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Page 1
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies.
Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, Pickering-Brown S, Halliwell N, Davidson Y, Gibbons L, Harris J, Sheerin UM, Bras J, Hardy J, Clark L, Marder K, Honig LS, Berg D, Maetzler W, Brockmann K, Gasser T, Novellino F, Quattrone A, Annesi G, De Marco EV, Rogaeva E, Masellis M, Black SE, Bilbao JM, Foroud T, Ghetti B, Nichols WC, Pankratz N, Halliday G, Lesage S, Klebe S, Durr A, Duyckaerts C, Brice A, Giasson BI, Trojanowski JQ, Hurtig HI, Tayebi N, Landazabal C, Knight MA, Keller M, Singleton AB, Wolfsberg TG, Sidransky E. Nalls MA, et al. Among authors: de marco ev. JAMA Neurol. 2013 Jun;70(6):727-35. doi: 10.1001/jamaneurol.2013.1925. JAMA Neurol. 2013. PMID: 23588557 Free PMC article. Clinical Trial.
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG. Sidransky E, et al. Among authors: de marco ev. N Engl J Med. 2009 Oct 22;361(17):1651-61. doi: 10.1056/NEJMoa0901281. N Engl J Med. 2009. PMID: 19846850 Free PMC article.
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
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease - a multicenter study.
von Otter M, Bergström P, Quattrone A, De Marco EV, Annesi G, Söderkvist P, Wettinger SB, Drozdzik M, Bialecka M, Nissbrandt H, Klein C, Nilsson M, Hammarsten O, Nilsson S, Zetterberg H. von Otter M, et al. Among authors: de marco ev. BMC Med Genet. 2014 Dec 12;15:131. doi: 10.1186/s12881-014-0131-4. BMC Med Genet. 2014. PMID: 25496089 Free PMC article.
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: de marco ev. 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
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.
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease.
Tarantino P, De Marco EV, Annesi G, Rocca FE, Annesi F, Civitelli D, Provenzano G, Scornaienchi V, Greco V, Colica C, Nicoletti G, Quattrone A. Tarantino P, et al. Among authors: de marco ev. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):104-7. doi: 10.1002/ajmg.b.31129. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184589
45 results