Open-label, expanded access study of taliglucerase alfa in patients with Gaucher disease requiring enzyme replacement therapy-Reference-Cited by-同舟云学术

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Open-label, expanded access study of taliglucerase alfa in patients with Gaucher disease requiring enzyme replacement therapy

Published:2020-05 Issue: Volume:82 Page:102418
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Kuter David J.,Wajnrajch Michael,Hernandez Betina,Wang Rong,Chertkoff Raul,Zimran Ari

Funder

Protalix Biotherapeutics

Pfizer

Publisher

Elsevier BV

Reference18 articles.

1. Gaucher disease and related lysosomal storage diseases;Zimran,2016

2. Gaucher disease;Grabowski,2010

3. Management of Gaucher disease: enzyme replacement therapy;Zimran;Pediatr. Endocrinol. Rev.,2014

4. Recommendations for the use of eliglustat in the treatment of adults with Gaucher disease type 1 in the United States;Balwani;Mol. Genet. Metab.,2016

5. How we manage Gaucher disease in the era of choices;Revel-Vilk;Br. J. Haematol.,2018

Cited by 4 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. Real-World Experiences with Taliglucerase Alfa Home Infusions for Patients with Gaucher Disease: A Global Cohort Study;Journal of Clinical Medicine;2023-09-12

2. Novel Therapeutic Approaches in Inherited Neuropathies: A Systematic Review;Pharmaceutics;2023-05-30

3. A Systematic Review and Meta-analyses of Longitudinal Studies on Drug Treatments for Gaucher Disease;Annals of Pharmacotherapy;2022-07-11

4. Enzyme Replacement Therapy for Genetic Disorders Associated with Enzyme Deficiency;Current Medicinal Chemistry;2022-02

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