They say knowledge is power, and a team of clinicians from our Network have set out to change the narrative around the treatment of FND and FS through the power of knowledge sharing.

A new RNA datatool aims to help patients with genetic diseases to receive a quicker diagnosis and improve their access to therapies.

New research has shown newborn bloodspot screening is more effective than conventional clinical diagnosis pathways for improving health outcomes in infants with SMA.

Experts are calling for research to look at how gene therapies can be adapted and scaled to become standard practices for people right around Australia.

A researcher’s vision to analyse genes of young cancer patients to personalise their treatment has now become a virtual reality.

Lockdowns led to a dramatic decrease in the number of young people taken to Sydney hospitals for their asthma during the pandemic.

A new study has found the number of Australian adults infected with COVID-19 at the end of February 2022, was at least twice as high as cases reported to authorities.

The number of teenage girls who presented to NSW Emergency Departments (ED) for self-harm or suicidal ideation has dramatically escalated during the pandemic, following a steady increase over the past decade.

The first ever clinical practice guidelines for children with Charcot-Marie-Tooth disease (CMT) have been published after a decade of work by an international team.

Two young sisters with a blinding eye condition will now have access to ocular gene therapy after a new pathway to the treatment was discovered.