Browsing by Author Bebbington, Ami

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Issue DateTitleAuthor(s)Citation
2011Altered attainment of developmental milestones influences the age of diagnosis of rett syndromeEllaway, Carolyn; Bebbington, Ami; Downs, Jenny A.; Fehr, Stephanie; Leonard, Helen; Rowe, Peter; Children's Hospital Westmead: Paediatrics & Child HealthAltered attainment of developmental milestones influences the age of diagnosis of rett syndrome, Journal of Child Neurology, vol.26, 8, 2011,pp 980-987
2011Autism and intellectual disability are differentially related to sociodemographic background at birthNassar, Natasha; Bebbington, Ami; Bourke, Jenny; Bower, Carol; Dixon, Glenys; Glasson, Emma J.; Jacoby, Peter; Leonard, Helen; Malacova, Eva; Stanley, Fiona J.; Whitehouse, Andrew; Northern Clinical School: Kolling InstituteAutism and intellectual disability are differentially related to sociodemographic background at birth, PLoS One, vol.6, 3, 2011,pp e17875 - 1-e17875 - 9
2009The common BDNF polymorphism may be a modifier of disease severity in Rett syndromeChristodoulou, John; Ho, Gladys; Bebbington, Ami; Ben Zeev, B; De Klerk, Nicholas H.; Gak, E; Leonard, Helen; Vecksler, M; Children's Hospital Westmead: Paediatrics & Child Health; Biological SciencesThe common BDNF polymorphism may be a modifier of disease severity in Rett syndrome, Neurology, vol.72, N/A,pp 1242-1247
2008The diagnosis of autism in a female: could it be Rett syndrome?Ellaway, Carolyn; Anderson, Alison; Bebbington, Ami; de Klerk, Nick; Kaufmann, Walter E; Kulkarni, Alpana; Leonard, Helen; Ravine, David; Young, Deidra; Children's Hospital Westmead: Paediatrics & Child HealthThe diagnosis of autism in a female: could it be Rett syndrome?, European Journal of Pediatrics, vol.167,(6),2008,pp 661-669
2011Trends in the Diagnosis of Rett Syndrome in AustraliaNassar, Natasha; Bebbington, Ami; de Klerk, Nicholas H.; Downs, Jenny; Fehr, Stephanie; Leonard, Helen; Ronen, Gabriel M.; Northern Clinical School: Kolling InstituteTrends in the Diagnosis of Rett Syndrome in Australia, Pediatric Research: international journal of human developmental biology, vol.70, 3, 2011,pp 313-319
2010Updating the profile of C-terminal MECP2 deletions in Rett syndromeChristodoulou, John; Anderson, Alison; Bahi-Buisson, Nadia; Bebbington, Ami; Ben Zeev, B; Ho, G; Jacoby, Peter; Leonard, Helen; Percy, Alan K.; Pineda, M; Ravine, David; Smeets, E; Children's Hospital Westmead: Paediatrics & Child HealthUpdating the profile of C-terminal MECP2 deletions in Rett syndrome, Journal of Medical Genetics, vol.47, N/A,pp 242-248