Rossetti S - Search Results

1

Cyst number but not the rate of cystic growth is associated with the mutated gene in autosomal dominant polycystic kidney disease.

Harris PC, Bae KT, Rossetti S, Torres VE, Grantham JJ, Chapman AB, Guay-Woodford LM, King BF, Wetzel LH, Baumgarten DA, Kenney PJ, Consugar M, Klahr S, Bennett WM, Meyers CM, Zhang QJ, Thompson PA, Zhu F, Miller JP. Harris PC, et al. Among authors: rossetti s. J Am Soc Nephrol. 2006 Nov;17(11):3013-9. doi: 10.1681/ASN.2006080835. Epub 2006 Oct 11. J Am Soc Nephrol. 2006. PMID: 17035604

2

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. 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

3

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: rossetti s. Am J Kidney Dis. 2003 Jan;41(1):90-4. doi: 10.1053/ajkd.2003.50027. Am J Kidney Dis. 2003. PMID: 12500225

4

Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype.

Rossetti S, Chauveau D, Kubly V, Slezak JM, Saggar-Malik AK, Pei Y, Ong AC, Stewart F, Watson ML, Bergstralh EJ, Winearls CG, Torres VE, Harris PC. Rossetti S, et al. Lancet. 2003 Jun 28;361(9376):2196-201. doi: 10.1016/S0140-6736(03)13773-7. Lancet. 2003. PMID: 12842373

5

A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees.

Rossetti S, Torra R, Coto E, Consugar M, Kubly V, Málaga S, Navarro M, El-Youssef M, Torres VE, Harris PC. Rossetti S, et al. Kidney Int. 2003 Aug;64(2):391-403. doi: 10.1046/j.1523-1755.2003.00111.x. Kidney Int. 2003. PMID: 12846734 Free article.

6

Molecular genetics of autosomal recessive polycystic kidney disease.

Harris PC, Rossetti S. Harris PC, et al. Among authors: rossetti s. Mol Genet Metab. 2004 Feb;81(2):75-85. doi: 10.1016/j.ymgme.2003.10.010. Mol Genet Metab. 2004. PMID: 14741187 Review.

7

Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease.

Consugar MB, Anderson SA, Rossetti S, Pankratz VS, Ward CJ, Torra R, Coto E, El-Youssef M, Kantarci S, Utsch B, Hildebrandt F, Sweeney WE, Avner ED, Torres VE, Cunningham JM, Harris PC. Consugar MB, et al. Among authors: rossetti s. Am J Kidney Dis. 2005 Jan;45(1):77-87. doi: 10.1053/j.ajkd.2004.09.009. Am J Kidney Dis. 2005. PMID: 15696446

8

Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD).

Adeva M, El-Youssef M, Rossetti S, Kamath PS, Kubly V, Consugar MB, Milliner DM, King BF, Torres VE, Harris PC. Adeva M, et al. Among authors: rossetti s. Medicine (Baltimore). 2006 Jan;85(1):1-21. doi: 10.1097/01.md.0000200165.90373.9a. Medicine (Baltimore). 2006. PMID: 16523049 Free article.

9

Loss of polycystin-1 in human cyst-lining epithelia leads to ciliary dysfunction.

Nauli SM, Rossetti S, Kolb RJ, Alenghat FJ, Consugar MB, Harris PC, Ingber DE, Loghman-Adham M, Zhou J. Nauli SM, et al. Among authors: rossetti s. J Am Soc Nephrol. 2006 Apr;17(4):1015-25. doi: 10.1681/ASN.2005080830. J Am Soc Nephrol. 2006. PMID: 16565258

10

Autosomal dominant polycystic kidney disease coexisting with cystic fibrosis.

Xu N, Glockner JF, Rossetti S, Babovich-Vuksanovic D, Harris PC, Torres VE. Xu N, et al. Among authors: rossetti s. J Nephrol. 2006 Jul-Aug;19(4):529-34. J Nephrol. 2006. PMID: 17048214

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