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Early Human Development|March 18, 2020
Early Childhood Attention Battery: Italian adaptation and new expanded normative dataGiorgia Coratti, Maria Mallardi, Carolina Coppola, et al.Orphanet Journal of Rare Diseases|April 7, 2020
Longitudinal natural history of type I spinal muscular atrophy: a critical reviewEugenio Mercuri, Simona Lucibello, Marco Perulli, et al.Journal of Inherited Metabolic Disease|September 11, 2019
Early neurodevelopmental characterization in children with cobalamin C/defectDaniela Ricci, Diego Martinelli, Gloria Ferrantini, et al.Neurology|August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational studyEugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.Pediatric Pulmonology|May 13, 2020
Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophyDanilo Buonsenso, Beatrice Berti, Concetta Palermo, et al.Neuromuscular Disorders : NMD|November 28, 2017
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophyRoberto De Sanctis, Marika Pane, Giorgia Coratti, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 11, 2020
Respiratory function and therapeutic expectations in DMD: families experience and perspectiveClaudia Brogna, Simona Lucibello, Giorgia Coratti, et al.Journal of Neuromuscular Diseases|May 24, 2021
Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New ModuleBeatrice Berti, Lavinia Fanelli, Roberto de Sanctis, et al.Plos One|January 17, 2018
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?Stefano Vicari, Giorgia Piccini, Eugenio Mercuri, et al.Journal of Clinical Medicine|January 21, 2023
A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable?Daniela P R Chieffo, Federica Moriconi, Marika Pane, et al.Pageof 4