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

Year Number of Results
2001 1
2002 1
2004 1
2006 1
2007 3
2008 4
2009 4
2010 4
2011 6
2012 6
2013 13
2014 11
2015 5
2016 6
2017 7
2018 5
2019 11
2020 9
2021 9
2022 6
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Search Results

94 results
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Page 1
Clinical neurogenetics: recent advances.
Pareyson D, Salsano E. Pareyson D, et al. Among authors: salsano e. J Neurol. 2012 Oct;259(10):2255-60. doi: 10.1007/s00415-012-6602-7. Epub 2012 Jul 21. J Neurol. 2012. PMID: 22820683 Review.
Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment.
Cortese A, Franciotta D, Alfonsi E, Visigalli N, Zardini E, Diamanti L, Prunetti P, Osera C, Gastaldi M, Berzero G, Pichiecchio A, Piccolo G, Lozza A, Piscosquito G, Salsano E, Ceroni M, Moglia A, Bono G, Pareyson D, Marchioni E. Cortese A, et al. Among authors: salsano e. J Neurol Sci. 2016 Apr 15;363:182-7. doi: 10.1016/j.jns.2016.02.022. Epub 2016 Feb 10. J Neurol Sci. 2016. PMID: 27000248
Hereditary predominantly motor neuropathies.
Pareyson D, Marchesi C, Salsano E. Pareyson D, et al. Among authors: salsano e. Curr Opin Neurol. 2009 Oct;22(5):451-9. doi: 10.1097/WCO.0b013e3283311dfd. Curr Opin Neurol. 2009. PMID: 19680125 Review.
Asymptomatic adrenoleukodystrophy in elderly males.
Benzoni C, Fenu S, Pensato V, Mauro E, Gellera C, Pareyson D, Salsano E. Benzoni C, et al. Among authors: salsano e. J Neurol. 2020 Jun;267(6):1849-1851. doi: 10.1007/s00415-020-09834-z. Epub 2020 Apr 20. J Neurol. 2020. PMID: 32307584 No abstract available.
Peripheral neuropathy in mitochondrial disorders.
Pareyson D, Piscosquito G, Moroni I, Salsano E, Zeviani M. Pareyson D, et al. Among authors: salsano e. Lancet Neurol. 2013 Oct;12(10):1011-24. doi: 10.1016/S1474-4422(13)70158-3. Lancet Neurol. 2013. PMID: 24050734 Review.
RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum.
Mendes MI, Green LMC, Bertini E, Tonduti D, Aiello C, Smith D, Salsano E, Beerepoot S, Hertecant J, von Spiczak S, Livingston JH, Emrick L, Fraser J, Russell L, Bernard G, Magri S, Di Bella D, Taroni F, Koenig MK, Moroni I, Cappuccio G, Brunetti-Pierri N, Rhee J, Mendelsohn BA, Helbig I, Helbig K, Muhle H, Ismayl O, Vanderver AL, Salomons GS, van der Knaap MS, Wolf NI. Mendes MI, et al. Among authors: salsano e. Ann Clin Transl Neurol. 2020 Jan;7(1):83-93. doi: 10.1002/acn3.50960. Epub 2019 Dec 8. Ann Clin Transl Neurol. 2020. PMID: 31814314 Free PMC article.
Metachromatic Leukodystrophy: Too Frequent (Mis)Diagnosis?
Politi LS, Salsano E, Biffi A. Politi LS, et al. Among authors: salsano e. JAMA Neurol. 2018 Aug 1;75(8):1027. doi: 10.1001/jamaneurol.2018.1515. JAMA Neurol. 2018. PMID: 29913002 No abstract available.
Hypomyelinating leukodystrophies in adults: Clinical and genetic features.
Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Di Bella D, et al. Among authors: salsano e. Eur J Neurol. 2021 Mar;28(3):934-944. doi: 10.1111/ene.14646. Epub 2020 Dec 3. Eur J Neurol. 2021. PMID: 33190326
Spinal cord involvement in adult-onset metabolic and genetic diseases.
Marelli C, Salsano E, Politi LS, Labauge P. Marelli C, et al. Among authors: salsano e. J Neurol Neurosurg Psychiatry. 2019 Feb;90(2):211-218. doi: 10.1136/jnnp-2018-318666. Epub 2018 Aug 27. J Neurol Neurosurg Psychiatry. 2019. PMID: 30150321 Review.
94 results