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Items: 9

1.

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.

Parkinsonism Relat Disord. 2012 Jun;18(5):651-3. doi: 10.1016/j.parkreldis.2011.08.017. Epub 2011 Sep 17.

PMID:
21925922
2.

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.

Hum Genet. 2010 Apr;127(4):463. No abstract available.

PMID:
21506293
3.

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.

Hum Genet. 2010 Apr;127(4):464. No abstract available.

PMID:
21488273
4.

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.

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

PMID:
21384276
5.

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.

Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):104-7. doi: 10.1002/ajmg.b.31129. Epub 2010 Nov 2.

PMID:
21184589
6.

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.

Hum Genet. 2010 Apr;127(4):463. doi: 10.1007/s00439-010-0788-5. No abstract available.

PMID:
20135149
7.

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.

Clin Genet. 2010 Feb;77(2):183-8. doi: 10.1111/j.1399-0004.2009.01310.x. Epub 2009 Nov 23.

PMID:
19968671
8.

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.

Hum Genet. 2009 Aug;126(2):337. No abstract available.

PMID:
19694011
9.

The mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspring.

Rose G, Passarino G, Scornaienchi V, Romeo G, Dato S, Bellizzi D, Mari V, Feraco E, Maletta R, Bruni A, Franceschi C, De Benedictis G.

BMC Genomics. 2007 Aug 29;8:293.

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