Adjunct Professor Peter Procopis AM

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

C29 - Children's Hospital Westmead
The University of Sydney
NSW 2006 Australia

T: +61 2 9845 2657
F: +61 2 9845 3376
E:

Publications

2014 | 2013 | 2011 | 2010

2014

   
  • Lim, S., Smith, K., Stroud, D., Compton, A., Tucker, E., Dasvarma, A., Gandolfo, L., Marum, J., McKenzie, M., Peters, H., Mowat, D., Procopis, P., Wilcken, B., Christodoulou, J., Brown, G., Ryan, M., Bahlo, M., Thorburn, D. (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. [Abstract]

2013

   
  • Suleiman, J., Wright, S., Gill, D., Brilot, F., Waters, P., Peacock, K., Procopis, P., Nibber, A., Vincent, A., Dale, R., Lang, B. (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. [Abstract]

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. [Abstract]

2010

   
  • Procopis, P. (2010), Heads Up: Benign paroxysmal torticollis of infancy. Journal of Paediatrics and Child Health. 46(6-7), 438.