Treatment regimens in Gaucher's disease
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. The clinical course of treated and untreated Gaucher disease: a study of 45 patients;Beutler;Blood Cell Mol Dis,1995
2. Low-dose enzyme replacement therapy for Gaucher's disease: effects of age, sex, genotype, and clinical features on response to treatment;Zimran;Am J Med,1994
3. Enzyme augmentation in moderate to life-threatening Gaucher disease;Fallet;Pediatr Res,1992
4. Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources;Grabowski;Ann Intern Med,1995
5. Enzyme replacement treatment in type 1 and type 3 Gaucher's disease;Bembi;Lancet,1994
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1. Quantitative assessment of the exposure–efficacy relationship of glucocerebrosidase using Markovian elements in Gaucher patients treated with enzyme replacement therapy;British Journal of Clinical Pharmacology;2022-01-10
2. Relationship Between Glucocerebrosidase Activity and Clinical Response to Enzyme Replacement Therapy in Patients With Gaucher Disease Type I;Basic & Clinical Pharmacology & Toxicology;2018-03-30
3. Cellular Uptake of Glucocerebrosidase in Gaucher Patients Receiving Enzyme Replacement Treatment;Clinical Pharmacokinetics;2016-04-15
4. Development and application to clinical practice of a validated HPLC method for the analysis of β-glucocerebrosidase in Gaucher disease;Journal of Pharmaceutical and Biomedical Analysis;2014-03
5. Uncoupling of osteoblast–osteoclast regulation in a chemical murine model of Gaucher disease;Gene;2013-12
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