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902 results

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Page 1
Olfactory dysfunction in Parkinsonism caused by PINK1 mutations.
Ferraris A, Ialongo T, Passali GC, Pellecchia MT, Brusa L, Laruffa M, Guidubaldi A, Paludetti G, Albanese A, Barone P, Dallapiccola B, Valente EM, Bentivoglio AR. Ferraris A, et al. Among authors: barone p. Mov Disord. 2009 Dec 15;24(16):2350-7. doi: 10.1002/mds.22816. Mov Disord. 2009. PMID: 19890973
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
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.
Ghezzi D, Marelli C, Achilli A, Goldwurm S, Pezzoli G, Barone P, Pellecchia MT, Stanzione P, Brusa L, Bentivoglio AR, Bonuccelli U, Petrozzi L, Abbruzzese G, Marchese R, Cortelli P, Grimaldi D, Martinelli P, Ferrarese C, Garavaglia B, Sangiorgi S, Carelli V, Torroni A, Albanese A, Zeviani M. Ghezzi D, et al. Among authors: barone p. Eur J Hum Genet. 2005 Jun;13(6):748-52. doi: 10.1038/sj.ejhg.5201425. Eur J Hum Genet. 2005. PMID: 15827561 Free article.
Progression of multiple system atrophy (MSA): a prospective natural history study by the European MSA Study Group (EMSA SG).
Geser F, Wenning GK, Seppi K, Stampfer-Kountchev M, Scherfler C, Sawires M, Frick C, Ndayisaba JP, Ulmer H, Pellecchia MT, Barone P, Kim HT, Hooker J, Quinn NP, Cardozo A, Tolosa E, Abele M, Klockgether T, Østergaard K, Dupont E, Schimke N, Eggert KM, Oertel W, Djaldetti R, Poewe W; European MSA Study Group. Geser F, et al. Among authors: barone p. Mov Disord. 2006 Feb;21(2):179-86. doi: 10.1002/mds.20678. Mov Disord. 2006. PMID: 16161136
Health-related quality of life in multiple system atrophy.
Schrag A, Geser F, Stampfer-Kountchev M, Seppi K, Sawires M, Köllensperger M, Scherfler C, Quinn N, Pellecchia MT, Barone P, Del Sorbo F, Albanese A, Ostergaard K, Dupont E, Cardozo A, Tolosa E, Nilsson CF, Widner H, Lindvall O, Giladi N, Gurevich T, Daniels C, Deuschl G, Coelho M, Sampaio C, Abele M, Klockgether T, Schimke N, Eggert KM, Oertel W, Djaldetti R, Colosimo C, Meco G, Poewe W, Wenning GK; European MSA-Study Group. Schrag A, et al. Among authors: barone p. Mov Disord. 2006 Jun;21(6):809-15. doi: 10.1002/mds.20808. Mov Disord. 2006. PMID: 16502399
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.
Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B; Italian PD Study Group. Marongiu R, et al. Among authors: barone p. Mov Disord. 2006 Aug;21(8):1232-5. doi: 10.1002/mds.20890. Mov Disord. 2006. PMID: 16622859
902 results