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The neuropathy in hereditary transthyretin amyloidosis: A narrative review.
Tozza S, Severi D, Spina E, Iovino A, Aruta F, Ruggiero L, Dubbioso R, Iodice R, Nolano M, Manganelli F. Tozza S, et al. J Peripher Nerv Syst. 2021 Jun;26(2):155-159. doi: 10.1111/jns.12451. Epub 2021 May 11. J Peripher Nerv Syst. 2021. PMID: 33960565 Free PMC article. Review.
Nerve conduction velocity in CMT1A: what else can we tell?
Manganelli F, Pisciotta C, Reilly MM, Tozza S, Schenone A, Fabrizi GM, Cavallaro T, Vita G, Padua L, Gemignani F, Laurà M, Hughes RA, Solari A, Pareyson D, Santoro L; CMT-TRIAAL and CMT-TRAUK Group. Manganelli F, et al. Among authors: tozza s. Eur J Neurol. 2016 Oct;23(10):1566-71. doi: 10.1111/ene.13079. Epub 2016 Jul 14. Eur J Neurol. 2016. PMID: 27412484 Free PMC article. Clinical Trial.
Postural instability in Charcot-Marie-Tooth 1A disease.
Tozza S, Aceto MG, Pisciotta C, Bruzzese D, Iodice R, Santoro L, Manganelli F. Tozza S, et al. Gait Posture. 2016 Sep;49:353-357. doi: 10.1016/j.gaitpost.2016.07.183. Epub 2016 Jul 28. Gait Posture. 2016. PMID: 27491052
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI.
Manganelli F, Parisi S, Nolano M, Tao F, Paladino S, Pisciotta C, Tozza S, Nesti C, Rebelo AP, Provitera V, Santorelli FM, Shy ME, Russo T, Zuchner S, Santoro L. Manganelli F, et al. Among authors: tozza s. Neurology. 2017 May 30;88(22):2132-2140. doi: 10.1212/WNL.0000000000003992. Epub 2017 May 3. Neurology. 2017. PMID: 28468842 Free PMC article.
Early predictive factors of disability in CIDP.
Spina E, Topa A, Iodice R, Tozza S, Ruggiero L, Dubbioso R, Esposito M, Bruzzese D, Santoro L, Manganelli F. Spina E, et al. Among authors: tozza s. J Neurol. 2017 Sep;264(9):1939-1944. doi: 10.1007/s00415-017-8578-9. Epub 2017 Aug 2. J Neurol. 2017. PMID: 28770373
79 results