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Molecular Genetics and Metabolism|February 22, 2023
Type I Alexander disease: Update and validation of the clinical evolution-based classificationYlenia Vaia, Eleonora Mura, Davide TondutiHandbook of Clinical Neurology|September 25, 2024
Rare forms of hypomyelination and delayed myelinationEleonora Mura, Cecilia Parazzini, Davide TondutiExpert Review of Clinical Immunology|December 20, 2019
Novel and emerging treatments for Aicardi-Goutières syndromeDavide Tonduti, Elisa Fazzi, Raffaele Badolato, et al.Expert Opinion on Emerging Drugs|December 20, 2024
Exploring emerging JAK inhibitors in the treatment of Aicardi-Goutières syndromeDavide Politano, Davide Tonduti, Roberta Battini, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 9, 2016
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander diseaseDavide Tonduti, Anna Ardissone, Isabella Ceccherini, et al.Pediatric Neurology|April 20, 2010
New case of 4H syndrome and a review of the literatureSimona Orcesi, Davide Tonduti, Carla Uggetti, et al.Journal of Child Neurology|April 25, 2015
Cerebrospinal Fluid Monoamine Metabolite Analysis in Pediatric Movement DisordersDavide Tonduti, Giovanna Zorzi, Daniele Ghezzi, et al.Neuropsychiatric Disease and Treatment|October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature ReviewNina-Maria Wilpert, Davide Tonduti, Ylenia Vaia, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|April 1, 2026
Early-Onset Hyperkinetic Movement Disorders Define the Most Severe Presentation of the ATP8A2-Related Phenotypic SpectrumFabio Bruschi, Clara E Antonello, Cecilia Parazzini, et al.Journal of Pediatric Psychology|August 25, 2025
The impact of leukodystrophies on parents' livesLaura Zampini, Laura Cordolcini, Lara Draghi, et al.Pageof 11