The University of Queensland

Environmental Determinants of Islet Autoimmunity (ENDIA) longitudinal prospective pregnancy to childhood cohort study of Australian children at risk of type 1 diabetes: parental demographics and birth information

Thomson, Rebecca L, Oakey, Helena, Haynes, Aveni, Craig, Maria E, Harrison, Leonard C, Wentworth, John M, Anderson, Amanda, Ashwood, Pat, Barry, Simon, Brittain, Bek, Brown, James D, Colman, Peter G, Davis, Elizabeth A, Hamilton-Williams, Emma, Huynh, Dao, Huynh, Tony, Kim, Ki-Wook, McGorm, Kelly J, Morahan, Grant, Rawlinson, William, Sinnott, Richard O, Soldatos, Georgia, Tye-Din, Jason A, Vuillermin, Peter J, Penno, Megan A S and Couper, Jennifer J (2024). Environmental Determinants of Islet Autoimmunity (ENDIA) longitudinal prospective pregnancy to childhood cohort study of Australian children at risk of type 1 diabetes: parental demographics and birth information. BMJ Open Diabetes Research & Care, 12 (4), e004130. doi: 10.1136/bmjdrc-2024-004130

Liver and pancreatic-targeted interleukin-22 as a therapeutic for metabolic dysfunction-associated steatohepatitis

Sajiir, Haressh, Keshvari, Sahar, Wong, Kuan Yau, Borg, Danielle J., Steyn, Frederik J., Fercher, Christian, Taylor, Karin, Taylor, Breten, Barnard, Ross T., Müller, Alexandra, Moniruzzaman, Md, Miller, Gregory, Wang, Ran, Fotheringham, Amelia, Schreiber, Veronika, Sheng, Yong Hua, Hancock, Janelle Louise, Loo, Dorothy, Burr, Lucy, Huynh, Tony, Lockett, Jack, Ramm, Grant A., Macdonald, Graeme A., Prins, Johannes B., McGuckin, Michael A. and Hasnain, Sumaira Z. (2024). Liver and pancreatic-targeted interleukin-22 as a therapeutic for metabolic dysfunction-associated steatohepatitis. Nature Communications, 15 (1) 4528, 4528. doi: 10.1038/s41467-024-48317-x

Growth During Pubertal Induction in Girls With Turner Syndrome: A Retrospective Cohort Analysis

Nicholls, Joshua, Harris, Mark, Hughes, Ian, Huynh, Tony and McMahon, Sarah K (2024). Growth During Pubertal Induction in Girls With Turner Syndrome: A Retrospective Cohort Analysis. The Journal of Clinical Endocrinology & Metabolism. doi: 10.1210/clinem/dgae071

Commentary on studies investigating low‐dose diazoxide in hyperinsulinism

Huynh, Tony (2024). Commentary on studies investigating low‐dose diazoxide in hyperinsulinism. Clinical Endocrinology, 100 (2), 138-139. doi: 10.1111/cen.14996

Paediatric perspectives in the diagnosis of polyuria‐polydipsia syndrome

Huynh, Tony, Signal, Dana and Christ‐Crain, Mirjam (2024). Paediatric perspectives in the diagnosis of polyuria‐polydipsia syndrome. Clinical Endocrinology. doi: 10.1111/cen.15011

Low-density lipoprotein cholesterol in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry

James, S., Donaghue, K. C., Perry, L., Lowe, J., Colman, P. G., Craig, M. 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, Fairchild, Jan, Fegan, Gerry, Fourlanos, Spiros, Glastras, Sarah, Goss, Peter, Gray, Leonie, Hamblin, Peter Shane, Hofman, Paul, Holmes-Walker, Dianne Jane, Huynh, Tony ... Zimmermann, Anthony (2023). Low-density lipoprotein cholesterol in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry. Diabetic Medicine, 40 (11) e15184. doi: 10.1111/dme.15184

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

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 ... Zimmermann, Anthony (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

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 ... Zimmermann, Anthony (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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort

