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Frontiers in Neurology|February 16, 2019
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the LiteratureDelia Gagliardi, Eleonora Mauri, Francesca Magri, et al.BMC Neurology|September 15, 2012
Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measuresAlberto Lerario, Serena Bonfiglio, MariaPia Sormani, et al.Neuromuscular Disorders : NMD|May 16, 2018
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literatureRoberta Brusa, Francesca Magri, Dimitra Papadimitriou, et al.Plos Genetics|March 29, 2014
An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selectionDiego Forni, Rachele Cagliani, Claudia Tresoldi, et al.Journal of the Neurological Sciences|April 24, 2012
Myotonia congenita: novel mutations in CLCN1 gene and functional characterizations in Italian patientsGianna Ulzi, Marzia Lecchi, Valeria Sansone, et al.Journal of Neurology|May 6, 2009
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degenerationChiara Villa, Eliana Venturelli, Chiara Fenoglio, et al.Molecular Biology and Evolution|February 8, 2013
Crohn's disease loci are common targets of protozoa-driven selectionRachele Cagliani, Uberto Pozzoli, Diego Forni, et al.Neuroscience Letters|April 30, 2011
GSK3β genetic variability in patients with Multiple SclerosisDaniela Galimberti, James Macmurray, Diego Scalabrini, et al.Journal of Neuroimmunology|May 6, 2014
No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosisFranca R Guerini, Mario Clerici, Rachele Cagliani, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosisFrancesca Magri, Roberta Brusa, Luca Bello, et al.Pageof 34