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Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry.
Pisciotta C, Bertini A, Tramacere I, Manganelli F, Fabrizi GM, Schenone A, Tozza S, Cavallaro T, Taioli F, Ferrarini M, Grandis M, Bellone E, Mandich P, Previtali SC, Falzone Y, Allegri I, Padua L, Pazzaglia C, Quattrone A, Valentino P, Gentile L, Russo M, Calabrese D, Moroni I, Pagliano E, Saveri P, Magri S, Baratta S, Taroni F, Mazzeo A, Santoro L, Vita G, Pareyson D; Italian CMT Network. Pisciotta C, et al. Among authors: pareyson d. Eur J Neurol. 2023 Aug;30(8):2461-2470. doi: 10.1111/ene.15860. Epub 2023 May 26. Eur J Neurol. 2023. PMID: 37170966
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.
The POEMS syndrome: report of six cases.
Pareyson D, Marazzi R, Confalonieri P, Mancardi GL, Schenone A, Sghirlanzoni A. Pareyson D, et al. Ital J Neurol Sci. 1994 Oct;15(7):353-8. doi: 10.1007/BF02339932. Ital J Neurol Sci. 1994. PMID: 7698893
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
322 results