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Page 1
Copy Number Variants in Alzheimer's Disease.
Cuccaro D, De Marco EV, Cittadella R, Cavallaro S. Cuccaro D, et al. Among authors: de marco ev. J Alzheimers Dis. 2017;55(1):37-52. doi: 10.3233/JAD-160469. J Alzheimers Dis. 2017. PMID: 27662298 Free PMC article. Review.
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in southern Italy.
Greco V, De Marco EV, Rocca FE, Annesi F, Civitelli D, Provenzano G, Tarantino P, Scornaienchi V, Pucci F, Salsone M, Novellino F, Morelli M, Paglionico S, Gambardella A, Quattrone A, Annesi G. Greco V, et al. Among authors: de marco ev. Neurol Sci. 2011 Jun;32(3):525-7. doi: 10.1007/s10072-011-0504-9. Epub 2011 Mar 8. Neurol Sci. 2011. PMID: 21384276
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.
Oliveri RL, Annesi G, Zappia M, Civitelli D, De Marco EV, Pasqua AA, Annesi F, Spadafora P, Gambardella A, Nicoletti G, Branca D, Caracciolo M, Aguglia U, Quattrone A. Oliveri RL, et al. Among authors: de marco ev. Mov Disord. 2000 Jan;15(1):127-31. doi: 10.1002/1531-8257(200001)15:1<120::aid-mds1019>3.0.co;2-s. Mov Disord. 2000. PMID: 10634251
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders.
La Cognata V, Morello G, Gentile G, Cavalcanti F, Cittadella R, Conforti FL, De Marco EV, Magariello A, Muglia M, Patitucci A, Spadafora P, D'Agata V, Ruggieri M, Cavallaro S. La Cognata V, et al. Among authors: de marco ev. Curr Genomics. 2018 Sep;19(6):431-443. doi: 10.2174/1389202919666180404105451. Curr Genomics. 2018. PMID: 30258275 Free PMC article.
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: de marco ev. Arch Neurol. 2005 Apr;62(4):601-5. doi: 10.1001/archneur.62.4.601. Arch Neurol. 2005. PMID: 15824260 Clinical Trial.
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: de marco ev. 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
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
Annesi G, Gambardella A, Carrideo S, Incorpora G, Labate A, Pasqua AA, Civitelli D, Polizzi A, Annesi F, Spadafora P, Tarantino P, Cirò Candiano IC, Romeo N, De Marco EV, Ventura P, LePiane E, Zappia M, Aguglia U, Pavone L, Quattrone A. Annesi G, et al. Among authors: de marco ev. Epilepsia. 2003 Sep;44(9):1257-8. doi: 10.1046/j.1528-1157.2003.22503.x. Epilepsia. 2003. PMID: 12919402 Free article. No abstract available.
45 results