Mucopolysaccharidosis type VI on enzyme replacement therapy since infancy: Six years follow-up of four children
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference22 articles.
1. Mucopolysaccharidosis VI;Valayannopoulos;Orphanet J Rare Dis.,2010
2. Mucopolysacharidoses type VI Maroteaux Lamy Syndrome;Wraith,2007
3. Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux–Lamy syndrome);Harmatz;J. Pediatr.,2004
4. Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study
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3. The importance of geographic and sociodemographic aspects in the characterization of mucopolysaccharidoses: a case series from Ceará state (Northeast Brazil);2024-02-21
4. The clinical and genotypic–phenotypic findings of mucopolysaccharidosis VI patients: an Iraqi single-study descriptive study;Annals of Medicine & Surgery;2023-09-06
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