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Neurofibromatosis type 1 (NF1) is a genetic condition associated with the development of tumours in the nervous system, such as the brain, spinal cord, or nerves that send signals throughout the body. There is currently no cure for NF1. As well as tumours, 80 per cent of children with NF1 will
The Genetic Support Network Victoria (GSNV) is a vibrant and active group committed to promoting the interests and well-being of people affected by genetic and rare conditions in Victoria. Murdoch Children's Research Institute is a proud supporter of the GSNV, along with the Department of Health
Victorian Clinical Genetics Services (VCGS) is a specialist prenatal, childhood and adult genetics service. VCGS is an Australian not-for-profit subsidiary of Murdoch Children’s Research Institute, and one of the largest contributors driving genetic healthcare, research and policy in
The Murdoch Institute's Animal Ethics Committee (AEC) is responsible for the consideration of projects under the following licences as issued by Animal Welfare Victoria: Murdoch Children's Research Institute and Royal Children's Hospital.
Content notice: This post contains information about violence and abuse.One in three Melbourne mothers experiences family violence before their first child’s 10th birthday, according to a new study. The study, led by the Murdoch Children’s Research Institute and the University of Melbourne,
Murdoch Children’s Research Institute (MCRI) researcher Dr Nicole Van Bergen has been recognised for a project that aims to use stem cell therapy to treat a severe neurological disorder in children.Dr Van Bergen received the $74,000 Victorian Near-Miss Award for her trial into improving
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Murdoch Children’s Research Institute researcher Associate Professor Brett Manley has been recognised for an international trial that aims to improve the long-term outcomes for extremely premature babies with a common chronic lung disease. Associate Professor Manley, who is also a Consultant
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