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The TANDEM investigation: efficacy and tolerability of levodopa-carbidopa intestinal gel in (LCIG) advanced Parkinson's disease patients.
Antonini A, Abbruzzese G, Berardelli A, Modugno N, Stroppa I, Tamma F, Sensi M, Mancini F, Cossu G, Stefani A, Tambasco N, Tessitore A, Fabbrini G, Pontieri FE, Solla P, Bentivoglio AR, Comi C, Minafra B, Riboldazzi G, Melchionda D, Martino T, Lopiano L. Antonini A, et al. Among authors: abbruzzese g. J Neural Transm (Vienna). 2020 Jun;127(6):881-891. doi: 10.1007/s00702-020-02175-1. Epub 2020 Mar 24. J Neural Transm (Vienna). 2020. PMID: 32212015
Epidemiology of primary dystonia.
Defazio G, Abbruzzese G, Livrea P, Berardelli A. Defazio G, et al. Among authors: abbruzzese g. Lancet Neurol. 2004 Nov;3(11):673-8. doi: 10.1016/S1474-4422(04)00907-X. Lancet Neurol. 2004. PMID: 15488460 Review.
Novel parkin mutations detected in patients with early-onset Parkinson's disease.
Bertoli-Avella AM, Giroud-Benitez JL, Akyol A, Barbosa E, Schaap O, van der Linde HC, Martignoni E, Lopiano L, Lamberti P, Fincati E, Antonini A, Stocchi F, Montagna P, Squitieri F, Marini P, Abbruzzese G, Fabbrini G, Marconi R, Dalla Libera A, Trianni G, Guidi M, De Gaetano A, Boff Maegawa G, De Leo A, Gallai V, de Rosa G, Vanacore N, Meco G, van Duijn CM, Oostra BA, Heutink P, Bonifati V; Italian Parkinson Genetics Network, MD. Bertoli-Avella AM, et al. Among authors: abbruzzese g. Mov Disord. 2005 Apr;20(4):424-431. doi: 10.1002/mds.20343. Mov Disord. 2005. PMID: 15584030
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: abbruzzese g. 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.
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
Di Fonzo A, Tassorelli C, De Mari M, Chien HF, Ferreira J, Rohé CF, Riboldazzi G, Antonini A, Albani G, Mauro A, Marconi R, Abbruzzese G, Lopiano L, Fincati E, Guidi M, Marini P, Stocchi F, Onofrj M, Toni V, Tinazzi M, Fabbrini G, Lamberti P, Vanacore N, Meco G, Leitner P, Uitti RJ, Wszolek ZK, Gasser T, Simons EJ, Breedveld GJ, Goldwurm S, Pezzoli G, Sampaio C, Barbosa E, Martignoni E, Oostra BA, Bonifati V; Italian Parkinson's Genetics Network. Di Fonzo A, et al. Among authors: abbruzzese g. Eur J Hum Genet. 2006 Mar;14(3):322-31. doi: 10.1038/sj.ejhg.5201539. Eur J Hum Genet. 2006. PMID: 16333314
A comparative study of primary and secondary hemifacial spasm.
Colosimo C, Bologna M, Lamberti S, Avanzino L, Marinelli L, Fabbrini G, Abbruzzese G, Defazio G, Berardelli A. Colosimo C, et al. Among authors: abbruzzese g. Arch Neurol. 2006 Mar;63(3):441-4. doi: 10.1001/archneur.63.3.441. Arch Neurol. 2006. PMID: 16533973
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: abbruzzese g. Ann Neurol. 2006 Nov;60(5):611-615. doi: 10.1002/ana.20956. Ann Neurol. 2006. PMID: 16958123
338 results