Skip to menu Skip to content Skip to footer

2013

Journal Article

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

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

2013

Journal Article

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

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

2009

Journal Article

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

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

2009

Journal Article

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.

Investigating maturity onset diabetes of the young

2009

Journal Article

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.

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

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