Bonuccelli U - Search Results

1

Expanding the clinical phenotype of DYT5 mutations: is multiple system atrophy a possible one?

Ceravolo R, Nicoletti V, Garavaglia B, Reale C, Kiferle L, Bonuccelli U. Ceravolo R, et al. Among authors: bonuccelli u. Neurology. 2013 Jul 16;81(3):301-2. doi: 10.1212/WNL.0b013e31829bfd7c. Epub 2013 Jun 14. Neurology. 2013. PMID: 23771491 No abstract available.

2

Orthostatic hypotension in de novo Parkinson disease.

Bonuccelli U, Lucetti C, Del Dotto P, Ceravolo R, Gambaccini G, Bernardini S, Rossi G, Piaggesi A. Bonuccelli U, et al. Arch Neurol. 2003 Oct;60(10):1400-4. doi: 10.1001/archneur.60.10.1400. Arch Neurol. 2003. PMID: 14568810 Clinical Trial.

3

Long-term clinical evaluation in patients with Parkinson's disease and early autonomic involvement.

Lucetti C, Gambaccini G, Del Dotto P, Ceravolo R, Logi C, Rossi G, Murri L, Bonuccelli U. Lucetti C, et al. Among authors: bonuccelli u. Parkinsonism Relat Disord. 2006 Jun;12(5):279-83. doi: 10.1016/j.parkreldis.2005.12.005. Epub 2006 Mar 23. Parkinsonism Relat Disord. 2006. PMID: 16549382

4

Multiple system atrophy is distinguished from idiopathic Parkinson's disease by the arginine growth hormone stimulation test.

Pellecchia MT, Longo K, Pivonello R, Lucetti C, Marchese R, Spampani A, Manfredi M, Epifanio A, Sensi M, Scaravilli T, Bracco F, Eleopra R, Morgante L, Donati E, Marconi R, Abbruzzese G, Bonuccelli U, Zappia M, Colao A, Barone P. Pellecchia MT, et al. Among authors: bonuccelli u. Ann Neurol. 2006 Nov;60(5):611-615. doi: 10.1002/ana.20956. Ann Neurol. 2006. PMID: 16958123

5

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

6

Influences of dopaminergic treatment on motor cortex in Parkinson disease: a MRI/MRS study.

Lucetti C, Del Dotto P, Gambaccini G, Ceravolo R, Logi C, Berti C, Rossi G, Bianchi MC, Tosetti M, Murri L, Bonuccelli U. Lucetti C, et al. Among authors: bonuccelli u. Mov Disord. 2007 Nov 15;22(15):2170-5. doi: 10.1002/mds.21576. Mov Disord. 2007. PMID: 17722082 Clinical Trial.

7

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: bonuccelli u. 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.

8

The safety of dopamine agonists in the treatment of Parkinson's disease.

Bonuccelli U, Ceravolo R. Bonuccelli U, et al. Expert Opin Drug Saf. 2008 Mar;7(2):111-27. doi: 10.1517/14740338.7.2.111. Expert Opin Drug Saf. 2008. PMID: 18324875 Review.

9

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

10

Predictive value of nigrostriatal dysfunction in isolated tremor: a clinical and SPECT study.

Ceravolo R, Antonini A, Volterrani D, Rossi C, Kiferle L, Frosini D, Lucetti C, Isaias IU, Benti R, Murri L, Bonuccelli U. Ceravolo R, et al. Among authors: bonuccelli u. Mov Disord. 2008 Oct 30;23(14):2049-54. doi: 10.1002/mds.22259. Mov Disord. 2008. PMID: 18759337

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