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Showing results for "mental health aboriginal"
The two-year study, which was the first in Australia to assess and diagnose young people in a youth custodial setting for Fetal Alcohol Spectrum Disorder.
Alexander David Martyn Larcombe Martino Symons BScEnv (Hons) PhD BSc PhD B.A. (Hons) PhD. Honorary Research Fellow Head, Chronic Diseases Research
This study will determine the rate of falls among older adults with ID living in community based settings, which will assist to identify the extent of this problem
Review of the available dental literature on assessment and management of the oral manifestations of Rett syndrome
The Kids Research Institute Australia researchers have urged Australia’s Food Safety Ministers to hold their nerve and resist alcohol industry efforts to water down health labels that will protect Australian babies from the lifelong effects of Fetal Alcohol Spectrum Disorder (FASD).
Every parent knows that physical activity and playtime are important elements of healthy growth and development. They're also a lot of fun.
Jenny Helen Kingsley Downs Leonard Wong BApplSci (physio) MSc PhD MBChB MPH MBBS, MPH, MMedStat Head, Child Disability Principal Research Fellow
This research focuses on understanding how maternal health, lifestyle, and fertility influence pregnancy outcomes and the early development of children.
Septo-optic dysplasia (SOD) is a congenital disorder affecting 1 in 10,000 births, defined by the presence of at least two of a clinical triad, consisting of optic nerve hypoplasia, midline brain defects and pituitary hormone deficiency. Children with SOD may have vision impairment, hormonal deficiencies, developmental disorders, or epilepsy, but the clinical picture is highly variable. The complexity of SOD, its interplay with family factors, and the need for multiple specialty commitments can make the diagnosis period a challenging time for families.
Children with complex needs and severe disability may undergo gastrostomy insertion to support feeding difficulties. Parent education programs are critical components of clinical care pathways but there is little information on parent-reported educational needs. This study describes the collaborative process that yielded a resource to assist parents considering gastrostomy tube placement for their children, and the evaluation of the resource.