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896 results

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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.
Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage S, Lin JJ, Lynch T, Mellick GD, de Nigris F, Opala G, Prigione A, Quattrone A, Ross OA, Satake W, Silburn PA, Tan EK, Toda T, Tomiyama H, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Maraganore DM; Genetic Epidemiology of Parkinson's disease consortium. Krüger R, et al. Among authors: quattrone a. Neurobiol Aging. 2011 Mar;32(3):548.e9-18. doi: 10.1016/j.neurobiolaging.2009.11.021. Epub 2009 Dec 24. Neurobiol Aging. 2011. PMID: 20036034 Free PMC article.
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: quattrone a. Neurosci Lett. 2004 Sep 16;368(1):21-4. doi: 10.1016/j.neulet.2004.06.049. Neurosci Lett. 2004. PMID: 15342126
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: quattrone a. Arch Neurol. 2005 Apr;62(4):601-5. doi: 10.1001/archneur.62.4.601. Arch Neurol. 2005. PMID: 15824260 Clinical Trial.
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
Valentino P, Annesi G, Cirò Candiano IC, Annesi F, Civitelli D, Tarantino P, Naso F, Spadafora P, Carrideo S, De Marco EV, Consoli D, Zappia M, Gambardella A, Quattrone A. Valentino P, et al. Among authors: quattrone a. Mov Disord. 2006 Feb;21(2):252-4. doi: 10.1002/mds.20681. Mov Disord. 2006. PMID: 16149094
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease.
Quattrone A, Bagnato A, Annesi G, Novellino F, Morgante L, Savettieri G, Zappia M, Tarantino P, Candiano IC, Annesi F, Civitelli D, Rocca FE, D'Amelio M, Nicoletti G, Morelli M, Petrone A, Loizzo P, Condino F. Quattrone A, et al. Mov Disord. 2008 Jan;23(1):21-7. doi: 10.1002/mds.21701. Mov Disord. 2008. PMID: 17975812
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease.
Savettieri G, Annesi G, Civitelli D, Cirò Candiano IC, Salemi G, Ragonese P, Annesi F, Tarantino P, Terruso V, D'Amelio M, Quattrone A. Savettieri G, et al. Among authors: quattrone a. Parkinsonism Relat Disord. 2008 Aug;14(6):509-12. doi: 10.1016/j.parkreldis.2007.10.014. Epub 2008 Mar 7. Parkinsonism Relat Disord. 2008. PMID: 18329316
896 results