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Journal of Neuropathology and Experimental Neurology|February 10, 2010
Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutationGaetano Vattemi, Francesca Gualandi, Arie Oosterhof, et al.Journal of Neuromuscular Diseases|May 18, 2020
Clinical Phenotypes of DMD Exon 51 Skip Equivalent Deletions: A Systematic ReviewMegan A Waldrop, Rabah Ben Yaou, Karin K Lucas, et al.Blood Transfusion = Trasfusione Del Sangue|October 13, 2012
Universal neonatal screening for sickle cell disease and other haemoglobinopathies in Ferrara, ItalyElisa Ballardini, Anna Tarocco, Maria Marsella, et al.Biomolecules|November 27, 2024
Restored Collagen VI Microfilaments Network in the Extracellular Matrix of CRISPR-Edited Ullrich Congenital Muscular Dystrophy FibroblastsDaniela Benati, Eleonora Cattin, Federico Corradi, et al.Matrix Biology : Journal of the International Society for Matrix Biology|January 10, 2012
Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosisPatrizia Sabatelli, Francesca Gualandi, Sudheer Kumar Gara, et al.Journal of Biomedicine & Biotechnology|October 24, 2012
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx miceElena Bassi, Sofia Falzarano, Marina Fabris, et al.Oxidative Medicine and Cellular Longevity|October 27, 2011
Cyclosporine A in Ullrich congenital muscular dystrophy: long-term resultsLuciano Merlini, Patrizia Sabatelli, Annarita Armaroli, et al.Neuromuscular Disorders : NMD|September 1, 2019
Autosomal recessive Bethlem myopathy: A clinical, genetic and functional studyFilomena Caria, Matilde Cescon, Francesca Gualandi, et al.Plos One|November 28, 2013
Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular DystrophyIrina T Zaharieva, Mattia Calissano, Mariacristina Scoto, et al.Human Mutation|March 25, 2009
Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophyElena Martoni, Anna Urciuolo, Patrizia Sabatelli, et al.Pageof 19