The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the International Collaborative Gaucher Group Gaucher Registry. Data were analyzed for 160 untreated patients and 342 ERT-treated patients. Imiglucerase significantly improves BMD in patients with GD, with 8 years of ERT leading to normal BMD. Introduction: The objective was to determine the effect of enzyme replacement therapy (ERT; Cerezyme, imiglucerase) on BMD in type 1 Gaucher disease (GD). Materials and Methods: The study population included all adults (men, 18–70 years; women, 18–50 years) enrolled in the International Collaborative Gaucher Group (ICGG) Gaucher Registry for whom lumbar spine BMD measurements were available. BMD data with up to 8 y...
Objective Eliglustat is an investigational oral substrate reduc-tion therapy for Gaucher disease typ...
AbstractGaucher disease is an inherited metabolic disease characterized by β-glucocerebrosidase defi...
Gaucher's disease (GD) is one of the most common lysosomal diseases in humans. It results from β-glu...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Progressive skeletal disease accounts for some of the most debilitating complications of type 1 Gauc...
Gaucher disease, a lysosomal storage disorder, is a multisystem disorder with variable and unpredict...
Copyright © 2013 Irina Tukan et al. This is an open access article distributed under the Creative Co...
Background: Gaucher disease (GD) type I is the most common type of GD. Its main clinical manifestati...
Bone involvement is one of the most disabling complications in patients with type 1 Gaucher disease ...
Dosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate a...
Background: In Gaucher disease (GD), acid-β-glucosidase (GBA1) gene mutations result in defective g...
Gaucher disease (GD) is a rare genetic lysosomal disorder which is sometimes complicated by bone eve...
25 pagesInternational audienceINTRODUCTION : Known biomarkers of Gaucher-disease activity are platel...
Gaucher disease (GD) is a lysosomal storage disorder; symptomatic patients with type 1 GD need long-...
Objective Eliglustat is an investigational oral substrate reduc-tion therapy for Gaucher disease typ...
AbstractGaucher disease is an inherited metabolic disease characterized by β-glucocerebrosidase defi...
Gaucher's disease (GD) is one of the most common lysosomal diseases in humans. It results from β-glu...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
The effect of ERT with imiglucerase on BMD in type 1 GD was studied using BMD data from the Internat...
Progressive skeletal disease accounts for some of the most debilitating complications of type 1 Gauc...
Gaucher disease, a lysosomal storage disorder, is a multisystem disorder with variable and unpredict...
Copyright © 2013 Irina Tukan et al. This is an open access article distributed under the Creative Co...
Background: Gaucher disease (GD) type I is the most common type of GD. Its main clinical manifestati...
Bone involvement is one of the most disabling complications in patients with type 1 Gaucher disease ...
Dosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate a...
Background: In Gaucher disease (GD), acid-β-glucosidase (GBA1) gene mutations result in defective g...
Gaucher disease (GD) is a rare genetic lysosomal disorder which is sometimes complicated by bone eve...
25 pagesInternational audienceINTRODUCTION : Known biomarkers of Gaucher-disease activity are platel...
Gaucher disease (GD) is a lysosomal storage disorder; symptomatic patients with type 1 GD need long-...
Objective Eliglustat is an investigational oral substrate reduc-tion therapy for Gaucher disease typ...
AbstractGaucher disease is an inherited metabolic disease characterized by β-glucocerebrosidase defi...
Gaucher's disease (GD) is one of the most common lysosomal diseases in humans. It results from β-glu...