Bibliografia e referências

Informações completas para prescrição de Aldurazyme® (solução de laronidase apenas para infusão intravenosa). BioMarin/Genzyme LLC.

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Byers S, Crawley AC, Brumfield LK, et al. Enzyme replacement therapy in a feline model of MPS VI: modification of enzyme structure and dose frequency. Pediatr Res. 2000;47:743-749.

Informações completas para prescrição de Cerezyme® (imiglucerase injetável). Genzyme Corporation.

Dangel JH. Cardiovascular changes in children with mucopolysaccharide storage diseases and related disordersclinical and echocardiographic findings in 64 patients. Eur J Pediatr. 1998;157:534-538.

Dados em arquivo, BioMarin Pharmaceutical Inc.

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Fisher A, Fox J. Newborn screening for lysosomal storage disorders [informativo]. National MPS Society, Inc. 2004. Disponível em: http://www.mpssociety.org/lib-factsheet.html. Acessado em 17 de dezembro de 2004.

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Swiedler SJ, Beck M, Bajbouj M, et al. Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). Am J Med Genet. A ser publicado.

TKT receives fast track designation for iduronate-2-sulfatase for Hunter syndrome [press release]. Cambridge, MA: Transkaryotic Therapies, Inc.; 15 de julho de 2004. Disponível em: http://www.tktx.com/newsbureau/press.htm. Acessado em 17 de dezembro de 2004.

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Yogalingam G, Muller V, Hopwood JJ, Anson DS. Regulation of N-acetylgalactosamine 4- sulfatase expression in retrovirus-transduced feline mucopolysaccharidosis type VI muscle cells. DNA Cell Biol. 1999;18:187-195.