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ANT1 is reduced in sporadic inclusion body myositis.
Barca E, Aguennouz M, Mazzeo A, Messina S, Toscano A, Vita GL, Portaro S, Parisi D, Rodolico C. Barca E, et al. Among authors: vita gl. Neurol Sci. 2013 Feb;34(2):217-24. doi: 10.1007/s10072-012-0976-2. Epub 2012 Feb 21. Neurol Sci. 2013. PMID: 22350218
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients.
Fiorillo C, Astrea G, Savarese M, Cassandrini D, Brisca G, Trucco F, Pedemonte M, Trovato R, Ruggiero L, Vercelli L, D'Amico A, Tasca G, Pane M, Fanin M, Bello L, Broda P, Musumeci O, Rodolico C, Messina S, Vita GL, Sframeli M, Gibertini S, Morandi L, Mora M, Maggi L, Petrucci A, Massa R, Grandis M, Toscano A, Pegoraro E, Mercuri E, Bertini E, Mongini T, Santoro L, Nigro V, Minetti C, Santorelli FM, Bruno C; Italian Network on Congenital Myopathies. Fiorillo C, et al. Among authors: vita gl. Orphanet J Rare Dis. 2016 Jul 7;11(1):91. doi: 10.1186/s13023-016-0476-1. Orphanet J Rare Dis. 2016. PMID: 27387980 Free PMC article.
Bone quality in Duchenne muscular dystrophy.
Catalano A, Vita GL, Messina S. Catalano A, et al. Among authors: vita gl. J Endocrinol Invest. 2022 Jun;45(6):1267-1268. doi: 10.1007/s40618-022-01784-9. Epub 2022 Mar 11. J Endocrinol Invest. 2022. PMID: 35277840 No abstract available.
Frequency, entity and determinants of fatigue in Charcot-Marie-Tooth disease.
Bellofatto M, Bertini A, Tramacere I, Manganelli F, Fabrizi GM, Schenone A, Santoro L, Cavallaro T, Grandis M, Previtali SC, Falzone Y, Allegri I, Padua L, Pazzaglia C, Calabrese D, Saveri P, Quattrone A, Valentino P, Tozza S, Gentile L, Russo M, Mazzeo A, Vita G, Piacentini S, Pisciotta C, Pareyson D; Italian CMT Network. Bellofatto M, et al. Eur J Neurol. 2023 Mar;30(3):710-718. doi: 10.1111/ene.15643. Epub 2022 Dec 2. Eur J Neurol. 2023. PMID: 36458502 Free PMC article.
Duchenne muscular dystrophy and epilepsy.
Pane M, Messina S, Bruno C, D'Amico A, Villanova M, Brancalion B, Sivo S, Bianco F, Striano P, Battaglia D, Lettori D, Vita GL, Bertini E, Gualandi F, Ricotti V, Ferlini A, Mercuri E. Pane M, et al. Among authors: vita gl. Neuromuscul Disord. 2013 Apr;23(4):313-5. doi: 10.1016/j.nmd.2013.01.011. Epub 2013 Mar 7. Neuromuscul Disord. 2013. PMID: 23465656
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy.
Shieh PB, Elfring G, Trifillis P, Santos C, Peltz SW, Parsons JA, Apkon S, Darras BT, Campbell C, McDonald CM; Members of the Ataluren Phase IIb Study Group; Members of the Ataluren Phase IIb Study Clinical Evaluator Training Group; Members of the ACT DMD Study Group; Members of the ACT DMD Clinical Evaluator Training Group. Shieh PB, et al. J Comp Eff Res. 2021 Dec;10(18):1337-1347. doi: 10.2217/cer-2021-0018. Epub 2021 Oct 25. J Comp Eff Res. 2021. PMID: 34693725 Free article.
70 results