Gaucher disease (GD) is an inborn error of metabolism that affects the recycling of cellular glycolipids. Glucosylceramide (also called glucocerebroside) accumulate within the lysosomes of cells. Gaucher%u2019s disease is most common lysosomal storage disease and its incidence is 1/75.000. Three types of this disease have been defined. During the course of disease, it was reported that hepatosplenomegaly, portal hypertension, hyperferritinemia, splenic infarcts and splenic nodules might develop. Therefore, as in our case; Gaucher%u2019s disease must be remembered in the setting of hepatosplenomegaly, portal hypertension, hyperferritinemia, splenic infarcts and splenic nodules of unknown etiology
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
Gaucher hastalığı beta glukoserobrozidaz genindeki mutasyon sonucunda gelişen, otozomal resesif kalı...
Gaucher's disease - an overview about a sphingolipidosis Abstract. Gaucher's disease is a sphingolip...
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...
Gaucher disease (GD), a rare lysosomal storage disorder caused by deficient glucocerebrosidase activ...
Gaucher disease (GD), a rare lysosomal storage disorder caused by deficient glucocerebrosidase activ...
A 21-year-old man with a history of sudden rectal hemorrhage was referred to our hospital. Examinati...
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease ...
In 1882, Philippe Gaucher described a 32-year-old woman with massive splenomegaly and unusually larg...
Background Gaucher’s Disease (G.D.) is an autosomal recessive disorder resulting from the accumulati...
Gaucher disease is a rare autosomal recessive genetic disorder. It is caused by the deficiency of ly...
Gaucher disease (GD) is a rare inherited lysosomal metabolism disorder, characterized by an accumula...
Summary Gaucher's disease is characterized by glucocerebroside accumulation in the cells of the reti...
Gaucher disease is a lysosomal storage disorder caused by abnormally low glucocerebrosidase enzy-mat...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
Gaucher hastalığı beta glukoserobrozidaz genindeki mutasyon sonucunda gelişen, otozomal resesif kalı...
Gaucher's disease - an overview about a sphingolipidosis Abstract. Gaucher's disease is a sphingolip...
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...
Gaucher disease (GD), a rare lysosomal storage disorder caused by deficient glucocerebrosidase activ...
Gaucher disease (GD), a rare lysosomal storage disorder caused by deficient glucocerebrosidase activ...
A 21-year-old man with a history of sudden rectal hemorrhage was referred to our hospital. Examinati...
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease ...
In 1882, Philippe Gaucher described a 32-year-old woman with massive splenomegaly and unusually larg...
Background Gaucher’s Disease (G.D.) is an autosomal recessive disorder resulting from the accumulati...
Gaucher disease is a rare autosomal recessive genetic disorder. It is caused by the deficiency of ly...
Gaucher disease (GD) is a rare inherited lysosomal metabolism disorder, characterized by an accumula...
Summary Gaucher's disease is characterized by glucocerebroside accumulation in the cells of the reti...
Gaucher disease is a lysosomal storage disorder caused by abnormally low glucocerebrosidase enzy-mat...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
Gaucher hastalığı beta glukoserobrozidaz genindeki mutasyon sonucunda gelişen, otozomal resesif kalı...
Gaucher's disease - an overview about a sphingolipidosis Abstract. Gaucher's disease is a sphingolip...