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Molecular Neurodegeneration|August 11, 2021
Decoding distinctive features of plasma extracellular vesicles in amyotrophic lateral sclerosisLaura Pasetto, Stefano Callegaro, Alessandro Corbelli, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 25, 2017
Trauma and amyotrophic lateral sclerosis: a european population-based case-control study from the EURALS consortiumElisabetta Pupillo, Marco Poloni, Elisa Bianchi, et al.
European Journal of Neurology|December 10, 2024
Sex-related differences in amyotrophic lateral sclerosis: A 2-[18F]FDG-PET studyAntonio Canosa, Alessio Martino, Umberto Manera, et al.
European Journal of Nuclear Medicine and Molecular Imaging|July 17, 2016
A PET/CT approach to spinal cord metabolism in amyotrophic lateral sclerosisCecilia Marini, Angelina Cistaro, Cristina Campi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 14, 2020
Telemedicine for patients with amyotrophic lateral sclerosis during COVID-19 pandemic: an Italian ALS referral center experienceRosario Vasta, Cristina Moglia, Fabrizio D'Ovidio, et al.
Archives of Neurology|January 12, 2011
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP geneAdriano Chiò, Giuseppe Borghero, Maura Pugliatti, et al.
Annals of Neurology|February 20, 2025
Brain Metabolic Features of FUS-ALS: A 2-[18F]FDG-PET StudyAntonio Canosa, Umberto Manera, Rosario Vasta, et al.
European Journal of Physical and Rehabilitation Medicine|September 1, 2016
Assessing and treating pain in movement disorders, amyotrophic lateral sclerosis, severe acquired brain injury, disorders of consciousness, dementia, oncology and neuroinfectivology. Evidence and recommendations from the Italian Consensus Conference on Pain in NeurorehabilitationMichelangelo Bartolo, Adriano Chiò, Sergio Ferrari, et al.
Annals of Clinical and Translational Neurology|April 25, 2025
KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral SclerosisArianna Manini, Rosario Vasta, Alberto Brusati, et al.
Neurobiology of Aging|July 26, 2015
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestryGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, et al.
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