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Revisiting mitochondrial ocular myopathies: a study from the Italian Network.
Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Federico A, Minetti C, Moggio M, Mongini T, Santorelli FM, Servidei S, Tonin P, Ardissone A, Bello L, Bruno C, Ienco EC, Diodato D, Filosto M, Lamperti C, Moroni I, Musumeci O, Pegoraro E, Primiano G, Ronchi D, Rubegni A, Salvatore S, Sciacco M, Valentino ML, Vercelli L, Toscano A, Zeviani M, Siciliano G, Mancuso M. Orsucci D, et al. Among authors: rubegni a. J Neurol. 2017 Aug;264(8):1777-1784. doi: 10.1007/s00415-017-8567-z. Epub 2017 Jul 10. J Neurol. 2017. PMID: 28695364
Tarlov cysts: clinical evaluation of an italian cohort of patients.
Marino D, Carluccio MA, Di Donato I, Sicurelli F, Chini E, Di Toro Mammarella L, Rossi F, Rubegni A, Federico A. Marino D, et al. Among authors: rubegni a. Neurol Sci. 2013 Sep;34(9):1679-82. doi: 10.1007/s10072-013-1321-0. Epub 2013 Feb 12. Neurol Sci. 2013. PMID: 23400656 Free article.
Centronuclear myopathies: genotype-phenotype correlation and frequency of defined genetic forms in an Italian cohort.
Fattori F, Maggi L, Bruno C, Cassandrini D, Codemo V, Catteruccia M, Tasca G, Berardinelli A, Magri F, Pane M, Rubegni A, Santoro L, Ruggiero L, Fiorini P, Pini A, Mongini T, Messina S, Brisca G, Colombo I, Astrea G, Fiorillo C, Bragato C, Moroni I, Pegoraro E, D'Apice MR, Alfei E, Mora M, Morandi L, Donati A, Evilä A, Vihola A, Udd B, Bernansconi P, Mercuri E, Santorelli FM, Bertini E, D'Amico A. Fattori F, et al. Among authors: rubegni a. J Neurol. 2015 Jul;262(7):1728-40. doi: 10.1007/s00415-015-7757-9. Epub 2015 May 10. J Neurol. 2015. PMID: 25957634
Hereditary spastic paraplegia type 11 with a very late onset.
Rubegni A, Storti E, Tessa A, Federico A, Santorelli FM. Rubegni A, et al. J Neurol. 2015 Aug;262(8):1987-9. doi: 10.1007/s00415-015-7854-9. Epub 2015 Jul 17. J Neurol. 2015. PMID: 26183056 No abstract available.
75 results