Biomarkers useful for diagnosis and evaluation of treatment for patients with Fabry disease are urgently needed. Recently, plasma globotriaosylsphingosine (lyso-Gb3) and lyso-Gb3-related analogues have attracted attention as promising biomarkers of Fabry disease. How-ever, the plasma concentrations of lyso-Gb3 and its analogues are extremely low or below the detection limits in some Fabry patients as well as in healthy subjects. In this paper, we introduce the novel application of a nano-liquid chromatography-tandemmass spectrome-try (nano-LC-MS/MS) system to the measurement of lyso-Gb3 and its analogues in plasma. Nano-LC-MS/MS requires smaller amounts of samples and is more sensitive than conven-tional techniques. Using this method, we me...
AbstractBackgroundPrevious studies revealed a high incidence of late-onset Fabry disease mutation, I...
Abstract Objectives Fabry disease (FD) is an X-l...
Fabry disease is a lysosomal storage disorder caused by deficiency of α-galactosidase A, resulting i...
Fabry disease is a multisystemic, X-linked lysosomal storage disorder caused by a deficit in α-galac...
BACKGROUND: Fabry disease (FD) is a rare X-linked lysosomal storage disorder due to mutations in the...
Background: Fabry disease is characterized by accumulation of glycosphingolipids, such as globotriao...
AbstractFabry disease is an X-linked lysosomal storage disorder due to deficiency of alpha-Galactosi...
Recently, lyso-globotriaosylsphingosine (lyso-Gb3) was found to be elevated in plasma of treatment n...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the α-galacto...
Recently, lyso-globotriaosylsphingosine (lyso-Gb3) was found to be elevated in plasma of treatment n...
Lyso-globotriaosylsphingosine (lyso-Gb(3)) is a useful biomarker in the diagnosis and monitoring of ...
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene act...
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galac...
Background: Fabry disease is an X-chromosomally inherited lysosomal storage disorder leading to accu...
Fabry disease (FD) is an X-linked lysosomal storage disorder where impaired α-galactosidase A enzyme...
AbstractBackgroundPrevious studies revealed a high incidence of late-onset Fabry disease mutation, I...
Abstract Objectives Fabry disease (FD) is an X-l...
Fabry disease is a lysosomal storage disorder caused by deficiency of α-galactosidase A, resulting i...
Fabry disease is a multisystemic, X-linked lysosomal storage disorder caused by a deficit in α-galac...
BACKGROUND: Fabry disease (FD) is a rare X-linked lysosomal storage disorder due to mutations in the...
Background: Fabry disease is characterized by accumulation of glycosphingolipids, such as globotriao...
AbstractFabry disease is an X-linked lysosomal storage disorder due to deficiency of alpha-Galactosi...
Recently, lyso-globotriaosylsphingosine (lyso-Gb3) was found to be elevated in plasma of treatment n...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the α-galacto...
Recently, lyso-globotriaosylsphingosine (lyso-Gb3) was found to be elevated in plasma of treatment n...
Lyso-globotriaosylsphingosine (lyso-Gb(3)) is a useful biomarker in the diagnosis and monitoring of ...
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene act...
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galac...
Background: Fabry disease is an X-chromosomally inherited lysosomal storage disorder leading to accu...
Fabry disease (FD) is an X-linked lysosomal storage disorder where impaired α-galactosidase A enzyme...
AbstractBackgroundPrevious studies revealed a high incidence of late-onset Fabry disease mutation, I...
Abstract Objectives Fabry disease (FD) is an X-l...
Fabry disease is a lysosomal storage disorder caused by deficiency of α-galactosidase A, resulting i...