Eggers, Stefanie, Sadedin, Simon, van den Bergen, Jocelyn A., Robevska, Gorjana, Ohnesorg, Thomas, Hewitt, Jacqueline, Lambeth, Luke, Bouty, Aurore, Knarston, Ingrid M., Tan, Tiong Yang, Cameron, Fergus, Werther, George, Hutson, John, O'Connell, Michele, Grover, Sonia R., Heloury, Yves, Zacharin, Margaret, Bergman, Philip, Kimber, Chris, Brown, Justin, Webb, Nathalie, Hunter, Matthew F., Srinivasan, Shubha, Titmuss, Angela, Verge, Charles F., Mowat, David, Smith, Grahame, Smith, Janine, Ewans, Lisa ... Sinclair, Andrew H. (2016). Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort. Genome Biology, 17 (1) 243, 243. doi: 10.1186/s13059-016-1105-y

Selective modulation through the glucocorticoid receptor ameliorates muscle pathology in mdx mice

Huynh, Tony, Uaesoontrachoon, Kitipong, Quinn, James L., Tatem, Kathleen S., Heier, Christopher R., Van Der Meulen, Jack H., Yu, Qing, Harris, Mark, Nolan, Christopher J., Haegeman, Guy, Grounds, Miranda D. and Nagaraju, Kanneboyina (2013). Selective modulation through the glucocorticoid receptor ameliorates muscle pathology in mdx mice. Journal of Pathology, 231 (2), 223-235. doi: 10.1002/path.4231

Omigapil Treatment Decreases Fibrosis and Improves Respiratory Rate in dy2J Mouse Model of Congenital Muscular Dystrophy

Yu, Qing, Sali, Arpana, van der Meulen, Jack, Creeden, Brittany K., Gordish-Dressman, Heather, Rutkowski, Anne, Rayavarapu, Sree, Uaesoontrachoon, Kitipong, Huynh, Tony, Nagaraju, Kanneboyina and Spurney, Christopher F. (2013). Omigapil Treatment Decreases Fibrosis and Improves Respiratory Rate in dy2J Mouse Model of Congenital Muscular Dystrophy. PLoS One, 8 (6) e65468, e65468.1-e65468.8. doi: 10.1371/journal.pone.0065468

VBP15, a Glucocorticoid Analogue, Is Effective at Reducing Allergic Lung Inflammation in Mice

Damsker, Jesse M., Dillingham, Blythe C., Rose, Mary C., Balsley, Molly A., Heier, Christopher R., Watson, Alan M., Stemmy, Erik J., Jurjus, Roslyn A., Huynh, Tony, Tatem, Kathleen, Uaesoontrachoon, Kitipong, Berry, Dana M., Benton, Angela S., Freishtat, Robert J., Hoffman, Eric P., McCall, John M., Gordish-Dressman, Heather, Constant, Stephanie L., Reeves, Erica K. M. and Nagaraju, Kanneboyina (2013). VBP15, a Glucocorticoid Analogue, Is Effective at Reducing Allergic Lung Inflammation in Mice. PLoS One, 8 (5) e63871, e63871.1-e63871.9. doi: 10.1371/journal.pone.0063871

Urine metabonomic profiling of a female adolescent with PIT-1 mutation before and during growth hormone therapy: insights into the metabolic effects of growth hormone

Abd Rahman, Shaffinaz, Schirra, Horst Joachim, Lichanska, Agnieszka M., Huynh, Tony and Leong, Gary M. (2013). Urine metabonomic profiling of a female adolescent with PIT-1 mutation before and during growth hormone therapy: insights into the metabolic effects of growth hormone. Growth Hormone & IGF Research, 23 (1-2), 29-36. doi: 10.1016/j.ghir.2012.12.001

Effects of Dantrolene therapy on disease phenotype in Dystrophin deficient mdx mice

