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Gaucher cells

Known as: Gaucher Cell, Gaucher's Cell, cells gaucher 
 
National Institutes of Health

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2018
2018
Deficiency of the lysosomal enzyme, β-glucocerebrosidase, and accumulation of its substrate in cells of the reticuloendothelial… Expand
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2015
2015
INTRODUCTION Gaucher cells (GCs), the lipid-laden storage macrophages, are the pathologic hallmark of Gaucher disease (GD). They… Expand
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2014
2014
Gaucher disease (GD) is a lysosomal storage disorder characterized by accumulation of glucosylceramide in macrophages, so-called… Expand
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2013
2013
OBJECTIVES To assess correlations of patient demographics, including enzyme replacement therapy (ERT) with bone histology, to… Expand
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2012
2012
Hemoglobin (Hb) E mutation is common in north-east part of our country. The natural history of Hb E thalassemia is highly… Expand
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2010
2010
Foamy transformation of macrophages is typically seen in lysosomal storage disorders in patients with Niemann-Pick disease, but… Expand
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2009
2009
SummaryWe report a female patient with Gaucher disease (GD) type I on ERT (imiglucerase) for 5 years, which led to a significant… Expand
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2006
2006
  • M. Elleder
  • Journal of Inherited Metabolic Disease
  • 2006
  • Corpus ID: 19837088
SummaryGaucher disease (GD), deficiency of acid glucosylceramidase (GlcCer-ase) is characterized by deficient degradation of beta… Expand
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Highly Cited
2004
Highly Cited
2004
Although the existence of anti-inflammatory alternatively activated macrophages (aamphi) has been accepted widely based on in… Expand
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1992
1992
  • M. Elleder
  • Zentralblatt fur Pathologie
  • 1992
  • Corpus ID: 22317089
Two cases of Gaucher's disease (Types I and III) are described with a substantial part of the storage cell population in several… Expand
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