Fletcher J - Search Results

1

The use of ocular abnormalities to diagnose X-linked Alport syndrome in children.

Zhang KW, Colville D, Tan R, Jones C, Alexander SI, Fletcher J, Savige J. Zhang KW, et al. Among authors: fletcher j. Pediatr Nephrol. 2008 Aug;23(8):1245-50. doi: 10.1007/s00467-008-0759-4. Epub 2008 Mar 15. Pediatr Nephrol. 2008. PMID: 18343956

2

Nephrotoxicity with cyclooxygenase 2 inhibitor use in children.

Fletcher JT, Graf N, Scarman A, Saleh H, Alexander SI. Fletcher JT, et al. Pediatr Nephrol. 2006 Dec;21(12):1893-7. doi: 10.1007/s00467-006-0252-x. Epub 2006 Sep 6. Pediatr Nephrol. 2006. PMID: 16955281

3

Chronic allograft nephropathy.

Fletcher JT, Nankivell BJ, Alexander SI. Fletcher JT, et al. Pediatr Nephrol. 2009 Aug;24(8):1465-71. doi: 10.1007/s00467-008-0869-z. Epub 2008 Jun 27. Pediatr Nephrol. 2009. PMID: 18584214 Free PMC article. Review.

4

Chronic allograft nephropathy in paediatric renal transplantation.

Alexander SI, Fletcher JT, Nankivell B. Alexander SI, et al. Pediatr Nephrol. 2007 Jan;22(1):17-23. doi: 10.1007/s00467-006-0219-y. Epub 2006 Aug 30. Pediatr Nephrol. 2007. PMID: 16944214 Review.

5

Prevalence of genetic renal disease in children.

Fletcher J, McDonald S, Alexander SI; Australian and New Zealand Pediatric Nephrology Association (ANZPNA). Fletcher J, et al. Pediatr Nephrol. 2013 Feb;28(2):251-6. doi: 10.1007/s00467-012-2306-6. Epub 2012 Sep 29. Pediatr Nephrol. 2013. PMID: 23052649

6

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: fletcher jt. 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.

7

Vesicoureteral reflux.

Williams G, Fletcher JT, Alexander SI, Craig JC. Williams G, et al. J Am Soc Nephrol. 2008 May;19(5):847-62. doi: 10.1681/ASN.2007020245. Epub 2008 Mar 5. J Am Soc Nephrol. 2008. PMID: 18322164

8

Bilateral Wilms tumor and early presentation in pediatric patients is associated with the truncation of the Wilms tumor 1 protein.

Hu M, Fletcher J, McCahon E, Catchpoole D, Zhang GY, Wang YM, Algar EM, Alexander SI. Hu M, et al. Among authors: fletcher j. J Pediatr. 2013 Jul;163(1):224-9. doi: 10.1016/j.jpeds.2012.12.080. Epub 2013 Feb 10. J Pediatr. 2013. PMID: 23403252

9

Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2.

Fletcher J, Hu M, Berman Y, Collins F, Grigg J, McIver M, Jüppner H, Alexander SI. Fletcher J, et al. J Am Soc Nephrol. 2005 Sep;16(9):2754-61. doi: 10.1681/ASN.2005030239. Epub 2005 Jul 27. J Am Soc Nephrol. 2005. PMID: 16049068 Review.

10

Long-term cardiac allograft survival across an MHC mismatch after "pruning" of alloreactive CD4 T cells.

Hu M, Watson D, Zhang GY, Graf N, Wang YM, Sartor M, Howden B, Fletcher J, Alexander SI. Hu M, et al. Among authors: fletcher j. J Immunol. 2008 May 15;180(10):6593-603. doi: 10.4049/jimmunol.180.10.6593. J Immunol. 2008. PMID: 18453578

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