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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 1
2014 3
2015 1
2016 3
2017 3
2018 5
2019 9
2020 15
2021 11
2022 18
2023 18
2024 7

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79 results

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Page 1
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: tozza s. Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
Telemedicine application to headache: a critical review.
Spina E, Tedeschi G, Russo A, Trojsi F, Iodice R, Tozza S, Iovino A, Iodice F, Abbadessa G, di Lorenzo F, Miele G, Maida E, Cerullo G, Sparaco M, Silvestro M, Leocani L, Bonavita S, Manganelli F, Lavorgna L; Digital Technologies, Web and Social Media Study Group of the Italian Society of Neurology (SIN). Spina E, et al. Among authors: tozza s. Neurol Sci. 2022 Jun;43(6):3795-3801. doi: 10.1007/s10072-022-05910-6. Epub 2022 Jan 24. Neurol Sci. 2022. PMID: 35075575 Free PMC article. Review.
RFC1 expansions are a common cause of idiopathic sensory neuropathy.
Currò R, Salvalaggio A, Tozza S, Gemelli C, Dominik N, Galassi Deforie V, Magrinelli F, Castellani F, Vegezzi E, Businaro P, Callegari I, Pichiecchio A, Cosentino G, Alfonsi E, Marchioni E, Colnaghi S, Gana S, Valente EM, Tassorelli C, Efthymiou S, Facchini S, Carr A, Laura M, Rossor AM, Manji H, Lunn MP, Pegoraro E, Santoro L, Grandis M, Bellone E, Beauchamp NJ, Hadjivassiliou M, Kaski D, Bronstein AM, Houlden H, Reilly MM, Mandich P, Schenone A, Manganelli F, Briani C, Cortese A. Currò R, et al. Among authors: tozza s. Brain. 2021 Jun 22;144(5):1542-1550. doi: 10.1093/brain/awab072. Brain. 2021. PMID: 33969391 Free PMC article.
Contribution of Skin Biopsy in Peripheral Neuropathies.
Nolano M, Tozza S, Caporaso G, Provitera V. Nolano M, et al. Among authors: tozza s. Brain Sci. 2020 Dec 15;10(12):989. doi: 10.3390/brainsci10120989. Brain Sci. 2020. PMID: 33333929 Free PMC article. Review.
Alemtuzumab in Covid era.
Iovino A, Olivieri N, Aruta F, Giaquinto E, Ruggiero L, Spina E, Tozza S, Manganelli F, Iodice R. Iovino A, et al. Among authors: tozza s. Mult Scler Relat Disord. 2021 Jun;51:102908. doi: 10.1016/j.msard.2021.102908. Epub 2021 Mar 18. Mult Scler Relat Disord. 2021. PMID: 33812222 Free PMC article.
How to manage with telemedicine people with neuromuscular diseases?
Spina E, Trojsi F, Tozza S, Iovino A, Iodice R, Passaniti C, Abbadessa G, Bonavita S, Leocani L, Tedeschi G, Manganelli F, Lavorgna L; Digital Technologies, Web and Social Media Study Group of the Italian Society of Neurology (SIN). Spina E, et al. Among authors: tozza s. Neurol Sci. 2021 Sep;42(9):3553-3559. doi: 10.1007/s10072-021-05396-8. Epub 2021 Jun 25. Neurol Sci. 2021. PMID: 34173087 Free PMC article. Review.
The neuropathy in hereditary transthyretin amyloidosis: A narrative review.
Tozza S, Severi D, Spina E, Iovino A, Aruta F, Ruggiero L, Dubbioso R, Iodice R, Nolano M, Manganelli F. Tozza S, et al. J Peripher Nerv Syst. 2021 Jun;26(2):155-159. doi: 10.1111/jns.12451. Epub 2021 May 11. J Peripher Nerv Syst. 2021. PMID: 33960565 Free PMC article. Review.
Uncalibrated, Two Source Photo-Polarimetric Stereo.
Tozza S, Zhu D, Smith WAP, Ramamoorthi R, Hancock ER. Tozza S, et al. IEEE Trans Pattern Anal Mach Intell. 2022 Sep;44(9):5747-5760. doi: 10.1109/TPAMI.2021.3078101. Epub 2022 Aug 4. IEEE Trans Pattern Anal Mach Intell. 2022. PMID: 33956625
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: tozza s. Eur J Neurol. 2023 Aug;30(8):2461-2470. doi: 10.1111/ene.15860. Epub 2023 May 26. Eur J Neurol. 2023. PMID: 37170966
79 results