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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.Eclinicalmedicine|July 1, 2026
Inter-centre heterogeneity, temporal evolution, and factors associated with treatment selection and outcomes in chronic inflammatory demyelinating polyradiculoneuropathy: a multicentre, combined prospective and retrospective observational studyAlberto De Lorenzo, Maria Margherita Sechi, Fiore Manganelli, et al.European Journal of Neurology|January 2, 2024
Impact of 2021 European Academy of Neurology/Peripheral Nerve Society diagnostic criteria on diagnosis and therapy of chronic inflammatory demyelinating polyradiculoneuropathy variantsAlberto De Lorenzo, Giuseppe Liberatore, Pietro Emiliano Doneddu, et al.Brain : a Journal of Neurology|February 28, 2012
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72Adriano Chiò, Giuseppe Borghero, Gabriella Restagno, et al.The Journal of Clinical Investigation|July 15, 2025
Sensory neuron-expressed FGF13 controls nociceptive signaling in diabetic neuropathy modelsAditya K Singh, Matteo Bernabucci, Nolan M Dvorak, et al.Cell Genomics|October 22, 2024
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic dataSara Saez-Atienzar, Cleide Dos Santos Souza, Ruth Chia, et al.Pageof 2