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2024 Conference Publication Deformation-aware GAN for Medical Image Synthesis with Substantially Misaligned PairsXin, Bowen, Young, Tony, Wainwright, Claire E., Blake, Tamara, Lebrat, Leo, Gaass, Thomas, Benkert, Thomas, Stemmer, Alto, Coman, David and Dowling, Jason (2024). Deformation-aware GAN for Medical Image Synthesis with Substantially Misaligned Pairs. ML Research Press. |
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2020 Conference Publication The Australian Genomic Health Alliance Mitochondrial Flagship - A national approach to genomic diagnosticsThorburn, D., Baker, N., Balasubramaniam, S., Bratkovic, D., Coman, D., Compton, A., Delatycki, M., Ellaway, C., Fahey, M., Fletcher, J., Frazier, A., Ghaoui, R., Goel, H., Hock, D., Kava, M., Lake, N., Lamont, P., Lee, J., Panetta, J., Phillips, L., Rius, R., Ryan, M., Smith, N., Stroud, D., Tchan, M., Walsh, M., Wallis, M., Welch, A., Wools, C. and Christodoulou, J. (2020). The Australian Genomic Health Alliance Mitochondrial Flagship - A national approach to genomic diagnostics. 53rd European Society of Human Genetics (ESHG) Conference, Virtual, 6–9 June 2020. London, United Kingdom: Nature Publishing Group. |
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2020 Conference Publication Quality of life of parents of children with phenylketonuria (PKU): Relationships with child behaviour and parenting indicatorsEtel, E., Morawska, A., Mitchell, A., Kirby, G., Inwood, A. and Coman, D. (2020). Quality of life of parents of children with phenylketonuria (PKU): Relationships with child behaviour and parenting indicators. Helping Families Change Conference, Brisbane, QLD Australia, 5 -7 February 2020. |
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2015 Conference Publication Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathySharwood, Erin F., McGill, Michael, Koorts, P. J., Coman, David and Conwell, Louise S. (2015). Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, Queensland, Australia, October 2015. |
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2015 Conference Publication Information processing in a child with Galactosaemia: an examination using behavioural and neuropysiological measuresLewis, Fiona M., Knueppfer, Christina and Coman, David J. (2015). Information processing in a child with Galactosaemia: an examination using behavioural and neuropysiological measures. Federation of European Societies of Neuropsychology, Tampere, Finland, 9-11 September 2015. doi: 10.13140/RG.2.1.3218.9923 |
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2015 Conference Publication Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathySharwood, E. F., McGill, M., Koorts, P. J., Coman, D. and Conwell, L. S. (2015). Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy. Children's Health Queensland Research Conference, Brisbane, Queensland, Australia, December 2015. |
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2012 Conference Publication Early communicative skills in galactosaemiaLewis, F. M., Coman, D. J., Kilcoyne, S., Syrmis, M. and Murdoch, B. E. (2012). Early communicative skills in galactosaemia. Developmental Neurorehabilitation Conference, Jasper, Canada, 15-16 December 2012. |
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2011 Conference Publication The emergence and development of language in infants and children with a diagnosis of galactosaemiaComan, David J., Lewis, Fiona M., Murdoch, Bruce E. and Syrmis, Maryann (2011). The emergence and development of language in infants and children with a diagnosis of galactosaemia. 3rd Annual Australasian Clinical Metabolic Meeting, Brisbane, QLD, Australia Australia, 18-19 March 2011. |
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2011 Conference Publication Stability of language skills despite marked leukoencephalopathic changes in a child with Leber Hereditary Optic Neuropathy following CNS-directed leukaemia treatmentLewis, Fiona M, Coman, David J and Murdoch, Bruce E (2011). Stability of language skills despite marked leukoencephalopathic changes in a child with Leber Hereditary Optic Neuropathy following CNS-directed leukaemia treatment. XX World Congress of Neurology, Marrakech, Morocco, 12-17 November 2011. |
