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Page 1
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
De Marco EV, Annesi G, Tarantino P, Rocca FE, Provenzano G, Civitelli D, Cirò Candiano IC, Annesi F, Carrideo S, Condino F, Nicoletti G, Messina D, Novellino F, Morelli M, Quattrone A. De Marco EV, et al. Among authors: annesi g, annesi f. Mov Disord. 2008 Feb 15;23(3):460-3. doi: 10.1002/mds.21892. Mov Disord. 2008. PMID: 18074383
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: annesi f. Neurosci Lett. 2004 Sep 16;368(1):21-4. doi: 10.1016/j.neulet.2004.06.049. Neurosci Lett. 2004. PMID: 15342126
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. Among authors: annesi g, annesi f. Mov Disord. 2008 Jan;23(1):21-7. doi: 10.1002/mds.21701. Mov Disord. 2008. PMID: 17975812
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.
Tarantino P, Civitelli D, Annesi F, De Marco EV, Rocca FE, Pugliese P, Nicoletti G, Carrideo S, Provenzano G, Annesi G, Quattrone A. Tarantino P, et al. Among authors: annesi g, annesi f. Parkinsonism Relat Disord. 2009 May;15(4):324-6. doi: 10.1016/j.parkreldis.2008.07.001. Epub 2008 Aug 22. Parkinsonism Relat Disord. 2009. PMID: 18722801
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: annesi g, annesi f. 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
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: annesi g, annesi 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
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: annesi f. 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.
Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the parkin gene.
Capecci M, Passamonti L, Annesi F, Annesi G, Bellesi M, Candiano IC, Ricciuti R, Iacoangeli M, Scerrati M, Zappia M, Tarantino P, De Marco EV, Civitelli D, Carrideo S, Provinciali L, Ceravolo MG, Quattrone A. Capecci M, et al. Among authors: annesi g, annesi f. Mov Disord. 2004 Dec;19(12):1450-2. doi: 10.1002/mds.20250. Mov Disord. 2004. PMID: 15390056
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: annesi g, annesi f. Arch Neurol. 2005 Apr;62(4):601-5. doi: 10.1001/archneur.62.4.601. Arch Neurol. 2005. PMID: 15824260 Clinical Trial.
78 results