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2011 1
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46 results

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Page 1
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.
Bello L, Sabbatini D, Fusto A, Gorgoglione D, Borin GU, Penzo M, Riguzzi P, Villa M, Vianello S, Calore C, Melacini P, Vio R, Barp A, D'Angelo G, Gandossini S, Politano L, Berardinelli A, Messina S, Vita GL, Pedemonte M, Bruno C, Albamonte E, Sansone V, Baranello G, Masson R, Astrea G, D'Amico A, Bertini E, Pane M, Lucibello S, Mercuri E, Spurney C, Clemens P, Morgenroth L, Gordish-Dressman H, McDonald CM, Hoffman EP; CINRG-DNHS Investigators; Pegoraro E. Bello L, et al. Among authors: lucibello s. J Neuromuscul Dis. 2024;11(2):285-297. doi: 10.3233/JND-230129. J Neuromuscul Dis. 2024. PMID: 38363615 Free PMC article.
Early Gross Motor Milestones in Duchenne Muscular Dystrophy.
Norcia G, Lucibello S, Coratti G, Onesimo R, Pede E, Ferrantini G, Brogna C, Cicala G, Carnicella S, Forcina N, Fanelli L, Pane M, Mercuri E. Norcia G, et al. Among authors: lucibello s. J Neuromuscul Dis. 2021;8(4):453-456. doi: 10.3233/JND-210640. J Neuromuscul Dis. 2021. PMID: 33935100 Free PMC article. Review.
Longitudinal natural history of type I spinal muscular atrophy: a critical review.
Mercuri E, Lucibello S, Perulli M, Coratti G, de Sanctis R, Pera MC, Pane M, Montes J, de Vivo DC, Darras BT, Kolb SJ, Finkel RS. Mercuri E, et al. Among authors: lucibello s. Orphanet J Rare Dis. 2020 Apr 5;15(1):84. doi: 10.1186/s13023-020-01356-1. Orphanet J Rare Dis. 2020. PMID: 32248834 Free PMC article. Review.
Language Development in Preschool Duchenne Muscular Dystrophy Boys.
Chieffo DPR, Moriconi F, Mastrilli L, Lino F, Brogna C, Coratti G, Altobelli M, Massaroni V, Norcia G, Ferraroli E, Lucibello S, Pane M, Mercuri E. Chieffo DPR, et al. Among authors: lucibello s. Brain Sci. 2022 Sep 16;12(9):1252. doi: 10.3390/brainsci12091252. Brain Sci. 2022. PMID: 36138988 Free PMC article.
Assessing Joint Hypermobility in Preschool-Aged Children.
Romeo DM, Lucibello S, Musto E, Brogna C, Ferrantini G, Velli C, Cota F, Ricci D, Mercuri E. Romeo DM, et al. Among authors: lucibello s. J Pediatr. 2016 Sep;176:162-6. doi: 10.1016/j.jpeds.2016.05.072. Epub 2016 Jun 20. J Pediatr. 2016. PMID: 27339250
Clinical Variability in Spinal Muscular Atrophy Type III.
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. Coratti G, et al. Among authors: lucibello s. Ann Neurol. 2020 Dec;88(6):1109-1117. doi: 10.1002/ana.25900. Epub 2020 Oct 2. Ann Neurol. 2020. PMID: 32926458
Joint Laxity in Preschool Children Born Preterm.
Romeo DM, Velli C, Lucibello S, Ferrantini G, Leo G, Brogna C, Cota F, Ricci D, Gallini F, Romagnoli C, Vento G, Mercuri E. Romeo DM, et al. Among authors: lucibello s. J Pediatr. 2018 Jun;197:104-108. doi: 10.1016/j.jpeds.2018.02.008. Epub 2018 Apr 9. J Pediatr. 2018. PMID: 29650414
Early neurodevelopmental characterization in children with cobalamin C/defect.
Ricci D, Martinelli D, Ferrantini G, Lucibello S, Gambardella M, Olivieri G, Chieffo D, Battaglia D, Diodato D, Iarossi G, Donati AM, Dionisi-Vici C, Battini R, Mercuri EM. Ricci D, et al. Among authors: lucibello s. J Inherit Metab Dis. 2020 Mar;43(2):367-374. doi: 10.1002/jimd.12171. Epub 2020 Jan 16. J Inherit Metab Dis. 2020. PMID: 31503356
Type I SMA "new natural history": long-term data in nusinersen-treated patients.
Pane M, Coratti G, Sansone VA, Messina S, Catteruccia M, Bruno C, Sframeli M, Albamonte E, Pedemonte M, D'Amico A, Bravetti C, Berti B, Palermo C, Leone D, Brigati G, Tacchetti P, Salmin F, De Sanctis R, Lucibello S, Pera MC, Piastra M, Genovese O, Bertini E, Vita G, Tiziano FD, Mercuri E; Italian EAP Working Group. Pane M, et al. Among authors: lucibello s. Ann Clin Transl Neurol. 2021 Mar;8(3):548-557. doi: 10.1002/acn3.51276. Epub 2021 Feb 6. Ann Clin Transl Neurol. 2021. PMID: 33547876 Free PMC article.
46 results