Taliglucerase alfa in Gaucher disease: Description of a Brazilian experience-Reference-Cited by-同舟云学术

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Taliglucerase alfa in Gaucher disease: Description of a Brazilian experience

Published:2018-02 Issue: Volume:68 Page:160-162
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Cravo R.,Rotman V.,Oliveira P.M.N.,Defendi H.G.T.,Conceição D.A.,Xavier J.R.,Chertkoff R.,Noronha T.G.,Maia M.L.S.

Funder

Oswaldo Cruz Foundation

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference10 articles.

1. Gaucher disease: lessons from a decade of therapy;Grabowski;J. Pediatr.,2004

2. Therapeutic approaches to bone pathology in Gaucher disease: past, present and future;Goker-Alpan;Mol. Genet. Metab.,2011

3. Gaucher disease: a prototype for molecular medicine;Grabowski;Crit. Rev. Oncol. Hematol.,1996

4. A plant-derived recombinant human glucocerebrosidase enzyme–a preclinical and phase I investigation;Aviezer;PLoS One,2009

5. [Package Insert] Pfizer Labs, New York, NY;Elelyso,2012

Cited by 1 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. Efficacy and Safety of Taliglucerase Alfa for the Treatment of Gaucher Disease: A 9-Year Experience;Journal of Inborn Errors of Metabolism and Screening;2022

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