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Journal of Neurology|April 6, 2019
Parkinsonian traits in amyotrophic lateral sclerosis (ALS): a prospective population-based studyAndrea Calvo, Adriano Chiò, Marco Pagani, et al.Journal of Neurology|November 17, 2025
Role of 2-[18F]FDG-PET as a biomarker of upper motor neuron involvement in amyotrophic lateral sclerosisSara Cabras, Umberto Manera, Francesca Di Pede, et al.Neurogenetics|April 3, 2013
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsAntonino Cannas, Giuseppe Borghero, Gian Luca Floris, et al.Journal of Neurology|October 26, 2016
Factors predicting survival in ALS: a multicenter Italian studyAndrea Calvo, Cristina Moglia, Christian Lunetta, et al.Journal of Neurology|August 22, 2025
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genesArianna Manini, Alberto Brusati, Maurizio Grassano, et al.European Journal of Nuclear Medicine and Molecular Imaging|December 11, 2025
Brain metabolic connectivity in ALS due to C9ORF72 hexanucleotide expansion: a [18F]FDG-PET studyAntonio Canosa, Stefano Callegaro, Umberto Manera, et al.Frontiers in Immunology|January 2, 2023
Markers of blood-brain barrier disruption increase early and persistently in COVID-19 patients with neurological manifestationsValentina Bonetto, Laura Pasetto, Ilaria Lisi, et al.Journal of Neurology|August 16, 2015
C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian populationAntonino Cannas, Paolo Solla, Giuseppe Borghero, et al.Neurobiology of Aging|August 16, 2014
Genetic architecture of ALS in SardiniaGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, et al.Nature Communications|August 17, 2023
Randomized, double-blind, placebo-controlled trial of rapamycin in amyotrophic lateral sclerosisJessica Mandrioli, Roberto D'Amico, Elisabetta Zucchi, et al.Pageof 25