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Human Pathology|February 3, 2007
Feasibility and diagnostic agreement in teledermatopathology using a virtual slide systemCesare Massone, H Peter Soyer, Gian Piero Lozzi, et al.Biochemical and Biophysical Research Communications|January 13, 2009
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6Natalia Cannelli, Barbara Garavaglia, Alessandro Simonati, et al.Plos One|May 7, 2014
Hyper-activation of Notch3 amplifies the proliferative potential of rhabdomyosarcoma cellsMaria De Salvo, Lavinia Raimondi, Serena Vella, et al.Human Mutation|January 30, 2009
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosisChiara Aiello, Alessandra Terracciano, Alessandro Simonati, et al.The European Respiratory Journal|June 2, 2019
Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertensionCsaba Galambos, Mary P Mullen, Joseph T Shieh, et al.Nutrients|November 9, 2017
Pediatric Chronic Intestinal Failure in Italy: Report from the 2016 Survey on Behalf of Italian Society for Gastroenterology, Hepatology and Nutrition (SIGENP)Antonella Diamanti, Teresa Capriati, Paolo Gandullia, et al.Pageof 10