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Expert Opinion on Orphan Drugs Volume 3, 2015 - Issue 2
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Review

Diagnosis and therapy options in mucopolysaccharidosis II (Hunter syndrome)

Roberto GiuglianiHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil+ 55 51 33598011; + 55 51 3359 8010; [email protected];Universidade Federal do Rio Grande do Sul, Department of Genetics, Porto Alegre, Brazil;Hospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil+ 55 51 33598011; + 55 51 3359 8010; [email protected]
,
Ana Carolina Brusius-FacchinHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil
,
Carolina Fischinger Moura de SouzaHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil
,
Gabriel CivalleroHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil
,
Maira BurinHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil
,
Sandra Leistner-SegalHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil
,
Guilherme BaldoHospital de Clínicas de Porto Alegre, Gene Therapy Center, Porto Alegre, Brazil;Universidade Federal do Rio Grande do Sul, Department of Physiology, Porto Alegre, Brazil
&
Filippo VairoHospital de Clínicas de Porto Alegre, Medical Genetics Service, Rua Ramiro Barcelos 2350, 90035 903 – Porto Alegre – RS, Brazil
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Pages 141-150 | Published online: 02 Feb 2015

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Read on this site (4)

David Millington, Scott Norton, Raj Singh, Rama Sista, Vijay Srinivasan & Vamsee Pamula. (2018) Digital microfluidics comes of age: high-throughput screening to bedside diagnostic testing for genetic disorders in newborns. Expert Review of Molecular Diagnostics 18:8, pages 701-712.
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Molly Stapleton, Francyne Kubaski, Robert W. Mason, Hiromasa Yabe, Yasuyuki Suzuki, Kenji E. Orii, Tadao Orii & Shunji Tomatsu. (2017) Presentation and treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome). Expert Opinion on Orphan Drugs 5:4, pages 295-307.
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Filippo Vairo, Andressa Federhen, Guilherme Baldo, Mariluce Riegel, Maira Burin, Sandra Leistner-Segal & Roberto Giugliani. (2015) Diagnostic and treatment strategies in mucopolysaccharidosis VI. The Application of Clinical Genetics 8, pages 245-255.
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Anna Tylki-Szymańska & Agnieszka Jurecka. (2015) Prospective therapies for mucopolysaccharidoses. Expert Opinion on Orphan Drugs 3:11, pages 1241-1253.
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Articles from other publishers (2)

Francyne Kubaski, Filippo Vairo, Guilherme Baldo, Fabiano de Oliveira Poswar, Amauri Dalla Corte & Roberto Giugliani. (2020) Therapeutic Options for Mucopolysaccharidosis II (Hunter Disease). Current Pharmaceutical Design 26:40, pages 5100-5109.
Crossref
Shifaza Mohamed, Qi Qi He, Arti A. Singh & Vito Ferro. 2020. 71 117 .

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