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Molecular Genetics and Metabolism|December 3, 2014
Development of cerebellar pathology in the canine model of mucopolysaccharidosis type IIIA (MPS IIIA)Sofia Hassiotis, Robert D Jolly, Kim M HemsleyArchives of Gerontology and Geriatrics|February 7, 2004
The analytical approach to the nature of lipofuscin (age pigment)Robert D Jolly, David N Palmer, Rosalind R DalefieldGenomics|February 7, 2002
Identification of a mutation causing mucopolysaccharidosis type IIIA in New Zealand Huntaway dogsGouri Yogalingam, Tony Pollard, Briony Gliddon, et al.Veterinary Pathology|January 3, 2022
An inherited night blindness in Wiltshire sheepHayley Hunt, Keren E Dittmer, Dorian J Garrick, et al.JIMD Reports|June 21, 2018
Evaluation of Disease Lesions in the Developing Canine MPS IIIA BrainLeanne K Winner, Neil R Marshall, Robert D Jolly, et al.Journal of Wildlife Diseases|August 23, 2021
MUCOPOLYSACCHARIDOSIS II (MPS II) IN A FREE-LIVING KAKA (NESTOR MERIDIONALIS) IN NEW ZEALANDRobert D Jolly, Stuart A Hunter, Maurice R Alley, et al.Journal of Inherited Metabolic Disease|November 26, 2014
Evaluation of enzyme dose and dose-frequency in ameliorating substrate accumulation in MPS IIIA Huntaway dog brainBarbara King, Neil Marshall, Helen Beard, et al.Veterinary Pathology|April 16, 2019
β-Mannosidosis in German Shepherd DogsRobert D Jolly, Keren E Dittmer, Dorian J Garrick, et al.Neurobiology of Disease|November 9, 2007
A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3Tony Frugier, Nadia L Mitchell, Imke Tammen, et al.Journal of Inherited Metabolic Disease|November 11, 2016
Slow, continuous enzyme replacement via spinal CSF in dogs with the paediatric-onset neurodegenerative disease, MPS IIIABarbara King, Neil R Marshall, Sofia Hassiotis, et al.Pageof 2