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2025

Conference Publication

Dynamic endocrine testing in children – can any laboratory be involved?

Huynh, Tony (2025). Dynamic endocrine testing in children – can any laboratory be involved?. Pathology Update 2025, Melbourne, VIC Australia, 21-23 February 2025. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.pathol.2024.12.409

Dynamic endocrine testing in children – can any laboratory be involved?

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

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.

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

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.

Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry

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.

Idiopathic Ductopaenia in a Paediatric Patient: A Case Report and Interesting Clinical Biochemistry

2016

Conference Publication

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

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

2013

Conference Publication

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.

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

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.

Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort

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

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