Quinn, James L., Huynh, Tony, Uaesoontrachoon, Kitipong, Tatem, Kathleen, Phadke, Aditi, Van der Meulen, Jack H., Yu, Qing and Nagaraju, Kannaboyina (2013). Effects of Dantrolene therapy on disease phenotype in Dystrophin deficient mdx mice. PLoS Currents (NOV). doi: 10.1371/currents.md.e246cf493a7edb1669f42fb735936b46

The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: Role of endogenous TLR ligands

Uaesoontrachoon, Kitipong, Cha, Hee-Jae, Ampong, Beryl, Sali, Arpana, Vandermeulen, Jack, Wei, Benjamin, Creeden, Brittany, Huynh, Tony, Quinn, James, Tatem, Kathleen, Rayavarapu, Sree, Hoffman, Eric P. and Nagaraju, Kanneboyina (2013). The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: Role of endogenous TLR ligands. Journal of Pathology, 231 (2), 199-209. doi: 10.1002/path.4207

VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects

Heier, Christopher R., Damsker, Jesse M., Yu, Qing, Dillingham, Blythe C., Huynh, Tony, Van der Meulen, Jack H., Sali, Arpana, Miller, Brittany K., Phadke, Aditi, Scheffer, Luana, Quinn, James, Tatem, Kathleen, Jordan, Sarah, Dadgar, Sherry, Rodriguez, Olga C., Albanese, Chris, Calhoun, Michael, Gordish-Dressman, Heather, Jaiswal, Jyoti K., Connor, Edward M., Mccall, John M., Hoffman, Eric P., Reeves, Eric K. M. and Nagaraju, Kanneboyina (2013). VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects. EMBO Molecular Medicine, 5 (10), 1569-1585. doi: 10.1002/emmm.201302621

Benefit of early commencement of growth hormone therapy in children with Prader-Willi syndrome

Nyunt, O., Harris, M., Hughes, I., Huynh, T., Davies, P. S. W. and Cotterill, A. M. (2009). Benefit of early commencement of growth hormone therapy in children with Prader-Willi syndrome. Journal of Pediatric Endocrinology and Metabolism, 22 (12), 1151-1158. doi: 10.1515/JPEM.2009.22.12.1151

Investigating maturity onset diabetes of the young

Nyunt, Ohn, Wu, Joyce Y, McGown, Ivan N, Harris, Mark, Huynh, Tony, Leong, Gary M, Cowley, David M and Cotterill, Andrew M (2009). Investigating maturity onset diabetes of the young. Clinical Biochemist Reviews, 30 (2), 67-74.

The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency

Huynh, Tony, McGown, Ivan, Cowley, David, Nyunt, Ohn, Leong, Gary M., Harris, Mark and Cotterill, Andrew M. (2009). The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency. Clinical Biochemist Reviews, 30 (2), 75-86.

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

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

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

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 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.

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.

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.

Insulin autoimmune syndrome in a child with type 1 diabetes: clinical, immunological, and biochemical correlations

Sharwood, Erin, Gous, Rehna, Cardinal, John, Hughes, Ian and Huynh, Tony (2016). Insulin autoimmune syndrome in a child with type 1 diabetes: clinical, immunological, and biochemical correlations. Endocrine Society's 98th Annual Meeting and Expo, Boston, MA United States, 1-4 April. London, United Kingdom: Lippincott Williams & Wilkins. doi: 10.1016/j.pathol.2015.12.247

Blocking Toll-Like Receptor Pathway Using an Antagonist of TLR7, 8 and 9 Reduces Inflammation in Dystrophin Deficient mdx Mice

Yu, Qing, Huynh, Tony, Sali, Arpana, Creeden, Brittany, Quinn, James, Vandermeulen, Jack, Spurney, Chris, Kandimalla, Ekambar, Agrawal, Sudhir and Nagaraju, Kanneboyina (2013). Blocking Toll-Like Receptor Pathway Using an Antagonist of TLR7, 8 and 9 Reduces Inflammation in Dystrophin Deficient mdx Mice. 65th Annual Meeting of the American-Academy-of-Neurology (AAN), San Diego Ca, Mar 16-23, 2013. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS.

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.

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.

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.