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Research

In this article, we examine the utility of a transdiagnostic, dimensional approach to very early identification and intervention for infants at risk of neurodevelopmental disorders

Research

Mental wellbeing was independently associated with academic achievement and perceived family support but not with physical health variables

Research

This study used qualitative methods to explore how adolescents with Duchenne muscular dystrophy used a powered wheelchair standing device in their daily lives

Research

The U-PART intervention was found to be feasible and effective in the short term in girls and women with Rett Syndrome

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

Research

To investigate modifiable child and caregiver factors influencing community participation among children with Down syndrome.

Research

To investigate developmental trajectories in early childhood and predictors of class assignment.

Research

MECP2 duplication syndrome (MDS) is a rare, X-linked, neurodevelopmental disorder caused by a duplication of the methyl-CpG-binding protein 2 (MECP2) gene-a gene in which loss-of-function mutations lead to Rett syndrome (RTT). MDS has an estimated live birth prevalence in males of 1/150,000.

Research

The developmental origins of handedness remain elusive, though very early emergence suggests individual differences manifesting in utero could play an important role. Prenatal testosterone and Vitamin D exposure are considered, yet findings and interpretations remain equivocal.

Research

To systematically identify and evaluate the measurement properties of patient-reported outcome measures (PROMs) and observer-reported outcome measures (parent proxy report) of pain coping tools that have been used with children and young adults (aged 0–24 years) with a neurodevelopmental disability.