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glycosphingolipid metabolic process

Known as: glycosphingolipid metabolism 
The chemical reactions and pathways involving glycosphingolipids, any compound with residues of sphingoid and at least one monosaccharide. [ISBN… 
National Institutes of Health

Papers overview

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2016
2016
Complex Vascular Involvement in Fabry Disease: An Unusual Case of Combined Critical Lower Limb Ischemia and Deep Vein Thrombosis
Complex Vascular Involvement in Fabry Disease: An Unusual Case of Combined Critical Lower Limb Ischemia and Deep Vein Thrombosis… 
2012
2012
Fabry Disease: from Diagnosis to Therapy
Fabry disease (FD) is an accelerating, X-linked hereditary disorder of glycosphingolipid metabolism which occurs due to improper… 
2010
2010
Nephropathy in Fabry disease and iatrogenic phospholipidosis mimicking Fabry disease
Fabry disease is a rare X-linked inborn error of th e glycosphingolipid metabolism caused by deficient activity of lysosomal… 
2008
2008
Preservation of renal function in a patient with Fabry nephropathy on enzyme replacement therapy.
Fabry disease is an X-linked recessive inborn error of glycosphingolipid metabolism caused by the deficient activity of the… 
2004
2004
Regulation of glycosphingolipid metabolism and consequent abnormal phenotypes in the mutant mice of glycosyltransferase genes.
1989
1989
[Transvenous permanent pacemaker implantation for Fabry's disease. 3 cases report].
Three men with Fabry's disease (angiokeratoma corporis diffusum universal ) are described. In the first patient, atrial… 
1988
1988
Modulation of glycosphingolipid metabolism in cell culture.
1981
1981
[Neuropathy associated with ichthyosis and splenomegaly in an adult patient. Possible relationship with altered glycosphingolipid metabolism (author's transl)].
The authors report on the case of a 40-year-old woman presenting with ichtyosiform erythroderma, central and peripheral… 
1976
1976
Fabry’s Disease—Angiokeratoma Corporis Diffusum Universale
Fabry’s disease is an inborn error of glycosphingolipid metabolism characterized by the deposition of the glycosphingolipids… 
1976
1976
Phospho- and glycosphingolipid metabolism in a rat neuri-noma clone (RN6) studied in tissue culture.
A serious drawback in neurochemistry still is the difficulty to resolve the complexity of cell types involved in the neuronal and… 
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