|
2015 Journal Article A protocol for the identification and validation of novel genetic causes of kidney diseaseMallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, Alexander, Stephen I., Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, McCarthy, Hugh J., Hyland, Valentine, Hoy, Wedy E., Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy H. and Little, Melissa (2015). A protocol for the identification and validation of novel genetic causes of kidney disease. BMC Nephrology, 16 (152) 148, 152. doi: 10.1186/s12882-015-0148-8 |
|
2015 Journal Article Genomics in the renal clinic - translating nephrogenetics for clinical practiceMallett, Andrew, Corney, Christopher, McCarthy, Hugh, Alexander, Stephen I. and Healy, Helen (2015). Genomics in the renal clinic - translating nephrogenetics for clinical practice. Human Genomics, 9 (13) 13, 13. doi: 10.1186/s40246-015-0035-1 |
|
2015 Journal Article End-Stage kidney disease due to fibrillary glomerulonephritis and immunotactoid glomerulopathy - outcomes in 66 consecutive ANZDATA registry casesMallett, Andrew, Tang, Wen, Hart, Gareth, McDonald, Stephen P., Hawley, Carmel M., Badve, Sunil V., Boudville, Neil, Brown, Fiona G., Campbell, Scott B., Clayton, Philip A. and Johnson, David W. (2015). End-Stage kidney disease due to fibrillary glomerulonephritis and immunotactoid glomerulopathy - outcomes in 66 consecutive ANZDATA registry cases. American Journal of Nephrology, 42 (3), 177-184. doi: 10.1159/000440815 |
|
2014 Journal Article End-stage kidney disease due to Alport syndrome: Outcomes in 296 consecutive Australia and New Zealand dialysis and transplant registry casesMallett, Andrew, Tang, Wen, Clayton, Philip A., Stevenson, Sarah, McDonald, Stephen P., Hawley, Carmel M., Badve, Sunil V., Boudville, Neil, Brown, Fiona G., Campbell, Scott B. and Johnson, David W. (2014). End-stage kidney disease due to Alport syndrome: Outcomes in 296 consecutive Australia and New Zealand dialysis and transplant registry cases. Nephrology Dialysis Transplantation, 29 (12), 2277-2286. doi: 10.1093/ndt/gfu254 |
|
2014 Journal Article NOS3 as a potential modifier of ADPKD phenotypic variability: progress towards an answerMallett, Andrew and Sandford, Richard (2014). NOS3 as a potential modifier of ADPKD phenotypic variability: progress towards an answer. Nephrology, 19 (12), 733-734. doi: 10.1111/nep.12331 |
|
2014 Journal Article The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in AustraliaMallett, Andrew, Patel, Chirag, Salisbury, Anne, Wang, Zaimin, Healy, Helen and Hoy, Wendy (2014). The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia. Orphanet Journal of Rare Diseases, 9 (1) 98. doi: 10.1186/1750-1172-9-98 |
|
2014 Journal Article Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplantStevenson, Sarah, Mallett, Andrew, Oliver, Kimberley, Hyland, Valentine, Hawley, Carmel, de Malmanche, Theo and Isbel, Nicole (2014). Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant. Nephrology, 19 (S1), 22-26. doi: 10.1111/nep.12195 |
|
2012 Journal Article Sustained remission of systemic lupus erythematosus related calciphylaxisMallett, A., John, G. T., Ranganathan, D., Kark, A., Berquier, I., Casey, J., Healy, H. and Francis, L. (2012). Sustained remission of systemic lupus erythematosus related calciphylaxis. Lupus, 21 (4), 441-444. doi: 10.1177/0961203311425526 |
