Mucolipidosis II and III alpha/beta in Brazil: Analysis of the GNPTAB gene by Cury, G.K., Matte, U., Artigalás, O., Alegra, T., Velho, R.V., Sperb, F., Burin, M.G., Ribeiro, E.M., Lourenço, C.M., Kim, C.A., Valadares, E.R., Galera, M.F., Acosta, A.X., Schwartz, I.V.D.

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CNS involvement in Fabry disease: Clinical and imaging studies before and after 12 months of enzyme replacement therapy by Jardim, L., Vedolin, L., Schwartz, I. V. D., Burin, M. G., Cecchin, C., Kalakun, L., Matte, U., Aesse, F., Pitta‐Pinheiro, C., Marconato, J., Giugliani, R.

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Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients by Petry, M. F. G., Nonemacher, K., Sebben, J. C., Schwartz, I. V. D., Azevedo, A. C. M., Burin, M. G., De Rezende, A. R., Kim, C. A., Giugliani, R., Leistner‐Segal, S.

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Nerve conduction studies, electromyography and sympathetic skin response in Fabry's disease by Gomes, Irenio, Nora, Daniel B., Becker, Jefferson, Ehlers, João Arthur C., Schwartz, Ida V.D., Giugliani, Roberto, Ashton-Prolla, Patricia, Jardim, Laura

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Sleep apnoea in patients with mucopolysaccharidoses by Canani, SF, Schwartz, IVD, Azevedo, AC, Fraga, JC, Barreto, SSM, Giugliani, R

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Effects of imilglucerase withdrawal on an adult with Gaucher disease by Schwartz, I V, Karam, S, Ashton-Prolla, P, Michelin, K, Coelho, J, Pires, R F, Pereira, M L, Giugliani, R

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Neurophysiological studies in Fabry disease by Becker, J, Gomes, I, Nora, D, Schwartz, IVD, Ashton-Prolla, P, Kalakun, L, Cecchin, C, Ehlers, JA, Giugliani, R, Jardim, L

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X-linked adrenoleukodystrophy: clinical and laboratory findings in 15 Brazilian patients by Vargas, Carmen R., Coelho, Daniella de M., Barschak, Alethéa G., Souza, Carolina F.M. de, Puga, Ana C.S., Schwartz, Ida V.D., Jardim, Laura, Giugliani, Roberto

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Clinical and molecular studies in five Brazilian cases of Friedreich ataxia by Schwartz, I V, Jardim, L B, Puga, A C, Cocozza, S, Leistner, S, Lima, L C

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