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News & Events

Accelerating Child Health Research: A Systems Biology Symposium

The integration of multi-omics approaches with clinical research will be, without doubt, a cornerstone of future innovation in medical practice.

News & Events

Child health a focus in national research grants

The Kids Research Institute Australia researchers have been awarded more than $8 million in prestigious project grants from the NHMRC.

News & Events

The Kids cancer researcher named a Superstar of STEM

The Kids Research Institute Australia brain cancer researcher, Dr Jessica Buck will today join the ranks of a select group of brilliant female scientists.

News & Events

How to support a friend who has type 1 diabetes

Clinical psychologist from the Children's Diabetes Centre Dr Keely Bebbington has some top tips on how to support a friend who has type 1 diabetes.

News & Events

Kids have a 'wild' time at diabetes camp

Kids living with type 1 diabetes got to hang out with peers and have a lot of fun at the Diabetes WA and Perth Children’s Hospital kids’ camp in Bicton recently.

News & Events

The reality of having a child with type 1 diabetes

At every meal, Candice Carlon counts the carbs in her daughter Mia’s food. When Mia started pre-kindy, she stayed with her every day for six months.

News & Events

Being a good friend to someone with diabetes

Teens with diabetes may sometimes feel alone and even embarrassed about their diabetes. We asked Professor Donna Cross, for her tips for being a good friend.

Maggie Dent on leaving a lasting legacy for kids

The legacy of beloved parenting author and educator Maggie Dent is set to live on well beyond her lifetime.

Research

NTNG1 mutations are a rare cause of Rett syndrome

A translocation that disrupted the netrin G1 gene (NTNG1) was recently reported in a patient with the early seizure variant of Rett syndrome (RTT).

Research

The phenotype associated with a large deletion on MECP2

Multiplex ligation-dependent Probe Amplification (MLPA) has become available for the detection of a large deletion on the MECP2 gene.