottini, Mario Turri-Zanoni, et al.Molecular Genetics and Metabolism|December 6, 2021
Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patientsEleonora Mura, Francesco Nicita, Silvia Masnada, et al.Molecular Genetics and Metabolism|December 31, 2021
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley SyndromeSilvia Masnada, Catherine Sarret, Clara Eleonora Antonello, et al.Pageof 1