AbstractThe concentration of globotriaosylceramide (ceramide trihexoside (CTH)) in the plasma of patients with Fabry disease has been determined quantitatively by tandem mass spectrometry (MS) using novel internal standards, [D4]C-16 CTH and C-17 CTH, which were synthesised enzymically from lyso-CTH using the reverse reaction of sphingolipid ceramide N-deacylase. C-17 CTH was also synthesised chemically from lyso-CTH. This strategy has also been used to prepare standards for the quantitative determination by MS of other glycosphingolipids
Fabry disease is a rare X-linked lysosomal storage disor-der resulting from a deficiency in the -gal...
Advanced mass spectrometry of glycosphingolipids takes the central stage in this...
Fabry disease is an X-linked lysosomal storage disease (LSD) caused by deficient activity of α-Galac...
AbstractThe concentration of globotriaosylceramide (ceramide trihexoside (CTH)) in the plasma of pat...
Background: Fabry disease is an X-chromosomally inherited lysosomal storage disorder leading to accu...
Identification of 19 molecular species of globotriaosylceramides (Gb3) in extracts from a Fabry''s p...
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene act...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the α-galacto...
Fabry disease is caused by a deficiency of a-galactosidase A which leads to the progressive intra-ly...
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galac...
Fabry disease is a multisystemic, X-linked lysosomal storage disorder caused by a deficit in α-galac...
Glycosphingolipid depletion in fabry disease lymphoblasts with potent inhibitors of glucosylceramide...
Biomarkers useful for diagnosis and evaluation of treatment for patients with Fabry disease are urge...
Free sphingoid bases (lysosphingolipids) of primary storage sphingolipids are increased in tissues a...
Abstract Objectives Fabry disease (FD) is an X-l...
Fabry disease is a rare X-linked lysosomal storage disor-der resulting from a deficiency in the -gal...
Advanced mass spectrometry of glycosphingolipids takes the central stage in this...
Fabry disease is an X-linked lysosomal storage disease (LSD) caused by deficient activity of α-Galac...
AbstractThe concentration of globotriaosylceramide (ceramide trihexoside (CTH)) in the plasma of pat...
Background: Fabry disease is an X-chromosomally inherited lysosomal storage disorder leading to accu...
Identification of 19 molecular species of globotriaosylceramides (Gb3) in extracts from a Fabry''s p...
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene act...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the α-galacto...
Fabry disease is caused by a deficiency of a-galactosidase A which leads to the progressive intra-ly...
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galac...
Fabry disease is a multisystemic, X-linked lysosomal storage disorder caused by a deficit in α-galac...
Glycosphingolipid depletion in fabry disease lymphoblasts with potent inhibitors of glucosylceramide...
Biomarkers useful for diagnosis and evaluation of treatment for patients with Fabry disease are urge...
Free sphingoid bases (lysosphingolipids) of primary storage sphingolipids are increased in tissues a...
Abstract Objectives Fabry disease (FD) is an X-l...
Fabry disease is a rare X-linked lysosomal storage disor-der resulting from a deficiency in the -gal...
Advanced mass spectrometry of glycosphingolipids takes the central stage in this...
Fabry disease is an X-linked lysosomal storage disease (LSD) caused by deficient activity of α-Galac...