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
ments form an integral part of the assessment of female reproductive function and have expanding rol...
Introduction Ceramide (Cer) is one of the most important sphingolipids subclasses actively involved ...
Assay of methyl umbell iferyl-a-galactosidase activity (MUM-a-Galase) in plasma reflects the activit...
AbstractThe concentration of globotriaosylceramide (ceramide trihexoside (CTH)) in the plasma of pat...
Fabry disease is caused by a deficiency of a-galactosidase A which leads to the progressive intra-ly...
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene act...
Background: Fabry disease is an X-chromosomally inherited lysosomal storage disorder leading to accu...
Free sphingoid bases (lysosphingolipids) of primary storage sphingolipids are increased in tissues a...
Identification of 19 molecular species of globotriaosylceramides (Gb3) in extracts from a Fabry''s p...
We developed a mass spectrometric procedure to quantify sphingosine-1-phosphate (S1P) in biologica...
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galac...
Fabry disease is an X-linked lysosomal storage disease (LSD) caused by deficient activity of α-Galac...
Monitoring the levels of the ceramides (Cer) d18:1/16:0, Cer d18:1/18:0, Cer d18:1/24:0, and Cer d18...
Fabry disease (FD) is an X-linked lysosomal storage disorder where impaired α-galactosidase A enzyme...
Fabry disease is a rare X-linked lysosomal storage disor-der resulting from a deficiency in the -gal...
ments form an integral part of the assessment of female reproductive function and have expanding rol...
Introduction Ceramide (Cer) is one of the most important sphingolipids subclasses actively involved ...
Assay of methyl umbell iferyl-a-galactosidase activity (MUM-a-Galase) in plasma reflects the activit...
AbstractThe concentration of globotriaosylceramide (ceramide trihexoside (CTH)) in the plasma of pat...
Fabry disease is caused by a deficiency of a-galactosidase A which leads to the progressive intra-ly...
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene act...
Background: Fabry disease is an X-chromosomally inherited lysosomal storage disorder leading to accu...
Free sphingoid bases (lysosphingolipids) of primary storage sphingolipids are increased in tissues a...
Identification of 19 molecular species of globotriaosylceramides (Gb3) in extracts from a Fabry''s p...
We developed a mass spectrometric procedure to quantify sphingosine-1-phosphate (S1P) in biologica...
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galac...
Fabry disease is an X-linked lysosomal storage disease (LSD) caused by deficient activity of α-Galac...
Monitoring the levels of the ceramides (Cer) d18:1/16:0, Cer d18:1/18:0, Cer d18:1/24:0, and Cer d18...
Fabry disease (FD) is an X-linked lysosomal storage disorder where impaired α-galactosidase A enzyme...
Fabry disease is a rare X-linked lysosomal storage disor-der resulting from a deficiency in the -gal...
ments form an integral part of the assessment of female reproductive function and have expanding rol...
Introduction Ceramide (Cer) is one of the most important sphingolipids subclasses actively involved ...
Assay of methyl umbell iferyl-a-galactosidase activity (MUM-a-Galase) in plasma reflects the activit...