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Journal of Neurology|September 5, 2023
Predictors for progression in amyotrophic lateral sclerosis associated to SOD1 mutation: insight from two population-based registriesIlaria Martinelli, Andrea Ghezzi, Elisabetta Zucchi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 25, 2022
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeatsAdriano Chio, Cristina Moglia, Antonio Canosa, et al.
Neurology|May 18, 2023
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and PrognosisAdriano Chiò, Cristina Moglia, Antonio Canosa, et al.
Annals of Clinical and Translational Neurology|January 18, 2024
Resting-state fMRI functional connectome of C9orf72 mutation statusMario Stanziano, Davide Fedeli, Umberto Manera, et al.
Brain : a Journal of Neurology|December 31, 2021
Defective cyclophilin A induces TDP-43 proteinopathy: implications for amyotrophic lateral sclerosis and frontotemporal dementiaLaura Pasetto, Maurizio Grassano, Silvia Pozzi, et al.
Neurology. Genetics|October 31, 2022
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral SclerosisAndrea Calvo, Antonio Canosa, Cristina Moglia, et al.
Neurology|September 25, 2025
Genetic Variants Associated With Neurodegenerative Disorders in Patients With Amyotrophic Lateral Sclerosis and Phenotypic VariabilityMaurizio Grassano, Emanuele Koumantakis, Francesca F Palumbo, et al.
Brain : a Journal of Neurology|May 8, 2026
King's stages of amyotrophic lateral sclerosis: an 18F-FDG-PET study of brain connectivityFrancesca Di Pede, Sara Cabras, Umberto Manera, et al.
Muscle & Nerve|January 22, 2011
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: clinical and biological results from a prospective multicenter studyAdriano Chiò, Gabriele Mora, Vincenzo La Bella, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|August 10, 2012
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: the Italian multicentre studyMario Sabatelli, Serena Lattante, Amelia Conte, et al.
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