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Cells|July 2, 2021
Redox Homeostasis in Muscular DystrophiesNicola Mosca, Sara Petrillo, Sara Bortolani, et al.
Muscle & Nerve|March 27, 2015
Magnetic resonance imaging pattern recognition in sporadic inclusion-body myositisGiorgio Tasca, Mauro Monforte, Chiara De Fino, et al.
Journal of Cachexia, Sarcopenia and Muscle|November 1, 2019
Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imagingMauro Monforte, Francesco Laschena, Pierfrancesco Ottaviani, et al.
International Journal of Molecular Sciences|January 5, 2021
Proteomics of Muscle Microdialysates Identifies Potential Circulating Biomarkers in Facioscapulohumeral Muscular DystrophyVictor Corasolla Carregari, Mauro Monforte, Giuseppe Di Maio, et al.
The Open Neurology Journal|November 3, 2011
An immunological analysis of dystroglycan subunits: lessons learned from a small cohort of non-congenital dystrophic patientsErnesto Pavoni, Francesca Sciandra, Giorgio Tasca, et al.
Frontiers in Neurology|February 27, 2019
Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and PerspectivesMatteo Paoletti, Anna Pichiecchio, Stefano Cotti Piccinelli, et al.
Clinical Neurology and Neurosurgery|January 6, 2023
ANCA-negative microscopic polyangiitis with neuromuscular involvement: When pathology could make the differenceFrancesca Vitali, Maria Ausilia Sciarrone, Giovanni Frisullo, et al.
Journal of Neurology|September 6, 2021
Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learningMauro Monforte, Sara Bortolani, Eleonora Torchia, et al.
Journal of the Neurological Sciences|May 12, 2009
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemiaGiorgio Tasca, Raffaele Iorio, Umberto Basile, et al.
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