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Preparing for your appointment

Find information on each session, and your pre-appointment checklist to ensure you are prepared.

Birth Sample Collection

Instructions on the various birth samples collected by the ORIGINS project and how to collect them.

One-Year Sample Collection

Get in Touch Dropping off a sample or attending a Kids Check appointment? Visit us at our Edgewater clinic. The Kids Joondalup Shop 51, Joondalup

Three-Year Sample Collection

Get in Touch Dropping off a sample or attending a Kids Check appointment? Visit us at our Edgewater clinic. The Kids Joondalup Shop 51, Joondalup

Withdrawing From the Study

Information about withdrawing from the study

FAQs

Find answers to frequently asked questions about ORIGINS.

Research

Urinary Ferritin as a Noninvasive Means of Assessing Iron Status in Young Children

Iron deficiency (ID) is the most common nutritional deficiency affecting young children. Serum ferritin concentration is the preferred biomarker for measuring iron status because it reflects iron stores; however, blood collection can be distressing for young children and can be logistically difficult. A noninvasive means to measure iron status would be attractive to either diagnose or screen for ID in young children.

Research

The feasibility of a digital health approach to facilitate remote dental screening among preschool children during COVID-19 and social restrictions

Tele-dentistry can be useful to facilitate screening of children, especially those living in rural and remote communities, and during the COVID-19 pandemic. This study evaluated the feasibility of tele-dental screening for the identification of early childhood caries (ECC) in preschoolers using an app operated by their parents with remote review by oral-health therapists.

Research

PKC activation promotes maturation of cord blood T cells towards a Th1 IFN-γ propensity

A significant number of babies present transiently with low protein kinase C zeta (PKCζ) levels in cord blood T cells, associated with reduced ability to transition from a neonatal Th2 to a mature Th1 cytokine bias, leading to a higher risk of developing allergic sensitisation, compared to neonates whose T cells have 'normal' PKCζ levels. However, the importance of PKCζ signalling in regulating their differentiation from a Th2 to a Th1 cytokine phenotype propensity remains undefined.