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galabiosylceramide

 
National Institutes of Health

Papers overview

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2017
2017
Fabry disease is an X-linked lysosomal storage disorder caused by α-galactosidase A (α-GAL A) deficiency. This enzyme contributes… Expand
2015
2015
AbstractFabry disease is an X-linked, complex, multisystemic lysosomal storage disorder presenting marked phenotypic and… Expand
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2010
2010
Fabry’s disease is an X-linked recessively inherited lysosomal storage disease, caused by a deficiency in catalytic activity or… Expand
1991
1991
Different concentrations of ionic and non-ionic detergents were examined for optimization of the in vitro degradations of… Expand
Highly Cited
1987
Highly Cited
1987
The cellular specificity of the Escherichia coli-derived verotoxin is of particular interest because of its extreme toxicity and… Expand
1985
1985
The glycosphingolipids of human thyroid were isolated and characterized by gas-liquid chromatography and sequential enzymic… Expand
1985
1985
The influence of Graves' disease in human thyroid neutral glycosphingolipids was investigated. The major alteration was in the… Expand
1985
1985
The neutral sphingolipids from chicken erythrocytes were characterized. The total concentration of neutral sphingolipids was… Expand
1985
1985
The neutral sphingolipids from chicken erythrocytes were characterized. The total concentration of neutral sphingo- lipids was… Expand
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1984
1984
Glycosphingolipids from the liver, kidney, and spleen of a patient with type 1 II3-N-acetylneuraminosylgangliotetraosylceramide… Expand