Valente EM - Search Results

1

TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study.

Percetti M, Franco G, Monfrini E, Caporali L, Minardi R, La Morgia C, Valentino ML, Liguori R, Palmieri I, Ottaviani D, Vizziello M, Ronchi D, Di Berardino F, Cocco A, Macao B, Falkenberg M, Comi GP, Albanese A, Giometto B, Valente EM, Carelli V, Di Fonzo A. Percetti M, et al. Among authors: valente em. Mov Disord. 2022 Sep;37(9):1938-1943. doi: 10.1002/mds.29139. Epub 2022 Jul 6. Mov Disord. 2022. PMID: 35792653 Free PMC article.

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

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.

Valente EM, Bentivoglio AR, Dixon PH, Ferraris A, Ialongo T, Frontali M, Albanese A, Wood NW. Valente EM, et al. Am J Hum Genet. 2001 Apr;68(4):895-900. doi: 10.1086/319522. Epub 2001 Mar 7. Am J Hum Genet. 2001. PMID: 11254447 Free PMC article.

4

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

5

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

6

Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study.

Khan NL, Valente EM, Bentivoglio AR, Wood NW, Albanese A, Brooks DJ, Piccini P. Khan NL, et al. Among authors: valente em. Ann Neurol. 2002 Dec;52(6):849-53. doi: 10.1002/ana.10417. Ann Neurol. 2002. PMID: 12447943

7

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: valente em. Adv Neurol. 2004;94:171-8. Adv Neurol. 2004. PMID: 14509671 No abstract available.

8

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

9

PINK1 mutations are associated with sporadic early-onset parkinsonism.

Valente EM, Salvi S, Ialongo T, Marongiu R, Elia AE, Caputo V, Romito L, Albanese A, Dallapiccola B, Bentivoglio AR. Valente EM, et al. Ann Neurol. 2004 Sep;56(3):336-41. doi: 10.1002/ana.20256. Ann Neurol. 2004. PMID: 15349860

10

A novel family with an unusual early-onset generalized dystonia.

Fabbrini G, Brancati F, Vacca L, Valente EM, Nemeth A, Meesaq A, Sykes N, Dallapiccola B, Berardelli A. Fabbrini G, et al. Among authors: valente em. Mov Disord. 2005 Jan;20(1):81-6. doi: 10.1002/mds.20267. Mov Disord. 2005. PMID: 15390042

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