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Showing results for "lung disease preterm"
This cross-sectional study examined parental well-being in caregivers of children with one of three genetic disorders associated with intellectual disability.
This study explores the role of infant sleep in early childhood development.
The ACE sub-project is investigating the impact of positive and negative maternal childhood experiences on pregnancy outcomes, and the health and wellbeing of children, with the aim to improve clinician screening and support available to families.
Rett syndrome is a genetically caused neurodevelopmental disorder associated with severe impairments and complex comorbidities. This study examined predictors of anxiety and depression in Rett syndrome, including genotype.
No validated oral health-related quality of life (OHRQOL) instrument currently exists for those with severe intellectual and developmental disabilities and who communicate non-verbally. This qualitative study aimed to explore the domains that were important to the oral health-related quality of life in individuals with Rett syndrome.
To describe trends, age-specific patterns, and factors influencing hospitalizations for 5 rare craniofacial anomalies.
This study aimed to validate qPCR assays for specific microbiota, for use on dental plaque samples stored on Whatman FTA cards to compare relative oral health risk in Rett syndrome.
Intellectual and developmental disabilities (IDD) are varied in their nature and presentation. Barriers to oral healthcare are reported in studies of general populations with IDD but these may not reflect the barriers experienced by individuals with rare disorders such as Rett syndrome.
To evaluate the effects of a physical activity programme on sedentary behaviour and physical activity in ambulant individuals with Rett syndrome.
Hand function is particularly affected and we discuss theoretical and practical perspectives for optimising hand function in Rett syndrome.