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52 results

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Page 1
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: taioli f. Eur J Neurol. 2023 Aug;30(8):2461-2470. doi: 10.1111/ene.15860. Epub 2023 May 26. Eur J Neurol. 2023. PMID: 37170966
CIDP, CMT1B, or CMT1B plus CIDP?
Cardellini D, Zanette G, Taioli F, Bertolasi L, Ferrari S, Cavallaro T, Fabrizi GM. Cardellini D, et al. Among authors: taioli f. Neurol Sci. 2021 Mar;42(3):1127-1130. doi: 10.1007/s10072-020-04789-5. Epub 2020 Oct 18. Neurol Sci. 2021. PMID: 33070202
Early-onset hereditary neuropathy with liability to pressure palsy.
Antonini G, Luchetti A, Mastrangelo M, Ciambra GL, Di Netta S, Taioli F, Fabrizi GM, Iannetti P. Antonini G, et al. Among authors: taioli f. Neuropediatrics. 2007 Feb;38(1):50-4. doi: 10.1055/s-2007-981451. Neuropediatrics. 2007. PMID: 17607607 Review.
Rare among Rare: Phenotypes of Uncommon CMT Genotypes.
Gentile L, Russo M, Taioli F, Ferrarini M, Aguennouz M, Rodolico C, Toscano A, Fabrizi GM, Mazzeo A. Gentile L, et al. Among authors: taioli f. Brain Sci. 2021 Dec 8;11(12):1616. doi: 10.3390/brainsci11121616. Brain Sci. 2021. PMID: 34942918 Free PMC article.
PMP22 related congenital hypomyelination neuropathy.
Fabrizi GM, Simonati A, Taioli F, Cavallaro T, Ferrarini M, Rigatelli F, Pini A, Mostacciuolo ML, Rizzuto N. Fabrizi GM, et al. Among authors: taioli f. J Neurol Neurosurg Psychiatry. 2001 Jan;70(1):123-6. doi: 10.1136/jnnp.70.1.123. J Neurol Neurosurg Psychiatry. 2001. PMID: 11118262 Free PMC article.
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy.
Bertini A, Gentile L, Cavallaro T, Tozza S, Saveri P, Russo M, Massucco S, Falzone YM, Bellone E, Taioli F, Geroldi A, Occhipinti G, Ferrarini M, Cavalca E, Crivellari L, Mandich P, Balistreri F, Magri S, Taroni F, Previtali SC, Schenone A, Grandis M, Manganelli F, Fabrizi GM, Mazzeo A, Pareyson D, Pisciotta C. Bertini A, et al. Among authors: taioli f. J Neurol Neurosurg Psychiatry. 2024 Jun 5:jnnp-2024-333842. doi: 10.1136/jnnp-2024-333842. Online ahead of print. J Neurol Neurosurg Psychiatry. 2024. PMID: 38839277 Free article.
52 results