Bonuccelli U - Search Results

1

Methylation analysis of DNA repair genes in Alzheimer's disease.

Coppedè F, Tannorella P, Stoccoro A, Chico L, Siciliano G, Bonuccelli U, Migliore L. Coppedè F, et al. Among authors: bonuccelli u. Mech Ageing Dev. 2017 Jan;161(Pt A):105-111. doi: 10.1016/j.mad.2016.04.003. Epub 2016 Apr 11. Mech Ageing Dev. 2017. PMID: 27080585 Clinical Trial.

2

Molecular implications of the human glutathione transferase A-4 gene (hGSTA4) polymorphisms in neurodegenerative diseases.

Coppedè F, Armani C, Bidia DD, Petrozzi L, Bonuccelli U, Migliore L. Coppedè F, et al. Among authors: bonuccelli u. Mutat Res. 2005 Nov 11;579(1-2):107-14. doi: 10.1016/j.mrfmmm.2005.02.020. Epub 2005 Jul 27. Mutat Res. 2005. PMID: 16054170

3

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: bonuccelli u. 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

4

Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype.

Mancuso M, Kiferle L, Petrozzi L, Nesti C, Rocchi A, Ceravolo R, Orsucci D, Maluccio MR, Bonuccelli U, Filosto M, Siciliano G, Murri L. Mancuso M, et al. Among authors: bonuccelli u. Neurosci Lett. 2008 Oct 17;444(1):83-6. doi: 10.1016/j.neulet.2008.08.013. Epub 2008 Aug 8. Neurosci Lett. 2008. PMID: 18706972

5

The hOGG1 Ser326Cys polymorphism is not associated with sporadic Parkinson's disease.

Coppedè F, Ceravolo R, Migheli F, Fanucchi F, Frosini D, Siciliano G, Bonuccelli U, Migliore L. Coppedè F, et al. Among authors: bonuccelli u. Neurosci Lett. 2010 Apr 12;473(3):248-51. doi: 10.1016/j.neulet.2010.02.059. Epub 2010 Mar 1. Neurosci Lett. 2010. PMID: 20193742

6

Vascular factors and mitochondrial dysfunction: a central role in the pathogenesis of Alzheimer's disease.

Orsucci D, Mancuso M, Ienco EC, Simoncini C, Siciliano G, Bonuccelli U. Orsucci D, et al. Among authors: bonuccelli u. Curr Neurovasc Res. 2013 Feb;10(1):76-80. doi: 10.2174/156720213804805972. Curr Neurovasc Res. 2013. PMID: 23151073 Review.

7

Levetiracetam-responsive myoclonus in spinocerebellar ataxia type 15.

Orsucci D, Ienco EC, Rocchi A, Siciliano G, Mancuso M, Bonuccelli U. Orsucci D, et al. Among authors: bonuccelli u. Mov Disord. 2013 Sep;28(10):1465. doi: 10.1002/mds.25433. Epub 2013 Mar 14. Mov Disord. 2013. PMID: 23495097 No abstract available.

8

Mapping cortical degeneration in ALS with magnetization transfer ratio and voxel-based morphometry.

Cosottini M, Cecchi P, Piazza S, Pesaresi I, Fabbri S, Diciotti S, Mascalchi M, Siciliano G, Bonuccelli U. Cosottini M, et al. Among authors: bonuccelli u. PLoS One. 2013 Jul 9;8(7):e68279. doi: 10.1371/journal.pone.0068279. Print 2013. PLoS One. 2013. PMID: 23874570 Free PMC article.

9

Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: a case report and an update on the state of art.

Kiferle L, Orsucci D, Mancuso M, Lo Gerfo A, Petrozzi L, Siciliano G, Ceravolo R, Bonuccelli U. Kiferle L, et al. Among authors: bonuccelli u. Neurosci Lett. 2013 Nov 27;556:1-4. doi: 10.1016/j.neulet.2013.09.034. Epub 2013 Sep 26. Neurosci Lett. 2013. PMID: 24076137 Review.

10

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany.

Orsucci D, Petrucci L, Ienco EC, Chico L, Simi P, Fogli A, Baldinotti F, Simoncini C, LoGerfo A, Carlesi C, Arnoldi A, Bassi MT, Siciliano G, Bonuccelli U, Mancuso M. Orsucci D, et al. Among authors: bonuccelli u. Clin Neurol Neurosurg. 2014 May;120:14-9. doi: 10.1016/j.clineuro.2014.02.002. Epub 2014 Feb 17. Clin Neurol Neurosurg. 2014. PMID: 24731568

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