Détail de l'auteur
Auteur Vita GL |
Documents disponibles écrits par cet auteur



![]()
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
Revue : Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 41, 7 Titre : Is it the right time for an infant screening for Duchenne muscular dystrophy? Type de document : Article Auteurs : Vita GL ; Vita G Année de publication : 07/2020 Pages : p 1677 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32112218 / DOI : 10.1007/s10072-020-04307-7
N° Profil MNM : 2020031 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32112218 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Revue : Annals of clinical and translational neurology Titre : Genetic modifiers of respiratory function in Duchenne muscular dystrophy Type de document : Article Auteurs : Bello L, Auteur ; D'Angelo G ; Villa M ; Fusto A ; Vianello S ; Merlo B ; Sabbatini D ; Barp A ; Gandossini S ; Magri F ; Comi GP ; Pedemonte M ; Tacchetti P ; Lanzillotta V ; Trucco F ; D'Amico A ; Bertini E ; Astrea G ; Politano L ; Masson R ; Baranello G ; Albamonte E ; De Mattia E ; Rao F ; Sansone VA ; Previtali S ; Messina S ; Vita GL ; Berardinelli A ; Mongini T ; Pini A ; Pane M ; Mercuri E ; Vianello A ; Bruno C ; Hoffman EP ; Morgenroth L ; Gordish-Dressman H ; McDonald CM ; Pegoraro E Editeur : United States Année de publication : 04/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32343055 / DOI : 10.1002/acn3.51046
N° Profil MNM : 2020051 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32343055 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Revue : Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Titre : Psychosocial impact of sport activity in neuromuscular disorders Type de document : Article Auteurs : Vita GL, Auteur ; Stancanelli C ; La Foresta S ; Faraone C ; Sframeli M ; Ferrero A ; Fattore C ; Galbo R ; Ferraro M ; Ricci G ; Cotti Piccinelli S ; Pizzighello S ; Filosto M ; Martinuzzi A ; Padua L ; Trimarchi G ; Siciliano G ; Mongini T ; Lombardo ME ; Berardinelli A ; Vita G Editeur : Italy Année de publication : 04/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32246354 / DOI : 10.1007/s10072-020-04345-1
N° Profil MNM : 2020041 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32246354 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
Clinical Variability in Spinal Muscular Atrophy Type III
Coratti G, Messina S, Lucibello S, et al.
Annals of neurology, 2020
Revue : Annals of neurology Titre : Clinical Variability in Spinal Muscular Atrophy Type III Type de document : Article Auteurs : Coratti G ; Messina S ; Lucibello S ; Pera MC ; Montes J ; Pasternak A ; Bovis F ; Exposito Escudero J ; Mazzone ES ; Mayhew A ; Glanzman AM ; Young SD ; Salazar R ; Duong T ; Muni Lofra R ; De Sanctis R ; Carnicella S ; Milev E ; Civitello M ; Pane M ; Scoto M ; Bettolo CM ; Antonaci L ; Frongia A ; Sframeli M ; Vita GL ; D'Amico A ; van den Hauwe M ; Albamonte E ; Goemans N ; Darras BT ; Bertini E ; Sansone V ; Day J ; Nascimento Osorio A ; Bruno C ; Muntoni F ; de Vivo DC ; Finkel RS ; Mercuri E Editeur : United States Année de publication : 2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32926458 / DOI : 10.1002/ana.25900
N° Profil MNM : 2020092 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32926458 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Revue : Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Titre : Practical approach to respiratory emergencies in neurological diseases Type de document : Article Auteurs : Racca F ; Vianello A ; Mongini T ; Ruggeri P ; Versaci A ; Vita GL ; Vita G Editeur : Italy Année de publication : 12/2019 Langues : Anglais (eng) Mots-clés : adolescent ; adulte ; article de synthèse ; insuffisance respiratoire aiguë ; maladie neuromusculaire ; médecine d'urgence ; physiopathologie ; prise en charge thérapeutique ; recommandation Pubmed / DOI : Pubmed : 31792719 / DOI : 10.1007/s10072-019-04163-0
N° Profil MNM : 2019121 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31792719 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
![]()
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
Permalink![]()
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
Permalink![]()
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data
Pane M, Coratti G, Brogna C, et al.
PLoS ONE, 2018, 13, 6
Permalink![]()
Sleep disorders in spinal muscular atrophy
Pera MC, Romeo DM, Graziano A, et al.
Sleep medicine, 2017, 30, p 160
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy
Barp A, Bello L, Politano L, et al.
PLoS ONE, 2015, 10, 10
Permalink![]()
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
Permalink![]()
"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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
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
Permalink![]()
Duchenne muscular dystrophy and epilepsy
Pane M, Messina S, D'Amico A, et al.
Neuromuscular disorders : NMD, 2013, 23, 4, p. 313-315
Permalink