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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
2023 1
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95 results
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Page 1
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach.
Engelen M, van Ballegoij WJC, Mallack EJ, Van Haren KP, Köhler W, Salsano E, van Trotsenburg ASP, Mochel F, Sevin C, Regelmann MO, Tritos NA, Halper A, Lachmann RH, Davison J, Raymond GV, Lund TC, Orchard PJ, Kuehl JS, Lindemans CA, Caruso P, Turk BR, Moser AB, Vaz FM, Ferdinandusse S, Kemp S, Fatemi A, Eichler FS, Huffnagel IC. Engelen M, et al. Among authors: salsano e. Neurology. 2022 Nov 22;99(21):940-951. doi: 10.1212/WNL.0000000000201374. Epub 2022 Sep 29. Neurology. 2022. PMID: 36175155 Free PMC article.
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
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.
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.
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.
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.
Caring for critically ill oldest old patients: a clinical review.
Vargas N, Tibullo L, Landi E, Carifi G, Pirone A, Pippo A, Alviggi I, Tizzano R, Salsano E, Di Grezia F, Vargas M. Vargas N, et al. Among authors: salsano e. Aging Clin Exp Res. 2017 Oct;29(5):833-845. doi: 10.1007/s40520-016-0638-y. Epub 2016 Oct 19. Aging Clin Exp Res. 2017. PMID: 27761759 Review.
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.
Epileptic syndrome with myoclonus as manifestation of adult-onset CblC deficiency.
Di Giacomo R, Salsano E, Deleo F, Pastori C, Didato G, Stabile A, Ferrario R, Giovagnoli AR, Benzoni C, Sarro L, Visani E, Canafoglia L. Di Giacomo R, et al. Among authors: salsano e. J Neurol. 2022 Sep;269(9):5173-5178. doi: 10.1007/s00415-022-11129-4. Epub 2022 Apr 11. J Neurol. 2022. PMID: 35403876 No abstract available.
95 results