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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: novellino f. JAMA Neurol. 2013 Jun;70(6):727-35. doi: 10.1001/jamaneurol.2013.1925. JAMA Neurol. 2013. PMID: 23588557 Free PMC article. Clinical Trial.
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease.
De Marco EV, Tarantino P, Rocca FE, Provenzano G, Civitelli D, De Luca V, Annesi F, Carrideo S, Cirò Candiano IC, Romeo N, Nicoletti G, Marconi R, Novellino F, Morelli M, Quattrone A, Annesi G. De Marco EV, et al. Among authors: novellino f. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 5;147(3):403-7. doi: 10.1002/ajmg.b.30611. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17918232
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. 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
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: novellino f. Neurol Sci. 2011 Jun;32(3):525-7. doi: 10.1007/s10072-011-0504-9. Epub 2011 Mar 8. Neurol Sci. 2011. PMID: 21384276
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: novellino f. 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
Connectivity Changes in Parkinson's Disease.
Cerasa A, Novellino F, Quattrone A. Cerasa A, et al. Among authors: novellino f. Curr Neurol Neurosci Rep. 2016 Oct;16(10):91. doi: 10.1007/s11910-016-0687-9. Curr Neurol Neurosci Rep. 2016. PMID: 27568202 Review.
80 results