Mucopolysaccharidosis type VI: A cardiologist's guide to diagnosis and treatment
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference66 articles.
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2. Mucopolysaccharidosis VI;Valayannopoulos;Orphanet J Rare Dis,2010
3. Cumulative incidence rates of the mucopolysaccharidoses in Germany;Baehner;J Inherit Metab Dis,2005
4. Mucopolysaccharidosis type VI: identification of novel mutations on the arylsulphatase B gene in South American patients;Petry;J Inherit Metab Dis,2005
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1. Evaluation of aortic elasticity properties in mucopolysaccharidosis patients; effect of enzyme replacement therapy (ERT) on aortic stiffness;Journal of Pediatric Endocrinology and Metabolism;2024-06-27
2. Generation of a novel disease model mouse for mucopolysaccharidosis type VI via c. 252T>C human ARSB mutation knock-in;Biochemistry and Biophysics Reports;2022-09
3. The Mucopolysaccharidoses;Lysosomal Storage Disorders;2022-07-21
4. Enzyme replacement therapy in mice lacking arylsulfatase B targets bone-remodeling cells, but not chondrocytes;Human Molecular Genetics;2020-01-15
5. Recommendations for the management of MPS VI: systematic evidence- and consensus-based guidance;Orphanet Journal of Rare Diseases;2019-05-29
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