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Frontiers in Neurology|February 15, 2021
Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple SclerosisMattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, et al.Molecular Therapy. Nucleic Acids|September 2, 2025
circARHGAP10 as a candidate biomarker and therapeutic target in myotonic dystrophy type 1Denisa Baci, Spyros Tastsoglou, Claudia Provenzano, et al.Journal of Neurology|March 13, 2012
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2Rosanna Cardani, Marzia Giagnacovo, Annalisa Botta, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 17, 2009
Common micro-RNA signature in skeletal muscle damage and regeneration induced by Duchenne muscular dystrophy and acute ischemiaSimona Greco, Marco De Simone, Claudia Colussi, et al.Plos One|June 4, 2016
"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 PatientsLaura Serra, Mara Cercignani, Michela Bruschini, et al.Frontiers in Neurology|May 16, 2020
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Na<sub>v</sub>1.4Serena Pagliarani, Sabrina Lucchiari, Marina Scarlato, et al.The Journal of Clinical Investigation|August 7, 2002
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)Martin Tristani-Firouzi, Judy L Jensen, Matthew R Donaldson, et al.Frontiers in Genetics|July 8, 2021
A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated <i>CNBP</i> AllelesAnnalisa Botta, Virginia Veronica Visconti, Luana Fontana, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|June 6, 2026
Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotoniaAnthony Frosio, Serena Calamaio, Serena Pagliarani, et al.Neurology. Clinical Practice|October 5, 2019
Consensus-based care recommendations for adults with myotonic dystrophy type 2Benedikt Schoser, Federica Montagnese, Guillaume Bassez, et al.Pageof 11