Stephen K. Duplock

North Terrace
Adelaide, SA 5001, Australia

Last Updated: 09/26/2026

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Found 10 publications

Is SGSH heterozygosity a risk factor for early-onset neurodegenerative disease?

Is SGSH heterozygosity a risk factor for early-onset neurodegenerative disease?

Journal: Journal of inherited metabolic disease

Published: October 19, 2020

Early disease course is unaltered in mucopolysaccharidosis type IIIA (MPS IIIA) mice lacking α-synuclein.

Early disease course is unaltered in mucopolysaccharidosis type IIIA (MPS IIIA) mice lacking α-synuclein.

Journal: Neuropathology and applied neurobiology

Published: September 12, 2018

Evaluation of Disease Lesions in the Developing Canine MPS IIIA Brain.

Evaluation of Disease Lesions in the Developing Canine MPS IIIA Brain.

Journal: JIMD reports

Published: May 02, 2017

A novel conditional Sgsh knockout mouse model recapitulates phenotypic and neuropathic deficits of Sanfilippo syndrome.

A novel conditional Sgsh knockout mouse model recapitulates phenotypic and neuropathic deficits of Sanfilippo syndrome.

Journal: Journal of inherited metabolic disease

Published: January 30, 2017

Glycosphingolipid analysis in a naturally occurring ovine model of acute neuronopathic Gaucher disease.

Glycosphingolipid analysis in a naturally occurring ovine model of acute neuronopathic Gaucher disease.

Journal: Neurobiology of disease

Published: November 13, 2015

Low-dose, continual enzyme delivery ameliorates some aspects of established brain disease in a mouse model of a childhood-onset neurodegenerative disorder.

Low-dose, continual enzyme delivery ameliorates some aspects of established brain disease in a mouse model of a childhood-onset neurodegenerative disorder.

Journal: Experimental neurology

Published: September 28, 2015

Delivery of therapeutic protein for prevention of neurodegenerative changes: comparison of different CSF-delivery methods.

Delivery of therapeutic protein for prevention of neurodegenerative changes: comparison of different CSF-delivery methods.

Journal: Experimental neurology

Published: May 08, 2014

Liquid chromatography/electrospray ionisation-tandem mass spectrometry quantification of GM2 gangliosides in human peripheral cells and plasma.

Liquid chromatography/electrospray ionisation-tandem mass spectrometry quantification of GM2 gangliosides in human peripheral cells and plasma.

Journal: Analytical biochemistry

Published: December 09, 2013

Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease.

Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease.

Journal: Journal of lipid research

Published: April 09, 2013

Mass spectrometric quantification of glycogen to assess primary substrate accumulation in the Pompe mouse.

Mass spectrometric quantification of glycogen to assess primary substrate accumulation in the Pompe mouse.

Journal: Analytical biochemistry

Published: December 02, 2011

Showing 1-10 of 10

Last Updated: 09/26/2026