Bibliyografi ve Referanslar

100 nüfusta tanı konan diyabetin ham ve yaşa göre düzeltilmiş prevalansı, Amerika Birleşik Devletleri, 1980-2002. Diyabet kamu sağlığı kaynağı, Hastalık Kontrol ve Önleme Merkezleri Web sitesi.
Şuradan görülebilir: http://www.cdc.gov/diabetes/statistics/prev/national/figage.htm. 17 Aralık 2004'te erişilmiştir.

Epilepsi: Ülkede en sık maluliyete yol açan nörolojik tablolardandır. Hastalık Kontrol ve Önleme Merkezleri Web sitesi. Şuradan görülebilir: http://www.cdc.gov/epilepsy. 17 Aralık 2004'te erişilmiştir.

Fisher A, Fox J. Newborn screening for lysosomal storage disorders [fact sheet]. National MPS Society, Inc. 2004. Available at: http://www.mpssociety.org/lib-factsheet.html. Accessed December 17, 2004.

Fletcher J, Pamula Y, Martin AJ. Reversing respiratory disease in MPS: lessons from bone marrow transplantation. Poster accessed at 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. [A new dysostosis with urinary elimination of chondroitin sulfate B]. Presse Med. 1963;71:1849-1852. French.

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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. April 2004. Available at: 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. Review.

Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. Vol 3. 8th ed. New York, NY: McGraw-Hill; 2001:3421-3452.

Paterson DE, Harper G, Weston HJ, Mattingley J. Maroteaux-Lamy syndrome, mild form—MPS 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.

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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. Review.

Wilcox WR. Lysosomal storage disorders: the need for better pediatric recognition and comprehensive care. J Pediatr. 2004;144(5 Suppl):S3-S14. Review.