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Year Number of Results
2015 1
2016 2
2018 2
2021 4
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9 results
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Page 1
EEG Patterns in Patients with Prader-Willi Syndrome.
Elia M, Rutigliano I, Sacco M, Madeo SF, Wasniewska M, Li Pomi A, Trifirò G, Di Bella P, De Lucia S, Vetri L, Iughetti L, Delvecchio M. Elia M, et al. Among authors: de lucia s. Brain Sci. 2021 Aug 6;11(8):1045. doi: 10.3390/brainsci11081045. Brain Sci. 2021. PMID: 34439664 Free PMC article.
Hierarchical Bayesian modelling of disease progression to inform clinical trial design in centronuclear myopathy.
Fouarge E, Monseur A, Boulanger B, Annoussamy M, Seferian AM, De Lucia S, Lilien C, Thielemans L, Paradis K, Cowling BS, Freitag C, Carlin BP, Servais L; NatHis-MTM Study Group. Fouarge E, et al. Among authors: de lucia s. Orphanet J Rare Dis. 2021 Jan 6;16(1):3. doi: 10.1186/s13023-020-01663-7. Orphanet J Rare Dis. 2021. PMID: 33407688 Free PMC article.
Autoimmune pituitary involvement in Prader-Willi syndrome: new perspective for further research.
Grugni G, Crinò A, De Bellis A, Convertino A, Bocchini S, Maestrini S, Cirillo P, De Lucia S, Delvecchio M; Italian Autoimmune Hypophysitis Network Study and of the Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinologyand Diabetology (ISPED). Grugni G, et al. Among authors: de lucia s. Endocrine. 2018 Dec;62(3):733-736. doi: 10.1007/s12020-018-1666-5. Epub 2018 Jul 2. Endocrine. 2018. PMID: 29968227
Ketogenic diet therapies in France: State of the use in 2018.
Dozières-Puyravel B, François L, de Lucia S, Goujon E, Danse M, Auvin S. Dozières-Puyravel B, et al. Among authors: de lucia s. Epilepsy Behav. 2018 Sep;86:204-206. doi: 10.1016/j.yebeh.2018.05.031. Epub 2018 Jul 8. Epilepsy Behav. 2018. PMID: 29997039
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international study.
Trucco F, Ridout D, Domingos J, Maresh K, Chesshyre M, Munot P, Sarkozy A, Robb S, Quinlivan R, Riley M, Wallis C, Chan E, Abel F, De Lucia S, Hogrel JY, Niks EH, de Groot I, Servais L, Straub V, Ricotti V, Manzur A, Muntoni F; UK NorthStar Clinical Network and AFM Network. Trucco F, et al. Among authors: de lucia s. Muscle Nerve. 2021 Oct 4. doi: 10.1002/mus.27427. Online ahead of print. Muscle Nerve. 2021. PMID: 34606104
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up.
Coratti G, Pane M, Brogna C, Ricotti V, Messina S, D'Amico A, Bruno C, Vita G, Berardinelli A, Mazzone E, Magri F, Ricci F, Mongini T, Battini R, Bello L, Pegoraro E, Baranello G, Previtali SC, Politano L, Comi GP, Sansone VA, Donati A, Hogrel JY, Straub V, De Lucia S, Niks E, Servais L, De Groot I, Chesshyre M, Bertini E, Goemans N, Muntoni F, Mercuri E; on behalf on the International DMD Group and the iMDEX Consortium. Coratti G, et al. Among authors: de lucia s. PLoS One. 2021 Jun 25;16(6):e0253882. doi: 10.1371/journal.pone.0253882. eCollection 2021. PLoS One. 2021. PMID: 34170974 Free PMC article.