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Extended follow-up of unruptured intracranial aneurysms detected by presymptomatic screening in patients with autosomal dominant polycystic kidney disease.
Irazabal MV, Huston J 3rd, Kubly V, Rossetti S, Sundsbak JL, Hogan MC, Harris PC, Brown RD Jr, Torres VE. Irazabal MV, et al. Among authors: harris pc. Clin J Am Soc Nephrol. 2011 Jun;6(6):1274-85. doi: 10.2215/CJN.09731110. Epub 2011 May 5. Clin J Am Soc Nephrol. 2011. PMID: 21551026 Free PMC article.
Mutation analysis of the entire PKD1 gene: genetic and diagnostic implications.
Rossetti S, Strmecki L, Gamble V, Burton S, Sneddon V, Peral B, Roy S, Bakkaloglu A, Komel R, Winearls CG, Harris PC. Rossetti S, et al. Among authors: harris pc. Am J Hum Genet. 2001 Jan;68(1):46-63. doi: 10.1086/316939. Epub 2000 Dec 12. Am J Hum Genet. 2001. PMID: 11115377 Free PMC article.
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.
Autosomal dominant polycystic kidney disease.
Torres VE, Harris PC. Torres VE, et al. Among authors: harris pc. Nefrologia. 2003;23 Suppl 1:14-22. Nefrologia. 2003. PMID: 12708359 Review. No abstract available.
389 results