Greco V - Search Results

1

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. Neurol Sci. 2011 Jun;32(3):525-7. doi: 10.1007/s10072-011-0504-9. Epub 2011 Mar 8. Neurol Sci. 2011. PMID: 21384276

2

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: greco v. 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

3

DJ-1 is a Parkinson's disease susceptibility gene in southern Italy.

De Marco EV, Annesi G, Tarantino P, Nicoletti G, Civitelli D, Messina D, Annesi F, Arabia G, Salsone M, Condino F, Novellino F, Provenzano G, Rocca FE, Colica C, Morelli M, Scornaienchi V, Greco V, Giofrè L, Quattrone A. De Marco EV, et al. Among authors: greco v. Clin Genet. 2010 Feb;77(2):183-8. doi: 10.1111/j.1399-0004.2009.01310.x. Epub 2009 Nov 23. Clin Genet. 2010. PMID: 19968671

4

Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy.

Provenzano G, Mannarino E, Annesi F, De Marco EV, Rocca FE, Greco V, Scornaienchi V, Tarantino P, Civitelli D, Quattrone A, Tortorella G, Annesi G. Provenzano G, et al. Among authors: greco v. Hum Genet. 2009 Aug;126(2):337. Hum Genet. 2009. PMID: 19694011 No abstract available.

5

Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson disease.

Scornaienchi V, Nicoletti G, Annesi F, Civitelli D, De Marco EV, Provenzano G, Greco V, Tarantino P, Rocca FE, Annesi G. Scornaienchi V, et al. Among authors: greco v. Hum Genet. 2010 Apr;127(4):464. Hum Genet. 2010. PMID: 21488273 No abstract available.

6

Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease.

Tarantino P, Annesi F, Scornaienchi V, Rocca FE, De Marco EV, Civitelli D, Provenzano G, Sproviero W, Greco V, Annesi G. Tarantino P, et al. Among authors: greco v. Hum Genet. 2010 Apr;127(4):463. Hum Genet. 2010. PMID: 21506293 No abstract available.

7

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: greco v. 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

8

Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancy.

Rocca FE, De Marco EV, Annesi F, Civitelli D, Provenzano G, Sproviero W, Scornaienchi V, Greco V, Tarantino P, Annesi G. Rocca FE, et al. Among authors: greco v. Hum Genet. 2010 Apr;127(4):463. doi: 10.1007/s00439-010-0788-5. Hum Genet. 2010. PMID: 20135149 No abstract available.

9

Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians.

Rose G, Passarino G, Carrieri G, Altomare K, Greco V, Bertolini S, Bonafè M, Franceschi C, De Benedictis G. Rose G, et al. Among authors: greco v. Eur J Hum Genet. 2001 Sep;9(9):701-7. doi: 10.1038/sj.ejhg.5200703. Eur J Hum Genet. 2001. PMID: 11571560

10

A novel VNTR enhancer within the SIRT3 gene, a human homologue of SIR2, is associated with survival at oldest ages.

Bellizzi D, Rose G, Cavalcante P, Covello G, Dato S, De Rango F, Greco V, Maggiolini M, Feraco E, Mari V, Franceschi C, Passarino G, De Benedictis G. Bellizzi D, et al. Among authors: greco v. Genomics. 2005 Feb;85(2):258-63. doi: 10.1016/j.ygeno.2004.11.003. Genomics. 2005. PMID: 15676284

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