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126 results

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Page 1
Complex phenotype in an Italian family with a novel mutation in SPG3A.
de Leva MF, Filla A, Criscuolo C, Tessa A, Pappatà S, Quarantelli M, Bilo L, Peluso S, Antenora A, Longo D, Santorelli FM, De Michele G. de Leva MF, et al. Among authors: peluso s. J Neurol. 2010 Mar;257(3):328-31. doi: 10.1007/s00415-009-5311-3. Epub 2009 Sep 19. J Neurol. 2010. PMID: 19768483
Be aware of Wolfram syndrome when examining ataxic patients.
Antenora A, Lieto M, Santorelli FM, Peluso S, Saccà F, De Michele G, Filla A. Antenora A, et al. Among authors: peluso s. J Neurol. 2016 Sep;263(9):1862-3. doi: 10.1007/s00415-016-8199-8. Epub 2016 Jun 17. J Neurol. 2016. PMID: 27314960 No abstract available.
SPG5 and multiple sclerosis: clinical and genetic overlap?
Criscuolo C, Carbone R, Lieto M, Peluso S, Guacci A, Filla A, Quarantelli M, Lanzillo R, Morra VB, De Michele G. Criscuolo C, et al. Among authors: peluso s. Acta Neurol Scand. 2016 Jun;133(6):410-4. doi: 10.1111/ane.12476. Epub 2015 Sep 15. Acta Neurol Scand. 2016. PMID: 26370385
Antiphospholipid-related chorea.
Peluso S, Antenora A, De Rosa A, Roca A, Maddaluno G, Brescia Morra V, De Michele G. Peluso S, et al. Front Neurol. 2012 Oct 22;3:150. doi: 10.3389/fneur.2012.00150. eCollection 2012. Front Neurol. 2012. PMID: 23097646 Free PMC article.
A case of restless leg syndrome in a family with LRRK2 gene mutation.
De Rosa A, Guacci A, Peluso S, Del Gaudio L, Massarelli M, Barbato S, Criscuolo C, De Michele G. De Rosa A, et al. Among authors: peluso s. Int J Neurosci. 2013 Apr;123(4):283-5. doi: 10.3109/00207454.2012.756485. Epub 2013 Feb 4. Int J Neurosci. 2013. PMID: 23227859
The magnetic apraxia of Denny-Brown.
Peluso S, De Michele G, Antenora A, De Rosa A, Bilo L. Peluso S, et al. Neurology. 2016 Aug 9;87(6):644. doi: 10.1212/WNL.0000000000002954. Neurology. 2016. PMID: 27502963 No abstract available.
126 results