Select Publications
Journal articles
1993, 'Single photon emission computed tomography in intractable infantile seizures.', Clinical and experimental neurology, 30, pp. 117 - 126
,1992, 'Video EEG analysis of non-ictal events in children.', Clin Exp Neurol, 29, pp. 92 - 98, https://www.ncbi.nlm.nih.gov/pubmed/1343877
,1990, 'Hereditary Sensory Neuropathy Type II, Without Trophic Changes', Developmental Medicine & Child Neurology, 32, pp. 164 - 167, http://dx.doi.org/10.1111/j.1469-8749.1990.tb16915.x
,1990, 'Commencement of a paediatric EEG-video telemetry service.', Clin Exp Neurol, 27, pp. 83 - 88, https://www.ncbi.nlm.nih.gov/pubmed/2129962
,1989, 'Epilepsy surgery in Sturge-Weber syndrome.', Aust Paediatr J, 25, pp. 103 - 105, http://dx.doi.org/10.1111/j.1440-1754.1989.tb01428.x
,1989, 'Selective epilepsy surgery in tuberous sclerosis.', Aust Paediatr J, 25, pp. 243 - 245, http://dx.doi.org/10.1111/j.1440-1754.1989.tb01465.x
,1983, 'The obesity hypoventilation syndrome and the Prader-Willi syndrome.', Aust Paediatr J, 19, pp. 251 - 255, http://dx.doi.org/10.1111/j.1440-1754.1983.tb02114.x
,Conference Papers
2014, 'Enterovirus 71 associated lower motor neuron disease in infants and children', Amsterdam, The Netherlands, presented at 13th International Child Neurology Congress, Amsterdam, The Netherlands
,2010, 'A RETROSPECTIVE REVIEW OF CHILDREN TREATED AT THE SYDNEY CHILDREN'S HOSPITAL/PRINCE OF WALES HOSPITAL', in NEURO-ONCOLOGY, OXFORD UNIV PRESS INC, AUSTRIA, Vienna, pp. II69 - II70, presented at 14th International Symposium on Pediatric Neuro-Oncology, AUSTRIA, Vienna, 20 June 2010 - 23 June 2010, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000278817700314&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'Quality of life of children with Benign Rolandic Epilepsy', in JOURNAL OF THE NEUROLOGICAL SCIENCES, ELSEVIER, AUSTRALIA, Sydney, pp. S119 - S119, presented at 18th World Congress of Neurology, AUSTRALIA, Sydney, 05 November 2005 - 11 November 2005, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000235088001096&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,1998, 'Bearing diagnostics by digital analysis techniques in high background noise situations', in Sas P (ed.), International Conference on Noise and Vibration Engineering 1998, Leuven, Belgium, pp. 1379 - 1386, presented at International Conference on Noise and Vibration Engineering 1998, Leuven, Belgium, 16 September 1998 - 18 September 1998
,Conference Posters
2019, 'The evaluation of an educational video counselling key messages for doctors and families following a first afebrile seizure', presented at Epilepsy Society of Australia 30th Annual Scientific Meeting, 6th – 8th November 2019, 06 November 2019 - 08 November 2019
,2019, 'Co-development of education and support resources for families with severe early-onset genetic epilepsy', Welcome Genome Campus, UK, presented at World Congress of Genetic Counselling, Welcome Genome Campus, UK, 02 October 2019 - 04 October 2019
,2017, 'Design and development of a novel App for adolescents with epilepsy', Perth, presented at Epilepsy Society of Australia 31st Annual Scientific Meeting, Perth, 01 November 2017 - 03 November 2017
,2015, 'The first unprovoked seizure: validation of a newly developed e-learning resource', Adelaide, South Australia, presented at Epilepsy Society of Australia 29th Annual Scientific Meeting, Adelaide, South Australia, 21 October 2015 - 23 October 2015
,2013, 'Does the severity of gliosis in hippocampal sclerosis correlate with epilepsy burden and predict outcome after temporal lobectomy?', Sydney, Australia, presented at Epilepsy Society of Australia, Sydney, Australia, 01 November 2013 - 04 November 2013
,Conference Presentations
2021, 'Evaluating positive psychology resources among caregivers of a child with a genetic epilepsy', presented at The Australian and New Zealand Child Neurology Society (ANZCNZ) 9th Annual Scientific Meeting, Held virtually, 13 September 2021 - 15 September 2021
,2017, 'Design, development and evaluation of an app for adolescents with epilepsy', presented at The Australian and New Zealand Child Neurology Society 6th Annual Scientific Meeting, Brisbane, QLD, 09 August 2017 - 11 August 2017
,2015, 'The first unprovoked seizure: validation of a newly developed e-learning resource.', presented at The Australian and New Zealand Child Neurology Society 4th Annual Scientific Meeting, Melbourne, Australia, 26 August 2015 - 28 August 2015
,2015, 'The first unprovoked seizure: validation of a newly developed e-learning resource', presented at The Australian and New Zealand Child Neurology Society 4th Annual Scientific Meeting, Melbourne, Australia, 26 August 2015 - 26 August 2015
,Conference Abstracts
2023, 'LGG-11. COGNITIVE, ACADEMIC, AND QUALITY OF LIFE OUTCOMES IN SURVIVORS OF PEDIATRIC LOW-GRADE GLIOMA: CHALLENGING THE ‘BENIGN TUMOR’ PERCEPTION', in Neuro-Oncology, Oxford University Press (OUP), Vol. 25, pp. i57 - i58, http://dx.doi.org/10.1093/neuonc/noad073.221
,2018, 'CRAN-27. PAEDIATRIC EXTRAVENTRICULAR NEUROCYTOMA: A SERIES AND A RARE COMPLICATION', in Neuro-Oncology, Oxford University Press (OUP), Vol. 20, pp. i42 - i42, http://dx.doi.org/10.1093/neuonc/noy059.063
,2013, 'TARGETED RESEQUENCING IN EPILEPTIC ENCEPHALOPATHIES REVEALS MARKED GENETIC HETEROGENEITY AND NOVEL GENES', in EPILEPSIA, WILEY-BLACKWELL, CANADA, Montreal, Vol. 54, pp. 16 - 16, presented at 30th International Epilepsy Congress, CANADA, Montreal, 23 June 2013 - 27 June 2013, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000320472000037&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2012, 'Change in cognitive functioning after paediatric temporal lobectomy', in Developmental Medicine and Child Neurology, Wiley, Brisbane, Australia, presented at International Child Neurology Congress, Brisbane, Australia
,Other
2019, Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)), Elsevier, http://dx.doi.org/10.1016/j.ajhg.2019.03.016
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