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Neuropediatrics|March 3, 2023
Expanding the Spectrum of NUBPL-Related LeukodystrophyDavide Tonduti, Alberto A Zambon, Daniele Ghezzi, et al.
Cerebrovascular Diseases (Basel, Switzerland)|March 21, 2015
Defining minor symptoms in acute ischemic strokeDavide Strambo, Alberto A Zambon, Luisa Roveri, et al.
Human Molecular Genetics|December 24, 2019
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutationFabiana Longo, Sara Benedetti, Alberto A Zambon, et al.
Annals of Clinical and Translational Neurology|August 30, 2023
Expanding the spectrum of neonatal-onset AIFM1-associated disordersAlberto A Zambon, Daniele Ghezzi, Cristina Baldoli, et al.
Brain : a Journal of Neurology|April 26, 2025
Effects of atidarsagene autotemcel gene therapy on peripheral nerves in late-infantile metachromatic leukodystrophyAlberto A Zambon, Paola M V Rancoita, Angelo Quattrini, et al.
Journal of Inherited Metabolic Disease|April 15, 2021
Metachromatic leukodystrophy: A single-center longitudinal study of 45 patientsFrancesca Fumagalli, Alberto A Zambon, Paola M V Rancoita, et al.
European Journal of Neurology|February 13, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13Alessandro Bertini, Mary M Reilly, Chiara Pisciotta, et al.
Brain : a Journal of Neurology|November 5, 2024
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severityDomenico Gorgoglione, Daniele Sabbatini, Pietro Riguzzi, et al.
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