Articles citing this paper
Obstacles in establishing a national disease registry in Australia: lessons from the development of the CHAANZ Congenital Heart Disease Registry
Larissa K. Lloyd A B C , Reeja Nasir B C , Calum Nicholson A B C , Geoff Strange A B C and David S. Celermajer A B C *
+ Author Affiliations
- Author Affiliations
A Clinical Research Group, Heart Research Institute, Sydney, NSW, Australia.
B Cardiology Department, Royal Prince Alfred Hospital, Camperdown, Sydney, NSW 2050, Australia.
C Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
* Correspondence to: david.celermajer@health.nsw.gov.au
Australian Health Review 47(4) 410-417 https://doi.org/10.1071/AH23063
Submitted: 14 March 2023 Accepted: 26 April 2023 Published: 16 May 2023
1 articles found in Crossref database.
The burdensome logistics of data linkage in Australia – the example of a national registry for congenital heart disease
Lloyd Larissa K.,
Nicholson Calum,
Strange Geoff, Celermajer David S.
Australian Health Review. 2023 48(1). p.8
