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This study aimed to define the active ingredients of a participation-focused physical activity intervention for children and youth with disabilities.
To define clinical common data elements (CDEs) and a mandatory minimum data set (MDS) for genomic studies of cerebral palsy (CP). Method: Candidate data elements were collated following a review of the literature and existing CDEs.
We have identified that CP registers often do not have quality data on congenital anomalies, necessitating linkage with congenital anomaly registers.
A downward trend in rates of CP in those born extremely preterm was evident over at least three consecutive periods across all three regions.
These findings will facilitate harmonization of data and collaborative research efforts, which are so necessary on account of the heterogeneity and...
Indigenous infants have a higher risk of CP than non-Indigenous infants, especially postneonatal CP.
This reconstructed total population cohort paper investigates the relationship between cerebral palsy & pregnancy induced hypertension.
The Australian Spasticity Assessment Scale complies with the definition of spasticity and is clinically feasible in paediatric settings
This paper is a timely reminder that we must recognise infants at high risk of cerebral palsy earlier using evidence-based assessments.
This article discusses the prenatal factors in singletons with cerebral palsy born at or near term.