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A 5-year clinical follow-up study from the Italian National Registry for FSHD.
Vercelli L, Mele F, Ruggiero L, Sera F, Tripodi S, Ricci G, Vallarola A, Villa L, Govi M, Maranda L, Di Muzio A, Scarlato M, Bucci E, Maggi L, Rodolico C, Moggio M, Filosto M, Antonini G, Previtali S, Angelini C, Berardinelli A, Pegoraro E, Siciliano G, Tomelleri G, Santoro L, Mongini T, Tupler R. Vercelli L, et al. Among authors: siciliano g. J Neurol. 2021 Jan;268(1):356-366. doi: 10.1007/s00415-020-10144-7. Epub 2020 Aug 19. J Neurol. 2021. PMID: 32813049 Free PMC article.
Phenotype modulators in myophosphorylase deficiency.
Martinuzzi A, Sartori E, Fanin M, Nascimbeni A, Valente L, Angelini C, Siciliano G, Mongini T, Tonin P, Tomelleri G, Toscano A, Merlini L, Bindoff LA, Bertelli S. Martinuzzi A, et al. Among authors: siciliano g. Ann Neurol. 2003 Apr;53(4):497-502. doi: 10.1002/ana.10499. Ann Neurol. 2003. PMID: 12666117
Absence of angiogenic genes modification in Italian ALS patients.
Del Bo R, Scarlato M, Ghezzi S, Martinelli-Boneschi F, Corti S, Locatelli F, Santoro D, Prelle A, Briani C, Nardini M, Siciliano G, Mancuso M, Murri L, Bresolin N, Comi GP. Del Bo R, et al. Among authors: siciliano g. Neurobiol Aging. 2008 Feb;29(2):314-6. doi: 10.1016/j.neurobiolaging.2006.10.008. Epub 2006 Nov 17. Neurobiol Aging. 2008. PMID: 17113198
Mitochondria and neurodegeneration.
Petrozzi L, Ricci G, Giglioli NJ, Siciliano G, Mancuso M. Petrozzi L, et al. Among authors: siciliano g. Biosci Rep. 2007 Jun;27(1-3):87-104. doi: 10.1007/s10540-007-9038-z. Biosci Rep. 2007. PMID: 17486441 Review.
Functional diagnostics in mitochondrial diseases.
Siciliano G, Volpi L, Piazza S, Ricci G, Mancuso M, Murri L. Siciliano G, et al. Biosci Rep. 2007 Jun;27(1-3):53-67. doi: 10.1007/s10540-007-9037-0. Biosci Rep. 2007. PMID: 17492503 Review.
618 results