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Page 1
Selective theory of mind impairment and cerebellar atrophy: a case report.
Parente A, Manfredi V, Tarallo A, Salsano E, Erbetta A, Pareyson D, Giovagnoli AR. Parente A, et al. Among authors: salsano e. J Neurol. 2013 Aug;260(8):2166-9. doi: 10.1007/s00415-013-6985-0. Epub 2013 Jun 16. J Neurol. 2013. PMID: 23771507 No abstract available.
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS, Pareyson D. Orthmann-Murphy JL, et al. Among authors: salsano e. Brain. 2009 Feb;132(Pt 2):426-38. doi: 10.1093/brain/awn328. Epub 2008 Dec 4. Brain. 2009. PMID: 19056803 Free PMC article.
Hereditary predominantly motor neuropathies.
Pareyson D, Marchesi C, Salsano E. Pareyson D, et al. Among authors: salsano e. Curr Opin Neurol. 2009 Oct;22(5):451-9. doi: 10.1097/WCO.0b013e3283311dfd. Curr Opin Neurol. 2009. PMID: 19680125 Review.
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial.
Pareyson D, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Vita G, Quattrone A, Padua L, Gemignani F, Visioli F, Laurà M, Radice D, Calabrese D, Hughes RA, Solari A; CMT-TRIAAL; CMT-TRAUK groups. Pareyson D, et al. Lancet Neurol. 2011 Apr;10(4):320-8. doi: 10.1016/S1474-4422(11)70025-4. Lancet Neurol. 2011. PMID: 21393063 Free PMC article. Clinical Trial.
108 results