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Page 1
HFE gene mutations in a population of Italian Parkinson's disease patients.
Biasiotto G, Goldwurm S, Finazzi D, Tunesi S, Zecchinelli A, Sironi F, Pezzoli G, Arosio P. Biasiotto G, et al. Among authors: zecchinelli a. Parkinsonism Relat Disord. 2008;14(5):426-30. doi: 10.1016/j.parkreldis.2007.10.011. Epub 2008 Mar 5. Parkinsonism Relat Disord. 2008. PMID: 18325820
Levodopa Equivalent Dose of Safinamide: A Multicenter, Longitudinal, Case-Control Study.
Cilia R, Cereda E, Piatti M, Pilotto A, Magistrelli L, Golfrè Andreasi N, Bonvegna S, Contaldi E, Mancini F, Imbalzano G, De Micco R, Colucci F, Braccia A, Bellini G, Brovelli F, Zangaglia R, Lazzeri G, Russillo MC, Olivola E, Sorbera C, Cereda V, Pinto P, Sucapane P, Gelosa G, Meloni M, Pistoia F, Sessa M, Canesi M, Modugno N, Pacchetti C, Brighina L, Pellecchia MT, Ceravolo R, Sensi M, Zibetti M, Comi C, Padovani A, Zecchinelli AL, Di Fonzo A, Tessitore A, Morgante F, Eleopra R. Cilia R, et al. Among authors: zecchinelli al. Mov Disord Clin Pract. 2023 Feb 15;10(4):625-635. doi: 10.1002/mdc3.13681. eCollection 2023 Apr. Mov Disord Clin Pract. 2023. PMID: 37070060 Free PMC article.
n-Hexane-induced parkinsonism: pathogenetic hypotheses.
Pezzoli G, Antonini A, Barbieri S, Canesi M, Perbellini L, Zecchinelli A, Mariani CB, Bonetti A, Leenders KL. Pezzoli G, et al. Among authors: zecchinelli a. Mov Disord. 1995 May;10(3):279-82. doi: 10.1002/mds.870100308. Mov Disord. 1995. PMID: 7651443
Hydrocarbon exposure and Parkinson's disease.
Pezzoli G, Canesi M, Antonini A, Righini A, Perbellini L, Barichella M, Mariani CB, Tenconi F, Tesei S, Zecchinelli A, Leenders KL. Pezzoli G, et al. Among authors: zecchinelli a. Neurology. 2000 Sep 12;55(5):667-73. doi: 10.1212/wnl.55.5.667. Neurology. 2000. PMID: 10980731
Tolerability of paroxetine in Parkinson's disease: a prospective study.
Tesei S, Antonini A, Canesi M, Zecchinelli A, Mariani CB, Pezzoli G. Tesei S, et al. Among authors: zecchinelli a. Mov Disord. 2000 Sep;15(5):986-9. doi: 10.1002/1531-8257(200009)15:5<986::aid-mds1034>3.0.co;2-i. Mov Disord. 2000. PMID: 11009210 Clinical Trial.
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor.
Goldwurm S, Di Fonzo A, Simons EJ, Rohé CF, Zini M, Canesi M, Tesei S, Zecchinelli A, Antonini A, Mariani C, Meucci N, Sacilotto G, Sironi F, Salani G, Ferreira J, Chien HF, Fabrizio E, Vanacore N, Dalla Libera A, Stocchi F, Diroma C, Lamberti P, Sampaio C, Meco G, Barbosa E, Bertoli-Avella AM, Breedveld GJ, Oostra BA, Pezzoli G, Bonifati V. Goldwurm S, et al. Among authors: zecchinelli a. J Med Genet. 2005 Nov;42(11):e65. doi: 10.1136/jmg.2005.035568. J Med Genet. 2005. PMID: 16272257 Free PMC article.
167 results