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Associate Professor Tony Huynh
Associate Professor

Tony Huynh

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Overview

Availability

Associate Professor Tony Huynh is:
Available for supervision

Research interests

  • Type 1 Diabetes

    Diabetes technology and immunotherapy

  • Steroidogenesis

    Measurement and quantification of various steroids

  • Newborn Screening

    Congenital hypothyroidism and congenital adrenal hyperplasia

Works

Search Professor Tony Huynh’s works on UQ eSpace

64 works between 2008 and 2025

61 - 64 of 64 works

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.

A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy

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

The association between ketoacidosis and 25(OH)-vitamin D-3 levels at presentation in children with type 1 diabetes mellitus

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

A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome

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.

Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene

Funding

Current funding

  • 2024 - 2028
    Klinefelter Syndrome Registry
    William Ivers Memorial Fund
    Open grant

Supervision

Availability

Associate Professor Tony Huynh is:
Available for supervision

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Media

Enquiries

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communications@uq.edu.au