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Hereditary transthyretin amyloidosis overview.
Manganelli F, Fabrizi GM, Luigetti M, Mandich P, Mazzeo A, Pareyson D. Manganelli F, et al. Among authors: pareyson d. Neurol Sci. 2022 Dec;43(Suppl 2):595-604. doi: 10.1007/s10072-020-04889-2. Epub 2020 Nov 14. Neurol Sci. 2022. PMID: 33188616 Free PMC article. Review.
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.
Bellone E, Mandich P, Mancardi GL, Schenone A, Uccelli A, Abbruzzese M, Sghirlanzoni A, Pareyson D, Ajmar F. Bellone E, et al. Among authors: pareyson d. J Med Genet. 1992 Jul;29(7):492-3. J Med Genet. 1992. PMID: 1640430 Free PMC article. No abstract available.
Hereditary motor and sensory neuropathy type I and type II.
Sghirlanzoni A, Pareyson D, Scaioli V, Marazzi R, Pacini L. Sghirlanzoni A, et al. Among authors: pareyson d. Ital J Neurol Sci. 1990 Oct;11(5):471-9. doi: 10.1007/BF02336567. Ital J Neurol Sci. 1990. PMID: 2272782
Homozygous hypertrophic hereditary motor and sensory neuropathies.
Sghirlanzoni A, Pareyson D, Marazzi R, Cavaletti G, Bellone E, Mandich P, Balestrini MR, Riva D. Sghirlanzoni A, et al. Among authors: pareyson d. Ital J Neurol Sci. 1994 Feb;15(1):5-14. doi: 10.1007/BF02343492. Ital J Neurol Sci. 1994. PMID: 8206746
Combined central and peripheral acute demyelination.
Pareyson D, Ciano C, Fiacchino F, Gemma M, Savoiardo M, Sghirlanzoni A. Pareyson D, et al. Ital J Neurol Sci. 1993 Jan;14(1):83-6. doi: 10.1007/BF02339047. Ital J Neurol Sci. 1993. PMID: 8386146
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol [EudraCT no.: 2006-000032-27].
Pareyson D, Schenone A, Fabrizi GM, Santoro L, Padua L, Quattrone A, Vita G, Gemignani F, Visioli F, Solari A; CMT-TRIAAL Group. Pareyson D, et al. Pharmacol Res. 2006 Dec;54(6):436-41. doi: 10.1016/j.phrs.2006.09.001. Epub 2006 Sep 9. Pharmacol Res. 2006. PMID: 17029975 Clinical Trial.
322 results