ARRK is a web-based database for Australia and New Zealand with two principle aims. Firstly to provide an information resource for patients, families and health professionals affected by rare and genetic kidney disease and secondly promoting research into these conditions by providing a platform to build national cohorts for secondary research studies with a single goal to improve the patient journey and overall outcomes.
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ARRK WEBSITE LAUNCHED
29th May 2019Read MoreWelcome to the website for the Australasian Registry of Rare and Genetic Kidney Disease (ARRK). This website will provide information about rare and genetic…
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ARRK REGISTRY APPROVED
29th May 2019Read MoreThe Australasian Registry of Rare and Genetic Kidney Disease (ARRK) has national ethics approval from the Sydney Children’s Hospitals Network (SCHN) for the next…
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ARRK FUNDING
29th May 2019Read MoreARRK FUNDED BY ANZSN AND AOOB Funding for the development of the ARRK website and ARRK registry was initially provided by Australia and New Zealand…