-
1
-
-
0034059944
-
Frequency of the DYT1 mutation in primary torsion dystonia without family history
-
Brassat D, Camuzat A,Vidailhet M et al. (2000) Frequency of the DYT1 mutation in primary torsion dystonia without family history. Arch Neurol 57:333-335
-
(2000)
Arch Neurol
, vol.57
, pp. 333-335
-
-
Brassat, D.1
Camuzat, A.2
Vidailhet, M.3
-
2
-
-
0024457283
-
Idiopathic dystonia among Ashkenazi Jews: Evidence for autosomal dominant inheritance
-
Bressman SB, de Leon D, Brin MF et al. (1989) Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Ann Neurol 26:612-620
-
(1989)
Ann Neurol
, vol.26
, pp. 612-620
-
-
Bressman, S.B.1
De Leon, D.2
Brin, M.F.3
-
3
-
-
0027988344
-
Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutation
-
Bressman SB, de Leon D, Kramer PL et al. (1994) Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation. Ann Neurol 36:771-777
-
(1994)
Ann Neurol
, vol.36
, pp. 771-777
-
-
Bressman, S.B.1
De Leon, D.2
Kramer, P.L.3
-
4
-
-
0034624938
-
The DYT1 phenotype and guidelines for diagnostic testing
-
Bressman SB, Sabatti C, Raymond D et al. (2000) The DYT1 phenotype and guidelines for diagnostic testing. Neurology 54:1746-1752
-
(2000)
Neurology
, vol.54
, pp. 1746-1752
-
-
Bressman, S.B.1
Sabatti, C.2
Raymond, D.3
-
5
-
-
0000613043
-
Classification and investigation of dystonia
-
Marsden CD, Fahn S (eds). Butterworths, London
-
Fahn S, Marsden CD, Calne DB (1987) Classification and investigation of dystonia. In: Marsden CD, Fahn S (eds) Movement Disorders, vol 2. Butterworths, London, pp 332-358
-
(1987)
Movement Disorders
, vol.2
, pp. 332-358
-
-
Fahn, S.1
Marsden, C.D.2
Calne, D.B.3
-
6
-
-
0031878303
-
Phenotypic expression of DYT1 mutation: A family with writer's cramp of juvenile onset
-
Gasser T, Windgassen K, Bereznai B, Kabus C, Ludoph AC (1998) Phenotypic expression of DYT1 mutation: a family with writer's cramp of juvenile onset. Ann Neurol 44:126-128
-
(1998)
Ann Neurol
, vol.44
, pp. 126-128
-
-
Gasser, T.1
Windgassen, K.2
Bereznai, B.3
Kabus, C.4
Ludoph, A.C.5
-
7
-
-
0028950638
-
Spread of symptoms in idiopathic torsion dystonia
-
Greene P, Kang UJ, Fahn S (1995) Spread of symptoms in idiopathic torsion dystonia. Mov Disord 10:143-152
-
(1995)
Mov Disord
, vol.10
, pp. 143-152
-
-
Greene, P.1
Kang, U.J.2
Fahn, S.3
-
8
-
-
0033435220
-
GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany
-
Kamm C, Castelon-Konkiewitz E, Naumann M et al. (1999) GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany. Mov Disord 14:681-683
-
(1999)
Mov Disord
, vol.14
, pp. 681-683
-
-
Kamm, C.1
Castelon-Konkiewitz, E.2
Naumann, M.3
-
9
-
-
7144256520
-
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia
-
Klein C, Brin MF, de Leon D et al. (1998) De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia. Hum Mol Genet 7:1133-1136
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1133-1136
-
-
Klein, C.1
Brin, M.F.2
De Leon, D.3
-
10
-
-
0029866764
-
Symptomatic dystonias associated with structural brain lesions: Report of 16 cases
-
Kostić VS, Stojanović M, Kačar A (1996) Symptomatic dystonias associated with structural brain lesions: report of 16 cases. Can J Neurol Sci 23:53-56
-
(1996)
Can J Neurol Sci
, vol.23
, pp. 53-56
-
-
Kostić, V.S.1
Stojanović, M.2
Kačar, A.3
-
11
-
-
0032951850
-
DYT1 mutation in French families with idiopathic torsion dystonia
-
Lebre AS, Durr A, Jedynak P et al. (1999) DYT1 mutation in French families with idiopathic torsion dystonia. Brain 122:41-45
-
(1999)
Brain
, vol.122
, pp. 41-45
-
-
Lebre, A.S.1
Durr, A.2
Jedynak, P.3
-
12
-
-
0032895322
-
Phenotype variability of the DYT1 mutation in German dystonia patients
-
Leube B, Kessler KR, Ferbert A et al. (1999) Phenotype variability of the DYT1 mutation in German dystonia patients. Acta Neurol Scand 99:248-251
-
(1999)
Acta Neurol Scand
, vol.99
, pp. 248-251
-
-
Leube, B.1
Kessler, K.R.2
Ferbert, A.3
-
13
-
-
0034624919
-
To test or not to test? That is the question (with a twist)
-
Lichter DG, Lang AE (2000) To test or not to test? That is the question (with a twist). Neurology 54:1718-1719
-
(2000)
Neurology
, vol.54
, pp. 1718-1719
-
-
Lichter, D.G.1
Lang, A.E.2
-
14
-
-
16944366666
-
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
-
Ozelius JL, Hewett JW, Page CE et al. (1997) The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet 17:40-48
-
(1997)
Nat Genet
, vol.17
, pp. 40-48
-
-
Ozelius, J.L.1
Hewett, J.W.2
Page, C.E.3
-
15
-
-
0033584562
-
A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia
-
Slominsky PA, Markova ED, Shadrina MI et al. (1999) A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia. Hum Mutat 14:269
-
(1999)
Hum Mutat
, vol.14
, pp. 269
-
-
Slominsky, P.A.1
Markova, E.D.2
Shadrina, M.I.3
-
16
-
-
0029052823
-
A genetic study of idiopathic focal dystonias
-
Stojanović M, Cvetković D, Kostić VS (1995) A genetic study of idiopathic focal dystonias. J Neurol 242:508-511
-
(1995)
J Neurol
, vol.242
, pp. 508-511
-
-
Stojanović, M.1
Cvetković, D.2
Kostić, V.S.3
-
17
-
-
0031797115
-
The role of DYT1 in primary torsion dystonia in Europe
-
Valente EM, Warner TT, Jarman PR et al. (1998) The role of DYT1 in primary torsion dystonia in Europe. Brain 121:2335-2339
-
(1998)
Brain
, vol.121
, pp. 2335-2339
-
-
Valente, E.M.1
Warner, T.T.2
Jarman, P.R.3
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