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

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2011
• April 2011

schemic stroke induced by thrombosis may be triggered by atherosclerotic plaque rupture and collagen-induced platelet activation. Collagen induces... ...

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2011
• February 2011

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

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2011
• February 2011

The objective of this study is to identify distinct age-related trajectory classes of body mass index (BMI) z-scores from childhood to adolescence ...

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2011
• January 2011

To examine the association of fetal alcohol exposure during pregnancy with child and adolescent behavioural development. ...

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2010
• August 2010

Association of pre-pregnancy weight, birth defects ...

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2010
• April 2010

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

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2009
• July 2009

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

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2008
• March 2008

Biostatistics is a vital component of almost every research project conducted at Telethon Kids. It is the application of statistical methodology within the areas of medical, biological and social sciences. ...

• 1. Telethon Kids Institute
• Our research
• Past teams

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. ...

• 1. Telethon Kids Institute
• Our research
• Reports and Findings
• 2021
• September 2021