-
1
-
-
4644244411
-
Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis
-
BANG OY, LEE PH, KIM SY, KIM HJ, HUH K. (2004). Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis. J Neurol Neurosurg Psychiatry, 75: 1452-1456.
-
(2004)
J Neurol Neurosurg Psychiatry
, vol.75
, pp. 1452-1456
-
-
BANG, O.Y.1
LEE, P.H.2
KIM, S.Y.3
KIM, H.J.4
HUH, K.5
-
2
-
-
6844254538
-
Molecular and clinical correlation in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)
-
DAVID G, DÜRR A, STEVANIN G et al. (1998). Molecular and clinical correlation in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). Hum Mol Genet, 7: 165-170.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 165-170
-
-
DAVID, G.1
DÜRR, A.2
STEVANIN, G.3
-
3
-
-
0028304397
-
Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: A clinical and genetic study of eight families
-
ENEVOLDSON TP, SANDERS M, HARDING A et al. (1994). Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: a clinical and genetic study of eight families. Brain, 117: 445-460.
-
(1994)
Brain
, vol.117
, pp. 445-460
-
-
ENEVOLDSON, T.P.1
SANDERS, M.2
HARDING, A.3
-
5
-
-
0033772042
-
Molecular and clinical study of spinocerebellar ataxia type 7 in chinese kindreds
-
GU W, WANG Y, LIU X et al. (2000). Molecular and clinical study of spinocerebellar ataxia type 7 in chinese kindreds. Arch Neurol, 57: 1513-1518.
-
(2000)
Arch Neurol
, vol.57
, pp. 1513-1518
-
-
GU, W.1
WANG, Y.2
LIU, X.3
-
6
-
-
0344875066
-
Cerebellar ataxia with oculomotor apraxia type 1: Clinical and genetic studies
-
LE BER I, MOREIRA MC, RIVAUD- PECHOUX S et al. (2003). Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies. Brain, 126: 2761-2772.
-
(2003)
Brain
, vol.126
, pp. 2761-2772
-
-
LE BER, I.1
MOREIRA, M.C.2
RIVAUD- PECHOUX, S.3
-
7
-
-
11144355513
-
Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: A clinical and genetic study in 18 patients
-
LE BER N, BOUSLAM S, RIVAUD- PECHOUX J et al. (2004). Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients. Brain, 127: 759-767.
-
(2004)
Brain
, vol.127
, pp. 759-767
-
-
LE BER, N.1
BOUSLAM, S.2
RIVAUD- PECHOUX, J.3
-
8
-
-
30444447681
-
Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes
-
MASCHKE M, GARY OEHLERT G, XIE TING-DONG et al. (2005). Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes. Mov Disord, 20: 1405-1412.
-
(2005)
Mov Disord
, vol.20
, pp. 1405-1412
-
-
MASCHKE, M.1
GARY OEHLERT, G.2
TING-DONG, X.3
-
9
-
-
0033996804
-
The clinical and genetic characteristics of spinocerebellar ataxia type 7 (SCA 7) in three Black South African families
-
MODI G, MODI M, MARTINUS I et al. (2000). The clinical and genetic characteristics of spinocerebellar ataxia type 7 (SCA 7) in three Black South African families. Acta Neurol Scand, 101: 177-182.
-
(2000)
Acta Neurol Scand
, vol.101
, pp. 177-182
-
-
MODI, G.1
MODI, M.2
MARTINUS, I.3
-
10
-
-
0141636410
-
Task specific focal dystonia: A presentation of spinocerebellar ataxia type 6
-
MUZAIMI MB, WILES CM, ROBERTSON NP. (2003). Task specific focal dystonia: a presentation of spinocerebellar ataxia type 6. J Neurol Neurosurg Psychiatry, 74: 1444-1446.
-
(2003)
J Neurol Neurosurg Psychiatry
, vol.74
, pp. 1444-1446
-
-
MUZAIMI, M.B.1
WILES, C.M.2
ROBERTSON, N.P.3
-
11
-
-
1542360717
-
Focal dystonia as a presenting sign of spinocerebellar ataxia 17
-
HAGENAH JM, ZUHLKE C, HELLENBROICH Y et al. (2004). Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Movement Disorders, 19: 217-220.
-
(2004)
Movement Disorders
, vol.19
, pp. 217-220
-
-
HAGENAH, J.M.1
ZUHLKE, C.2
HELLENBROICH, Y.3
-
12
-
-
0344406278
-
Slowly progressive cerebellar ataxia and cervical dystonia: Clinical presentation of a new form of spinocerebellar ataxia
-
KUOPPAMÄKI M, GIUNTI P, QUINN N et al. (2003). Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia. Mov Disord, 18: 200-206.
-
(2003)
Mov Disord
, vol.18
, pp. 200-206
-
-
KUOPPAMÄKI, M.1
GIUNTI, P.2
QUINN, N.3
-
13
-
-
1342347394
-
Prevalence of primary late-onset focal dystonia in the Belgrade population
-
PEKMEZOVI T, IVANOVI N, SVETEL M et al. (2003). Prevalence of primary late-onset focal dystonia in the Belgrade population. Movement disorders, 11: 1389-1392.
-
(2003)
Movement disorders
, vol.11
, pp. 1389-1392
-
-
PEKMEZOVI, T.1
IVANOVI, N.2
SVETEL, M.3
-
14
-
-
0033772440
-
Extrapyramidal motor signs in degenerative ataxias
-
SCHÖLS L, PETERS S, SZYMANSKI S et al. (2000). Extrapyramidal motor signs in degenerative ataxias. Arch Neurol, 57: 1495-1500.
-
(2000)
Arch Neurol
, vol.57
, pp. 1495-1500
-
-
SCHÖLS, L.1
PETERS, S.2
SZYMANSKI, S.3
-
15
-
-
11144356369
-
Autosomal dominant cerebellar ataxias: Clinical features, genetics, and pathogenesis
-
SCHÖLS L, BAUER P, SCHMIDT Y et al. (2004). Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol, 3: 291-304.
-
(2004)
Lancet Neurol
, vol.3
, pp. 291-304
-
-
SCHÖLS, L.1
BAUER, P.2
SCHMIDT, Y.3
-
16
-
-
0036460973
-
Dystonia in spinocerebellar ataxia type 6
-
SETHI KD, JANKOVIC J. (2002). Dystonia in spinocerebellar ataxia type 6. Mov Disord, 17: 150-153.
-
(2002)
Mov Disord
, vol.17
, pp. 150-153
-
-
SETHI, K.D.1
JANKOVIC, J.2
-
18
-
-
4544320300
-
Dystonia as a presenting sign of spinocerebellar ataxia type 1
-
WU YR, LEE-CHEN GJ, LANG AE et al. (2003). Dystonia as a presenting sign of spinocerebellar ataxia type 1. Mov Disord, 19: 586-587.
-
(2003)
Mov Disord
, vol.19
, pp. 586-587
-
-
WU, Y.R.1
LEE-CHEN, G.J.2
LANG, A.E.3
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