Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17(297 views) Salvatore E, Varrone A, Sansone V, Nolano M, Bruni AC, De Rosa A, Santoro L, Pappata S, Filla A, De Michele G
Department of Neurological Sciences, University of Naples Federico II, Via S. Pansini 5, 80131 Naples, Italy
Biostructure and Bioimaging Institute, CNR, Naples, Italy
Department of Biomorphological and Functional Sciences, University of Naples Federico II, Via S. Pansini 5, 80131 Naples, Italy
IRCCS Fondazione S. Maugeri, Telese, Italy
Regional Neurogenetic Center AS6, Lamezia Terme, Italy
References: Nakamura, K., Jeong, S.Y., Uchihara, T., SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein (2001) Hum Mol Genet, 10, pp. 1441-144
Wu, Y.R., Lin, H.Y., Chen, C.M., Genetic testing in spinocerebellar ataxia in Taiwan: Expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease (2004) Clin Genet, 65, pp. 209-214
Bruni, A.C., Takahashi-Fujigasaki, J., Maltecca, F., Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation (2004) Arch Neurol, 61, pp. 1441-1443
Rolfs, A., Koeppen, A.H., Bauer, I., Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17) (2003) Ann Neurol, 54, pp. 367-375
Toyoshima, Y., Yamada, M., Onodera, O., SCA17 homozygote showing Huntington's disease-like phenotype (2004) Ann Neurol, 55, pp. 281-286
Marshall, V., Grosset, D., Role of dopamine transporter imaging in routine clinical practice (2003) Mov Disord, 18, pp. 1415-1423
Maltecca, F., Filla, A., Castaldo, I., Intergenerational instability and marked anticipation in SCA-17 (2003) Neurology, 61, pp. 1441-1443
Trouillas, P., Takayanagi, T., Haller, M., International cooperative ataxia rating scale for pharmacological assessment of the cerebellar syndrome (1997) J Neurol Sci, 145, pp. 205-211
Comella, C.L., Leurgans, S., Wuu, J., Stebbins, G.T., Chmura, T., Rating scales for dystonia: A multicenter assessment (2003) Mov Disord, 18, pp. 303-312. , Dystonia Study Group
Fahn, S., Elton, R.L., Unified Parkinson's Disease Rating (1987) Recent Developments in Parkinson's Disease, 2, pp. 153-163. , members of the UPDRS Development Committee. Scale Fahn S, Marsden CD, Calne DB, Goldstein M, editors. Florham Park, NJ: MacMillian Health Care Information
Lane, R.D., Glazer, W.M., Hansen, T.E., Berman, W.H., Kramer, S.I., Assessment of tardive dyskinesia using the Abnormal Involuntary Movement Scale (1985) J Nerv Ment Dis, 173, pp. 353-357
Varrone, A., Salvatore, E., De Michele, G., Reduced striatal [123I]FP-CIT binding in SCA2 patients without parkinsonism (2004) Ann Neurol, 55, pp. 426-430
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 (2004) J Neurol, 251, pp. 896-897
Yen, T.C., Tzen, K.Y., Chen, M.C., Dopamine transporter concentration is reduced in asymptomatic Machado-Joseph disease gene carriers (2002) Nucl Med, 43, pp. 153-159
Benamer, H.T.S., Patterson, J., Wyper, D.J., Correlation of Parkinson's disease severity and duration with 123I-FP-CIT SPECT striatal uptake (2000) Mov Disord, 15, pp. 692-698
Van Laere, K., De Ceuninck, L., Dom, R., Dopamine transporter SPECT using fast kinetic ligands: 123I-FP-beta-CIT versus 99mTc-TRODAT-1 (2004) Eur J Nucl Med Mol Imaging, 31, pp. 1119-1127
Wu, Y. R., Lin, H. Y., Chen, C. M., Genetic testing in spinocerebellar ataxia in Taiwan: Expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease (2004) Clin Genet, 65, pp. 209-214
Bruni, A. C., Takahashi-Fujigasaki, J., Maltecca, F., Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation (2004) Arch Neurol, 61, pp. 1441-1443
Comella, C. L., Leurgans, S., Wuu, J., Stebbins, G. T., Chmura, T., Rating scales for dystonia: A multicenter assessment (2003) Mov Disord, 18, pp. 303-312. , Dystonia Study Group
Lane, R. D., Glazer, W. M., Hansen, T. E., Berman, W. H., Kramer, S. I., Assessment of tardive dyskinesia using the Abnormal Involuntary Movement Scale (1985) J Nerv Ment Dis, 173, pp. 353-357
Yen, T. C., Tzen, K. Y., Chen, M. C., Dopamine transporter concentration is reduced in asymptomatic Machado-Joseph disease gene carriers (2002) Nucl Med, 43, pp. 153-159
Benamer, H. T. S., Patterson, J., Wyper, D. J., Correlation of Parkinson's disease severity and duration with 123I-FP-CIT SPECT striatal uptake (2000) Mov Disord, 15, pp. 692-698
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17
Antonini A, Vitale C, Barone P, Cilia R, Righini A, Bonuccelli U, Abbruzzese G, Ramat S, Petrone A, Quatrale R, Marconi R, Ceravolo R, Stefani A, Lopiano L, Zappia M, Capus L, Morgante L, Tamma F, Tinazzi M, Colosimo C, Guerra UP, Valzania F, Fagioli G, Distefano A, Bagnato A, Feggi L, Anna S, Maria Teresa Rosaria De Cr, Nobili F, Mazzuca N, Baldari S, Eleopra R, Bestetti A, Benti R, Varrone A, Volterrani D, Massa R, Stocchi F, Schillaci O, Dore F, Zibetti M, Castellano G, Battista SG, Giorgetti G * The relationship between cerebral vascular disease and parkinsonism: The VADO study(498 views) Parkinsonism Relat D (ISSN: 1353-8020, 1873-5126, 1873-5126electronic), 2012; 18(6): 775-780. Impact Factor:3.274 ViewExport to BibTeXExport to EndNote