Bibliografia e referências
Crude and age-adjusted prevalence of diagnosed diabetes per 100 population, Estados Unidos, 1980-2002. Recurso de saúde pública sobre diabetes, site dos Centros de Controle e Prevenção de Doenças. Disponível em: http://www.cdc.gov/diabetes/statistics/prev/national/figage.htm. Acessado em 17 de dezembro de 2004.
Epilepsy: One of the nation's most common disabling neurological conditions. Site dos Centros de Controle e Prevenção de Doenças. Disponível em: http://www.cdc.gov/epilepsy. Acessado em 17 de dezembro de 2004.
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.
Fletcher J, Pamula Y, Martin AJ. Reversing respiratory disease in MPS: lessons from bone marrow transplantation. Poster acessado em www.chempathadelaide.com.au.
Harmatz P, Whitley CB, Waber L, et al. Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) J Pediatr. 2004;144:574-580.
Lee V, Li CK, Shing MM, et al. Umbilical cord blood transplantation for Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Bone Marrow Transplant. 2000;26:455-458.
Maroteaux P, Leveque B, Marie J, Lamy M. [Nova disostose com eliminação urinária de sulfato de condroitina B] Presse Med. 1963;71:1849-1852. Francês.
McGovern MM, Ludman MD, Short MP, et al. Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMT. Birth Defects Orig Artic Ser. 1986;22:41-53.
Meikle PJ, Hopwood JJ, Clague AE, Carey WF. Prevalence of lysosomal storage disorders.
JAMA. 1999;281:249-254.
Miller G, Partridge A. Mucopolysaccharidosis type VI presenting in infancy with endocardial fibroelastosis and heart failure. Pediatr Cardiol. 1983;4:61-62.
MPS I survey results: patterns in the referral, diagnosis, and management of individuals with MPS
I. National MPS Society and Genzyme Corporation. Abril de 2004. Disponível em:
http://www.mpssociety.org/library.html.
Muenzer J. The mucopolysaccharidoses: a heterogeneous group of disorders with variable
pediatric presentations. J Pediatr. 2004;144(5 Suppl):S27-S34. Revisão.
Neufeld EF, Muenzer J. The mucopolysaccharidoses. Em: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. Vol 3. 8ª. edição Nova York, NY: McGraw-Hill; 2001:3421-3452.
Paterson DE, Harper G, Weston HJ, Mattingley J. Maroteaux-Lamy syndrome, mild formMPS vi
b. Br J Radiol. 1982;55:805-812.
Poorthuis BJ, Wevers RA, Kleijer WJ, et al. The frequency of lysosomal storage diseases in The
Netherlands. Hum Genet. 1999;105:151-156.
Rhodes L, Bailey CM, Moorman JE. Asthma prevalence and control characteristics by
race/ethnicityUnited States, 2002. Morbidity and Mortality Weekly Report. 27 de fevereiro de 2004; 53:145-148. Disponível em: http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5307a1.htm.
Acessado em 17 de dezembro de 2004.
Sjogren P, Pedersen T, Steinmetz H. Mucopolysaccharidoses and anaesthetic risks. Acta
Anaesthesiol Scand. 1987;31:214-218. Revisão.
Smith KS, Hallett KB, Hall RK, et al. Mucopolysaccharidosis: MPS VI and associated delayed
tooth eruption. Int J Oral Maxillofac Surg. 1995;24:176-180.
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; 2005:134A:144-150.
Vougioukas VI, Berlis A, Kopp MV, et al. Neurosurgical interventions in children with Maroteaux-
Lamy syndrome. Case report and review of the literature. Pediatr Neurosurg. 2001;35:35-38.
Revisão.
Wilcox WR. Lysosomal storage disorders: the need for better pediatric recognition and
comprehensive care. J Pediatr. 2004;144(5 Suppl):S3-S14. Revisão.
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