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Annals of Neurology|October 24, 1997
Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's diseaseR Schiffmann, M P Heyes, J M Aerts, et al.
Journal of Inherited Metabolic Disease|May 30, 2025
A Multiomic Network Approach to Uncover Disease Modifying Mechanisms of Inborn Errors of MetabolismAaron Bender, Pablo Ranea-Robles, Evan G Williams, et al.
Human Mutation|January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic valueR G Boot, C E Hollak, M Verhoek, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2025
A multiomic network approach uncovers disease modifying mechanisms of inborn errors of metabolismAaron Bender, Pablo Ranea-Robles, Evan G Williams, et al.
Hepatology (Baltimore, Md.)|May 16, 2009
Inhibiting glycosphingolipid synthesis ameliorates hepatic steatosis in obese miceHongmei Zhao, Malgorzata Przybylska, I-Huan Wu, et al.
Diabetes|February 9, 2007
Pharmacological inhibition of glucosylceramide synthase enhances insulin sensitivityJohannes M Aerts, Roelof Ottenhoff, Andrew S Powlson, et al.
Molecular Genetics and Metabolism|January 12, 2016
Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disordersMaria J Ferraz, André R A Marques, Paulo Gaspar, et al.
FEBS Letters|February 23, 2016
Lysosomal glycosphingolipid catabolism by acid ceramidase: formation of glycosphingoid bases during deficiency of glycosidasesMaria J Ferraz, André R A Marques, Monique D Appelman, et al.
FEBS Letters|March 29, 2005
SKN1, a novel plant defensin-sensitivity gene in Saccharomyces cerevisiae, is implicated in sphingolipid biosynthesisKarin Thevissen, Jola Idkowiak-Baldys, Yang-Ju Im, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|September 25, 2009
Proteomic profiling of plasma and serum in elderly patients with deliriumBarbara C van Munster, Marielle J van Breemen, Perry D Moerland, et al.
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