Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical and laboratory parameters after two, five and ten years of treatment. Methods: data were collected from patient records and analyzed using BioEstat software (version 5.0). Student's t-test, Analysis of Variance (ANOVA), Wilcoxon test and Kruskal–Wallis test were used for statistical analysis. Hepatomegaly and splenomegaly were analyzed using the Kappa test. Results: there was a significant increase in hemoglobin levels (p-value <0.01) and platelet counts (p-value = 0.01) within two years of therapy. At the same time, the frequencies of splenomegaly (p-value <0.01) and hepatomegaly (p-value <0.05) reduced. These results were similar...
Taliglucerase alfa is the first available plant cell-expressed human recombinant therapeutic protein...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
Enzyme replacement therapy is the stan-dard of care for symptomatic Gaucher disease. Velaglucerase a...
Purpose: To determine whether enzyme therapy with imiglucerase/ alglucerase demonstrates dose-respon...
Gaucher disease; enzyme replacement; inherited; metabolic.AimTo study the effectiveness of a specifi...
For three decades, enzyme replacement therapy (ERT), and more recently, substrate reduction therapy,...
Abstract Background Previous studies have provided eq...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
BACKGROUND We retrospectively compared biochemical responses in type 1 Gaucher disease patients to t...
Long-term complications and associated conditions of type 1 Gaucher Disease (GD) can include splenec...
Deborah Elstein, Ari ZimranGaucher Clinic, Shaare Zedek Medical Center, Jerusalem, IsraelAbstract: M...
Gaucher disease (GD) is a rare recessively inherited disorder caused by deficiency of a lysosomal en...
Dosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate a...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Taliglucerase alfa is the first available plant cell-expressed human recombinant therapeutic protein...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
Enzyme replacement therapy is the stan-dard of care for symptomatic Gaucher disease. Velaglucerase a...
Purpose: To determine whether enzyme therapy with imiglucerase/ alglucerase demonstrates dose-respon...
Gaucher disease; enzyme replacement; inherited; metabolic.AimTo study the effectiveness of a specifi...
For three decades, enzyme replacement therapy (ERT), and more recently, substrate reduction therapy,...
Abstract Background Previous studies have provided eq...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
BACKGROUND We retrospectively compared biochemical responses in type 1 Gaucher disease patients to t...
Long-term complications and associated conditions of type 1 Gaucher Disease (GD) can include splenec...
Deborah Elstein, Ari ZimranGaucher Clinic, Shaare Zedek Medical Center, Jerusalem, IsraelAbstract: M...
Gaucher disease (GD) is a rare recessively inherited disorder caused by deficiency of a lysosomal en...
Dosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate a...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Taliglucerase alfa is the first available plant cell-expressed human recombinant therapeutic protein...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
Enzyme replacement therapy is the stan-dard of care for symptomatic Gaucher disease. Velaglucerase a...