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Journal of Child Neurology|September 15, 2005
Sturge-Weber syndrome: altered blood vessel fibronectin expression and morphologyAnne M Comi, Catherine J C Weisz, Bridget H Highet, et al.Life Sciences|May 4, 2025
Age-progressive stratification of Becker muscular dystrophy patients: a focus on muscle biopsy fibrosis, inflammation and capillary networkSimona Zanotti, Patrizia Ciscato, Laura Napoli, et al.Stem Cell Reports|November 14, 2025
Advances and challenges in modeling Charcot-Marie-Tooth type 2A using iPSC-derived modelsMafalda Rizzuti, Elisa Pagliari, Martina D'Agostino, et al.Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|December 6, 2013
Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patientS Lucchiari, G Ulzi, F Magri, et al.Journal of Neurology|November 14, 2013
Assessment of cardiac safety during fingolimod treatment initiation in a real-world relapsing multiple sclerosis population: a phase 3b, open-label studyRalf Gold, Giancarlo Comi, Jacqueline Palace, et al.Brain and Language|July 30, 2013
Disruption of structural connectivity along the dorsal and ventral language pathways in patients with nonfluent and semantic variant primary progressive aphasia: a DT MRI study and a literature reviewFederica Agosta, Sebastiano Galantucci, Elisa Canu, et al.Neuroimage|December 25, 2007
The topographical distribution of tissue injury in benign MS: a 3T multiparametric MRI studyAntonia Ceccarelli, Maria A Rocca, Elisabetta Pagani, et al.Journal of the Neurological Sciences|May 13, 2014
Clinical and MRI correlates of disease progression in a case of nonfluent/agrammatic variant of primary progressive aphasia due to progranulin (GRN) Cys157LysfsX97 mutationFrancesca Caso, Federica Agosta, Giuseppe Magnani, et al.European Journal of Immunology|August 26, 1998
IL-12 is involved in the induction of experimental autoimmune myasthenia gravis, an antibody-mediated diseaseL Moiola, F Galbiati, G Martino, et al.European Thyroid Journal|October 8, 2024
Role of genetics and epigenetics in Graves' orbitopathyMichele Marinò, Giovanna Rotondo Dottore, Francesca Menconi, et al.Pageof 253