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Frontiers in Neurology|August 28, 2020
Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in <i>SCN4A</i> in a Large Cohort of Italian PatientsLorenzo Maggi, Raffaella Brugnoni, Eleonora Canioni, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravisNili Avidan, Rozen Le Panse, Hanne F Harbo, et al.
Acta Neuropathologica Communications|April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population studyAurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Orphanet Journal of Rare Diseases|June 14, 2012
The empowerment of translational research: lessons from laminopathiesSara Benedetti, Pia Bernasconi, Enrico Bertini, et al.
Frontiers in Genetics|March 21, 2020
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide StudyMarcella Neri, Rachele Rossi, Cecilia Trabanelli, et al.
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