Petrozzi L - Search Results

1

The mtDNA A8344G "MERRF" mutation is not a common cause of sporadic Parkinson disease in Italian population.

Mancuso M, Nesti C, Petrozzi L, Orsucci D, Frosini D, Kiferle L, Bonuccelli U, Ceravolo R, Murri L, Siciliano G. Mancuso M, et al. Among authors: petrozzi l. Parkinsonism Relat Disord. 2008;14(4):381-2. doi: 10.1016/j.parkreldis.2007.10.001. Epub 2007 Nov 13. Parkinsonism Relat Disord. 2008. PMID: 17993288 No abstract available.

2

Cytogenetic analysis oxidative damage in lymphocytes of Parkinson's disease patients.

Petrozzi L, Lucetti C, Gambaccini G, Bernardini S, Del Dotto P, Migliore L, Scarpato R, Bonuccelli U. Petrozzi L, et al. Neurol Sci. 2001 Feb;22(1):83-4. doi: 10.1007/s100720170058. Neurol Sci. 2001. PMID: 11487213

3

Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.

Ghezzi D, Marelli C, Achilli A, Goldwurm S, Pezzoli G, Barone P, Pellecchia MT, Stanzione P, Brusa L, Bentivoglio AR, Bonuccelli U, Petrozzi L, Abbruzzese G, Marchese R, Cortelli P, Grimaldi D, Martinelli P, Ferrarese C, Garavaglia B, Sangiorgi S, Carelli V, Torroni A, Albanese A, Zeviani M. Ghezzi D, et al. Among authors: petrozzi l. Eur J Hum Genet. 2005 Jun;13(6):748-52. doi: 10.1038/sj.ejhg.5201425. Eur J Hum Genet. 2005. PMID: 15827561 Free article.

4

A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's disease.

Coppedè F, Mancuso M, Lo Gerfo A, Manca ML, Petrozzi L, Migliore L, Siciliano G, Murri L. Coppedè F, et al. Among authors: petrozzi l. Neurosci Lett. 2007 Mar 13;414(3):282-5. doi: 10.1016/j.neulet.2006.12.035. Epub 2006 Dec 29. Neurosci Lett. 2007. PMID: 17240059

5

MERRF syndrome without ragged-red fibers: the need for molecular diagnosis.

Mancuso M, Petrozzi L, Filosto M, Nesti C, Rocchi A, Choub A, Pistolesi S, Massetani R, Fontanini G, Siciliano G. Mancuso M, et al. Among authors: petrozzi l. Biochem Biophys Res Commun. 2007 Mar 23;354(4):1058-60. doi: 10.1016/j.bbrc.2007.01.099. Epub 2007 Jan 26. Biochem Biophys Res Commun. 2007. PMID: 17275787

6

Mitochondria and neurodegeneration.

Petrozzi L, Ricci G, Giglioli NJ, Siciliano G, Mancuso M. Petrozzi L, et al. Biosci Rep. 2007 Jun;27(1-3):87-104. doi: 10.1007/s10540-007-9038-z. Biosci Rep. 2007. PMID: 17486441 Review.

7

Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.

Coppedè F, Mancuso M, Lo Gerfo A, Carlesi C, Piazza S, Rocchi A, Petrozzi L, Nesti C, Micheli D, Bacci A, Migliore L, Murri L, Siciliano G. Coppedè F, et al. Among authors: petrozzi l. Neurosci Lett. 2007 Jun 13;420(2):163-8. doi: 10.1016/j.neulet.2007.04.067. Epub 2007 May 5. Neurosci Lett. 2007. PMID: 17531381

8

Lack of association between mtDNA haplogroups and Alzheimer's disease in Tuscany.

Mancuso M, Nardini M, Micheli D, Rocchi A, Nesti C, Giglioli NJ, Petrozzi L, Rossi C, Ceravolo R, Bacci A, Choub A, Ricci G, Tognoni G, Manca ML, Siciliano G, Murri L. Mancuso M, et al. Among authors: petrozzi l. Neurol Sci. 2007 Jun;28(3):142-7. doi: 10.1007/s10072-007-0807-z. Epub 2007 Jun 30. Neurol Sci. 2007. PMID: 17603766

9

Visual hallucinations in Parkinson's disease are not influenced by polymorphisms of serotonin 5-HT2A receptor and transporter genes.

Kiferle L, Ceravolo R, Petrozzi L, Rossi C, Frosini D, Rocchi A, Siciliano G, Bonuccelli U, Murri L. Kiferle L, et al. Among authors: petrozzi l. Neurosci Lett. 2007 Jul 18;422(3):228-31. doi: 10.1016/j.neulet.2007.06.028. Epub 2007 Jun 22. Neurosci Lett. 2007. PMID: 17614196

10

CSF phosporylated TAU protein levels correlate with cerebral glucose metabolism assessed with PET in Alzheimer's disease.

Ceravolo R, Borghetti D, Kiferle L, Tognoni G, Giorgetti A, Neglia D, Sassi N, Frosini D, Rossi C, Petrozzi L, Siciliano G, Murri L. Ceravolo R, et al. Among authors: petrozzi l. Brain Res Bull. 2008 May 15;76(1-2):80-4. doi: 10.1016/j.brainresbull.2008.01.010. Epub 2008 Feb 11. Brain Res Bull. 2008. PMID: 18395614

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