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Items: 16

1.

Longitudinal natural history in young boys with Duchenne muscular dystrophy.

Coratti G, Brogna C, Norcia G, Ricotti V, Abbott L, D'Amico A, Berardinelli A, Vita GL, Lucibello S, Messina S, Sansone V, Albamonte E, Colia G, Salmin F, Gardani A, Manzur A, Main M, Baranello G, Arnoldi MT, Parsons J, Carry T, Connolly AM, Bertini E, Muntoni F, Pane M, Mercuri E.

Neuromuscul Disord. 2019 Sep 26. pii: S0960-8966(19)31130-7. doi: 10.1016/j.nmd.2019.09.010. [Epub ahead of print]

PMID:
31629611
2.

Early neurodevelopmental characterization in children with cobalamin C/defect.

Ricci D, Martinelli D, Ferrantini G, Lucibello S, Gambardella ML, Olivieri G, Chieffo D, Battaglia D, Diodato D, Iarossi G, Donati A, Dionisi-Vici C, Battini R, Mercuri E.

J Inherit Metab Dis. 2019 Sep 10. doi: 10.1002/jimd.12171. [Epub ahead of print]

PMID:
31503356
3.

Long-term progression in type II spinal muscular atrophy: A retrospective observational study.

Mercuri E, Lucibello S, Pera MC, Carnicella S, Coratti G, de Sanctis R, Messina S, Mazzone E, Forcina N, Fanelli L, Norcia G, Antonaci L, Frongia AL, Pane M.

Neurology. 2019 Sep 24;93(13):e1241-e1247. doi: 10.1212/WNL.0000000000008166. Epub 2019 Aug 26.

PMID:
31451515
4.

Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world data.

Pane M, Coratti G, Sansone VA, Messina S, Bruno C, Catteruccia M, Sframeli M, Albamonte E, Pedemonte M, D'Amico A, Bravetti C, Berti B, Brigati G, Tacchetti P, Salmin F, de Sanctis R, Lucibello S, Piastra M, Genovese O, Bertini E, Vita G, Tiziano FD, Mercuri E; Italian Expanded Access Program Working Group.

Ann Neurol. 2019 Sep;86(3):443-451. doi: 10.1002/ana.25533. Epub 2019 Jul 8.

PMID:
31228281
5.

Brain morphometry of preschool age children affected by autism spectrum disorder: Correlation with clinical findings.

Lucibello S, Verdolotti T, Giordano FM, Lapenta L, Infante A, Piludu F, Tartaglione T, Chieffo D, Colosimo C, Mercuri E, Battini R.

Clin Anat. 2019 Jan;32(1):143-150. doi: 10.1002/ca.23252.

PMID:
30113100
6.

An observational study of functional abilities in infants, children, and adults with type 1 SMA.

Pane M, Palermo C, Messina S, Sansone VA, Bruno C, Catteruccia M, Sframeli M, Albamonte E, Pedemonte M, D'Amico A, Brigati G, de Sanctis R, Coratti G, Lucibello S, Bertini E, Vita G, Danilo Tiziano F, Mercuri E; Italian EAP Working Group.

Neurology. 2018 Aug 21;91(8):e696-e703. doi: 10.1212/WNL.0000000000006050. Epub 2018 Jul 25.

7.

Nusinersen in type 1 SMA infants, children and young adults: Preliminary results on motor function.

Pane M, Palermo C, Messina S, Sansone VA, Bruno C, Catteruccia M, Sframeli M, Albamonte E, Pedemonte M, D'Amico A, Brigati G, de Sanctis R, Coratti G, Lucibello S, Bertini E, Vita G, Tiziano FD, Mercuri E; Italian EAP working group.

Neuromuscul Disord. 2018 Jul;28(7):582-585. doi: 10.1016/j.nmd.2018.05.010. Epub 2018 Jun 1.

PMID:
29960818
8.

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.

J Pediatr. 2018 Jun;197:104-108. doi: 10.1016/j.jpeds.2018.02.008. Epub 2018 Apr 9.

PMID:
29650414
9.

Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?

Vicari S, Piccini G, Mercuri E, Battini R, Chieffo D, Bulgheroni S, Pecini C, Lucibello S, Lenzi S, Moriconi F, Pane M, D'Amico A, Astrea G, Baranello G, Riva D, Cioni G, Alfieri P.

PLoS One. 2018 Jan 16;13(1):e0191164. doi: 10.1371/journal.pone.0191164. eCollection 2018.

10.

Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions.

Battini R, Chieffo D, Bulgheroni S, Piccini G, Pecini C, Lucibello S, Lenzi S, Moriconi F, Pane M, Astrea G, Baranello G, Alfieri P, Vicari S, Riva D, Cioni G, Mercuri E.

Neuromuscul Disord. 2018 Feb;28(2):122-128. doi: 10.1016/j.nmd.2017.11.018. Epub 2017 Dec 6.

PMID:
29305139
11.

Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy.

De Sanctis R, Pane M, Coratti G, Palermo C, Leone D, Pera MC, Abiusi E, Fiori S, Forcina N, Fanelli L, Lucibello S, Mazzone ES, Tiziano FD, Mercuri E.

Neuromuscul Disord. 2018 Jan;28(1):24-28. doi: 10.1016/j.nmd.2017.09.015. Epub 2017 Oct 10.

PMID:
29174525
12.

Inter and intra-rater reliability and minimal detectable difference of Movement Disorder-Childhood Rating Scale.

Sgandurra G, Olivieri I, Casarano M, DI Pietro R, Menici V, Velli C, Sini F, Lucibello S, Romeo DM, Cioni G, Battini R.

Eur J Phys Rehabil Med. 2018 Feb;54(1):48-57. doi: 10.23736/S1973-9087.17.04661-5. Epub 2017 Jul 13.

13.

Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy.

Pera MC, Coratti G, Forcina N, Mazzone ES, Scoto M, Montes J, Pasternak A, Mayhew A, Messina S, Sframeli M, Main M, Lofra RM, Duong T, Ramsey D, Dunaway S, Salazar R, Fanelli L, Civitello M, de Sanctis R, Antonaci L, Lapenta L, Lucibello S, Pane M, Day J, Darras BT, De Vivo DC, Muntoni F, Finkel R, Mercuri E.

BMC Neurol. 2017 Feb 23;17(1):39. doi: 10.1186/s12883-017-0790-9.

14.

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.

J Pediatr. 2016 Sep;176:162-6. doi: 10.1016/j.jpeds.2016.05.072. Epub 2016 Jun 20.

PMID:
27339250
15.

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.

Epilepsy Behav. 2016 Jan;54:30-3. doi: 10.1016/j.yebeh.2015.10.027. Epub 2015 Nov 26.

PMID:
26630186
16.

Galectin-3 plasma levels and coronary artery disease: a new possible biomarker of acute coronary syndrome.

Falcone C, Lucibello S, Mazzucchelli I, Bozzini S, D'Angelo A, Schirinzi S, Totaro R, Falcone R, Bondesan M, Pelissero G.

Int J Immunopathol Pharmacol. 2011 Oct-Dec;24(4):905-13.

PMID:
22230397

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