Ferraris 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: ferraris a. Mov Disord. 2013 Jun;28(6):813-7. doi: 10.1002/mds.25518. Epub 2013 Jun 6. Mov Disord. 2013. PMID: 23744550

2

Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families.

Ricciardi L, Petrucci S, Guidubaldi A, Ialongo T, Serra L, Ferraris A, Spanò B, Bozzali M, Valente EM, Bentivoglio AR. Ricciardi L, et al. Among authors: ferraris a. Mov Disord. 2014 Oct;29(12):1561-6. doi: 10.1002/mds.25994. Epub 2014 Aug 27. Mov Disord. 2014. PMID: 25164310

3

Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families.

Bentivoglio AR, Cortelli P, Valente EM, Ialongo T, Ferraris A, Elia A, Montagna P, Albanese A. Bentivoglio AR, et al. Among authors: ferraris a. Mov Disord. 2001 Nov;16(6):999-1006. doi: 10.1002/mds.10034. Mov Disord. 2001. PMID: 11748730

4

Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements.

Scarciolla O, Brancati F, Valente EM, Ferraris A, De Angelis MV, Valbonesi S, Garavaglia B, Uncini A, Palka G, Stuppia L, Dallapiccola B. Scarciolla O, et al. Among authors: ferraris a. Mov Disord. 2007 Nov 15;22(15):2274-8. doi: 10.1002/mds.21532. Mov Disord. 2007. PMID: 17914726

5

Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study.

Gelmetti V, Ferraris A, Brusa L, Romano F, Lombardi F, Barzaghi C, Stanzione P, Garavaglia B, Dallapiccola B, Valente EM. Gelmetti V, et al. Among authors: ferraris a. Mov Disord. 2008 Apr 30;23(6):881-5. doi: 10.1002/mds.21960. Mov Disord. 2008. PMID: 18307263

6

Olfactory dysfunction in Parkinsonism caused by PINK1 mutations.

Ferraris A, Ialongo T, Passali GC, Pellecchia MT, Brusa L, Laruffa M, Guidubaldi A, Paludetti G, Albanese A, Barone P, Dallapiccola B, Valente EM, Bentivoglio AR. Ferraris A, et al. Mov Disord. 2009 Dec 15;24(16):2350-7. doi: 10.1002/mds.22816. Mov Disord. 2009. PMID: 19890973

7

Mutation screening of the DYT6/THAP1 gene in Italy.

Bonetti M, Barzaghi C, Brancati F, Ferraris A, Bellacchio E, Giovanetti A, Ialongo T, Zorzi G, Piano C, Petracca M, Albanese A, Nardocci N, Dallapiccola B, Bentivoglio AR, Garavaglia B, Valente EM. Bonetti M, et al. Among authors: ferraris a. Mov Disord. 2009 Dec 15;24(16):2424-7. doi: 10.1002/mds.22861. Mov Disord. 2009. PMID: 19908325

8

Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria.

Carecchio M, Magliozzi M, Copetti M, Ferraris A, Bernardini L, Bonetti M, Defazio G, Edwards MJ, Torrente I, Pellegrini F, Comi C, Bhatia KP, Valente EM. Carecchio M, et al. Among authors: ferraris a. Mov Disord. 2013 Jun;28(6):787-94. doi: 10.1002/mds.25506. Epub 2013 May 15. Mov Disord. 2013. PMID: 23677909

9

Heterozygous mutations in genes causing parkinsonism: monogenic disorders go complex.

Valente EM, Ferraris A. Valente EM, et al. Among authors: ferraris a. Lancet Neurol. 2007 Jul;6(7):576-8. doi: 10.1016/S1474-4422(07)70158-8. Lancet Neurol. 2007. PMID: 17582354 No abstract available.

10

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. Among authors: ferraris a. Hum Mutat. 2008 Apr;29(4):565. doi: 10.1002/humu.20719. Hum Mutat. 2008. PMID: 18330912 Free article.

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