Valente EM - Search Results

1

Defective temporal processing of sensory stimuli in DYT1 mutation carriers: a new endophenotype of dystonia?

Fiorio M, Gambarin M, Valente EM, Liberini P, Loi M, Cossu G, Moretto G, Bhatia KP, Defazio G, Aglioti SM, Fiaschi A, Tinazzi M. Fiorio M, et al. Among authors: valente em. Brain. 2007 Jan;130(Pt 1):134-42. doi: 10.1093/brain/awl283. Epub 2006 Nov 14. Brain. 2007. PMID: 17105745

2

Dopa-responsive dystonia: a clinical and molecular genetic study.

Bandmann O, Valente EM, Holmans P, Surtees RA, Walters JH, Wevers RA, Marsden CD, Wood NW. Bandmann O, et al. Among authors: valente em. Ann Neurol. 1998 Oct;44(4):649-56. doi: 10.1002/ana.410440411. Ann Neurol. 1998. PMID: 9778264

3

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

4

Primary torsion dystonia: the search for genes is not over.

Jarman PR, del Grosso N, Valente EM, Leube B, Cassetta E, Bentivoglio AR, Waddy HM, Uitti RJ, Maraganore DM, Albanese A, Frontali M, Auburger G, Bressman SB, Wood NW, Nygaard TG. Jarman PR, et al. Among authors: valente em. J Neurol Neurosurg Psychiatry. 1999 Sep;67(3):395-7. doi: 10.1136/jnnp.67.3.395. J Neurol Neurosurg Psychiatry. 1999. PMID: 10449567 Free PMC article.

5

Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.

Valente EM, Povey S, Warner TT, Wood NW, Davis MB. Valente EM, et al. Ann Hum Genet. 1999 Jan;63(Pt 1):1-8. doi: 10.1046/j.1469-1809.1999.6310001.x. Ann Hum Genet. 1999. PMID: 10738516

6

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.

7

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

8

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

9

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

10

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

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