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        "The problem with running"-Comparing the propulsion strategy of children with Developmental Coordination Disorder and typically developing children

        This study compared strategies of propulsion and power generation at the ankle during late stance/early swing in both walking and running in children with... ...

        Research

        Health of mothers of children with intellectual disability or autism spectrum disorder: a review of the literature

        The deficits associated with intellectual disability (ID) and autism spectrum disorder (ASD)place a burden on their co-residing families which may impact... ...

        Research

        Initial assessment of the StepWatch Activity Monitor™ to measure walking activity in Rett syndrome

        In girls and women with Rett syndrome, we assessed the accuracy of the StepWatch Activity Monitor™ and investigated relationships between daily step counts,... ...

        Research

        The relationship between MECP2 mutation type and health status and service use trajectories over time in a Rett syndrome population

        This study aimed to investigate the trajectories over time of health status and health service use in Rett syndrome by mutation... ...

        Research

        Bone mineral content and density in Rett syndrome and their contributing factors

        This study used densitometry to investigate the areal bone mineral density (aBMD) and bone mineral content (BMC) in an Australian Rett syndrome cohort... ...

        Research

        Variation over time in medical conditions and health service utilization of children with Down syndrome

        Variation over time in medical conditions and health service utilization of children with Down syndrome. ...

        Research

        Monitoring child abuse and neglect at a population level: patterns of hospital admissions for maltreatment and assault

        To investigate the prevalence, trends, and characteristics of maltreatment and assault related hospital admissions and deaths among children; ...

        Research

        Unpacking the complex nature of the autism epidemic

        This paper discusses changes in diagnostic criteria, decreasing age at diagnosis, improved case ascertainment, diagnostic substitution, and social influences. ...

        Research

        The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

        Rett syndrome (RTT) is caused by mutations in the transcriptional repressor methyl CpG-binding protein 2 (MECP2). ...

        Research

        Siblings of children with disabilities: challenges and opportunities

        Siblings of children with disabilities: challenges and opportunities ...

        Research

        Investigating genotype-phenotype relationships in Rett syndrome using an international data set

        This study uses data from a large international database, InterRett, to examine genotype-phenotype relationships and compares these with previous findings in... ...

        Research

        Associations Between Hyperphagia, Symptoms of Sleep Breathing Disorder, Behaviour Difficulties and Caregiver Well-Being in Prader-Willi Syndrome: A Preliminary Study

        Prader-Willi syndrome (PWS) is a rare genetic disorder characterised by neurodevelopmental delays, hyperphagia, difficulties with social communication and challenging behaviours. Individuals require intensive supervision from caregivers which may negatively affect caregiver quality of life. This study used data collected in the Australasian PWS Registry to evaluate associations between child behaviours and caregiver mental well-being. ...

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