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Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation.
Saveri P, De Luca M, Nisi V, Pisciotta C, Romano R, Piscosquito G, Reilly MM, Polke JM, Cavallaro T, Fabrizi GM, Fossa P, Cichero E, Lombardi R, Lauria G, Magri S, Taroni F, Pareyson D, Bucci C. Saveri P, et al. Among authors: piscosquito g. Cells. 2020 Apr 21;9(4):1028. doi: 10.3390/cells9041028. Cells. 2020. PMID: 32326241 Free PMC article.
Adult-onset leukodystrophies from respiratory chain disorders: do they exist?
Salsano E, Farina L, Lamperti C, Piscosquito G, Salerno F, Morandi L, Carrara F, Lamantea E, Zeviani M, Uziel G, Savoiardo M, Pareyson D. Salsano E, et al. Among authors: piscosquito g. J Neurol. 2013 Jun;260(6):1617-23. doi: 10.1007/s00415-013-6844-z. Epub 2013 Jan 29. J Neurol. 2013. PMID: 23358625 Review.
Peripheral neuropathy in mitochondrial disorders.
Pareyson D, Piscosquito G, Moroni I, Salsano E, Zeviani M. Pareyson D, et al. Among authors: piscosquito g. Lancet Neurol. 2013 Oct;12(10):1011-24. doi: 10.1016/S1474-4422(13)70158-3. Lancet Neurol. 2013. PMID: 24050734 Review.
Inherited neuropathies: an update.
Sagnelli A, Piscosquito G, Pareyson D. Sagnelli A, et al. Among authors: piscosquito g. J Neurol. 2013 Oct;260(10):2684-90. doi: 10.1007/s00415-013-7113-x. Epub 2013 Sep 24. J Neurol. 2013. PMID: 24061768 Review.
Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.
Pensato V, Castellotti B, Gellera C, Pareyson D, Ciano C, Nanetti L, Salsano E, Piscosquito G, Sarto E, Eoli M, Moroni I, Soliveri P, Lamperti E, Chiapparini L, Di Bella D, Taroni F, Mariotti C. Pensato V, et al. Among authors: piscosquito g. Brain. 2014 Jul;137(Pt 7):1907-20. doi: 10.1093/brain/awu121. Epub 2014 May 15. Brain. 2014. PMID: 24833714
Mitochondrial dynamics and inherited peripheral nerve diseases.
Pareyson D, Saveri P, Sagnelli A, Piscosquito G. Pareyson D, et al. Among authors: piscosquito g. Neurosci Lett. 2015 Jun 2;596:66-77. doi: 10.1016/j.neulet.2015.04.001. Epub 2015 Apr 3. Neurosci Lett. 2015. PMID: 25847151 Review.
A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders.
Ardissone A, Piscosquito G, Legati A, Langella T, Lamantea E, Garavaglia B, Salsano E, Farina L, Moroni I, Pareyson D, Ghezzi D. Ardissone A, et al. Among authors: piscosquito g. Neurology. 2015 May 26;84(21):2193-5. doi: 10.1212/WNL.0000000000001613. Epub 2015 May 1. Neurology. 2015. PMID: 25934856 Free PMC article. No abstract available.
61 results