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Page 1
Analysis of ferritin genes in Parkinson disease.
Foglieni B, Ferrari F, Goldwurm S, Santambrogio P, Castiglioni E, Sessa M, Volontè MA, Lalli S, Galli C, Wang XS, Connor J, Sironi F, Canesi M, Biasiotto G, Pezzoli G, Levi S, Ferrari M, Arosio P, Cremonesi L. Foglieni B, et al. Among authors: sironi f. Clin Chem Lab Med. 2007;45(11):1450-6. doi: 10.1515/CCLM.2007.307. Clin Chem Lab Med. 2007. PMID: 17970701
Parkin analysis in early onset Parkinson's disease.
Sironi F, Primignani P, Zini M, Tunesi S, Ruffmann C, Ricca S, Brambilla T, Antonini A, Tesei S, Canesi M, Zecchinelli A, Mariani C, Meucci N, Sacilotto G, Cilia R, Isaias IU, Garavaglia B, Ghezzi D, Travi M, Decarli A, Coviello DA, Pezzoli G, Goldwurm S. Sironi F, et al. Parkinsonism Relat Disord. 2008;14(4):326-33. doi: 10.1016/j.parkreldis.2007.10.003. Epub 2007 Nov 19. Parkinsonism Relat Disord. 2008. PMID: 18519021
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: sironi f. 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
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene.
Guella I, Pistocchi A, Asselta R, Rimoldi V, Ghilardi A, Sironi F, Trotta L, Primignani P, Zini M, Zecchinelli A, Coviello D, Pezzoli G, Del Giacco L, Duga S, Goldwurm S. Guella I, et al. Among authors: sironi f. Neurobiol Aging. 2011 Nov;32(11):1994-2005. doi: 10.1016/j.neurobiolaging.2009.12.016. Epub 2010 Jan 8. Neurobiol Aging. 2011. PMID: 20060621
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: sironi f. J Med Genet. 2005 Nov;42(11):e65. doi: 10.1136/jmg.2005.035568. J Med Genet. 2005. PMID: 16272257 Free PMC article.
alpha-Synuclein multiplication analysis in Italian familial Parkinson disease.
Sironi F, Trotta L, Antonini A, Zini M, Ciccone R, Della Mina E, Meucci N, Sacilotto G, Primignani P, Brambilla T, Coviello DA, Pezzoli G, Goldwurm S. Sironi F, et al. Parkinsonism Relat Disord. 2010 Mar;16(3):228-31. doi: 10.1016/j.parkreldis.2009.09.008. Epub 2009 Oct 14. Parkinsonism Relat Disord. 2010. PMID: 19833540
LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample.
Goldwurm S, Zini M, Di Fonzo A, De Gaspari D, Siri C, Simons EJ, van Doeselaar M, Tesei S, Antonini A, Canesi M, Zecchinelli A, Mariani C, Meucci N, Sacilotto G, Cilia R, Isaias IU, Bonetti A, Sironi F, Ricca S, Oostra BA, Bonifati V, Pezzoli G. Goldwurm S, et al. Among authors: sironi f. Parkinsonism Relat Disord. 2006 Oct;12(7):410-9. doi: 10.1016/j.parkreldis.2006.04.001. Epub 2006 Jun 5. Parkinsonism Relat Disord. 2006. PMID: 16750929
54 results