BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase is efficacious, well-tolerated and safe. However, cost considerations, visits to medical facilities, potentially duration of theray for life, are issues of major concern to a proportion of treated patients and has, in some cases, led to the withdrawal of therapy. AIMS: To elucidate whether an extension of the interval between enzyme infusions to once every three weeks is as effective in maintaining the clinical responses achieved with the bi-monthly regimen. MATERIALS AND METHODS: Four patients with an optimal response to ERT (at 30 units/kg every two weeks for an average of 27 months), were subjected to enzyme dose/frequency changes that ess...
Long-term complications and associated conditions of type 1 Gaucher Disease (GD) can include splenec...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
Switching between enzyme replacement therapies (ERT) and substrate reduction therapies (SRT) in pati...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
Purpose: To determine whether enzyme therapy with imiglucerase/ alglucerase demonstrates dose-respon...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Background: Children with Gaucher disease type I (GD1) are usually treated with enzyme replacement ...
Dosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate a...
Purpose: In Gaucher disease, diminished activity of the lysosomal enzyme, acid β-glucosidase, leads ...
Gaucher disease; enzyme replacement; inherited; metabolic.AimTo study the effectiveness of a specifi...
Gaucher disease (GD) is a lysosomal storage disorder; symptomatic patients with type 1 GD need long-...
Abstract Background Previous studies have provided eq...
For three decades, enzyme replacement therapy (ERT), and more recently, substrate reduction therapy,...
International audienceBackground: In 2009, a worldwide supply constraint of imiglucerase led to trea...
Deborah Elstein, Ari ZimranGaucher Clinic, Shaare Zedek Medical Center, Jerusalem, IsraelAbstract: M...
Long-term complications and associated conditions of type 1 Gaucher Disease (GD) can include splenec...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
Switching between enzyme replacement therapies (ERT) and substrate reduction therapies (SRT) in pati...
BACKGROUND: Enzyme replacement therapy (ERT) for Gaucher's disease with alglucerase or imiglucerase ...
Purpose: To determine whether enzyme therapy with imiglucerase/ alglucerase demonstrates dose-respon...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Background: Children with Gaucher disease type I (GD1) are usually treated with enzyme replacement ...
Dosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate a...
Purpose: In Gaucher disease, diminished activity of the lysosomal enzyme, acid β-glucosidase, leads ...
Gaucher disease; enzyme replacement; inherited; metabolic.AimTo study the effectiveness of a specifi...
Gaucher disease (GD) is a lysosomal storage disorder; symptomatic patients with type 1 GD need long-...
Abstract Background Previous studies have provided eq...
For three decades, enzyme replacement therapy (ERT), and more recently, substrate reduction therapy,...
International audienceBackground: In 2009, a worldwide supply constraint of imiglucerase led to trea...
Deborah Elstein, Ari ZimranGaucher Clinic, Shaare Zedek Medical Center, Jerusalem, IsraelAbstract: M...
Long-term complications and associated conditions of type 1 Gaucher Disease (GD) can include splenec...
The quantification of enzyme activity in the patient treated with enzyme replacement therapy (ERT) h...
Switching between enzyme replacement therapies (ERT) and substrate reduction therapies (SRT) in pati...