Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused by mutations in the galactosylceramidase (GALC) gene. Deficiency of GALC results in the accumulation of a highly cytotoxic metabolite galactosylsphingosine (psychosine). In the present study, we describe the development and validation of a sensitive and specific LC–ESI-tandem-MS method for the determination of psychosine in the serum of twitcher mice, the naturally occurring animal model of this disease. The method was validated in terms of accuracy, precision, specificity, linearity and sensitivity. Calibration plots were linear over the concentration range of 2.5–50 ng/mL. Recovery of psychosine from serum was in the range 94.20–98.02%...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Galactosylceramidase (GALC) is the lysosomal β-galactosidase responsible for the hydrolysis of galac...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused by...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused by...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused b...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused b...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused b...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
The Twitcher (Twi) mouse is a neurological Krabbe disease (KD, or globoid cell leukodystrophy) spont...
Abstract Krabbe disease (KD) and metachromatic leukodystrophy (MLD) are caused by accumulation of th...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Galactosylceramidase (GALC) is the lysosomal β-galactosidase responsible for the hydrolysis of galac...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused by...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused by...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused b...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused b...
Globoid cell leukodystrophy or Krabbe disease is an inherited autosomal recessive disorder caused b...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
Krabbe disease (KD, or globoid cell leukodystrophy; OMIM #245200) is an inherited neurodegenerative ...
The Twitcher (Twi) mouse is a neurological Krabbe disease (KD, or globoid cell leukodystrophy) spont...
Abstract Krabbe disease (KD) and metachromatic leukodystrophy (MLD) are caused by accumulation of th...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Galactosylceramidase (GALC) is the lysosomal β-galactosidase responsible for the hydrolysis of galac...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...