Modeling changes in biomarkers in Gaucher disease patients receiving enzyme replacement therapy using a pathophysiological model-Reference-Cited by-同舟云学术

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Modeling changes in biomarkers in Gaucher disease patients receiving enzyme replacement therapy using a pathophysiological model

Published:2014 Issue:1 Volume:9 Page:95
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Vigan Marie,Stirnemann Jérôme,Caillaud Catherine,Froissart Roseline,Boutten Anne,Fantin Bruno,Belmatoug Nadia,Mentré France

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Reference34 articles.

1. Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's disease

2. Gaucher Disease

3. Recent clinical progress in Gaucher disease

4. Gaucher disease: pathological mechanisms and modern management

5. Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease

Cited by 9 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. Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients;International Journal of Molecular Sciences;2023-09-22

2. A 20-Year Longitudinal Study of Plasma Chitotriosidase Activity in Treated Gaucher Disease Type 1 and 3 Patients—A Qualitative and Quantitative Approach;Biomolecules;2023-02-24

3. Metabolomic Study Using Time-of-Flight Mass Spectrometry Reveals Novel Urinary Biomarkers for Gaucher Disease Type 1;Journal of Proteome Research;2022-03-29

4. A Quantitative Systems Pharmacology Model of Gaucher Disease Type 1 Provides Mechanistic Insight Into the Response to Substrate Reduction Therapy With Eliglustat;CPT: Pharmacometrics & Systems Pharmacology;2020-06-19

5. Effect of velaglucerase alfa enzyme replacement therapy on red blood cell properties in Gaucher disease;American Journal of Hematology;2017-07-19

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