UNLABELLED: The therapeutic options for lysosomal storage diseases (LSDs) have expanded greatly over the past decade, although for many disorders there is still no effective treatment. Given that the majority of LSDs involve pathological changes in both the brain and peripheral tissues, effective treatment of central nervous system (CNS) and peripheral manifestations still remains a considerable technical challenge. Type 1 Gaucher disease has two approved treatment modalities - enzyme replacement therapy (ERT) and substrate reduction therapy (SRT) - which have unique, independent and potentially complementary mechanisms of action. The availability of these two therapies has greatly increased the options for the effective clinical management...
Gaucher disease is caused by a deficiency of the lysosomal enzyme glucocerebrosidase (acid βâ gluc...
The lysosomal storage diseases (LSDs) are a group of inherited metabolic disorders caused by the de...
Substrate reduction therapy is a novel approach to treating glycosphingolipid (GSL) lysosomal storag...
The concept of enzyme replacement as a potential therapeutic approach to ameliorate lysosomal storag...
Lysosomal storage diseases (LSDs) are a group of rare, life-threatening genetic disorders, usually c...
Lysosomal storage diseases (LSDs) are a group of rare, life-threatening genetic disorders, usually c...
Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as...
Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as...
Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as...
Glycosphingolipid lysosomal storage diseases are a small but challenging group of human disorders to...
Lysosomal storage diseases (LSDs) are a group of rare genetic multisystemic disorders, resulting in ...
Lysosomal storage diseases are a group of rare genetic disorders characterized by the accumulation o...
Lysosomal storage diseases are a group of rare genetic disorders characterized by the accumulation o...
Abstract In this article, we review specific therapies that tackle the basic biochemical defects of ...
Glycosphingolipid (GSL) lysosomal storage disorders are a small but challenging group of human disea...
Gaucher disease is caused by a deficiency of the lysosomal enzyme glucocerebrosidase (acid βâ gluc...
The lysosomal storage diseases (LSDs) are a group of inherited metabolic disorders caused by the de...
Substrate reduction therapy is a novel approach to treating glycosphingolipid (GSL) lysosomal storag...
The concept of enzyme replacement as a potential therapeutic approach to ameliorate lysosomal storag...
Lysosomal storage diseases (LSDs) are a group of rare, life-threatening genetic disorders, usually c...
Lysosomal storage diseases (LSDs) are a group of rare, life-threatening genetic disorders, usually c...
Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as...
Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as...
Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as...
Glycosphingolipid lysosomal storage diseases are a small but challenging group of human disorders to...
Lysosomal storage diseases (LSDs) are a group of rare genetic multisystemic disorders, resulting in ...
Lysosomal storage diseases are a group of rare genetic disorders characterized by the accumulation o...
Lysosomal storage diseases are a group of rare genetic disorders characterized by the accumulation o...
Abstract In this article, we review specific therapies that tackle the basic biochemical defects of ...
Glycosphingolipid (GSL) lysosomal storage disorders are a small but challenging group of human disea...
Gaucher disease is caused by a deficiency of the lysosomal enzyme glucocerebrosidase (acid βâ gluc...
The lysosomal storage diseases (LSDs) are a group of inherited metabolic disorders caused by the de...
Substrate reduction therapy is a novel approach to treating glycosphingolipid (GSL) lysosomal storag...