Overview
Availability
- Associate Professor Tony Huynh is:
- Available for supervision
Research interests
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Type 1 Diabetes
Diabetes technology and immunotherapy
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Steroidogenesis
Measurement and quantification of various steroids
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Newborn Screening
Congenital hypothyroidism and congenital adrenal hyperplasia
Works
Search Professor Tony Huynh’s works on UQ eSpace
2009
Conference Publication
Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort
Huynh, Tony, McGown, Ivan, Cowley, David, Harris, Mark, Leong, Gary M. and Cotterill, Andrew M. (2009). Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort. BASEL: KARGER.
2009
Conference Publication
A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy
Huynh, Tony, Trebbin, Andrea, Cowley, David, Bowling, Francis, Leong, Gary M., Cotterill, Andrew M., Harris, Mark, De Bosscher, Karolien, Haegeman, Guy and Hoey, Andrew J. (2009). A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy. BASEL: KARGER.
2009
Journal Article
The association between ketoacidosis and 25(OH)-vitamin D-3 levels at presentation in children with type 1 diabetes mellitus
Huynh, Tony, Greer, Ristan M., Nyunt, Ohn, Bowling, Francis, Cowley, David, Leong, Gary M., Cotterill, Andrew M. and Harris, Mark (2009). The association between ketoacidosis and 25(OH)-vitamin D-3 levels at presentation in children with type 1 diabetes mellitus. Pediatric Diabetes, 10 (1), 38-43. doi: 10.1111/j.1399-5448.2008.00439.x
2009
Journal Article
A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome
Cotterill, A. M., Cowley, D., Harris, M., Huynh, T., Leong, G. M., McGown, I. and Nyunt, O. (2009). A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome. Clinical Pediatric Endocrinology, 18 (2), 73-75. doi: 10.1297/cpe.18.73
2008
Conference Publication
Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene
Cotterill, A. M., Cowley, D., Dahiya, R., Greer, R. M., Harris, M., Huynh, T., Leong, G., McGown, I., Nyunt, O., Venter, D. J. and Walker, R. (2008). Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra, ACT, Australia, 17-19 November 2008.
Funding
Current funding
Supervision
Availability
- Associate Professor Tony Huynh is:
- Available for supervision
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Media
Enquiries
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