Morphological damage in Sertoli, myoid and interstitial cells in a mouse model of mucopolysaccharidosis type I (MPS I)

Author:

do Nascimento Cinthia CastroORCID,Aguiar OdairORCID,Viana Gustavo MonteiroORCID,D’Almeida VâniaORCID

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Associação Fundo de Incentivo à Pesquisa

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Reference42 articles.

1. Neufeld EF, Meunzer J (2001) The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) Metabolic and molecular basis of inherited disease. McGraw-Hill, New York, pp 3421–3452

2. Clarke LA (2008) The mucopolysaccharidoses: a success of molecular medicine. Expert Rev Mol Med 10:1–18. https://doi.org/10.1017/S1462399408000550

3. Muenzer J, Wraith JE, Clarke LA (2009) Mucopolysaccharidosis I : Management and treatment guidelines. Pediatrics 123:12–29. https://doi.org/10.1542/peds.2008-0416

4. Kakkis ED, Muenzer J, Tiller GE (2001) Enzyme-replacement therapy in mucopolysaccharidosis I. N Engl J Med 344(3):182–188. https://doi.org/10.1056/NEJM200101183440304

5. Castorina M, Antuzzi D, Richards SM, Cox GF, Xue Y (2015) Successful pregnancy and breastfeeding in a woman with mucopolysaccharidosis type I while receiving laronidase enzyme replacement therapy. Clin Exp Obstet Gynecol 42(1):108–113

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