Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions von Souza, G.N., Kersting, N., Krum-Santos, A.C., Santos, A.S.P., Furtado, G.V., Pacheco, D., Gonçalves, T.A., Saute, J.A., Schuler-Faccini, L., Mattos, E.P., Saraiva-Pereira, M.L., Jardim, L.B.

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Genetic aspects of Huntington's disease in Latin America. A systematic review von Castilhos, R.M., Augustin, M.C., Santos, J.A., Perandones, C., Saraiva-Pereira, M.L., Jardim, L.B.

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Huntington disease and Huntington disease-like in a case series from Brazil von Castilhos, R.M., Souza, A.F.D., Furtado, G.V., Gheno, T.C., Silva, A.L., Vargas, F.R., Lima, M.-A.F.D., Barsottini, O., Pedroso, J.L., Godeiro Jr, C., Salarini, D., Pereira, E.T., Lin, K., Toralles, M.-B., Saute, J.A.M., Rieder, C.R., Quintas, M., Sequeiros, J., Alonso, I., Saraiva-Pereira, M.L., Jardim, L.B.

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Does DNA methylation in the promoter region of the ATXN3 gene modify age at onset in MJD (SCA3) patients? von Emmel, VE, Alonso, I, Jardim, LB, Saraiva-Pereira, ML, Sequeiros, J

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Survival estimates for patients with Machado-Joseph disease (SCA3) von Kieling, C, Prestes, PR, Saraiva-Pereira, ML, Jardim, LB

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MR Imaging in Spinocerebellar Ataxias: A Systematic Review von Klaes, A, Reckziegel, E, Franca, Jr, M C, Rezende, T J R, Vedolin, L M, Jardim, L B, Saute, J A

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Age at onset prediction in spinocerebellar ataxia type 3 changes according to population of origin von de Mattos, E. P., Leotti, V. B., Soong, B.‐W., Raposo, M., Lima, M., Vasconcelos, J., Fussiger, H., Souza, G. N., Kersting, N., Furtado, G. V., Saute, J. A. M., Camey, S. A., Saraiva‐Pereira, M. L., Jardim, L. B.

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SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil von França Jr, M.C., Dogini, D.B., D'Abreu, A., Teive, H.A.G., Munhoz, R.P., Raskin, S., Moro, A., Melo, C.C., Gomes, A.P., Saute, J.A.M., Jardim, L.B., Lopes-Cendes, I.

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Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10 von ALONSO, I, JARDIM, L. B, ARTIGALAS, O, SARAIUA-PEREIRA, M. L, MATSUURA, T, ASHIZAWA, T, SEQUEIROS, J, SILVEIRA, I

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ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease von DI FONZO, A, CHIEN, H. F, MARINI, P, SQUITIERI, F, HORSTINK, M. W, MONTAGNA, P, DALLA LIBERA, A, STOCCHI, F, GOLDWURM, S, FERREIRA, J. J, MECO, G, MARTIGNONI, E, SOCAL, M, LOPIANO, L, JARDIM, L. B, OOSTRA, B. A, BARBOSA, E. R, BONIFATI, V, GIRAUDO, S, TASSORELLI, C, ILICETO, G, FABBRINI, G, MARCONI, R, FINCATI, E, ABBRUZZESE, G

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Improvement of sympathetic skin responses under enzyme replacement therapy in Fabry disease von Jardim, L. B., Gomes, I., Netto, C. B. O., Nora, D. B., Matte, U. S., Pereira, F., Burin, M. G., Kalakun, L., Giugliani, R., Becker, J.

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Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil von Gheno, T. C., Furtado, G. V., Saute, J. A. M., Donis, K. C., Fontanari, A. M. V., Emmel, V. E., Pedroso, J. L., Barsottini, O., Godeiro‐Junior, C., Linden, H., Ternes Pereira, E., Cintra, V. P., Marques, W., Castilhos, R. M., Alonso, I., Sequeiros, J., Cornejo‐Olivas, M., Mazzetti, P., Leotti, V. B., Jardim, L. B., Saraiva‐Pereira, M. L.

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Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutations von Servelhere, K. R., Faber, I., Saute, J. A. M., Moscovich, M., D'Abreu, A., Jardim, L. B., Teive, H. A. G., Lopes-Cendes, I., Franca Jr, M. C.

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Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings von Trott, A, Jardim, LB, Ludwig, HT, Saute, JAM, Artigalás, O, Kieling, C, Wanderley, HYC, Rieder, CRM, Monte, TL, Socal, M, Alonso, I, Ferro, A, Carvalho, T, Do Céu Moreira, M, Mendonça, P, Ferreirinha, F, Silveira, I, Sequeiros, J, Giugliani, R, Saraiva-Pereira, ML

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Intrafamilial variability of Parkinson phenotype in SCAs: Novel cases due to SCA2 and SCA3 expansions von Socal, M.P, Emmel, V.E, Rieder, C.R.M, Hilbig, A, Saraiva-Pereira, M.L, Jardim, L.B

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A neurological examination score for the assessment of spinocerebellar ataxia 3 (SCA3) von Kieling, C., Rieder, C. R. M., Silva, A. C. F., Saute, J. A. M., Cecchin, C. R., Monte, T. L., Jardim, L. B.

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Severity score system for progressive myelopathy: development and validation of a new clinical scale von Castilhos, R M, Blank, D, Netto, C B O, Souza, C F M, Fernandes, L N T, Schwartz, I V D, Giugliani, R, Jardim, L B

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Occupational therapy in spinocerebellar ataxia type 3: an open-label trial von Silva, R C R, Saute, J A M, Silva, A C F, Coutinho, A C O, Saraiva-Pereira, M L, Jardim, L B

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Glucocerebrosidase gene variants in parkinsonian patients with Machado Joseph/spinocerebellar ataxia 3 von Siebert, M, Donis, K.C, Socal, M, Rieder, C.R.M, Emmel, V.E, Vairo, F, Michelin-Tirelli, K, França, M, D’Abreu, A.C, Bettencourt, C, Lima, M, Lopes Cendes, I, Saraiva-Pereira, M.L, Jardim, L.B

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Depressive Symptoms in Machado-Joseph Disease (SCA3) Patients and Their Relatives von Cecchin, C.R., Pires, A.P., Rieder, C.R., Monte, T.L., Silveira, I., Carvalho, T., Saraiva-Pereira, M.L., Sequeiros, J., Jardim, L.B.

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