Add to ORKGWe describe, with a brief thematic review, the case of a 47-year-old woman that was hospitalized to study a clinical picture characterized by massive splenomegaly with asthenia, postprandial fullness, weight loss and edema in the left lower extremity, in which Gaucher disease was diagnosed.We describe, with a brief thematic review, the case of a 47-year-old woman that was hospitalized to study a clinical picture characterized by massive splenomegaly with asthenia, postprandial fullness, weight loss and edema in the left lower extremity, in which Gaucher disease was diagnosed
Five recent cases of Gaucher's disease seen at Groote Schuur Hospital illustrate the haematological ...
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it...
Gaucher disease (GD) is the most common lysosomal disorder resulting from deficient activity of the ...
Gaucher disease is the most common lysosomal storage disease. It is caused by the defective activity...
Gaucher disease is the most common lysosomal storage disease. It is caused by the defective activity...
Objectives: Thrombocytopenia and splenomegaly are common features in several haematological disorder...
Summary Gaucher's disease is characterized by glucocerebroside accumulation in the cells of the reti...
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease ...
Background Gaucher’s Disease (G.D.) is an autosomal recessive disorder resulting from the accumulati...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
BACKGROUND: The Gaucher Investigative Therapy Evaluation is a national clinical cohort of 250 patien...
A review of the pathology of t 2 cases of non-neuronopathic type Gaucher's disease, diagnosed over ...
Five recent cases of Gaucher's disease seen at Groote Schuur Hospital illustrate the haematological ...
Gaucher disease (GD, ORPHA355) is a rare, autosomal recessive genetic disorder. It is caused by a de...
In 1882, Philippe Gaucher described a 32-year-old woman with massive splenomegaly and unusually larg...
Five recent cases of Gaucher's disease seen at Groote Schuur Hospital illustrate the haematological ...
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it...
Gaucher disease (GD) is the most common lysosomal disorder resulting from deficient activity of the ...
Gaucher disease is the most common lysosomal storage disease. It is caused by the defective activity...
Gaucher disease is the most common lysosomal storage disease. It is caused by the defective activity...
Objectives: Thrombocytopenia and splenomegaly are common features in several haematological disorder...
Summary Gaucher's disease is characterized by glucocerebroside accumulation in the cells of the reti...
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease ...
Background Gaucher’s Disease (G.D.) is an autosomal recessive disorder resulting from the accumulati...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
BACKGROUND: The Gaucher Investigative Therapy Evaluation is a national clinical cohort of 250 patien...
A review of the pathology of t 2 cases of non-neuronopathic type Gaucher's disease, diagnosed over ...
Five recent cases of Gaucher's disease seen at Groote Schuur Hospital illustrate the haematological ...
Gaucher disease (GD, ORPHA355) is a rare, autosomal recessive genetic disorder. It is caused by a de...
In 1882, Philippe Gaucher described a 32-year-old woman with massive splenomegaly and unusually larg...
Five recent cases of Gaucher's disease seen at Groote Schuur Hospital illustrate the haematological ...
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it...
Gaucher disease (GD) is the most common lysosomal disorder resulting from deficient activity of the ...