Fasano A - Search Results

1

Alpha-synuclein gene duplication: marked intrafamilial variability in two novel pedigrees.

Elia AE, Petrucci S, Fasano A, Guidi M, Valbonesi S, Bernardini L, Consoli F, Ferraris A, Albanese A, Valente EM. Elia AE, et al. Among authors: fasano a. Mov Disord. 2013 Jun;28(6):813-7. doi: 10.1002/mds.25518. Epub 2013 Jun 6. Mov Disord. 2013. PMID: 23744550

2

Clinical presentation and progression of sporadic and familial primary torsion dystonia in Italy.

Bentivoglio AR, Elia AE, Filippini G, Valente EM, Fasano A, Albanese A. Bentivoglio AR, et al. Among authors: fasano a. Adv Neurol. 2004;94:171-8. Adv Neurol. 2004. PMID: 14509671 No abstract available.

3

Analysis of blink rate in patients with blepharospasm.

Bentivoglio AR, Daniele A, Albanese A, Tonali PA, Fasano A. Bentivoglio AR, et al. Among authors: fasano a. Mov Disord. 2006 Aug;21(8):1225-9. doi: 10.1002/mds.20889. Mov Disord. 2006. PMID: 16622858

4

Punding and computer addiction in Parkinson's disease.

Fasano A, Elia AE, Soleti F, Guidubaldi A, Bentivoglio AR. Fasano A, et al. Mov Disord. 2006 Aug;21(8):1217-8. doi: 10.1002/mds.20787. Mov Disord. 2006. PMID: 16637024

5

Non-DYT1 early-onset primary torsion dystonia: comparison with DYT1 phenotype and review of the literature.

Fasano A, Nardocci N, Elia AE, Zorzi G, Bentivoglio AR, Albanese A. Fasano A, et al. Mov Disord. 2006 Sep;21(9):1411-8. doi: 10.1002/mds.21000. Mov Disord. 2006. PMID: 16773641 Review.

6

Onset and progression of primary torsion dystonia in sporadic and familial cases.

Elia AE, Filippini G, Bentivoglio AR, Fasano A, Ialongo T, Albanese A. Elia AE, et al. Among authors: fasano a. Eur J Neurol. 2006 Oct;13(10):1083-8. doi: 10.1111/j.1468-1331.2006.01387.x. Eur J Neurol. 2006. PMID: 16987160

7

Dystonia gravidarum: a new case with a long follow-up.

Fasano A, Elia AE, Guidubaldi A, Tonali PA, Bentivoglio AR. Fasano A, et al. Mov Disord. 2007 Mar 15;22(4):564-6. doi: 10.1002/mds.21310. Mov Disord. 2007. PMID: 17260334

8

Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.

Fasano A, Colosimo C, Miyajima H, Tonali PA, Re TJ, Bentivoglio AR. Fasano A, et al. Mov Disord. 2008 Apr 15;23(5):751-5. doi: 10.1002/mds.21938. Mov Disord. 2008. PMID: 18200628

9

PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum.

Marongiu R, Ferraris A, Ialongo T, Michiorri S, Soleti F, Ferrari F, Elia AE, Ghezzi D, Albanese A, Altavista MC, Antonini A, Barone P, Brusa L, Cortelli P, Martinelli P, Pellecchia MT, Pezzoli G, Scaglione C, Stanzione P, Tinazzi M, Zecchinelli A, Zeviani M, Cassetta E, Garavaglia B, Dallapiccola B, Bentivoglio AR, Valente EM; Italian PD Study Group. Marongiu R, et al. Hum Mutat. 2008 Apr;29(4):565. doi: 10.1002/humu.20719. Hum Mutat. 2008. PMID: 18330912 Free article.

10

High frequency extradural motor cortex stimulation transiently improves axial symptoms in a patient with Parkinson's disease.

Fasano A, Piano C, De Simone C, Cioni B, Di Giuda D, Zinno M, Daniele A, Meglio M, Giordano A, Bentivoglio AR. Fasano A, et al. Mov Disord. 2008 Oct 15;23(13):1916-9. doi: 10.1002/mds.21977. Mov Disord. 2008. PMID: 18709668

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