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International Journal of Molecular Sciences|February 15, 2020
Metabolomics to Improve the Diagnostic Efficiency of Inborn Errors of MetabolismDylan Mordaunt, David Cox, Maria Fuller
Journal of Neuroscience Methods|June 17, 2019
Collection of cerebrospinal fluid from murine lateral ventricles for biomarker determination in mucopolysaccharidosis type IIIAChantelle McIntyre, Jennifer Saville, Maria Fuller
Molecular Genetics and Metabolism Reports|June 19, 2023
Neurocognitive testing in a murine model of mucopolysaccharidosis type IIIAKleopatra Pericleous, Chantelle McIntyre, Maria Fuller
Journal of Lipid Research|April 9, 2013
Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher diseaseLeanne K Hein, Stephen Duplock, Maria Fuller
International Journal of Molecular Sciences|October 1, 2020
Value of Glucosylsphingosine (Lyso-Gb1) as a Biomarker in Gaucher Disease: A Systematic Literature ReviewShoshana Revel-Vilk, Maria Fuller, Ari Zimran
Molecular Genetics and Metabolism|December 24, 2017
Glycosaminoglycan fragments as a measure of disease burden in the mucopolysaccharidosis type I mouseJennifer T Saville, Belinda K McDermott, Maria Fuller
Metabolites|December 17, 2014
Distribution of Heparan Sulfate Oligosaccharides in Murine Mucopolysaccharidosis Type IIIAKerryn Mason, Peter Meikle, John Hopwood, et al.
Biochemical and Biophysical Research Communications|November 14, 2013
Lipid composition of membrane rafts, isolated with and without detergent, from the spleen of a mouse model of Gaucher diseaseKathryn J Hattersley, Leanne K Hein, Maria Fuller
Glycobiology|January 14, 2004
Glycosaminoglycan degradation fragments in mucopolysaccharidosis IMaria Fuller, Peter J Meikle, John J Hopwood
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 2, 2015
Rapid, single-phase extraction of glucosylsphingosine from plasma: A universal screening and monitoring toolMaria Fuller, Jeff Szer, Samantha Stark, et al.
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