The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) has been suggested as a tool for dosage individualization, so we conducted a study to evaluate the relationship between glucocerebrosidase activity and clinical response in patients with Gaucher disease type I (GD1) to ERT. The study included patients diagnosed with GD1, who were being treated with ERT, and healthy individuals. Markers based on glucocerebrosidase activity measurement in patients' leucocytes were studied: enzyme activity at 15 min. post-infusion (Act75 ) reflects the amount of enzyme that is distributed in the body post-ERT infusion, and accumulated glucocerebrosidase activity during ERT infusion (Act75-0 ) indicates the total ...
AbstractPurposeIn Gaucher disease, diminished activity of the lysosomal enzyme, acid β-glucosidase, ...
Gaucher disease (GD) is the most common lysosomal storage disorder (LSD). Based on a deficient β-glu...
Gaucher disease is a lysosomal storage disorder characterized by a deficiency of the enzyme acid bet...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
BACKGROUND We retrospectively compared biochemical responses in type 1 Gaucher disease patients to t...
Gaucher disease (GD) is a rare recessively inherited disorder caused by deficiency of a lysosomal en...
For three decades, enzyme replacement therapy (ERT), and more recently, substrate reduction therapy,...
Purpose: To determine whether enzyme therapy with imiglucerase/ alglucerase demonstrates dose-respon...
Background: Gaucher disease (GD) is the most common glycosphingolipidosis resulting in accumulation ...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Objectives: The aim of the study was to evaluate the efficiency of the biomarkers chitotriosidase (C...
Gaucher disease (GD) patients often present with abnormalities in immune response that may be the re...
Background: Gaucher disease (GD) is the most common lysosomal storage disorder (LSD). Based on a def...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
<div><p>Gaucher disease (GD) patients often present with abnormalities in immune response that may b...
AbstractPurposeIn Gaucher disease, diminished activity of the lysosomal enzyme, acid β-glucosidase, ...
Gaucher disease (GD) is the most common lysosomal storage disorder (LSD). Based on a deficient β-glu...
Gaucher disease is a lysosomal storage disorder characterized by a deficiency of the enzyme acid bet...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
BACKGROUND We retrospectively compared biochemical responses in type 1 Gaucher disease patients to t...
Gaucher disease (GD) is a rare recessively inherited disorder caused by deficiency of a lysosomal en...
For three decades, enzyme replacement therapy (ERT), and more recently, substrate reduction therapy,...
Purpose: To determine whether enzyme therapy with imiglucerase/ alglucerase demonstrates dose-respon...
Background: Gaucher disease (GD) is the most common glycosphingolipidosis resulting in accumulation ...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Objectives: The aim of the study was to evaluate the efficiency of the biomarkers chitotriosidase (C...
Gaucher disease (GD) patients often present with abnormalities in immune response that may be the re...
Background: Gaucher disease (GD) is the most common lysosomal storage disorder (LSD). Based on a def...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
<div><p>Gaucher disease (GD) patients often present with abnormalities in immune response that may b...
AbstractPurposeIn Gaucher disease, diminished activity of the lysosomal enzyme, acid β-glucosidase, ...
Gaucher disease (GD) is the most common lysosomal storage disorder (LSD). Based on a deficient β-glu...
Gaucher disease is a lysosomal storage disorder characterized by a deficiency of the enzyme acid bet...