Long-term complications and associated conditions of type 1 Gaucher Disease (GD) can include splenectomy, bone complications, pulmonary hypertension, Parkinson disease and malignancies. Enzyme replacement therapy (ERT) reverses cytopenia and reduces organomegaly. To study the effects of ERT on long-term complications and associated conditions, the course of Gaucher disease was modelle
Gaucher disease (GD) is a rare genetic lysosomal disorder which is sometimes complicated by bone eve...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Gaucher’s syndrome is the distinguished prevailing disorder characterized under the lysosomal reposi...
Gaucher disease is an autosomal recessively inherited lysosomal storage disorder (LSD). Type I Gauch...
Gaucher disease; enzyme replacement; inherited; metabolic.AimTo study the effectiveness of a specifi...
To determine the effectiveness of enzyme replacement therapies (ERT) for adults with Gaucher disease...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Enzyme replacement therapy (ERT) for Gaucher disease with mannose-terminated glucocerebrosidase has ...
Treatment of Gaucher Disease (GD) is now beset with the abundance of therapeutic options for an indi...
AbstractGaucher disease is an inherited metabolic disease characterized by β-glucocerebrosidase defi...
Gaucher disease (GD) is a rare recessively inherited disorder caused by deficiency of a lysosomal en...
To determine the effectiveness of enzyme replacement therapies (ERT) for children with Gaucher disea...
Gaucher disease, a lysosomal storage disorder, is a multisystem disorder with variable and unpredict...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Gaucher disease (GD) is an autosomal recessive disease which if undiagnosed or diagnosed late result...
Gaucher disease (GD) is a rare genetic lysosomal disorder which is sometimes complicated by bone eve...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Gaucher’s syndrome is the distinguished prevailing disorder characterized under the lysosomal reposi...
Gaucher disease is an autosomal recessively inherited lysosomal storage disorder (LSD). Type I Gauch...
Gaucher disease; enzyme replacement; inherited; metabolic.AimTo study the effectiveness of a specifi...
To determine the effectiveness of enzyme replacement therapies (ERT) for adults with Gaucher disease...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Enzyme replacement therapy (ERT) for Gaucher disease with mannose-terminated glucocerebrosidase has ...
Treatment of Gaucher Disease (GD) is now beset with the abundance of therapeutic options for an indi...
AbstractGaucher disease is an inherited metabolic disease characterized by β-glucocerebrosidase defi...
Gaucher disease (GD) is a rare recessively inherited disorder caused by deficiency of a lysosomal en...
To determine the effectiveness of enzyme replacement therapies (ERT) for children with Gaucher disea...
Gaucher disease, a lysosomal storage disorder, is a multisystem disorder with variable and unpredict...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Gaucher disease (GD) is an autosomal recessive disease which if undiagnosed or diagnosed late result...
Gaucher disease (GD) is a rare genetic lysosomal disorder which is sometimes complicated by bone eve...
Objective: to evaluate the impact of enzyme replacement therapy for Gaucher Disease on clinical a...
Gaucher’s syndrome is the distinguished prevailing disorder characterized under the lysosomal reposi...