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European Journal of Neurology|January 20, 2025
Mitochondrial DNA (mtDNA) as fluid biomarker in neurodegenerative disorders: A systematic reviewBarbara Risi, Alberto Imarisio, Giada Cuconato, et al.Frontiers in Neurology|October 23, 2023
Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathyLoris Poli, Beatrice Labella, Stefano Cotti Piccinelli, et al.Nutrition Research Reviews|April 24, 2026
Diet and nutrition in patients with neuromuscular disorders, as lifestyle factors affecting clinical parameters and quality of life: a narrative systematic reviewSilvia Marconi, Giulia Gilberti, Barbara Zanini, et al.Journal of Clinical Medicine|August 12, 2023
Prognostic Usefulness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral SclerosisBarbara Risi, Stefano Cotti Piccinelli, Stefano Gazzina, et al.Biomolecules|September 28, 2023
A Comprehensive Update on Late-Onset Pompe DiseaseBeatrice Labella, Stefano Cotti Piccinelli, Barbara Risi, et al.Brain Sciences|August 26, 2023
Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the <i>ACADVL</i> GeneBeatrice Labella, Gaetana Lanzi, Stefano Cotti Piccinelli, et al.Biomedicines|September 28, 2023
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological StudyStefano Cotti Piccinelli, Matteo Tagliapietra, Tiziana Cavallaro, et al.Brain Sciences|November 27, 2024
Gold Coast Criteria in ALS Diagnosis: A Real-World ExperienceLucia Ferullo, Barbara Risi, Filomena Caria, et al.Clinical Genetics|August 11, 2025
The Role of Whole-Exome Sequencing and Methylation Analysis in Untangling Complex Facioscapulo-Humeral Muscular Dystrophy CasesFrancesca Torri, Claudia Strafella, Liliana Vercelli, et al.Journal of Medical Case Reports|February 20, 2025
SELENON-related myopathy as a cause of acute respiratory failure in middle age: a case reportBarbara Risi, Filomena Caria, Simona Damioli, et al.Pageof 3