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Journal of Neurology|August 23, 2023
Sensory neuropathy in amyotrophic lateral sclerosis: a systematic reviewAlessandro Bombaci, Antonino Lupica, Federico Emanuele Pozzi, et al.
Scientific Reports|August 12, 2022
Deep learning methods to predict amyotrophic lateral sclerosis disease progressionCorrado Pancotti, Giovanni Birolo, Cesare Rollo, et al.
Clinical Genetics|December 13, 2023
A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's diseaseAntonio Canosa, Sara Cabras, Francesca Di Pede, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2014
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year courseAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
CNS & Neurological Disorders Drug Targets|August 18, 2023
Mycotoxins and Amyotrophic Lateral Sclerosis: Food Exposure, Nutritional Implications and Dietary SolutionsUmberto Manera, Enrico Matteoni, Antonio Canosa, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 9, 2021
Can amyotrophic lateral sclerosis progression really pause? A cohort study using the medical research council scaleRosario Vasta, Luca Solero, Francesca Palumbo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 12, 2019
Early weight loss in amyotrophic lateral sclerosis: outcome relevance and clinical correlates in a population-based cohortCristina Moglia, Andrea Calvo, Maurizio Grassano, et al.
European Journal of Neurology|December 14, 2020
Neck flexor weakness at diagnosis predicts respiratory impairment in amyotrophic lateral sclerosisRosario Vasta, Maria Claudia Torrieri, Fabrizio D'Ovidio, et al.
Computer Methods and Programs in Biomedicine|February 12, 2022
Causal associations of genetic factors with clinical progression in amyotrophic lateral sclerosisMeysam Ahangaran, Adriano Chiò, Fabrizio D'Ovidio, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutationAntonio Canosa, Maurizio Grassano, Marco Barberis, et al.
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