-
1
-
-
0035393427
-
SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
-
Nakamura K, Jeong SY, Uchihara T, et al. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum Mol Genet 2001; 10: 1441-1448.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1441-1448
-
-
Nakamura, K.1
Jeong, S.Y.2
Uchihara, T.3
-
2
-
-
11144356369
-
Autosomal dominant cerebellar ataxias: Clinical features, genetics, and pathogenesis
-
Schols L, Bauer P, Schmidt T, Schulte T, Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol 2004;3:291-304.
-
(2004)
Lancet Neurol
, vol.3
, pp. 291-304
-
-
Schols, L.1
Bauer, P.2
Schmidt, T.3
Schulte, T.4
Riess, O.5
-
3
-
-
10744231577
-
Genetic testing in spinocerebellar ataxia in Taiwan: Expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease
-
Wu YR, Lin HY, Chen CM, et al. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease. Clin Genet 2004;65:209-214.
-
(2004)
Clin Genet
, vol.65
, pp. 209-214
-
-
Wu, Y.R.1
Lin, H.Y.2
Chen, C.M.3
-
4
-
-
4043175666
-
Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation
-
Bruni AC, Takahashi-Fujigasaki J, Maltecca F, et al. Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation. Arch Neurol 2004;61:1441-1443.
-
(2004)
Arch Neurol
, vol.61
, pp. 1441-1443
-
-
Bruni, A.C.1
Takahashi-Fujigasaki, J.2
Maltecca, F.3
-
5
-
-
0042837890
-
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)
-
Rolfs A, Koeppen AH, Bauer I, et al. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). Ann Neurol 2003;54:367-375.
-
(2003)
Ann Neurol
, vol.54
, pp. 367-375
-
-
Rolfs, A.1
Koeppen, A.H.2
Bauer, I.3
-
6
-
-
0842282678
-
SCA17 homozygote showing Huntington's disease-like phenotype
-
Toyoshima Y, Yamada M, Onodera O, et al. SCA17 homozygote showing Huntington's disease-like phenotype. Ann Neurol 2004; 55:281-286.
-
(2004)
Ann Neurol
, vol.55
, pp. 281-286
-
-
Toyoshima, Y.1
Yamada, M.2
Onodera, O.3
-
7
-
-
0345770368
-
Role of dopamine transporter imaging in routine clinical practice
-
Marshall V, Grosset D. Role of dopamine transporter imaging in routine clinical practice. Mov Disord 2003;18:1415-1423.
-
(2003)
Mov Disord
, vol.18
, pp. 1415-1423
-
-
Marshall, V.1
Grosset, D.2
-
8
-
-
10744221735
-
Intergenerational instability and marked anticipation in SCA-17
-
Maltecca F, Filla A, Castaldo I, et al. Intergenerational instability and marked anticipation in SCA-17. Neurology 2003;61: 1441-1443.
-
(2003)
Neurology
, vol.61
, pp. 1441-1443
-
-
Maltecca, F.1
Filla, A.2
Castaldo, I.3
-
9
-
-
0030939011
-
International cooperative ataxia rating scale for pharmacological assessment of the cerebellar syndrome
-
Trouillas P, Takayanagi T, Haller M, et al. International cooperative ataxia rating scale for pharmacological assessment of the cerebellar syndrome. J Neurol Sci 1997;145:205-211.
-
(1997)
J Neurol Sci
, vol.145
, pp. 205-211
-
-
Trouillas, P.1
Takayanagi, T.2
Haller, M.3
-
10
-
-
0037354472
-
Rating scales for dystonia: A multicenter assessment
-
Dystonia Study Group
-
Comella CL, Leurgans S, Wuu J, Stebbins GT, Chmura T, Dystonia Study Group. Rating scales for dystonia: a multicenter assessment. Mov Disord 2003;18:303-312.
-
(2003)
Mov Disord
, vol.18
, pp. 303-312
-
-
Comella, C.L.1
Leurgans, S.2
Wuu, J.3
Stebbins, G.T.4
Chmura, T.5
-
11
-
-
0000224448
-
Unified Parkinson's Disease Rating
-
members of the UPDRS Development Committee. Scale Fahn S, Marsden CD, Calne DB, Goldstein M, editors. Florham Park, NJ: MacMillian Health Care Information
-
Fahn S, Elton RL, members of the UPDRS Development Committee. Unified Parkinson's Disease Rating Scale. In: Fahn S, Marsden CD, Calne DB, Goldstein M, editors. Recent developments in Parkinson's disease, vol. 2. Florham Park, NJ: MacMillian Health Care Information; 1987. p 153-163.
-
(1987)
Recent Developments in Parkinson's Disease
, vol.2
, pp. 153-163
-
-
Fahn, S.1
Elton, R.L.2
-
12
-
-
0021846840
-
Assessment of tardive dyskinesia using the Abnormal Involuntary Movement Scale
-
Lane RD, Glazer WM, Hansen TE, Berman WH, Kramer SI. Assessment of tardive dyskinesia using the Abnormal Involuntary Movement Scale. J Nerv Ment Dis 1985;173:353-357.
-
(1985)
J Nerv Ment Dis
, vol.173
, pp. 353-357
-
-
Lane, R.D.1
Glazer, W.M.2
Hansen, T.E.3
Berman, W.H.4
Kramer, S.I.5
-
14
-
-
3442890310
-
Basal ganglia involvement of a patient with SCA 17-a new form of autosomal dominant spinocerebellar ataxia
-
Gunther P, Storch A, Schwarz J, Sabri O, Steinbach P, Wagner A, Hesse S. Basal ganglia involvement of a patient with SCA 17-a new form of autosomal dominant spinocerebellar ataxia. J Neurol 2004;251:896-897.
-
(2004)
J Neurol
, vol.251
, pp. 896-897
-
-
Gunther, P.1
Storch, A.2
Schwarz, J.3
Sabri, O.4
Steinbach, P.5
Wagner, A.6
Hesse, S.7
-
15
-
-
0036169407
-
Dopamine transporter concentration is reduced in asymptomatic Machado-Joseph disease gene carriers
-
Yen TC, Tzen KY, Chen MC, et al. Dopamine transporter concentration is reduced in asymptomatic Machado-Joseph disease gene carriers. Nucl Med 2002;43:153-159.
-
(2002)
Nucl Med
, vol.43
, pp. 153-159
-
-
Yen, T.C.1
Tzen, K.Y.2
Chen, M.C.3
-
17
-
-
3943111027
-
Dopamine transporter SPECT using fast kinetic ligands: 123I-FP-beta-CIT versus 99mTc-TRODAT-1
-
Van Laere K, De Ceuninck L, Dom R, et al. Dopamine transporter SPECT using fast kinetic ligands: 123I-FP-beta-CIT versus 99mTc-TRODAT-1. Eur J Nucl Med Mol Imaging 2004;31:1119-1127.
-
(2004)
Eur J Nucl Med Mol Imaging
, vol.31
, pp. 1119-1127
-
-
Van Laere, K.1
De Ceuninck, L.2
Dom, R.3
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