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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

21 - 40 of 64 works

2023

Journal Article

Continuous glucose monitoring has an increasing role in pre-symptomatic type 1 diabetes: advantages, limitations, and comparisons with laboratory-based testing

Joshi, Kriti, Harris, Mark, Cotterill, Andrew, Wentworth, John M., Couper, Jennifer J., Haynes, Aveni, Davis, Elizabeth A., Lomax, Kate E. and Huynh, Tony (2023). Continuous glucose monitoring has an increasing role in pre-symptomatic type 1 diabetes: advantages, limitations, and comparisons with laboratory-based testing. Clinical Chemistry and Laboratory Medicine, 62 (1) 107585, 41-49. doi: 10.1515/cclm-2023-0234

Continuous glucose monitoring has an increasing role in pre-symptomatic type 1 diabetes: advantages, limitations, and comparisons with laboratory-based testing

2023

Journal Article

Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone: data from the Australasian Diabetes Data Network (ADDN) registry

James, Steven, Perry, Lin, Lowe, Julia, Donaghue, Kim C., Pham-Short, Anna, Craig, Maria E., Ambler, Geoff, Anderson, Kym, Andrikopoulos, Sof, Batch, Jenny, Brown, Justin, Cameron, Fergus, Colman, Peter G., Conwell, Louise, Cotterill, Andrew, Couper, Jennifer, Davis, Elizabeth, de Bock, Martin, Fairchild, Jan, Fegan, Gerry, Fourlanos, Spiros, Glastras, Sarah, Goss, Peter, Gray, Leonie, Hamblin, Peter Shane, Hofman, Paul, Holmes-Walker, Dianne Jane, Huynh, Tony, Isaacs, Sonia ... the ADDN Study Group (2023). Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone: data from the Australasian Diabetes Data Network (ADDN) registry. Acta Diabetologica, 60 (11), 1471-1477. doi: 10.1007/s00592-023-02113-z

Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone: data from the Australasian Diabetes Data Network (ADDN) registry

2023

Journal Article

Blood pressure in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry

James, Steven, Perry, Lin, Lowe, Julia, Harris, Margaret, Colman, Peter G., Craig, Maria E., Anderson, Kym, Andrikopoulos, Sof, Ambler, Geoff, Barrett, Helen, Batch, Jenny, Bergman, Philip, Cameron, Fergus, Conwell, Louise, Cotterill, Andrew, Cooper, Chris, Couper, Jennifer, Davis, Elizabeth, de Bock, Martin, Donaghue, Kim, Fairchild, Jan, Fegan, Gerry, Fourlanos, Spiros, Glastras, Sarah, Goss, Peter, Gray, Leonie, Hamblin, Peter Shane, Hofman, Paul, Holmes-Walker, Dianne Jane ... Australasian Diabetes Data Network Study Group (2023). Blood pressure in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry. Acta Diabetologica, 60 (6), 797-803. doi: 10.1007/s00592-023-02057-4

Blood pressure in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry

2023

Journal Article

Correction to: Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone: data from the Australasian Diabetes Data Network (ADDN) registry (Acta Diabetologica, (2023), 10.1007/s00592-023-02113-z)

James, Steven, Perry, Lin, Lowe, Julia, Donaghue, Kim C., Pham-Short, Anna, Craig, Maria E., Ambler, Geoff, Anderson, Kym, Andrikopoulos, Sof, Batch, Jenny, Brown, Justin, Cameron, Fergus, Colman, Peter G., Conwell, Louise, Cotterill, Andrew, Couper, Jennifer, Davis, Elizabeth, de Bock, Martin, Fairchild, Jan, Fegan, Gerry, Fourlanos, Spiros, Glastras, Sarah, Goss, Peter, Gray, Leonie, Hamblin, Peter Shane, Hofman, Paul, Holmes-Walker, Dianne Jane, Huynh, Tony, Isaacs, Sonia ... Zimmermann, Anthony (2023). Correction to: Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone: data from the Australasian Diabetes Data Network (ADDN) registry (Acta Diabetologica, (2023), 10.1007/s00592-023-02113-z). Acta Diabetologica, 60 (11), 1479-1479. doi: 10.1007/s00592-023-02160-6

Correction to: Coexisiting type 1 diabetes and celiac disease is associated with lower Hba1c when compared to type 1 diabetes alone: data from the Australasian Diabetes Data Network (ADDN) registry (Acta Diabetologica, (2023), 10.1007/s00592-023-02113-z)

2022

Journal Article

ISPAD Clinical Practice Consensus Guidelines 2022: Glycemic targets and glucose monitoring for children, adolescents, and young people with diabetes

de Bock, Martin, Codner, Ethel, Craig, Maria E., Huynh, Tony, Maahs, David M., Mahmud, Farid H., Marcovecchio, Loredana and DiMeglio, Linda A. (2022). ISPAD Clinical Practice Consensus Guidelines 2022: Glycemic targets and glucose monitoring for children, adolescents, and young people with diabetes. Pediatric Diabetes, 23 (8), 1270-1276. doi: 10.1111/pedi.13455

ISPAD Clinical Practice Consensus Guidelines 2022: Glycemic targets and glucose monitoring for children, adolescents, and young people with diabetes

2022

Journal Article

Mapping care provision for type 1 diabetes throughout Australia: a protocol for a mixed-method study

Carrigan, Ann, Lake, Rebecca, Zoungas, Sophia, Huynh, Tony, Couper, Jennifer, Davis, Elizabeth, Jones, Timothy, Bloom, David, Braithwaite, Jeffrey and Zurynski, Yvonne (2022). Mapping care provision for type 1 diabetes throughout Australia: a protocol for a mixed-method study. BMJ Open, 12 (12) e067209, 1-6. doi: 10.1136/bmjopen-2022-067209

Mapping care provision for type 1 diabetes throughout Australia: a protocol for a mixed-method study

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

An unusual presentation of autoimmune primary adrenal insufficiency

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

Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation

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

Long-term efficacy of T3 analogue triac in children and adults with MCT8 deficiency: a real-life retrospective cohort study

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

Pre-analytical mysteries: a case of severe hypervitaminosis D and mild hypercalcaemia

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

Challenges of managing congenital hyperinsulinism in remote Aboriginal Australian communities

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

A Rare and Unusual Cause of Unilateral Ureteric Obstruction in a Child

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

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

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

Clinical and laboratory aspects of insulin autoantibody-mediated glycaemic dysregulation and hyperinsulinaemic hypoglycaemia: insulin autoimmune syndrome and exogenous insulin antibody syndrome

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.

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12

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.

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12

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

An unusual cause of metabolic alkalosis and hypocalcemia in childhood

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

A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report

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

Immunoassay interference secondary to therapeutic high-dose biotin: a paediatric case report

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

Therapeutic plasma exchange normalizes insulin-mediated response in a child with type 1 diabetes and insulin autoimmune syndrome

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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