Peter Procopis
Professor
Paediatrics
University of Sydney
Australia
Biography
Dr.Peter Procopis is a Professor of Paediatrics & Child Health, Children's Hospital, Westmead
Research Interest
Paediatrics
Publications
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Baker, P., Friederich, M., Swanson, M., Shaikh, T., Bhattacharya, K., Scharer, G., Aicher, J., Creadon-Swindell, G., Geiger, E., Maclean, K., Procopis, P., et al (2014). Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5. Brain, 137(2), 366-379
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Lim, S., Smith, K., Stroud, D., Compton, A., Tucker, E., Dasvarma, A., Gandolfo, L., Marum, J., McKenzie, M., Peters, H., Procopis, P., Wilcken, B., Christodoulou, J., et al (2014). A Founder Mutation in PET100 Causes Isolated Complex IV Deficiency in Lebanese Individuals with Leigh Syndrome. The American Journal of Human Genetics, 94(2), 209-222.
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Ka, A., Britton, P., Troedson, C., Webster, R., Procopis, P., Ging, J., Chua, Y., Buckmaster, A., Wood, N., Jones, C., Dale, R. (2015). Mild encephalopathy with reversible splenial lesion: an important differential of encephalitis. European Journal of Paediatric Neurology, 19(3), 377-382
