Professor Peter Procopis

AM
Adjunct Professor
Paediatrics & Child Health, Children's Hospital, Westmead

Telephone +61 2 9845 2657
Fax +61 2 9845 3376

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Clinical Specialty

Paediatrics

Selected publications

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Journals

  • 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. [More Information]
  • 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. American Journal of Human Genetics, 94(2), 209-222. [More Information]
  • 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. [More Information]
  • Suleiman, J., Wright, S., Gill, D., Brilot-Turville, F., Waters, P., Peacock, K., Procopis, P., Nibber, A., Vincent, A., Dale, R., et al (2013). Autoantibodies to neuronal antigens in children with new-onset seizures classified according to the revised ILAE organization of seizures and epilepsies. Epilepsia, 54(12), 2091-2100. [More Information]
  • Compton, A., Troedson, C., Wilson, M., Procopis, P., Li, F., Brundage, E., Yamazaki, T., Thorburn, D., Wong, L. (2011). Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome. Mitochondrion, 11(1), 104-107. [More Information]
  • Procopis, P. (2010). Heads Up: Benign paroxysmal torticollis of infancy. Journal of Paediatrics and Child Health, 46, 438.
  • Chiong, M., Procopis, P., Wilcken, B. (2007). Late-Onset Nonketotic Hyperglycinemia With Leukodystrophy and an Unusual Clinical Course. Pediatric Neurology, 37(4), 283-286. [More Information]

2015

  • 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. [More Information]

2014

  • 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. American Journal of Human Genetics, 94(2), 209-222. [More Information]
  • 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. [More Information]

2013

  • Suleiman, J., Wright, S., Gill, D., Brilot-Turville, F., Waters, P., Peacock, K., Procopis, P., Nibber, A., Vincent, A., Dale, R., et al (2013). Autoantibodies to neuronal antigens in children with new-onset seizures classified according to the revised ILAE organization of seizures and epilepsies. Epilepsia, 54(12), 2091-2100. [More Information]

2011

  • Compton, A., Troedson, C., Wilson, M., Procopis, P., Li, F., Brundage, E., Yamazaki, T., Thorburn, D., Wong, L. (2011). Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome. Mitochondrion, 11(1), 104-107. [More Information]

2010

  • Procopis, P. (2010). Heads Up: Benign paroxysmal torticollis of infancy. Journal of Paediatrics and Child Health, 46, 438.

2007

  • Chiong, M., Procopis, P., Wilcken, B. (2007). Late-Onset Nonketotic Hyperglycinemia With Leukodystrophy and an Unusual Clinical Course. Pediatric Neurology, 37(4), 283-286. [More Information]

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