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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 5, 2020
Psychosocial impact of sport activity in neuromuscular disordersGian Luca Vita, Claudia Stancanelli, Stefania La Foresta, et al.Sleep Medicine|February 21, 2017
Sleep disorders in spinal muscular atrophyMaria C Pera, Domenico M Romeo, Alessandra Graziano, et al.Plos One|October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated CardiomyopathyAndrea Barp, Luca Bello, Luisa Politano, et al.European Journal of Human Genetics : EJHG|October 18, 2012
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker studyFrancesco D Tiziano, Rosa Lomastro, Lorena Di Pietro, et al.Neuromuscular Disorders : NMD|October 21, 2019
Longitudinal natural history in young boys with Duchenne muscular dystrophyGiorgia Coratti, Claudia Brogna, Giulia Norcia, et al.Neuromuscular Disorders : NMD|February 27, 2016
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort studySonia Messina, Gian Luca Vita, Maria Sframeli, et al.Muscle & Nerve|November 4, 2014
Burden, professional support, and social network in families of children and young adults with muscular dystrophiesLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative studyLorenza Magliano, Maria Grazia D'Angelo, Giuseppe Vita, et al.Journal of Neurology|November 9, 2013
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophyLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.Neuromuscular Disorders : NMD|January 19, 2016
Patterns of disease progression in type 2 and 3 SMA: Implications for clinical trialsEugenio Mercuri, Richard Finkel, Jacqueline Montes, et al.Pageof 6