Evaluation of idursulfase for the treatment of mucopolysaccharidosis II (Hunter syndrome)
Author:
Publisher
Informa Healthcare
Subject
Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Link
http://www.tandfonline.com/doi/pdf/10.1517/21678707.2013.738182
Reference54 articles.
1. The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase
2. The frequency of lysosomal storage diseases in The Netherlands
3. Cumulative incidence rates of the mucopolysaccharidoses in Germany
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2. Mucopolysaccharidosis type II (Hunter syndrome): Clinical and biochemical aspects of the disease and approaches to its diagnosis and treatment;Advances in Carbohydrate Chemistry and Biochemistry;2020
3. Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future;Drug Design, Development and Therapy;2017-08
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