Mallett AJ - Search Results

1

Wu Y, Jayasinghe K, Stark Z, Quinlan C, Patel C, McCarthy H, Mallawaarachchi AC, Kerr PG, Alexander SI, Mallett AJ, Goranitis I; KidGen Collaborative investigators. Wu Y, et al. Among authors: mallett aj. Genet Med. 2024 Jan;26(1):100989. doi: 10.1016/j.gim.2023.100989. Epub 2023 Sep 28. Genet Med. 2024. PMID: 37777873 No abstract available.

2

The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia.

Mallett A, Patel C, Salisbury A, Wang Z, Healy H, Hoy W. Mallett A, et al. Orphanet J Rare Dis. 2014 Jun 30;9:98. doi: 10.1186/1750-1172-9-98. Orphanet J Rare Dis. 2014. PMID: 24980890 Free PMC article.

3

Genomics in the renal clinic - translating nephrogenetics for clinical practice.

Mallett A, Corney C, McCarthy H, Alexander SI, Healy H. Mallett A, et al. Hum Genomics. 2015 Jun 24;9(1):13. doi: 10.1186/s40246-015-0035-1. Hum Genomics. 2015. PMID: 26104748 Free PMC article.

4

Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease.

Tong A, Tunnicliffe DJ, Lopez-Vargas P, Mallett A, Patel C, Savige J, Campbell K, Patel M, Tchan MC, Alexander SI, Lee V, Craig JC, Fassett R, Rangan GK. Tong A, et al. Nephrology (Carlton). 2016 Feb;21(2):122-32. doi: 10.1111/nep.12579. Nephrology (Carlton). 2016. PMID: 26235729

5

A protocol for the identification and validation of novel genetic causes of kidney disease.

Mallett A, Patel C, Maier B, McGaughran J, Gabbett M, Takasato M, Cameron A, Trnka P, Alexander SI, Rangan G, Tchan MC, Caruana G, John G, Quinlan C, McCarthy HJ, Hyland V, Hoy WE, Wolvetang E, Taft R, Simons C, Healy H, Little M. Mallett A, et al. BMC Nephrol. 2015 Sep 15;16:152. doi: 10.1186/s12882-015-0148-8. BMC Nephrol. 2015. PMID: 26374634 Free PMC article.

6

KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease.

Rangan GK, Alexander SI, Campbell KL, Dexter MA, Lee VW, Lopez-Vargas P, Mai J, Mallett A, Patel C, Patel M, Tchan MC, Tong A, Tunnicliffe DJ, Vladica P, Savige J. Rangan GK, et al. Among authors: mallett a. Nephrology (Carlton). 2016 Aug;21(8):705-16. doi: 10.1111/nep.12658. Nephrology (Carlton). 2016. PMID: 26511892 Review. No abstract available.

7

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis.

Tchan M, Savige J, Patel C, Mallett A, Tong A, Tunnicliffe DJ, Rangan GK. Tchan M, et al. Semin Nephrol. 2015 Nov;35(6):545-549.e2. doi: 10.1016/j.semnephrol.2015.10.007. Semin Nephrol. 2015. PMID: 26718157 Review. No abstract available.

8

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetics and Genetic Counseling.

Patel C, Tchan M, Savige J, Mallett A, Tong A, Tunnicliffe DJ, Rangan GK. Patel C, et al. Semin Nephrol. 2015 Nov;35(6):550-556.e1. doi: 10.1016/j.semnephrol.2015.10.003. Semin Nephrol. 2015. PMID: 26718158 Review. No abstract available.

9

A multidisciplinary renal genetics clinic improves patient diagnosis.

Mallett A, Fowles LF, McGaughran J, Healy H, Patel C. Mallett A, et al. Med J Aust. 2016 Feb 1;204(2):58-9. doi: 10.5694/mja15.01157. Med J Aust. 2016. PMID: 26821098 No abstract available.

10

Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to a CD46 mutation in the setting of SMARCAL1-mediated inherited kidney disease.

Chan S, Mallett AJ, Patel C, Francis RS, Johnson DW, Mudge DW, Isbel NM. Chan S, et al. Among authors: mallett aj. Nephrology (Carlton). 2017 Feb;22 Suppl 1:11-14. doi: 10.1111/nep.12933. Nephrology (Carlton). 2017. PMID: 28176476 Review.

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