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Correction to: Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy.
Gentile L, Mazzeo A, Briani C, Casagrande S, De Luca M, Fabrizi GM, Gagliardi C, Gemelli C, Forcina F, Grandis M, Guglielmino V, Iabichella G, Leonardi L, Lozza A, Manganelli F, Mussinelli R, My F, Occhipinti G, Fenu S, Russo M, Romano A, Salvalaggio A, Tagliapietra M, Tozza S, Palladini G, Obici L, Luigetti M. Gentile L, et al. Among authors: fabrizi gm. Neurol Sci. 2024 Aug 2. doi: 10.1007/s10072-024-07717-z. Online ahead of print. Neurol Sci. 2024. PMID: 39090357 No abstract available.
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype.
Luigetti M, Fabrizi GM, Madia F, Ferrarini M, Conte A, Del Grande A, Tasca G, Tonali PA, Sabatelli M. Luigetti M, et al. Among authors: fabrizi gm. J Neurol Sci. 2010 Nov 15;298(1-2):114-7. doi: 10.1016/j.jns.2010.09.008. Epub 2010 Sep 25. J Neurol Sci. 2010. PMID: 20870250
Autonomic nervous system involvement in a new CMT2B family.
Manganelli F, Pisciotta C, Provitera V, Taioli F, Iodice R, Topa A, Fabrizi GM, Nolano M, Santoro L. Manganelli F, et al. Among authors: fabrizi gm. J Peripher Nerv Syst. 2012 Sep;17(3):361-4. doi: 10.1111/j.1529-8027.2012.00415.x. J Peripher Nerv Syst. 2012. PMID: 22971099
Considerable post-partum worsening in a patient with CMT2E.
Gentile L, Taioli F, Fabrizi GM, Russo M, Stancanelli C, Mazzeo A. Gentile L, et al. Among authors: fabrizi gm. Neurol Sci. 2013 Oct;34(10):1813-4. doi: 10.1007/s10072-013-1296-x. Epub 2013 Feb 15. Neurol Sci. 2013. PMID: 23412702 No abstract available.
171 results