Harris PC - Search Results

1

Prognostic enrichment design in clinical trials for autosomal dominant polycystic kidney disease: the HALT-PKD clinical trial.

Irazabal MV, Abebe KZ, Bae KT, Perrone RD, Chapman AB, Schrier RW, Yu AS, Braun WE, Steinman TI, Harris PC, Flessner MF, Torres VE; HALT Investigators. Irazabal MV, et al. Among authors: harris pc. Nephrol Dial Transplant. 2017 Nov 1;32(11):1857-1865. doi: 10.1093/ndt/gfw294. Nephrol Dial Transplant. 2017. PMID: 27484667 Free PMC article.

2

Identification of a gene for autosomal dominant polycystic kidney disease: implications for understanding the pathogenesis and treatment of the disease.

Harris PC. Harris PC. Nephrol Dial Transplant. 1996 Feb;11(2):258-62. doi: 10.1093/oxfordjournals.ndt.a027250. Nephrol Dial Transplant. 1996. PMID: 8700362 Review. No abstract available.

3

Autosomal dominant polycystic kidney disease: neoplasia in disguise?

Harris PC, Watson ML. Harris PC, et al. Nephrol Dial Transplant. 1997 Jun;12(6):1089-90. doi: 10.1093/ndt/12.6.1089. Nephrol Dial Transplant. 1997. PMID: 9198029 No abstract available.

4

Neonatal presentation of autosomal dominant polycystic kidney disease with a maternal history of tuberous sclerosis.

Griffin MD, Gamble V, Milliner DS, Gomez MR, Harris PC, Torres VE. Griffin MD, et al. Among authors: harris pc. Nephrol Dial Transplant. 1997 Nov;12(11):2284-8. doi: 10.1093/ndt/12.11.2284. Nephrol Dial Transplant. 1997. PMID: 9394312

5

Treatment prospects for autosomal-dominant polycystic kidney disease.

Qian Q, Harris PC, Torres VE. Qian Q, et al. Among authors: harris pc. Kidney Int. 2001 Jun;59(6):2005-22. doi: 10.1046/j.1523-1755.2001.00716.x. Kidney Int. 2001. PMID: 11380803 Free article. Review.

6

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein.

Ward CJ, Hogan MC, Rossetti S, Walker D, Sneddon T, Wang X, Kubly V, Cunningham JM, Bacallao R, Ishibashi M, Milliner DS, Torres VE, Harris PC. Ward CJ, et al. Among authors: harris pc. Nat Genet. 2002 Mar;30(3):259-69. doi: 10.1038/ng833. Epub 2002 Feb 4. Nat Genet. 2002. PMID: 11919560

7

The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease.

Rossetti S, Burton S, Strmecki L, Pond GR, San Millán JL, Zerres K, Barratt TM, Ozen S, Torres VE, Bergstralh EJ, Winearls CG, Harris PC. Rossetti S, et al. Among authors: harris pc. J Am Soc Nephrol. 2002 May;13(5):1230-7. doi: 10.1097/01.asn.0000013300.11876.37. J Am Soc Nephrol. 2002. PMID: 11961010

8

A complete mutation screen of the ADPKD genes by DHPLC.

Rossetti S, Chauveau D, Walker D, Saggar-Malik A, Winearls CG, Torres VE, Harris PC. Rossetti S, et al. Among authors: harris pc. Kidney Int. 2002 May;61(5):1588-99. doi: 10.1046/j.1523-1755.2002.00326.x. Kidney Int. 2002. PMID: 11967008 Free article.

9

The ENOS polymorphism is not associated with severity of renal disease in polycystic kidney disease 1.

Walker D, Consugar M, Slezak J, Rossetti S, Torres VE, Winearls CG, Harris PC. Walker D, et al. Among authors: harris pc. Am J Kidney Dis. 2003 Jan;41(1):90-4. doi: 10.1053/ajkd.2003.50027. Am J Kidney Dis. 2003. PMID: 12500225

10

PKHDL1, a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression.

Hogan MC, Griffin MD, Rossetti S, Torres VE, Ward CJ, Harris PC. Hogan MC, et al. Among authors: harris pc. Hum Mol Genet. 2003 Mar 15;12(6):685-98. Hum Mol Genet. 2003. PMID: 12620974

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

376 results

Search Page