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
2022
Journal Article
An unusual presentation of autoimmune primary adrenal insufficiency
Hobbs, Annabelle, Odutolu, Oluwatoyin and Huynh, Tony (2022). An unusual presentation of autoimmune primary adrenal insufficiency. Clinical Chemistry, 68 (11), 1374-1378. doi: 10.1093/clinchem/hvac165
2022
Journal Article
Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation
Huynh, Tony, Greaves, Ronda, Mawad, Nazha, Greed, Lawrence, Wotton, Tiffany, Wiley, Veronica, Ranieri, Enzo, Rankin, Wayne, Ungerer, Jacobus, Price, Ricky, Webster, Dianne and Heather, Natasha (2022). Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation. Clinical Chemistry and Laboratory Medicine (CCLM), 60 (10), 1551-1561. doi: 10.1515/cclm-2022-0403
2022
Journal Article
Long-term efficacy of T3 analogue triac in children and adults with MCT8 deficiency: a real-life retrospective cohort study
van Geest, Ferdy S., Groeneweg, Stefan, van den Akker, Erica L T, Bacos, Iuliu, Barca, Diana, van den Berg, Sjoerd A A, Bertini, Enrico, Brunner, Doris, Brunetti-Pierri, Nicola, Cappa, Marco, Cappuccio, Gerarda, Chatterjee, Krishna, Chesover, Alexander D., Christian, Peter, Coutant, Régis, Craiu, Dana, Crock, Patricia, Dewey, Cheyenne, Dica, Alice, Dimitri, Paul, Dubey, Rachana, Enderli, Anina, Fairchild, Jan, Gallichan, Jonathan, Garibaldi, Luigi R., George, Belinda, Hackenberg, Annette, Heinrich, Bianka, Huynh, Tony ... Visser, W Edward (2022). Long-term efficacy of T3 analogue triac in children and adults with MCT8 deficiency: a real-life retrospective cohort study. The Journal of Clinical Endocrinology and Metabolism, 107 (3), e1136-e1147. doi: 10.1210/clinem/dgab750
2021
Journal Article
Pre-analytical mysteries: a case of severe hypervitaminosis D and mild hypercalcaemia
Whittle, Emma, de Waal, Elzahn, Huynh, Tony, Treacy, Oliver and Morton, Adam (2021). Pre-analytical mysteries: a case of severe hypervitaminosis D and mild hypercalcaemia. Biochemia Medica, 31 (1) 011001, 011001-155. doi: 10.11613/bm.2021.011001
2020
Journal Article
Challenges of managing congenital hyperinsulinism in remote Aboriginal Australian communities
Musthaffa, Yassmin, Papadimos, Emily R., Fairchild, Jan, Titmuss, Angela, Corpus, Sumaria, Huynh, Tony and Conwell, Louise S. (2020). Challenges of managing congenital hyperinsulinism in remote Aboriginal Australian communities. Journal of Paediatrics and Child Health, 57 (5) jpc.14984, 727-731. doi: 10.1111/jpc.14984
2020
Journal Article
A Rare and Unusual Cause of Unilateral Ureteric Obstruction in a Child
Fowler, Dallas, Irving, Helen, Borzi, Peter, Trnka, Peter and Huynh, Tony (2020). A Rare and Unusual Cause of Unilateral Ureteric Obstruction in a Child. Clinical Chemistry, 66 (8), 1006-1009. doi: 10.1093/clinchem/hvaa059
2020
Journal Article
Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study
Groeneweg, Stefan, van Geest, Ferdy S., Abacı, Ayhan, Alcantud, Alberto, Ambegaonkar, Gautem P., Armour, Christine M., Bakhtiani, Priyanka, Barca, Diana, Bertini, Enrico S., van Beynum, Ingrid M., Brunetti-Pierri, Nicola, Bugiani, Marianna, Cappa, Marco, Cappuccio, Gerarda, Castellotti, Barbara, Castiglioni, Claudia, Chatterjee, Krishna, de Coo, Irenaeus F. M., Coutant, Régis, Craiu, Dana, Crock, Patricia, DeGoede, Christian, Demir, Korcan, Dica, Alice, Dimitri, Paul, Dolcetta-Capuzzo, Anna, Dremmen, Marjolein H. G., Dubey, Rachana, Enderli, Anina ... Visser, W. Edward (2020). Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. The Lancet Diabetes and Endocrinology, 8 (7), 594-605. doi: 10.1016/S2213-8587(20)30153-4
2020
Journal Article
Clinical and laboratory aspects of insulin autoantibody-mediated glycaemic dysregulation and hyperinsulinaemic hypoglycaemia: insulin autoimmune syndrome and exogenous insulin antibody syndrome
Huynh, Tony (2020). Clinical and laboratory aspects of insulin autoantibody-mediated glycaemic dysregulation and hyperinsulinaemic hypoglycaemia: insulin autoimmune syndrome and exogenous insulin antibody syndrome. Clinical Biochemist Reviews, 41 (3), 93-102. doi: 10.33176/AACB-20-00008
2019
Conference Publication
Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12
Conwell, Louise S., Harraway, James R., Williams, Mark G., Joy, Christopher, Scurry, Bonnie M., Lee, Kevin, McBride, Craig A., Choo, Kelvin, Huynh, Tony, Ng, Carolyn G.L. and Flanagan, Sarah E. (2019). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12. The European Society of Paediatric Endocrinology Annual Meeting, Vienna, Austria, 19-21 September 2019.
