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Molecular Genetics and Metabolism|May 24, 2017
Lipid composition of microdomains is altered in neuronopathic Gaucher disease sheep brain and spleenLeanne K Hein, Tina Rozaklis, Melissa K Adams, et al.Pediatric Research|September 7, 2004
Disease-specific markers for the mucopolysaccharidosesMaria Fuller, Tina Rozaklis, Steven L Ramsay, et al.Molecular Genetics and Metabolism|December 29, 2007
Glucosylceramide accumulation is not confined to the lysosome in fibroblasts from patients with Gaucher diseaseMaria Fuller, Tina Rozaklis, Melanie Lovejoy, et al.Experimental Neurology|August 3, 2010
Allogeneic stem cell transplantation does not improve neurological deficits in mucopolysaccharidosis type IIIA miceAdeline A Lau, Hanan Hannouche, Tina Rozaklis, et al.JIMD Reports|December 2, 2015
Continual Low-Dose Infusion of Sulfamidase Is Superior to Intermittent High-Dose Delivery in Ameliorating Neuropathology in the MPS IIIA Mouse BrainHelen Beard, Sofia Hassiotis, Amanda J Luck, et al.Clinical Chemistry|December 26, 2001
Determination of oligosaccharides in Pompe disease by electrospray ionization tandem mass spectrometryTina Rozaklis, Steven L Ramsay, Phillip D Whitfield, et al.Clinical Chemistry|February 8, 2005
Urinary lipid profiling for the identification of fabry hemizygotes and heterozygotesMaria Fuller, Peter C Sharp, Tina Rozaklis, et al.Journal of Neurochemistry|January 15, 2016
Low-dose, continuous enzyme replacement therapy ameliorates brain pathology in the neurodegenerative lysosomal disorder mucopolysaccharidosis type IIIABarbara King, Sofia Hassiotis, Tina Rozaklis, et al.Neurobiology of Disease|March 16, 2016
Glycosphingolipid analysis in a naturally occurring ovine model of acute neuronopathic Gaucher diseaseLitsa Karageorgos, Leanne Hein, Tina Rozaklis, et al.The European Journal of Neuroscience|March 24, 2009
Examination of intravenous and intra-CSF protein delivery for treatment of neurological diseaseKim M Hemsley, Amanda J Luck, Allison C Crawley, et al.Pageof 2