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Oncotarget|December 10, 2017
Epstein-Barr virus in tumor-infiltrating B cells of myasthenia gravis thymoma: an innocent bystander or an autoimmunity mediator?Paola Cavalcante, Stefania Marcuzzo, Sara Franzi, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|September 5, 2017
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expressionSamuele Gherardi, Matteo Bovolenta, Chiara Passarelli, et al.
Experimental Neurology|March 30, 2017
A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosisStefania Marcuzzo, Silvia Bonanno, Matteo Figini, et al.
Frontiers in Immunology|June 24, 2021
Next-Generation Sequencing Identifies Extended HLA Class I and II Haplotypes Associated With Early-Onset and Late-Onset Myasthenia Gravis in Italian, Norwegian, and Swedish PopulationsLisa E Creary, Sridevi Gangavarapu, Stacy J Caillier, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 22, 2016
Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathiesPaola Imbrici, Concetta Altamura, Giulia Maria Camerino, et al.
Cells|June 27, 2020
Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease PredictionCristina Cappelletti, Irene Tramacere, Paola Cavalcante, et al.
International Journal of Molecular Sciences|June 2, 2021
Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human PatientsClaudia Malacarne, Mariarita Galbiati, Eleonora Giagnorio, et al.
Nucleus (Austin, Tex.)|April 26, 2018
Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processesPia Bernasconi, Nicola Carboni, Giulia Ricci, et al.
Neuromuscular Disorders : NMD|February 12, 2021
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patientsRaffaella Brugnoni, Lorenzo Maggi, Eleonora Canioni, et al.
Neurology|October 3, 2014
LMNA-associated myopathies: the Italian experience in a large cohort of patientsLorenzo Maggi, Adele D'Amico, Antonella Pini, et al.
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