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Page 1
Long-Term Safety and Efficacy Data of Golodirsen in Ambulatory Patients with Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A First-in-human, Multicenter, Two-Part, Open-Label, Phase 1/2 Trial.
Servais L, Mercuri E, Straub V, Guglieri M, Seferian AM, Scoto M, Leone D, Koenig E, Khan N, Dugar A, Wang X, Han B, Wang D, Muntoni F; SKIP-NMD Study Group. Servais L, et al. Nucleic Acid Ther. 2022 Feb;32(1):29-39. doi: 10.1089/nat.2021.0043. Epub 2021 Nov 17. Nucleic Acid Ther. 2022. PMID: 34788571 Free PMC article. Clinical Trial.
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: ferrantini g. J Neuromuscul Dis. 2021;8(4):453-456. doi: 10.3233/JND-210640. J Neuromuscul Dis. 2021. PMID: 33935100 Free PMC article. Review.
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: ferrantini g. J Pediatr. 2016 Sep;176:162-6. doi: 10.1016/j.jpeds.2016.05.072. Epub 2016 Jun 20. J Pediatr. 2016. PMID: 27339250
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: ferrantini g. J Pediatr. 2018 Jun;197:104-108. doi: 10.1016/j.jpeds.2018.02.008. Epub 2018 Apr 9. J Pediatr. 2018. PMID: 29650414
Disorders of early language development in Dravet syndrome.
Chieffo D, Battaglia D, Lucibello S, Gambardella ML, Moriconi F, Ferrantini G, Leo G, Dravet C, Mercuri E, Guzzetta F. Chieffo D, et al. Among authors: ferrantini g. Epilepsy Behav. 2016 Jan;54:30-3. doi: 10.1016/j.yebeh.2015.10.027. Epub 2015 Nov 26. Epilepsy Behav. 2016. PMID: 26630186
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: ferrantini g. 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
Body mass index in type 2 spinal muscular atrophy: a longitudinal study.
Ferrantini G, Coratti G, Onesimo R, Lucibello S, Bompard S, Turrini I, Cicala G, Caprarelli M, Pera MC, Bravetti C, Berti B, Giorgio V, Bruno C, Brolatti N, Panicucci C, D'Amico A, Longo A, Leoni C, Sansone VA, Albamonte E, Messina S, Sframeli M, Bertini E, Pane M, Mercuri E; Italian ISMAC study group. Ferrantini G, et al. Eur J Pediatr. 2022 May;181(5):1923-1932. doi: 10.1007/s00431-021-04325-3. Epub 2022 Jan 19. Eur J Pediatr. 2022. PMID: 35048179 Free PMC article.
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen.
Sansone VA, Coratti G, Pera MC, Pane M, Messina S, Salmin F, Albamonte E, De Sanctis R, Sframeli M, Di Bella V, Morando S, d'Amico A, Frongia AL, Antonaci L, Pirola A, Pedemonte M, Bertini E, Bruno C, Mercuri E; Italian ISMAC group. Sansone VA, et al. Eur J Neurol. 2021 Feb;28(2):602-608. doi: 10.1111/ene.14567. Epub 2020 Oct 31. Eur J Neurol. 2021. PMID: 33012052 Free article.
15 results