Highly-sensitive simultaneous quantitation of glucosylsphingosine and galactosylsphingosine in human cerebrospinal fluid by liquid chromatography/tandem mass spectrometry

Author:

Matsumoto Shin-ichi,Sato Sho,Otake Kentaro,Kosugi Yohei

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference35 articles.

1. Value of glucosylsphingosine (lyso-Gb1) as a biomarker in Gaucher disease: a systematic literature review;Revel-Vilk;Int. J. Mol. Sci.,2020

2. The metabolism of glucocerebrosides. I. Purification and properties of a glucocerebroside-cleaving enzyme from spleen tissue;Brady;J. Biol. Chem.,1965

3. Gaucher disease and Fabry disease: new markers and insights in pathophysiology for two distinct glycosphingolipidoses;Ferraz;Biochim. Biophys. Acta,1841

4. Elevated globotriaosylsphingosine is a hallmark of Fabry disease;Aerts;Proc. Natl. Acad. Sci. U.S.A.,2008

5. Krabbe disease: a galactosylsphingosine (psychosine) lipidosis;Svennerholm;J. Lipid Res,1980

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