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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 FullerThe Clinical Journal of Pain|June 19, 2007
Nature and prevalence of pain in Fabry disease and its response to enzyme replacement therapy--a retrospective analysis from the Fabry Outcome SurveyBjoern Hoffmann, Michael Beck, Gere Sunder-Plassmann, et al.The British Journal of Ophthalmology|September 16, 2006
Ocular manifestations of Fabry's disease: data from the Fabry Outcome SurveyAndrea Sodi, Alexander S Ioannidis, Atul Mehta, et al.British Journal of Haematology|March 29, 2002
Fluoro-deoxyglucose positron emission tomography imaging for the detection of occult disease in multiple myelomaKim Orchard, Sally Barrington, John Buscombe, et al.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 ZimranMuscle & Nerve|July 9, 2005
Evidence for motor axon depolarization in Fabry diseaseStella V Tan, Philip J Lee, Richard J L Walters, et al.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 FullerMetabolites|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 FullerGlycobiology|January 14, 2004
Glycosaminoglycan degradation fragments in mucopolysaccharidosis IMaria Fuller, Peter J Meikle, John J HopwoodPageof 24