2019
Conference Publication
Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12
Conwell, Louise S., Harraway, James R., Williams, Mark G., Joy, Christopher, Scurry, Bonnie M., Lee, Kevin, McBride, Craig A., Choo, Kelvin, Huynh, Tony, Ng, Carolyn G.L. and Flanagan, Sarah E. (2019). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12. Updates in Diagnosis and Management of Hyperinsulinism and Neonatal Hypoglycemia Conference, Philadelphia, PA United States, 5-6 September 2019.
2019
Journal Article
An unusual cause of metabolic alkalosis and hypocalcemia in childhood
Huynh, Tony and Wilgen, Urs (2019). An unusual cause of metabolic alkalosis and hypocalcemia in childhood. Clinical Chemistry, 65 (4), 514-517. doi: 10.1373/clinchem.2018.287136
2018
Journal Article
A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
Watanabe, Y., Sharwood, E., Goodwin, B., Creech, M. K., Hassan, H. Y., Netea, M. G., Jaeger, M., Dumitrescu, A., Refetoff, S., Huynh, T. and Weiss, R. E. (2018). A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report. BMC Medical Genetics, 19 (1) 69, 69. doi: 10.1186/s12881-018-0588-7
2018
Journal Article
Immunoassay interference secondary to therapeutic high-dose biotin: a paediatric case report
Evans, Natalie, Yates, Jason, Tobin, Jacinta, McGill, Jim and Huynh, Tony (2018). Immunoassay interference secondary to therapeutic high-dose biotin: a paediatric case report. Journal of Paediatrics and Child Health, 54 (5), 572-575. doi: 10.1111/jpc.13857
2018
Journal Article
Therapeutic plasma exchange normalizes insulin-mediated response in a child with type 1 diabetes and insulin autoimmune syndrome
Sharwood, Erin F., Hughes, Ian P., Pretorius, Carel J., Trnka, Peter, Peake, Jane and Huynh, Tony (2018). Therapeutic plasma exchange normalizes insulin-mediated response in a child with type 1 diabetes and insulin autoimmune syndrome. Pediatric Diabetes, 48 (1), S89-179. doi: 10.1111/pedi.12522
2018
Journal Article
Diabetes in a child on growth hormone therapy: questions
Aldridge, Melanie, Huynh, Tony, Prado, Jose and McTaggart, Steven J. (2018). Diabetes in a child on growth hormone therapy: questions. Pediatric Nephrology, 33 (1), 77-78. doi: 10.1007/s00467-017-3645-0
2018
Conference Publication
Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12
Conwell, Louise S., Harroway, James, Williams, Mark, Joy, Christopher, Scurry, Bonnie, Lee, Kevin, McBride, Craig, Choo, Kelvin, Huynh, Tony and Ng, Carolyn G. L. (2018). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12. Australasian Paediatric Endocrine Group Annual Scientific Meetings, Newcastle, Australia, July 2018.
2017
Journal Article
Diabetes in a child on growth hormone therapy: Answers
Aldridge, Melanie, Huynh, Tony, Prado, Jose and McTaggart, Steven J. (2017). Diabetes in a child on growth hormone therapy: Answers. Pediatric Nephrology, 33 (1), 79-80. doi: 10.1007/s00467-017-3651-2
2017
Journal Article
Virilisation in siblings secondary to transdermal ‘bioidentical’ testosterone exposure
Huynh, Tony and Stewart, Catherine I. (2017). Virilisation in siblings secondary to transdermal ‘bioidentical’ testosterone exposure. Journal of Paediatrics and Child Health, 53 (3), 301-305. doi: 10.1111/jpc.13466
2017
Conference Publication
Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry
Ruddell, Richard G., Burgess, Christopher, Huynh, Tony, Conwell, Louise S., Balouch, Fariha, Burke, Matthew and Pretorius, Carel (2017). Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry. Clinical Lipidology (3rd World Congress), Brisbane, QLD, Australia, unknown.
2017
Conference Publication
Idiopathic Ductopaenia in a Paediatric Patient: A Case Report and Interesting Clinical Biochemistry
Ruddell, Richard G., Burgess, Christopher, Huynh, Tony, Conwell, Louise S., Balouch, Fariha, Burke, Matthew and Pretorius, Carel (2017). Idiopathic Ductopaenia in a Paediatric Patient: A Case Report and Interesting Clinical Biochemistry. Royal College of Pathology Australia Update, Sydney, NSW, Australia, 24 – 26 February 2017.
Funding
Current funding
Supervision
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- Associate Professor Tony Huynh is:
- Available for supervision
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