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Page 1
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism.
Scornaienchi V, Civitelli D, De Marco EV, Annesi G, Tarantino P, Rocca FE, Greco V, Provenzano G, Annesi F, Nicoletti G, Colica C, Uncini A, Salsone M, Novellino F, Morelli M, Arabia G, Gambardella A, Quattrone A. Scornaienchi V, et al. Among authors: arabia g. Parkinsonism Relat Disord. 2012 Jun;18(5):651-3. doi: 10.1016/j.parkreldis.2011.08.017. Epub 2011 Sep 17. Parkinsonism Relat Disord. 2012. PMID: 21925922
Association of tau gene polymorphism with Parkinson's disease.
Zappia M, Annesi G, Nicoletti G, Serra P, Arabia G, Pugliese P, Messina D, Caracciolo M, Romeo N, Annesi F, Pasqua AA, Spadafora P, Civitelli D, Romeo N, Epifanio A, Morgante L, Quattrone A. Zappia M, et al. Among authors: arabia g. Neurol Sci. 2003 Oct;24(3):223-4. doi: 10.1007/s10072-003-0141-z. Neurol Sci. 2003. PMID: 14600827
FRAXE intermediate alleles are associated with Parkinson's disease.
Annesi G, Nicoletti G, Tarantino P, Cutuli N, Annesi F, Marco EV, Zappia M, Morgante L, Arabia G, Pugliese P, Condino F, Carrideo S, Civitelli D, Caracciolo M, Romeo N, Spadafora P, Candiano IC, Quattrone A. Annesi G, et al. Among authors: arabia g. Neurosci Lett. 2004 Sep 16;368(1):21-4. doi: 10.1016/j.neulet.2004.06.049. Neurosci Lett. 2004. PMID: 15342126
The fragile X premutation presenting as postprandial hypotension.
Pugliese P, Annesi G, Cutuli N, Arabia G, Nicoletti G, Annesi F, Tarantino P, Gambardella A, Valentino P, Zappia M, Quattrone A. Pugliese P, et al. Among authors: arabia g. Neurology. 2004 Dec 14;63(11):2188-9. doi: 10.1212/01.wnl.0000145709.61117.08. Neurology. 2004. PMID: 15596781 No abstract available.
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study.
Zappia M, Annesi G, Nicoletti G, Arabia G, Annesi F, Messina D, Pugliese P, Spadafora P, Tarantino P, Carrideo S, Civitelli D, De Marco EV, Cirò-Candiano IC, Gambardella A, Quattrone A. Zappia M, et al. Among authors: arabia g. Arch Neurol. 2005 Apr;62(4):601-5. doi: 10.1001/archneur.62.4.601. Arch Neurol. 2005. PMID: 15824260 Clinical Trial.
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.
Annesi G, Savettieri G, Pugliese P, D'Amelio M, Tarantino P, Ragonese P, La Bella V, Piccoli T, Civitelli D, Annesi F, Fierro B, Piccoli F, Arabia G, Caracciolo M, Cirò Candiano IC, Quattrone A. Annesi G, et al. Among authors: arabia g. Ann Neurol. 2005 Nov;58(5):803-7. doi: 10.1002/ana.20666. Ann Neurol. 2005. PMID: 16240358
Cardiac MIBG scintigraphy in Primary Progressive Freezing Gait.
Salsone M, Bagnato A, Novellino F, Cascini GL, Paglionico S, Cipullo S, Morelli M, Pugliese P, Nicoletti G, Messina D, Condino F, Arabia G, Morgante L, Quattrone A. Salsone M, et al. Among authors: arabia g. Parkinsonism Relat Disord. 2009 Jun;15(5):365-9. doi: 10.1016/j.parkreldis.2008.08.008. Epub 2008 Nov 5. Parkinsonism Relat Disord. 2009. PMID: 18980855
Myocardial (123)I-MIBG scintigraphy for differentiation of Lewy bodies disease from FTD.
Novellino F, Bagnato A, Salsone M, Cascini GL, Nicoletti G, Arabia G, Pugliese P, Morelli M, Paglionico S, Cipullo S, Manna I, De Marco EV, Condino F, Chiriaco C, Morgante L, Zappia M, Quattrone A. Novellino F, et al. Among authors: arabia g. Neurobiol Aging. 2010 Nov;31(11):1903-11. doi: 10.1016/j.neurobiolaging.2008.11.009. Epub 2009 Jan 9. Neurobiol Aging. 2010. PMID: 19135762
161 results