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Is it the right time for an infant screening for Duchenne muscular dystrophy?
Vita GL, Vita G
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020, 41, 7, p 1677
Genetic modifiers of respiratory function in Duchenne muscular dystrophy
Bello L, D'Angelo G, Villa M, et al.
Annals of clinical and translational neurology, 2020
Psychosocial impact of sport activity in neuromuscular disorders
Vita GL, Stancanelli C, La Foresta S, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Clinical Variability in Spinal Muscular Atrophy Type III
Coratti G, Messina S, Lucibello S, et al.
Annals of neurology, 2020
Practical approach to respiratory emergencies in neurological diseases
Racca F, Vianello A, Mongini T, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019
Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 2: diseases of motor neuron and skeletal muscle
Vita G, Vita GL, Musumeci O, et al.
Neurological sciences, 2019, 40, 4, p 671
Intrathecal administration of Nusinersen in type 1 SMA: successful psychological program in a single Italian center
La Foresta S, Faraone C, Sframeli M, et al.
Neurological sciences, 2018, 39, 11, p 1961
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data
Pane M, Coratti G, Brogna C, et al.
PLoS ONE, 2018, 13, 6
Sleep disorders in spinal muscular atrophy
Pera MC, Romeo DM, Graziano A, et al.
Sleep medicine, 2017, 30, p 160
Histological effects of givinostat in boys with Duchenne muscular dystrophy
Bettica P, Petrini S, D'Oria V, et al.
Neuromuscular disorders : NMD, 2016, 26, 10, p 643
Patterns of disease progression in type 2 and 3 SMA: Implications for clinical trials
Mercuri E, Finkel R, Montes J, et al.
Neuromuscular disorders : NMD, 2016, 26, 2, p 126
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study
Messina S, Vita GL, Sframeli M, et al.
Neuromuscular disorders : NMD, 2016, 26, 3, p 189
Sport activity in Charcot-Marie-Tooth disease: A case study of a Paralympic swimmer
Vita G, La Foresta S, Russo M, et al.
Neuromuscular disorders : NMD, 2016, 26, 9, p 614
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients
Fiorillo C, Astrea G, Savarese M, et al.
Orphanet journal of rare diseases, 2016, 11, 1, p 91
Effects of teriparatide on bone mineral density and quality of life in Duchenne muscular dystrophy related osteoporosis: a case report
Catalano A, Vita GL, Russo M, et al.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2016, 27, 12, p 3655
Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular Dystrophy
Mercuri E, Coratti G, Messina S, et al.
PLoS ONE, 2016, 11, 8
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test
Pane M, Fanelli L, Mazzone ES, et al.
Neuromuscular disorders : NMD, 2015, 25, 10, p 749
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
Barp A, Bello L, Politano L, et al.
PLoS ONE, 2015, 10, 10
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study
Magliano L, D'Angelo MG, Vita G, et al.
Acta myologica, 2014, 33, 3, p 136
"I have got something positive out of this situation" : psychological benefits of caregiving in relatives of young people with muscular dystrophy
Magliano L, Patalano M, Sagliocchi A, et al.
Journal of neurology, 2014, 261, 1, p. 188-195
Burden, professional support, and social network in families of children and young adults with muscular dystrophies
Magliano L, Patalano M, Sagliocchi A, et al.
Muscle & Nerve, 2014, 52, 1, p 13
The 6 minute walk test and performance of upper limb in ambulant Duchenne Muscular Dystrophy boys
Pane M, Mazzone ES, Sivo S, et al.
PLoS Currents, 2014, 6
6 minute walk test in duchenne MD patients with different mutations : 12 month changes
Pane M, Mazzone ES, Sormani MP, et al.
PLoS ONE, 2014, 9, 1, e83400, p. 1-7
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study
Tiziano FD, Lomastro R, Di Pietro L, et al.
European journal of human genetics, 2013, 21, 6, p. 630-636
Duchenne muscular dystrophy and epilepsy
Pane M, Messina S, D'Amico A, et al.
Neuromuscular disorders : NMD, 2013, 23, 4, p. 313-315
