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Expert Opinion on Orphan Drugs Volume 1, 2013 - Issue 1
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Drug Evaluations

Evaluation of idursulfase for the treatment of mucopolysaccharidosis II (Hunter syndrome)

Maurizio ScarpaUniversity of Padova, Department of Pediatrics, Via Giustiniani 3, 35128 Padova, Italy+39 049 8213505; +39 049 8213502; [email protected]
, MD PhD
Pages 89-98 | Published online: 17 Dec 2012

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David AH Whiteman & Alan Kimura. (2017) Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future. Drug Design, Development and Therapy 11, pages 2467-2480.
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Articles from other publishers (3)

Marialaura Marchetti, Serena Faggiano & Andrea Mozzarelli. (2022) Enzyme Replacement Therapy for Genetic Disorders Associated with Enzyme Deficiency. Current Medicinal Chemistry 29:3, pages 489-525.
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Shifaza Mohamed, Qi Qi He, Arti A. Singh & Vito Ferro. 2020. 71 117 .
Yo Kyung Chung, Young Bae Sohn, Jong Mun Sohn, Jieun Lee, Mi Sun Chang, Younghee Kwun, Chi Hwa Kim, Jin Young Lee, Yeon Joo Yook, Ah-Ra Ko & Dong-Kyu Jin. (2014) A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome. Glycoconjugate Journal 31:4, pages 309-315.
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