Patel C - Search Results

1

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. Among authors: patel c. 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.

2

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. Among authors: patel m, patel c. Nephrology (Carlton). 2016 Feb;21(2):122-32. doi: 10.1111/nep.12579. Nephrology (Carlton). 2016. PMID: 26235729

3

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. Among authors: patel c. BMC Nephrol. 2015 Sep 15;16:152. doi: 10.1186/s12882-015-0148-8. BMC Nephrol. 2015. PMID: 26374634 Free PMC article.

4

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: patel m, patel c. Nephrology (Carlton). 2016 Aug;21(8):705-16. doi: 10.1111/nep.12658. Nephrology (Carlton). 2016. PMID: 26511892 Review. No abstract available.

5

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. Among authors: patel c. 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.

6

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.

7

A multidisciplinary renal genetics clinic improves patient diagnosis.

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

8

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: patel c. Nephrology (Carlton). 2017 Feb;22 Suppl 1:11-14. doi: 10.1111/nep.12933. Nephrology (Carlton). 2017. PMID: 28176476 Review.

9

Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders.

Mallett AJ, McCarthy HJ, Ho G, Holman K, Farnsworth E, Patel C, Fletcher JT, Mallawaarachchi A, Quinlan C, Bennetts B, Alexander SI. Mallett AJ, et al. Among authors: patel c. Kidney Int. 2017 Dec;92(6):1493-1506. doi: 10.1016/j.kint.2017.06.013. Epub 2017 Aug 23. Kidney Int. 2017. PMID: 28844315 Free article.

10

Meeting report of the 2017 KidGen Renal Genetics Symposium.

Jayasinghe K, Quinlan C, Stark Z, Patel C, Sampson MG, Saleem M, Mallett AJ; KidGen Collaborative. Jayasinghe K, et al. Among authors: patel c. Hum Genomics. 2018 Jan 30;12(1):5. doi: 10.1186/s40246-018-0137-7. Hum Genomics. 2018. PMID: 29382385 Free PMC article.

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