Valente EM - Search Results

1

X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.

Di Lazzaro G, Magrinelli F, Estevez-Fraga C, Valente EM, Pisani A, Bhatia KP. Di Lazzaro G, et al. Among authors: valente em. Mov Disord. 2021 Jul;36(7):1511-1525. doi: 10.1002/mds.28565. Epub 2021 May 7. Mov Disord. 2021. PMID: 33960519 Review.

2

The role of DYT1 in primary torsion dystonia in Europe.

Valente EM, Warner TT, Jarman PR, Mathen D, Fletcher NA, Marsden CD, Bhatia KP, Wood NW. Valente EM, et al. Brain. 1998 Dec;121 ( Pt 12):2335-9. doi: 10.1093/brain/121.12.2335. Brain. 1998. PMID: 9874484

3

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.

Münchau A, Valente EM, Shahidi GA, Eunson LH, Hanna MG, Quinn NP, Schapira AH, Wood NW, Bhatia KP. Münchau A, et al. Among authors: valente em. J Neurol Neurosurg Psychiatry. 2000 May;68(5):609-14. doi: 10.1136/jnnp.68.5.609. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766892 Free PMC article.

4

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB. Valente EM, et al. Brain. 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. Brain. 2000. PMID: 11004121

5

A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.

Münchau A, Valente EM, Davis MB, Stinton V, Wood NW, Quinn NP, Bhatia KP. Münchau A, et al. Among authors: valente em. Mov Disord. 2000 Sep;15(5):954-9. doi: 10.1002/1531-8257(200009)15:5<954::aid-mds1028>3.0.co;2-i. Mov Disord. 2000. PMID: 11009204

6

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

7

Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia.

Brancati F, Defazio G, Caputo V, Valente EM, Pizzuti A, Livrea P, Berardelli A, Dallapiccola B. Brancati F, et al. Among authors: valente em. Mov Disord. 2002 Mar;17(2):392-7. doi: 10.1002/mds.10077. Mov Disord. 2002. PMID: 11921130

8

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.

Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW. Spacey SD, et al. Among authors: valente em. Mov Disord. 2002 Jul;17(4):717-25. doi: 10.1002/mds.10126. Mov Disord. 2002. PMID: 12210861

9

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

10

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

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