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Research

A systematic review of risk factors for cerebral palsy in children born at term in developed countries

The aim of this study was to conduct a systematic review in order to identify the risk factors for cerebral palsy (CP) in children born at term.

Research

Validation of a model for optimal birth weight: A prospective study using serial ultrasounds

The aim of this study was to validate a model for optimal birth weight derived from neonatal records, and to test the assumption that preterm births may be...

Germs!

Discover resources and science activities for kids for the topic 'Germs!'.

News & Events

Keelan has ‘survived and thrived’, thanks to research

Ten-year-old Keelan Mullins is known to his mum Clare Hindle as her ‘miracle baby’. Keelan was born in March 2013 at 26 weeks’ gestation and weighing just 1096 grams.

Working with the community

Community involvement plays an integral role in guiding our research - find out how.

START Phage WA

START Phage WA was formed to pave the way towards treating AMR infections with phage therapy in Western Australia.

Effect of Posture on Lung Ventilation distribution and Associations with Structure in Children with Cystic Fibrosis

Effect of Posture on Lung Ventilation distribution and Associations with Structure in Children with Cystic Fibrosis Effect of Posture on Lung

Alpha-1 Antitrypsin Mitigates the Inhibition of Airway Epithelial Cell Repair by Neutrophil Elastase

Alpha-1 Antitrypsin Mitigates the Inhibition of Airway Epithelial Cell Repair by Neutrophil Elastase Abstract Neutrophil elastase (NE) activity is

Interleukin-1 is associated with inflammation and structural lung disease in young children with cystic fibrosis

Interleukin-1 is associated with inflammation and structural lung disease in young children with cystic fibrosis Early diagnosis and treatment in

Psychosocial characteristics and predictors of health-care use in families of young children with cystic fibrosis in Western Australia

Psychosocial characteristics and predictors of health-care use in families of young children with cystic fibrosis in Western Australia Abstract