Valente EM - Search Results

1

Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.

Di Fonzo A, Percetti M, Monfrini E, Palmieri I, Albanese A, Avenali M, Bartoletti-Stella A, Blandini F, Brescia G, Calandra-Buonaura G, Campopiano R, Capellari S, Colangelo I, Comi GP, Cuconato G, Ferese R, Galandra C, Gambardella S, Garavaglia B, Gaudio A, Giardina E, Invernizzi F, Mandich P, Mineri R, Panteghini C, Reale C, Trevisan L, Zampatti S, Cortelli P, Valente EM; PARKNET study group. Di Fonzo A, et al. Among authors: valente em. Mov Disord. 2023 Dec;38(12):2241-2248. doi: 10.1002/mds.29617. Epub 2023 Sep 26. Mov Disord. 2023. PMID: 37750340

2

Italian family with cranial cervical dystonia: clinical and genetic study.

Cassetta E, Del Grosso N, Bentivoglio AR, Valente EM, Frontali M, Albanese A. Cassetta E, et al. Among authors: valente em. Mov Disord. 1999 Sep;14(5):820-5. doi: 10.1002/1531-8257(199909)14:5<820::aid-mds1015>3.0.co;2-i. Mov Disord. 1999. PMID: 10495044

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: valente em. Mov Disord. 2001 Nov;16(6):999-1006. doi: 10.1002/mds.10034. Mov Disord. 2001. PMID: 11748730

4

Phenotypic variability of DYT1-PTD: does the clinical spectrum include psychogenic dystonia?

Bentivoglio AR, Loi M, Valente EM, Ialongo T, Tonali P, Albanese A. Bentivoglio AR, et al. Among authors: valente em. Mov Disord. 2002 Sep;17(5):1058-63. doi: 10.1002/mds.10236. Mov Disord. 2002. PMID: 12360559

5

Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity.

Valente EM, Misbahuddin A, Brancati F, Placzek MR, Garavaglia B, Salvi S, Nemeth A, Shaw-Smith C, Nardocci N, Bentivoglio AR, Berardelli A, Eleopra R, Dallapiccola B, Warner TT. Valente EM, et al. Mov Disord. 2003 Sep;18(9):1047-51. doi: 10.1002/mds.10476. Mov Disord. 2003. PMID: 14502674

6

Phenotypic characterization of DYT13 primary torsion dystonia.

Bentivoglio AR, Ialongo T, Contarino MF, Valente EM, Albanese A. Bentivoglio AR, et al. Among authors: valente em. Mov Disord. 2004 Feb;19(2):200-6. doi: 10.1002/mds.10634. Mov Disord. 2004. PMID: 14978677

7

Hereditary early-onset Parkinson's disease caused by mutations in PINK1.

Valente EM, Abou-Sleiman PM, Caputo V, Muqit MM, Harvey K, Gispert S, Ali Z, Del Turco D, Bentivoglio AR, Healy DG, Albanese A, Nussbaum R, González-Maldonado R, Deller T, Salvi S, Cortelli P, Gilks WP, Latchman DS, Harvey RJ, Dallapiccola B, Auburger G, Wood NW. Valente EM, et al. Science. 2004 May 21;304(5674):1158-60. doi: 10.1126/science.1096284. Epub 2004 Apr 15. Science. 2004. PMID: 15087508

8

The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease.

Albanese A, Valente EM, Romito LM, Bellacchio E, Elia AE, Dallapiccola B. Albanese A, et al. Among authors: valente em. Neurology. 2005 Jun 14;64(11):1958-60. doi: 10.1212/01.WNL.0000163999.72864.FD. Neurology. 2005. PMID: 15955954

9

Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.

Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B; Italian PD Study Group. Marongiu R, et al. Among authors: valente em. Mov Disord. 2006 Aug;21(8):1232-5. doi: 10.1002/mds.20890. Mov Disord. 2006. PMID: 16622859

10

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: valente em. Mov Disord. 2007 Nov 15;22(15):2274-8. doi: 10.1002/mds.21532. Mov Disord. 2007. PMID: 17914726

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