Disease burden, management patterns and multidisciplinary clinical approaches for patients with MPS IVA and VI in selected Latin American Countries-Reference-Cited by-同舟云学术

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Disease burden, management patterns and multidisciplinary clinical approaches for patients with MPS IVA and VI in selected Latin American Countries

Published:2021-09 Issue: Volume:28 Page:100769
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Solano Villarreal M,Mandujano Claudia Yazmín Cossío,Avila-Rejon Carmen Amor,Espin Victor Hugo,Montaño Hector Paul Quintero

Funder

BioMarin Pharmaceutical

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference44 articles.

1. Mucopolysaccharidosis, Medscape;Bittar,2020

2. Changes in cellular processes occurring in mucopolysaccharidoses as underestimated pathomechanisms of these diseases;Gaffke;Cell Biol. Int.,2020

3. Clinical findings in 12 patients with MPS IV A (Morquio’s disease);Nelson;Clin. Genet.,2008

4. Online Mendelian Inheritance in Man (OMIM). Mucopolysaccharidosis type VI;Johns Hopkins University,2018

5. Mucopolusaccharidosis Type IVA, Online Mendelian Inherit. Man (OMIM);Vernon,2020

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Safety outcomes and patients’ preferences for home-based intravenous enzyme replacement therapy (ERT) in pompe disease and mucopolysaccharidosis type I (MPS I) disorder: COVID-19 and beyond;Orphanet Journal of Rare Diseases;2023-10-27

2. Difficulties Associated with Enzyme Replacement Therapy for Mucopolysaccharidoses;Turkish Archives of Pediatrics;2021-11-19

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