Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature-Reference-Cited by-同舟云学术

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Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature

Published:2010-11 Issue:11 Volume:12 Page:668-679
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Lidove Olivier,West Michael L.,Pintos-Morell Guillem,Reisin Ricardo,Nicholls Kathy,Figuera Luis E.,Parini Rossella,Carvalho Luiz R.,Kampmann Christoph,Pastores Gregory M.,Mehta Atul

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference104 articles.

Cited by 101 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. Fabry disease management: Current status, therapeutic challenges, and future horizons in drug delivery and artificial intelligence assisted diagnosis;Journal of Drug Delivery Science and Technology;2024-10

2. Comparative study on incorporation of three recombinant human α-galactosidase A drugs (agalsidases) into cultured fibroblasts and organs/tissues of Fabry mice;Molecular Genetics and Metabolism Reports;2024-09

3. Pegunigalsidase alfa: a novel, pegylated recombinant alpha-galactosidase enzyme for the treatment of Fabry disease;Frontiers in Genetics;2024-04-12

4. Safety and efficacy of pegunigalsidase alfa in patients with Fabry disease who were previously treated with agalsidase alfa: results from BRIDGE, a phase 3 open-label study;Orphanet Journal of Rare Diseases;2023-10-21

5. Successful Desensitization in a Patient with Fabry Disease with Agalsidase Beta Anaphylaxis: A Rare Case Report;Asthma Allergy Immunology;2023-04-07

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