De Marco EV - Search Results

1

Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.

Cirò Candiano IC, Annesi F, Rocca EF, Carrideo S, Tarantino P, Provenzano G, Civitelli D, De Marco EV, Quattrone A, Annesi G. Cirò Candiano IC, et al. Among authors: de marco ev. Hum Genet. 2007 Nov;122(3-4):416. Hum Genet. 2007. PMID: 18350653 No abstract available.

2

Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.

Tarantino P, Cirò Candiano IC, Annesi F, Rocca FE, Carrideo S, Provenzano G, Civitelli D, De Marco EV, Quattrone A, Annesi G. Tarantino P, et al. Among authors: de marco ev. Hum Genet. 2007 Nov;122(3-4):415. Hum Genet. 2007. PMID: 18350649 No abstract available.

3

Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.

Rocca FE, Annesi F, Cirò Candiano IC, Carrideo S, Tarantino P, Provenzano G, Civitelli D, De Marco EV, Quattrone A, Annesi G. Rocca FE, et al. Among authors: de marco ev. Hum Genet. 2007 Nov;122(3-4):415. Hum Genet. 2007. PMID: 18350651 No abstract available.

4

Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease.

Annesi F, Rocca EF, Cirò Candiano IC, Carrideo S, Tarantino P, Provenzano G, Civitelli D, De Marco EV, Quattrone A, Annesi G. Annesi F, et al. Among authors: de marco ev. Hum Genet. 2007 Nov;122(3-4):415. Hum Genet. 2007. PMID: 18350652 No abstract available.

5

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: de marco ev. Hum Genet. 2009 Aug;126(2):337. Hum Genet. 2009. PMID: 19694011 No abstract available.

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. Rocca FE, et al. Among authors: de marco ev. Hum Genet. 2010 Apr;127(4):463. doi: 10.1007/s00439-010-0788-5. Hum Genet. 2010. PMID: 20135149 No abstract available.

7

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: de marco ev. Hum Genet. 2010 Apr;127(4):464. Hum Genet. 2010. PMID: 21488273 No abstract available.

8

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: de marco ev. Hum Genet. 2010 Apr;127(4):463. Hum Genet. 2010. PMID: 21506293 No abstract available.

9

LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease.

Civitelli D, Tarantino P, Nicoletti G, Cirò Candiano IC, Annesi F, De Marco EV, Carrideo S, Rocca FE, Condino F, Spadafora P, Pugliese P, D'Asero S, Morelli M, Paglionico S, Annesi G, Quattrone A. Civitelli D, et al. Among authors: de marco ev. Clin Genet. 2007 Apr;71(4):367-70. doi: 10.1111/j.1399-0004.2007.00771.x. Clin Genet. 2007. PMID: 17470139 No abstract available.

10

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: de luca v. 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

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