Christodoulou, J. GENE DISCOVERY FOR ORPHAN DISEASES. Pathology 45(&NA;) : s30 2013
view publication
Armani, R, Archer, H, Clarke, A, Vasudevan, P, Zweier, C, Ho, G, Williamson, S, Cloosterman, D, Yang, N, Christodoulou, J. Transcription Factor 4 and Myocyte Enhancer Factor 2C mutations are not common causes of Rett syndrome. American Journal of Medical Genetics Part A 158A(4) : 713 -719 2012
view publication
Ho, G, Walter, JH, Christodoulou, J. Costeff optic atrophy syndrome: New clinical case and novel molecular findings. Journal of Inherited Metabolic Disease 31(S2) : 419 -423 2008
view publication
Schindeler, S, Ghosh-Jerath, S, Thompson, S, Rocca, A, Joy, P, Kemp, A, Rae, C, Green, K, Wilcken, B, Christodoulou, J. The effects of large neutral amino acid supplements in PKU: An MRS and neuropsychological study. Molecular Genetics and Metabolism 91(1) : 48 -54 2007
view publication
Pelka, GJ, Watson, CM, Radziewic, T, Hayward, M, Lahooti, H, Christodoulou, J, Tam, PPL. Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice. Brain 129(4) : 887 -898 2006
view publication