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578 results

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Page 1
Validation of the Italian version of the PSP Quality of Life questionnaire.
Picillo M, Cuoco S, Amboni M, Bonifacio FP, Bruschi F, Carotenuto I, De Micco R, De Rosa A, Del Prete E, Di Biasio F, Elifani F, Erro R, Fabbri M, Falla M, Franco G, Frosini D, Galantucci S, Lazzeri G, Magistrelli L, Malaguti MC, Milner AV, Minafra B, Olivola E, Pilotto A, Rascunà C, Rizzetti MC, Schirinzi T, Borroni B, Ceravolo R, Di Fonzo A, Marchese R, Mercuri NB, Modugno N, Nicoletti A, Padovani A, Santangelo G, Stefani A, Tessitore A, Volontè MA, Zangaglia R, Zappia M, Zibetti M, Barone P. Picillo M, et al. Among authors: de rosa a, de micco r. Neurol Sci. 2019 Dec;40(12):2587-2594. doi: 10.1007/s10072-019-04010-2. Epub 2019 Jul 26. Neurol Sci. 2019. PMID: 31350659
The heterogeneity of early Parkinson's disease: a cluster analysis on newly diagnosed untreated patients.
Erro R, Vitale C, Amboni M, Picillo M, Moccia M, Longo K, Santangelo G, De Rosa A, Allocca R, Giordano F, Orefice G, De Michele G, Santoro L, Pellecchia MT, Barone P. Erro R, et al. Among authors: de rosa a, de michele g. PLoS One. 2013 Aug 1;8(8):e70244. doi: 10.1371/journal.pone.0070244. Print 2013. PLoS One. 2013. PMID: 23936396 Free PMC article.
Gender differences in non-motor symptoms in early, drug naïve Parkinson's disease.
Picillo M, Amboni M, Erro R, Longo K, Vitale C, Moccia M, Pierro A, Santangelo G, De Rosa A, De Michele G, Santoro L, Orefice G, Barone P, Pellecchia MT. Picillo M, et al. Among authors: de rosa a, de michele g. J Neurol. 2013 Nov;260(11):2849-55. doi: 10.1007/s00415-013-7085-x. Epub 2013 Aug 30. J Neurol. 2013. PMID: 23989344
Is serum uric acid related to non-motor symptoms in de-novo Parkinson's disease patients?
Moccia M, Picillo M, Erro R, Vitale C, Longo K, Amboni M, Santangelo G, Spina E, De Rosa A, De Michele G, Santoro L, Barone P, Pellecchia MT. Moccia M, et al. Among authors: de rosa a, de michele g. Parkinsonism Relat Disord. 2014 Jul;20(7):772-5. doi: 10.1016/j.parkreldis.2014.03.016. Epub 2014 Mar 25. Parkinsonism Relat Disord. 2014. PMID: 24725754
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family.
Olgiati S, De Rosa A, Quadri M, Criscuolo C, Breedveld GJ, Picillo M, Pappatà S, Quarantelli M, Barone P, De Michele G, Bonifati V. Olgiati S, et al. Among authors: de rosa a, de michele g. Neurogenetics. 2014 Aug;15(3):183-8. doi: 10.1007/s10048-014-0406-0. Epub 2014 May 10. Neurogenetics. 2014. PMID: 24816432
578 results