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1,326 results

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Page 1
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.
Mantuano E, Romano S, Veneziano L, Gellera C, Castellotti B, Caimi S, Testa D, Estienne M, Zorzi G, Bugiani M, Rajabally YA, Barcina MJ, Servidei S, Panico A, Frontali M, Mariotti C. Mantuano E, et al. Among authors: romano s. J Neurol Sci. 2010 Apr 15;291(1-2):30-6. doi: 10.1016/j.jns.2010.01.010. Epub 2010 Feb 2. J Neurol Sci. 2010. PMID: 20129625
Impaired vasoreactivity in mildly disabled CADASIL patients.
Campolo J, De Maria R, Frontali M, Taroni F, Inzitari D, Federico A, Romano S, Puca E, Mariotti C, Tomasello C, Pantoni L, Pescini F, Dotti MT, Stromillo ML, De Stefano N, Tavani A, Parodi O. Campolo J, et al. Among authors: romano s. J Neurol Neurosurg Psychiatry. 2012 Mar;83(3):268-74. doi: 10.1136/jnnp-2011-300080. Epub 2011 Nov 9. J Neurol Neurosurg Psychiatry. 2012. PMID: 22072702
Effects of sapropterin on endothelium-dependent vasodilation in patients with CADASIL: a randomized controlled trial.
De Maria R, Campolo J, Frontali M, Taroni F, Federico A, Inzitari D, Tavani A, Romano S, Puca E, Orzi F, Francia A, Mariotti C, Tomasello C, Dotti MT, Stromillo ML, Pantoni L, Pescini F, Valenti R, Pelucchi C, Parolini M, Parodi O; CADASIL Study Investigators. De Maria R, et al. Among authors: romano s. Stroke. 2014 Oct;45(10):2959-66. doi: 10.1161/STROKEAHA.114.005937. Epub 2014 Sep 2. Stroke. 2014. PMID: 25184356 Clinical Trial.
Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial.
Romano S, Coarelli G, Marcotulli C, Leonardi L, Piccolo F, Spadaro M, Frontali M, Ferraldeschi M, Vulpiani MC, Ponzelli F, Salvetti M, Orzi F, Petrucci A, Vanacore N, Casali C, Ristori G. Romano S, et al. Lancet Neurol. 2015 Oct;14(10):985-91. doi: 10.1016/S1474-4422(15)00201-X. Epub 2015 Aug 25. Lancet Neurol. 2015. PMID: 26321318 Clinical Trial.
Analyzing the Effects of a G137V Mutation in the FXN Gene.
Faggianelli N, Puglisi R, Veneziano L, Romano S, Frontali M, Vannocci T, Fortuni S, Testi R, Pastore A. Faggianelli N, et al. Among authors: romano s. Front Mol Neurosci. 2015 Nov 25;8:66. doi: 10.3389/fnmol.2015.00066. eCollection 2015. Front Mol Neurosci. 2015. PMID: 26635519 Free PMC article.
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia.
Coarelli G, Romano S, Travaglini L, Ferraldeschi M, Nicita F, Spadaro M, Fornasiero A, Frontali M, Salvetti M, Bertini E, Ristori G. Coarelli G, et al. Among authors: romano s. Clin Neurol Neurosurg. 2018 May;168:60-63. doi: 10.1016/j.clineuro.2018.02.042. Epub 2018 Mar 3. Clin Neurol Neurosurg. 2018. PMID: 29524657
1,326 results