Salsano E - Search Results

1

Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.

Rossi G, Bastone A, Piccoli E, Morbin M, Mazzoleni G, Fugnanesi V, Beeg M, Del Favero E, Cantù L, Motta S, Salsano E, Pareyson D, Erbetta A, Elia AE, Del Sorbo F, Silani V, Morelli C, Salmona M, Tagliavini F. Rossi G, et al. Among authors: salsano e. Neurobiol Aging. 2014 Feb;35(2):408-17. doi: 10.1016/j.neurobiolaging.2013.08.004. Epub 2013 Sep 7. Neurobiol Aging. 2014. PMID: 24018212

2

Late-onset sporadic ataxia, pontine lesion, and retroperitoneal fibrosis: a case of Erdheim-Chester disease.

Salsano E, Savoiardo M, Nappini S, Maderna E, Pollo B, Chinaglia D, Guerra U, Finocchiaro G, Pareyson D. Salsano E, et al. Neurol Sci. 2008 Sep;29(4):263-7. doi: 10.1007/s10072-008-0978-2. Epub 2008 Sep 20. Neurol Sci. 2008. PMID: 18810602

3

Neurological pictures. Adult-onset leukoencephalopathy with calcifications associated with primary antiphospholipid syndrome.

Salsano E, Chiapparini L, Finocchiaro G, Pareyson D, Savoiardo M. Salsano E, et al. J Neurol Neurosurg Psychiatry. 2008 Nov;79(11):1215-7. doi: 10.1136/jnnp.2007.128579. J Neurol Neurosurg Psychiatry. 2008. PMID: 18940989 No abstract available.

4

Tonic pupil following the use of dermatoscope.

Salsano E, Pareyson D, Politi LS. Salsano E, et al. Acta Neurol Taiwan. 2009 Jun;18(2):148-50. Acta Neurol Taiwan. 2009. PMID: 19673371

5

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.

6

Immunological reactivity against neuronal and non-neuronal antigens in sporadic adult-onset cerebellar ataxia.

Fancellu R, Pareyson D, Corsini E, Salsano E, Laurà M, Bernardi G, Antozzi C, Andreetta F, Colecchia M, Di Donato S, Mariotti C. Fancellu R, et al. Among authors: salsano e. Eur Neurol. 2009;62(6):356-61. doi: 10.1159/000242010. Epub 2009 Sep 26. Eur Neurol. 2009. PMID: 19786780

7

Mitochondrial dementia: a sporadic case of progressive cognitive and behavioral decline with hearing loss due to the rare m.3291T>C MELAS mutation.

Salsano E, Giovagnoli AR, Morandi L, Maccagnano C, Lamantea E, Marchesi C, Zeviani M, Pareyson D. Salsano E, et al. J Neurol Sci. 2011 Jan 15;300(1-2):165-8. doi: 10.1016/j.jns.2010.09.022. Epub 2010 Oct 12. J Neurol Sci. 2011. PMID: 20943236

8

Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene.

Marchesi C, Ciano C, Salsano E, Nanetti L, Milani M, Gellera C, Taroni F, Fabrizi GM, Uncini A, Pareyson D. Marchesi C, et al. Among authors: salsano e. Neuromuscul Disord. 2011 Feb;21(2):129-31. doi: 10.1016/j.nmd.2010.09.009. Epub 2010 Oct 14. Neuromuscul Disord. 2011. PMID: 20951041

9

Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.

Salsano E, Fancellu R, Di Fede G, Ciano C, Scaioli V, Nanetti L, Politi LS, Tagliavini F, Mariotti C, Pareyson D. Salsano E, et al. J Neurol Sci. 2011 Mar 15;302(1-2):85-8. doi: 10.1016/j.jns.2010.11.019. Epub 2010 Dec 16. J Neurol Sci. 2011. PMID: 21167505

10

Vertical supranuclear gaze palsy in Niemann-Pick type C disease.

Salsano E, Umeh C, Rufa A, Pareyson D, Zee DS. Salsano E, et al. Neurol Sci. 2012 Dec;33(6):1225-32. doi: 10.1007/s10072-012-1155-1. Epub 2012 Jul 19. Neurol Sci. 2012. PMID: 22810120 Review.

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