-
1
-
-
0142135448
-
An epidemiologic survey of dystonia within the entire population of northeast England over the past nine years
-
Butler AG, Duffey PO, Hawthorne MR, Barnes MP. An epidemiologic survey of dystonia within the entire population of northeast England over the past nine years. Adv Neurol 2004;94: 95-99.
-
(2004)
Adv Neurol
, vol.94
, pp. 95-99
-
-
Butler, A.G.1
Duffey, P.O.2
Hawthorne, M.R.3
Barnes, M.P.4
-
2
-
-
0344896723
-
Candidate gene studies in focal dystonia
-
Sibbing D, Asmus F, Konig IR, et al. Candidate gene studies in focal dystonia. Neurology 2003;61:1097-1101.
-
(2003)
Neurology
, vol.61
, pp. 1097-1101
-
-
Sibbing, D.1
Asmus, F.2
Konig, I.R.3
-
3
-
-
18244406025
-
Torsin A haplotype predisposes to idiopathic dystonia
-
Clarimon J, Asgeirsson H, Singleton A, Jakobsson F, Hjaltason H, Hardy J, Sveinbjornsdottir S. Torsin A haplotype predisposes to idiopathic dystonia. Ann Neurol 2005;57:765-767.
-
(2005)
Ann Neurol
, vol.57
, pp. 765-767
-
-
Clarimon, J.1
Asgeirsson, H.2
Singleton, A.3
Jakobsson, F.4
Hjaltason, H.5
Hardy, J.6
Sveinbjornsdottir, S.7
-
4
-
-
33845398122
-
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia
-
Kamm C, Asmus F, Mueller J, et al. Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia. Neurology 2006;67:1857-1859.
-
(2006)
Neurology
, vol.67
, pp. 1857-1859
-
-
Kamm, C.1
Asmus, F.2
Mueller, J.3
-
5
-
-
33746922348
-
Clinical characterization and evaluation of DYT1 gene in Indian primary dystonia patients
-
Naiya T, Biswas A, Neogi R, et al. Clinical characterization and evaluation of DYT1 gene in Indian primary dystonia patients. Acta Neurol Scand 2006;114:210-215.
-
(2006)
Acta Neurol Scand
, vol.114
, pp. 210-215
-
-
Naiya, T.1
Biswas, A.2
Neogi, R.3
-
6
-
-
33847762857
-
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm
-
Clarimon J, Brancati F, Peckham E, et al. Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm. Mov Disord 2007;22:162-166.
-
(2007)
Mov Disord
, vol.22
, pp. 162-166
-
-
Clarimon, J.1
Brancati, F.2
Peckham, E.3
-
7
-
-
33645827756
-
Lack of association with TorsinA haplotype in German patients with sporadic dystonia
-
Hague S, Klaffke S, Clarimon J, et al. Lack of association with TorsinA haplotype in German patients with sporadic dystonia. Neurology 2006;66:951-952.
-
(2006)
Neurology
, vol.66
, pp. 951-952
-
-
Hague, S.1
Klaffke, S.2
Clarimon, J.3
-
8
-
-
67449158938
-
The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
-
Bruggemann N, Kock N, Lohmann K, et al. The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases? Neurology 2009;72:1441-1443.
-
(2009)
Neurology
, vol.72
, pp. 1441-1443
-
-
Bruggemann, N.1
Kock, N.2
Lohmann, K.3
-
9
-
-
78649359143
-
Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia
-
Sharma N, Franco RA Jr, Kuster JK, et al. Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia. Mov Disord 2010;25:2183-2187.
-
(2010)
Mov Disord
, vol.25
, pp. 2183-2187
-
-
Sharma, N.1
Franco Jr, R.A.2
Kuster, J.K.3
-
10
-
-
4143145303
-
Meta-analysis of genetic association studies
-
Munafo MR, Flint J. Meta-analysis of genetic association studies. Trends Genet 2004;20:439-444.
-
(2004)
Trends Genet
, vol.20
, pp. 439-444
-
-
Munafo, M.R.1
Flint, J.2
-
13
-
-
67651165237
-
The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasm
-
Defazio G, Matarin M, Peckham EL, et al. The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasm. Mov Disord 2009;24:613-616.
-
(2009)
Mov Disord
, vol.24
, pp. 613-616
-
-
Defazio, G.1
Matarin, M.2
Peckham, E.L.3
-
14
-
-
44949188596
-
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism
-
Kamm C, Fischer H, Garavaglia B, et al. Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism. Neurology 2008;70:2261-2262.
-
(2008)
Neurology
, vol.70
, pp. 2261-2262
-
-
Kamm, C.1
Fischer, H.2
Garavaglia, B.3
-
15
-
-
34250872219
-
Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia
-
Risch NJ, Bressman SB, Senthil G, Ozelius LJ. Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia. Am J Hum Genet 2007;80:1188-1193.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 1188-1193
-
-
Risch, N.J.1
Bressman, S.B.2
Senthil, G.3
Ozelius, L.J.4
-
16
-
-
33645814863
-
Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier
-
Kock N, Naismith TV, Boston HE, Ozelius LJ, Corey DP, Breakefield XO, Hanson PI. Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier. Hum Mol Genet 2006;15:1355-1364.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1355-1364
-
-
Kock, N.1
Naismith, T.V.2
Boston, H.E.3
Ozelius, L.J.4
Corey, D.P.5
Breakefield, X.O.6
Hanson, P.I.7
|