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862 results

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Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Periquet M, et al. Among authors: barone p. Brain. 2003 Jun;126(Pt 6):1271-8. doi: 10.1093/brain/awg136. Brain. 2003. PMID: 12764050
Reduced striatal [123 I]FP-CIT binding in SCA2 patients without parkinsonism.
Varrone A, Salvatore E, De Michele G, Barone P, Sansone V, Pellecchia MT, Castaldo I, Coppola G, Brunetti A, Salvatore M, Pappatà S, Filla A. Varrone A, et al. Among authors: barone p. Ann Neurol. 2004 Mar;55(3):426-30. doi: 10.1002/ana.20054. Ann Neurol. 2004. PMID: 14991822
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: barone p. J Neurol. 2013 Nov;260(11):2849-55. doi: 10.1007/s00415-013-7085-x. Epub 2013 Aug 30. J Neurol. 2013. PMID: 23989344
Impulsive-compulsive behaviors in parkin-associated Parkinson disease.
Morgante F, Fasano A, Ginevrino M, Petrucci S, Ricciardi L, Bove F, Criscuolo C, Moccia M, De Rosa A, Sorbera C, Bentivoglio AR, Barone P, De Michele G, Pellecchia MT, Valente EM. Morgante F, et al. Among authors: barone p. Neurology. 2016 Oct 4;87(14):1436-1441. doi: 10.1212/WNL.0000000000003177. Epub 2016 Sep 2. Neurology. 2016. PMID: 27590295 Free PMC article.
Subclinical sensory abnormalities in unaffected PINK1 heterozygotes.
Fiorio M, Valente EM, Gambarin M, Bentivoglio AR, Ialongo T, Albanese A, Barone P, Pellecchia MT, Brancati F, Moretto G, Fiaschi A, Tinazzi M. Fiorio M, et al. Among authors: barone p. J Neurol. 2008 Sep;255(9):1372-7. doi: 10.1007/s00415-008-0923-6. Epub 2008 Jul 3. J Neurol. 2008. PMID: 18584234 Clinical Trial.
862 results